Next Article in Journal
Genome-Wide Identification and Analysis of the WRKY Transcription Factor Family Associated with Leaf Senescence in Alfalfa
Previous Article in Journal
Plant-Derived Alkaloids as a Potential Source of Treatment for Colorectal Cancer over the Past Five Years: A Comprehensive Review
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Ziziphus jujuba: Applications in the Pharmacy and Food Industry

by
Desislava Popstoyanova
1,
Anelia Gerasimova
2,
Galia Gentscheva
3,*,
Stoyanka Nikolova
4,
Anna Gavrilova
5 and
Krastena Nikolova
1,*
1
Department of Physics and Biophysics, Faculty of Pharmacy, Medical University of Varna, 9002 Varna, Bulgaria
2
Department of Chemistry, Faculty of Pharmacy, Medical University of Varna, 9000 Varna, Bulgaria
3
Department of Chemistry and Biochemistry, Medical University-Pleven, 5800 Pleven, Bulgaria
4
Department of Organic Chemistry, Faculty of Chemistry, University of Plovdiv Paisii Hilendarski, 4000 Plovdiv, Bulgaria
5
Department of Pharmaceutical Chemistry and Pharmacognosy, Medical University-Pleven, 5800 Pleven, Bulgaria
*
Authors to whom correspondence should be addressed.
Plants 2024, 13(19), 2724; https://doi.org/10.3390/plants13192724 (registering DOI)
Submission received: 11 August 2024 / Revised: 18 September 2024 / Accepted: 25 September 2024 / Published: 29 September 2024

Abstract

:
Ziziphus jujuba has been used since ancient times in traditional Eastern medicine. It is widely cultivated in numerous countries between the tropical and temperate climatic zones due to its high ecological plasticity and resilience to adverse weather. The different classes of chemical compounds contained in the plant are the reason for its medicinal properties. Research shows that every part of Ziziphus jujuba, the leaves, fruits and seeds, demonstrate therapeutic properties. This review focuses on the chemical composition in order to establish the relationship between the plant and its clinical use. Various biological effects are summarized and discussed: anticancer, anti-inflammatory, immunostimulating, antioxidant, hepatoprotective, gastrointestinal, etc. Apart from medicinal uses, the fruits of Ziziphus jujuba are edible and used in fresh and dried form. This literature review reveals possible medical applications of Ziziphus jujuba and its great potential for improving the diet of people in areas where the plant is abundant.

1. Introduction

Since ancient times, plants have been used not only for food but also for the treatment of people and animals. Over time, many plant species have spread far from their original place of origin. Such is the case with the plant known as Ziziphus jujuba Mill, commonly known as red date. It belongs to the Rhamnaceae family [1,2,3,4]. The species originates from China and has over 4000 years of history. It is considered one of the most valuable plants in Chinese traditional medicine [3,4,5,6]. The first scientific description of the species was made in 1753 by Carolus Linnaeus, misclassifying it as Rhamnus ziziphus. But in 1768, the error was corrected and the plant was designated as a new species [7]. There are around 40 jujube species known around the world [1]. Some of the most popular are Ziziphus jujuba (China), Ziziphus mauritiana Lam., Ziziphus nummularia (Burm.f.), Ziziphus celata, Ziziphus lotus (L.) Lam. (India), Ziziphus obtusifolia (US, Mexico), Ziziphus parryi Torr. (US, Mexico), Ziziphus reticulata (Vahl) DC., Ziziphus rignonii (Indonesia), and Ziziphus taylorii (Britton) [8].
In China, India, and other South Asian countries, the plant is considered a superfood. Moreover, it plays a role in local traditions and is among the five most valuable fruits according to the Huangdi Neijing (475–221 BC). There are four medicinally important species—Ziziphus jujuba, Ziziphus glaberata, Ziziphus mauritiana, and Ziziphus rugosa [9]. The first presents great interest to researchers as it is the fastest-growing of the four.
Ziziphus jujuba (Z. jujuba) has spread in different countries around the world. It could be found in many Asian countries: Afghanistan, Armenia, Azerbaijan, Bangladesh, Burma, China, India, Iraq, Iran, Israel, Japan, Kyrgyzstan, Lebanon, Malaysia, Mongolia, Pakistan, Palestine, South Korea, Syria, Thailand, Turkey, Turkmenistan, and Uzbekistan. In Europe, the plant grows in all southern countries, France, Germany, the Czech Republic, England, and Ukraine. In Africa, Ziziphus jujuba is found in Egypt, Tanzania, and Tunisia, as well as in Canada, the USA, Australia, and New Zealand [6]. However, China is still the only one that exports jujube as it grows 1.5 million hectares [10]. The annual sum of the dried plant has a value of around USD 5 million [11].

Taxonometry

Ziziphus jujuba is classified as follows [8]:
Domain: Eukaryota;
Kingdom: Plantae;
Subkingdom: Viridiplantae;
Phylum: Spermatophyta;
Subphylum: Angiospermae;
Superdivision: Embryophyta;
Division: Tracheophyta;
Subdivision: Spermatophytina;
Class: Magnoliopsida;
Superorder: Rosanae;
Order: Rosales;
Family: Rhamnaceae;
Genus: Ziziphus;
Species: Ziziphus jujuba
A thorough description of the plant was made by Shahrajabian et al. [6]. The height of the plant is from 457 to 1070 cm on average and it spreads for 305 to 915 cm. The crown of the tree is oval, with irregularities in the silhouette and open density. The growth rate is classified as medium. The leaves have alternating arrangement, simple form, crenate or serrulate margins, ovate shape, and bowed venation. Their color is green in spring and summer and turns brown before shedding in autumn. The length reaches 10.5 cm. The plant blooms in spring with small yellow flowers that are hard to notice. The fruits are oval and 2.5 to 12.5 cm in length. Their color ranges from red to black. They are easy to spot on the tree, have fleshy texture, and attract animals. Stefania et al. [3] investigated the pathogen species found on the fruit after harvest. Most of them belonged to the Rhizopus spp. Others were Alternaria genus, Monilinia spp., Fusarium spp. The tree grows in full sun or partial shade. The plant can survive drought and lives in clay or sandy, well-drained soil [6,12]. All parts of the jujube have medicinal effects [13]. The literature includes reviews that examine the bioactivity of jujube extracts and the results of some in vitro and in vivo studies [14], antibacterial, phytotoxic, and hemagglutination activities [9], pharmacological effects and potential active ingredients [15], and the chemical components and biological activities of its fruits [16]. The purpose of this review is to summarize the chemical composition of Ziziphus jujuba Mill, its pharmacological and toxicological effects, its applications in the food industry, as well as other unconventional uses that have not been covered in other reviews but contribute to the understanding of its benefits.

2. Methodology

In the literature review, data and information regarding the botanical description of the species Ziziphus jujuba, its chemical composition and nutritional value, pharmacological action, and unconventional ecological applications have been collected, summarized, and analyzed. The articles used for Z. jujuba Mill. were sourced from Web of Science, Scopus, PubMed, ScienceDirect, SpringerLink, and Google Scholar. The search period covers articles published between 1976 and 2024. The following keywords were used: Ziziphus jujuba Mill., chemical composition, pharmacological application, ecological application, and botanical origin. About 200 literature sources were reviewed, of which approximately 132 were used in the review, while 68 were irrelevant as they dealt with other species of the studied plant.

3. Chemical Content

The chemical content of Ziziphus jujuba has been the objective of many studies. The richness in amino acids, such as tryptophan, is important for mental health and the optimal function of the brain [3]. The presence of many compounds such as tannin, saponins, flavonoids, terpenoids, phenolic compounds, alkaloids, amino acids, sugar, protein, fats, calcium, potassium, phosphate, and iron have been reported in the literature [1,17,18,19]. A thorough review of the various compounds was conducted by Aafi et al. [20], where they are sorted by class. The authors examined some of them in order to establish the relationship between the plant and its medicinal uses.
Flavonoids are a class of substances with some pronounced health benefits. The extraction method affects the total amount of flavonoids. The highest values were achieved with the extractant—chloroform—and the lowest were achieved with hexane in the leaves and methanol in the fruits [8].
Others types of substances that are found in the plant are quercetin glycosides (quercetin-3-glucoside, quercetin-3-rhamnoside), rutin (quercetin 3-O-rutinoside), quercetin 3-O-β-D-galactoside, kaempferol 3-O-robinobioside, quercetin 3-O-β-D-glucoside, kaempferol 3-rutinoside, 3′,5′-Di-C-β-D-glucosylphloretin, catechin, epicatechin, and procyanidin B2 [21,22,23,24].
Using FCR analysis, Hossain, M.A. determined the phenolic content of the plant, the best results being obtained with the ethyl acetate extract [8]. The results obtained suggest that the antioxidant effect of the plant can be explained by the content of flavonoids and polysaccharides [25,26,27]. Furthermore, the fruit contains vital vitamins in high concentrations—A, B1, B12, and C [17,27,28,29]. Data from the World Health Organization and Food and Agriculture Organization suggests that one fruit could be sufficient for the daily requirement of five different vitamins.
The polysaccharide content of Ziziphus jujuba also affects its uses. Jingya Ruan and others have conducted studies of this type of molecule in the plant. Forty-six types of polysaccharides are contained in the Ziziphus jujuba plant. Some of them have antioxidant, anti-fatigue, anti-inflammatory, liver protecting, and other healing properties. Such examples contain monosaccharides such as uronic acid, galactose, xylose, arabinose, galacturonic acid, etc. [30,31].
The alkaloids in Z. jujuba, identified by Zhao et al., were asimilobine, isoboldine, juziphine, juzirine, and norisoboldine [31]. The chemical content of Z. jujuba is presented in Figure 1. The structure formulas of the main compounds are shown in Figure 2.
Table 1, Table 2, Table 3 and Table 4 present various chemical compounds and their concentrations reported for different countries around the world, indicating that climate and geographical region matter.

4. Pharmacological and Toxicological Effects

According to the literature, fruit and leaf extracts show pharmacological and toxicological effects depending on the polarity of the solvent [17,29,46,47,48]. The influence of jujube has been tested in vitro, however, there are few clinical trials to prove a real pharmacological application [20].
Its antioxidant activity has an important pharmacological application. It was determined by a modified radical scavenging method by several authors [1,2,49,50]. Z. jujuba exhibited reduction activity over iron and lipid peroxidation assays [20]. The authors [20] found that the highest antioxidant activity was shown by the fruit extracts with chloroform. The scavenging activity decreased with the polarity of the sample. Another paper determined that the peel had the highest antioxidant activity [51]. The reason for this activity is linked directly to the chemical content of the sample—uronic acid, flavonoids, and phenolic compounds in particular. The influence of uronic acid and how it affects the antioxidant potential of polysaccharides was studied by Li et al. [27]. Fruit quality varies depending on different growing conditions and harvesting methods. It is suggested that high-stress environments and higher altitudes increase the antioxidant activity [52]. Sun et al. [35] conducted a comprehensive evaluation of the total antioxidants and antioxidant activity in relation to environmental conditions by examining samples from ten different regions with varying latitudes and altitudes in China. They found a positive correlation between altitude and the levels of polyphenols, anthocyanins, saponins, flavonoids, and polysaccharides while observing a negative correlation with vitamin C. Annual rainfall had a strong negative impact on the content of flavonoids, polyphenols, saponins, polysaccharides, and carotenoids, but a positive effect on the content of vitamin C.
According to the results of experiments on rats, the polysaccharides reduced the trauma on the liver due to CCl4 poisoning. The levels of 3,4-methylenedioxyamphetamine (MDA) were also reduced, and the activity of the antioxidant proteins stayed within normal limits [9]. Another study suggests that the levels of antioxidant enzymes (superoxide dismutase (SOD) and catalase (CAT)) and glutathione (GSH) were increased, and the levels of aminotransferase enzymes (ALT and AST) and MDA were decreased. The histological activity was also improved [53,54,55]. Some neurodegenerative diseases, such as Parkinson’s and Alzheimer’s, are greatly influenced by oxidative stress as their progression is accelerated. Experiments with neuronal cell lines (PC12) investigating the protective properties of jujube water extract against tert-butyl hydroperoxide-induced oxidative damage have had positive results. The fraction further reduces the reactive oxygen species formed from the agent [56]. Z. jujuba was tested in vivo against ischemic damage in the gerbil hippocampus; the effect was attributed to the upregulation of superoxide dismutase and reduced lipid peroxidation [57].
Another useful property of Z. jujuba is its anti-inflammatory activity. It was observed in experiments with mice in acute and chronic cases. The inhibition was achieved by interaction and deactivation of COX, NO, and histamine. The most active compounds of the plant were the terpenoid acids [58].
Al-Saeedi et al. studied the antimicrobial activity of Z. jujuba by tests performed on Gram-positive and Gram-negative bacteria. The extracts of the plant showed potency against the tested strains. The inhibition depends on the ingredients of the drug solution. The authors found that the best results were obtained using the hexane extracts. This suggests that this type of extraction contains the biggest concentration of bioactive compounds. There is a difference between studies due to the extraction methods, bacterial stains, doses, etc. Other experiments showed antimicrobial activity against Escherichia coli and Staphylococcus aureus [59]. The ethyl acetate extract has antimicrobial effects against Bacillus pumalis, Pseudomonas aeruginosa, Salmonella typhi, and Staphylococcus epidermidis. For example, the n-hexane fraction of Z. jujuba is significantly active against B. pumalis, while an aqueous fraction is active against P. aerugenoza [9]. Snakin-Z is a peptide derived from Z. jujuba that showed antimicrobial effect on E. coli, K. pneumonia, B. subtilis, S. aureus, Aspergillus niger, Candida albicans, Phomopsis azadirachtae, and Pythium ultimum with higher activity on Gram-positive bacteria [60]. Betulinic acid extracted from the plant shows an activity against the influenza virus in experiments with mice [61].
The fruit of Z. jujuba expresses neuroprotective effects in in vitro experiments. Glucose-induced neurotoxicity is reduced in a model of diabetic neuropathy [62]. Taati et al. found that consumption of the fruit lowers ethanol-induced spatial memory loss and oxidative stress [63]. Moreover, some experiments in the literature suggest that water fruit extract is beneficial to neuron differentiation. The effect was observed in vitro and was modeled using PC12 cell lines. After 72 h, proliferation and stimulated expression of certain neurofilament proteins were induced [56]. Another important part of the nervous system is played by astrocytes. They produce neurotropic factors such as NT3, NT4/5, BDNF, and GDNF. Their upregulation is vital to the cell as it plays an important role throughout its whole living cycle. There have been some in vitro experiments on the effect of Z. jujuba on astrocyte cellular lines. The result was a dose-dependent elevated expression of the above-mentioned factors while the morphology of the cells remained unaffected [64]. Jujube was also observed to improve the signaling pathway cAMP-PKA-CREB, which is connected to neuron differentiation. This effect and the improvement in the expression of neurotrophic factors can both be inhibited by the addition of H89 [64,65].
One of the promising substances that could be used against Alzheimer’s disease is oleamide. It has been extracted from jujube fruits and could be used for treatment [66]. Snakin-Z has the properties to treat this disease. Its neurobiological activity has been studied, and in addition, it also has antioxidant and cholinesterase inhibition activity [67].
Another application of Z. jujuba has been suggested to be antiepileptic activity. The hydroalcoholic extract from the fruit reduced the seizures expressed by rats. Anticonvulsant activity was observed with both types of seizures—tonic-clonic and tonic hindlimb extension. The fruit also increased the learning ability and memory of mice [68]. The synergy with antiepileptic drugs on the market has also been examined. The concentrations of the drugs were not changed by the addition of the plant extract. In two cases—with phenobarbital and phenytoin—Z. jujuba improved the effect. No change was observed with simultaneous administration of carbamazepine and the fruit [69].
Ziziphus jujuba is used in traditional Chinese medicine to battle insomnia [70]. This was confirmed in experiments with mice as jujube increased sleep time and decreased the movement of the subjects [71]. Other research on jujube seeds reports similar results in both mice and rats [72]. An extract of flavonoids and saponins from the seed decreases coordinated movement and prolongs sleep [73]. Another effect of jujube is the improvement in learning ability and memory, as mentioned above. An increase in estrogen in the blood and nitric oxide and acetylcholine in the brain was probably the cause in the ovariectomized rat model [74]. Enhancement in memory from the intake of Z. jujuba extract was reported in alcohol-induced disorders, and improvement in learning ability was observed [75].
The polyphenols in jujube can have cardioprotective activity. The results from rat experiments show reduced MDA activity and inhibited expression of ST-segment in ECG. They enhance SOD, GPx in the hearts of the tested animals. The myofibrillar degeneration of the left ventricle is reduced [76].
The hydroalcoholic extract from the jujube fruit was tested using two intake methods—topical gel and oral consumption—against ulcerative colitis in rats. Both were found to be effective; however, the gel had more potency—around 40%. The colon tissue histopathology was enhanced, and the levels of interleukin-1β (IL-1β), myeloperoxidase, and GPx were reduced [77]. There was a clinical trial on the effect of jujube against constipation. The test group was 50 patients, and the period was 12 weeks. The treatment had a significant effect on the group that received jujube compared to the placebo group. This method positively influenced the cases of chronic idiopathic constipation, bloating, and abdominal pain [78]. Ziziphus jujuba also reduces inflammation and progression of colon cancer [79].
In total, 70% of ethanolic extracts of Z. jujuba were evaluated using Caco2 cells and a mouse model and demonstrated their efficacy in IBD (inflammatory bowel disease) [80].
Due to its content of flavonoids and steroidal saponins, Z. jujuba also has a protective activity against allergies and asthma. Its effect has different mechanisms of positive interaction, including stabilization of mast cells, immunomodulation, antihistamine effect, etc. [81,82].
Another application is in the healing of second-degree burn wounds. The fruit extracts significantly accelerate the process [83].
Ziziphus jujuba is also used in ginseng paste as an adjuvant to improve the treatment of hyperuricemia. This is a disease caused by the overproduction of uric acid. It was shown that the ginseng–jujube pair could have a positive influence on the illness through interaction with CCL2, TNF-α, IL-1β, and VEGFA. The effect of hydroalcoholic extracts of Z. jujuba leaves on the prevention/treatment of kidney stones was evaluated and found to reduce the formation of calcium oxalate crystals and the effective dose was 500 mg/kg [84].
A brine shrimp lethality assay was used by Al-Saeedi et al. to determine the cytotoxicity of Z. jujuba extracts. It was shown that butanol leaf extract had the highest toxicity. This characteristic depends on the ingredients of the sample. These results were confirmed by Hoshyar and Alhakmani [44,85].
Moreover, the fruits of Ziziphus jujuba have an immunostimulatory effect. One of the water-soluble fractions, ZSP3, which has a lot of pectin, shows a potential immunological response with 49% esterification [27]. The effect of Ziziphus jujuba fruit extract on the non-specific immune parameters of skin mucus and the mRNA levels of immune-related genes in the skin of small carp was investigated. Feeding of 0.5 and 1% Ziziphus jujuba fruit extract was found to significantly increase the protease activity of skin mucus, and gene expression studies in skin showed a significant increase in Il1b expression. [86]. This part of the plant is used in aesthetics and medical cosmetics [87]. The healing properties of Ziziphus jujuba have also been tested on wounds. Breastfeeding is negatively affected by nipple fissure pain. Several lactating women have tested lotion with an extract of the plant’s fruit and reported that the pain subsided between one and two weeks after using it [88].
According to the literature, essential oil extracted from Ziziphus jujuba enhances skin elasticity and enables bigger elastic deformations. Miwa suggested that it could be used to improve the treatment of acne and psoriasis [89]. Later, Pazyar noted the potential of the oil for acne treatment due to its positive keratoplastic effect [82]. Furthermore, some pharmaceutical advancements have improved the penetration capability of drugs or the delivery efficiency to the target area due to the inclusion of the jujube’s oil. An example is the enhancement of the flow of the medication olanzapine through the skin in transdermal patches. It is often used in the emulsification of alginate beads with hydrogels for the production of vaccines in order to improve their stability [90]. For instance, the vaccine Calmette-Guérin is stable at room temperature for as long as a year after dehydration using freezing of such beads [91]. The essential oil of jujube is included in a lot of pharmaceutical products. In Figure 3, an example of three of them is presented.
Lee et al. [94] found that Zizyphus jujuba var. inermis (Korea) essential oil is a rich source of 3-pentadecylcatechol, ρ-menth3-ene, γ-bisabolene, and vomifoliol, as well as β-sitosterol, stigmasterol, stigmasta-5,23-dien-3β-ol, stigmast-4-en-3-one, lupeol, betulinic acid and its derivatives, alphitolic acid and its derivatives, zizyberanalic acid, ceanothic acid, oleanolic acid, and maslinic acid and its derivatives.
Elaloui et al. [95] identified thirteen fatty acids from the pulps’ essential oil of four Tunisian Ziziphus jujuba ecotypes (Sfax, Choutrana, Mahres, and Mandia). The authors found that Mahres and Choutrana were the richest sources of oleic acid compared to the other ecotypes. The Sfax ecotype’s most significant chemical compound was palmitic acid. For each ecotype, the percentage of unsaturated fatty acids ranged from 62.63% to 72.40% of total fatty acids. The unsaturated/saturated (U/S) ratio therefore ranged from 1.68 to 2.37. Beta-sitosterol and stigmasterol were found to be the major sterols.
Out of the 20 compounds found in the essential oil from Ziziphus jujuba seeds [96], the most abundant ones were 13-Heptadecyn-1-ol (12.95%), 7-Ethyl-4-decen-6-one (9.73%), Lineoleoyl chloride (8.54%), Linoleic acid (6.37%), 2,5-Octadecadiynoic acid, methyl ester (5.57%), and Palatinol A (4.81%).

5. Applications in Foods

The jujube’s fruits have a short shelf-life—around 10 days in fresh form. The pulp of the jujube is usually eaten fresh, but the fruit could also be dried and included in other recipes [97]. The remarkable healing potential of Ziziphus jujuba renders it a staple in traditional cuisine and an increasingly popular choice as a functional food. Its incorporation into culinary practices not only enhances flavor profiles but also infuses dishes with a myriad of health benefits, contributing to its growing prominence as a sought-after ingredient in both traditional and modern dietary contexts [98]. It can be added to improve the taste or to enhance the nutritional value. Rashwan et al. reviewed the content of more than 30 food products incorporating jujube. Some examples are tea, cake, yogurt, bread, etc. A couple of the jujube’s products have been investigated further in order to evaluate their medicinal properties. The powdered form exhibited high levels of phenolic compounds. Moreover, it expressed antimicrobial, antioxidant, and anticancer activity. This form has already found its application in the treatment of dyslipidemia and insulin resistance [92,93,94,95,96,97,98,99,100,101,102]. The jujube vinegar expressed anticancer properties and a positive effect on the gastrointestinal system. It is used in insomnia treatment and normalizes blood pressure. The vinegar also contains vitamin C [103,104,105]. Another product—jujube fermented juice—has the potential to be used in non-dairy probiotic food. It has an abundance of phenolic compounds. The same characteristics are applicable to jujube wine [105,106,107,108,109,110]. Fresh juice is rich in Vitamin C and has antioxidant properties [104,105,111].
In order to avoid fast spoilage, food processing is used to prevent bacteria, yeast, and fungi from developing on the product. This improves the storage time of the culinary item. On the other hand, the process has to be optimized to ensure that the item retains its valuable qualities. According to Zozio et al., jujubes’ shelf life is around 10 days in uncontrolled conditions [112]. Sensory evaluation and chemical analysis were performed by Shin and co-authors. It was concluded that powder, dried fruits, extracts, juices, and jam showed the greatest preserving potential [113]. A solely sensory evaluation of different products after various preservation methods (cloying with honey, vinegar infusion, compote, and drying) was made by Krška [97]. On their scale, the compote was ranked the highest. The jam, jelly, and pickled jujube have been tested for their physicochemical and sensory characteristics by Uddin and Hussein in 2012. The nutrition in these forms was retained; they complied with food standards and were satisfactory [114].
Drying food is considered a suitable preservation process that maintains the flavor, aroma, and color of the Z. jujuba fruits. This is a reason to investigate some innovative techniques further. Some examples use infrared and microwave radiation, vacuum, freezing, or a combination of these methods. They increase the speed of the process while sustaining the qualities [115,116,117,118].
Juices are easy to consume and are a suitable addition to food supplements. The extraction method can vary in parameters. A study showed that when using hot water, the optimal conditions are 70–80 °C and 40 min in a fruit-to-water ratio of 1:7. Enhanced effect is achieved by following this procedure by pectinase treatment [98].
Another common beverage is Z. jujuba wine. However, research on its ideal preparation conditions is scarce compared to the above-mentioned examples. Liu et al. and Zhao et al. concluded that suitable conditions are 18% sugar content, pH = 4.0, 24 °C, and 12.5% vol. alcohol in the wine produced [119]. Jujube’s brandy (50% vol.) is a popular drink in China. The evaluation of such beverages is based on the content of volatile organic components (VOC) as they are major components of the aroma. This characteristic can be altered with variations of the processing methods. For example, thermal treatment increases VOC while decreasing phenolic and flavonoid compounds by around 20%. Some of the contents of jujube wine include 16 amino acids and seven organic acids. Their quantity was increased with the process of fermentation, which indicates they improved the taste [98]. Jujube’s vinegar is another available product. It has high nutritional value as well as increased content of antioxidant components. This classifies it as functional vinegar [105].
Candied Z. jujuba is one of the more well-known products in China. This form has a longer storage time and could be prepared with different sweeteners in order to lower the sugar content [98]. Different methods vary in the retention of valuable substances such as vitamin C. Zhao et al. investigated different recipes that are used to prepare jam and jelly from jujube’s fruit [118,119]. Pectin obtained from Z. jujuba at different ripeness was studied, and it was found that it can be used to increase the amount of vitamin C in kefir [120].
Some artificial food additives can be substituted with jujube to decrease health hazards. Some examples are the addition of bread or meat to improve the preparation process [121].
Since quinoa, although a complete food, due to its bad taste, is not a good option for direct consumption (cake), this shortcoming was overcome by adding jujube fruit powder [122].
In Chinese alternative medicine, there is an increasing focus on functional foods that meet the needs of the population. Bae et al. studied yogurt with added fermented seeds of Ziziphus jujuba using Lactobacillus brevis L-32 [123]. The authors reported that the resulting fermented beverage was high in γ-aminobutyric acid (GABA), which promotes sleep. The addition of pulp from Ziziphus jujuba fruits improves the taste of goat yogurt [124]. Furthermore, the addition of polysaccharides extracted from the pulp of Ziziphus jujuba fruits enhances the density and firmness of the casein matrix structure in goat cheese [125].

6. Other Applications Related to Zero-Waste Technologies and Ecology

Recently, special attention has been paid to the waste-free use of plant resources, from composting to the production of non-conventional adsorbents.
The pulp of Ziziphus jujuba fruits can be used to extract condensed tannins [126]. Research by the author team has shown that these substances effectively inhibit the monophenolase and diphenolase activities of tyrosinase. Therefore, Ziziphus jujuba pulp is a natural tyrosinase inhibitor with potential applications in food preservation and skin-whitening cosmetics.
Steam-pyrolyzed at 1000 °C, Ziziphus jujuba seeds have been used to produce granular activated carbon with twice the adsorption capacity of commercially available options [127]. When the surface of the plant seeds is modified with ultrasound and sulfuric acid, they become suitable for the absorption of toxic metals such as cadmium, copper, zinc, lead, nickel, and others [128].
The chemical modification of Ziziphus jujuba stones (ZJS) with ortho-phosphoric acid (ZJS-H3PO4) was found to have an adsorption capacity of 179.83 mg g−1 of methylene blue, and they could be used as efficient adsorbents for organic dyes [129]. Jujube kernel fibers (JKF) can serve as a renewable and environmentally friendly wastewater adsorbent after modification of their microstructure. JKF treated with mixed enzymatic hydrolysis and acetylation can adsorb oil, while JKF treated with mixed enzymatic hydrolysis and carboxymethylation have high adsorption ability for heavy metals [130]. Gavade et al. reported a one-step biogenic synthesis of silver nanoparticles (AgNPs) by using Ziziphus jujuba leaf extract as a reducing and stabilizing agent. These particles can be used in environmental applications to reduce the anthropogenic pollutant 4-nitrophenol (4-NP) and methylene blue (MB), and they also show good antimicrobial activity against Escherichia coli [131]. A study investigated the mechanical properties of hybrid composites prepared from Holoptelea integrifolia bark fiber (HIBF) reinforced with Ziziphus jujuba seed particles (ZJSP) for bio-based epoxy resin (BBER) [132]. A highly porous, economical, and sustainable carbon electrode based on a waste material (Ziziphus jujuba seeds) has been developed, which can be useful for energy storage [133].
Due to their high energy value, jujube fruits have shown a positive effect when used as an alternative additive in diets for poultry in egg production, which further helped reduce feed [134].

7. Conclusions

In conclusion, this review presents a description of the main chemical compounds found in the plant Z. jujuba with pharmacological importance. Attention has been given to its application in the food industry. Our evaluation shows that all its parts—leaves, fruits, and seeds—have medicinal potential. However, further clinical studies of the effects of various Z. jujuba extracts are lacking for most reported uses. It has been noted that the fruit retains some of its valuable constituents after drying, and these properties can be used in herbal mixtures. In addition, Z. jujuba has other applications: as a sorbent, animal feed, and a composite material.

Author Contributions

Conceptualization, K.N. and G.G.; resources, A.G. (Anelia Gerasimova); data curation, G.G. and A.G. (Anelia Gerasimova); writing—original draft preparation, D.P.; writing—review and editing, S.N. and A.G. (Anna Gavrilova); visualization, A.G. (Anna Gavrilova); supervision, K.N.; project administration, K.N.; funding acquisition, K.N. All authors have read and agreed to the published version of the manuscript.

Funding

This study is financed by the European Union NextGenerationEU, through the National Recovery and Resilience Plan of the Republic of Bulgaria, project № BG-RRP-2.004-0009--C02.

Data Availability Statement

The data presented in this study are available on request from the corresponding authors.

Acknowledgments

Special thanks to the Medical University of Varna and the European Union for the financial support provided for the publication of this paper.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Al-Saeedi, A.H.; Ghafri, M.T.H.A.; Hossain, M.A. Comparative evaluation of total phenols, flavonoids content and antioxidant potential of leaf and fruit extracts of Omani Ziziphus jujuba L. Pac. Sci. Rev. ANat. Sci. Eng. 2016, 18, 78–83. [Google Scholar] [CrossRef]
  2. Al-Saeedi, A.H.; Al-Ghafri, M.T.H.; Hossain, M.A. Brine shrimp toxicity of various polarities leaves and fruits crude fractions of Ziziphus jujuba native to Oman and their antimicrobial potency. Sustain. Chem. Pharm. 2017, 5, 122–126. [Google Scholar] [CrossRef]
  3. Stefania, G.; Vâtcă, S.; Vâtcă, A. The use of medicinal plants in the human civilization. Agric. Sci. Pract. 2016, 3–4, 46–50. [Google Scholar]
  4. Feng, R.; Wang, N.; Kou, J.; An, X.; Meng, F.-H.; Zheng, X.; Wang, W.; Wang, L.; Ze-He, W.; Liu, M.; et al. Sulfated Modification, Characterization and Potential Bioactivities of Polysaccharide From Ziziphus jujuba cv. Jinsixiaozao. Nat. Product. Commun. 2021, 16, 1–14. [Google Scholar] [CrossRef]
  5. Li, H.; Feng, L.; Wang, L.; Sheng, J.; Xin, Z.; Zhao, L.; Xiao, H.; Zheng, Y.; Hu, Q. Effect of nano-packing on preservation quality of Chinese jujube (Ziziphus jujuba Mill. var. inermis (Bunge) Rehd). Food Chem. 2009, 114, 547–552. [Google Scholar] [CrossRef]
  6. Shahrajabian, M.H.; Khoshkharam, M.; Zandi, P.; Sun, W.; Cheng, Q. Jujube, a super-fruit in traditional Chinese medicine, heading for modern pharmacological science. J. Med. Plants Stud. 2019, 7, 173–178. [Google Scholar]
  7. Bean, W.J. Trees and Shrubs Hardy in the British Isles: Eighth Edition Revised Four Volumes with Supplement, 1st ed.; John Murray: London, UK, 1976; Available online: https://www.abebooks.co.uk/servlet/BookDetailsPL?bi=31138500847&searchurl=an%3Dbean%26attrs%3Dhc%2Bdj%26bi%3Dh%26dj%3Don%26ds%3D30%26rollup%3Don%26sortby%3D1%26tn%3Dtrees%2Band%2Bshrubs%2Bhardy%2Bin%2Bthe%2Bbritish%2Bisles&cm_sp=snippet-_-srp0-_-image1 (accessed on 5 June 2024).
  8. Hossain, M.A. A phytopharmacological review on the Omani medicinal plant: Ziziphus jujuba. J. King Saud. Univ. Sci. 2019, 31, 1352–1357. [Google Scholar] [CrossRef]
  9. Ahmad, B.; Khan, I.; Bashir, S.; Azam, S.; Hussain, F. Screening of Zizyphus jujuba for antibacterial, phytotoxic and haemagglutination activities. Afr. J. Biotechnol. 2011, 10, 2514–2519. [Google Scholar]
  10. Yi, X.; Wu, W.; Zhang, Y.; Li, J.; Luo, H. Thin-Layer drying characteristics and modeling of Chinese jujubes. Math. Probl. Eng. 2012, 2012, 386214. [Google Scholar] [CrossRef]
  11. Liu, M.; Wang, Y. cAMP contents of Zizyphus jujuba Mill., Zizyphus spinosus hu. and other twelve horticultural plants. J. Agric. Univ. Hebei 1991, 14, 20–23. [Google Scholar]
  12. Yao, S. Past, present, and future of Jujubes-Chinese dates in the United States. Hortscience 2013, 48, 672–680. [Google Scholar] [CrossRef]
  13. Djeuzong, E.; Kandeda, A.K.; Djiogue, S.; Stéphanie, L.; Nguedia, D.; Ngueguim, F.T.; Djientcheu, J.P.; Kouamouo, J.; Dimo, T. Antiamnesic and Neuroprotective Effects of an Aqueous Extract of Ziziphus jujuba Mill. (Rhamnaceae) on Scopolamine-Induced Cognitive Impairments in Rats. Evid.-Based Complement. Altern. Med. 2021, 2021, 5577163. [Google Scholar] [CrossRef] [PubMed]
  14. Agrawal, P.; Singh, T.; Pathak, D.; Chopra, H. An updated review of Ziziphus jujube: Major focus on its phytochemicals and pharmacological properties. Pharmacol. Res.-Mod. Chin. Med. 2023, 8, 100297. [Google Scholar] [CrossRef]
  15. Zhu, D.; Jiang, N.; Wang, N.; Zhao, Y.; Liu, X. A Literature Review of the Pharmacological Effects of Jujube. Foods 2024, 13, 193. [Google Scholar] [CrossRef] [PubMed]
  16. Lu, Y.; Bao, T.; Mo, J.; Ni, J.; Chen, W. Research advances in bioactive components and health benefits of jujube (Ziziphus jujuba Mill.) fruit. J. Zhejiang Univ.-Sci. B 2021, 22, 431–449. [Google Scholar] [CrossRef]
  17. Singh, V.; Guizani, N.; Essa, M.M.; Rahman, M.S.; Subash, S. In vitro Antioxidant Activities of Ziziphus spina-christi Fruits (Red Date) Grown in Oman. Biotechnology 2012, 11, 209–216. [Google Scholar] [CrossRef]
  18. Elaloui, M.; Laamouri, A.; Fabre, J.-C.; Mathieu, C.; Vilarem, G.; Hasnaoui, B. Distribution of free amino acids, polyphenols and sugars of Ziziphus jujuba pulps harvested from plants grown in Tunisia. Nat. Product. Res. 2015, 29, 94–97. [Google Scholar] [CrossRef] [PubMed]
  19. Elaloui, M.; Ghazghazi, H.; Ennajah, A.; Manaa, S.; Guezmir, W.; Karray, N.; Laamouri, A. Phenolic profile, antioxidant capacity of five Ziziphus spina-christi (L.) Willd provenances and their allelopathic effects on Trigonella foenum-graecum L. and Lens culinaris L. seeds. Nat. Product. Res. 2016, 31, 1209–1213. [Google Scholar] [CrossRef]
  20. Aafi, E.; Reza, M.T.; Mirabzadeh, M. Jujube (Ziziphus jujuba Mill. (Rhamnaceae)): A review on its pharmacological properties and phytochemistry. Tradit. Med. Res. 2022, 7, 38. [Google Scholar] [CrossRef]
  21. Gao, Q.; Wu, C.; Wang, M. The Jujube (Ziziphus jujuba Mill.) fruit: A review of current knowledge of fruit composition and health benefits. J. Agric. Food Chem. 2013, 61, 3351–3363. [Google Scholar] [CrossRef] [PubMed]
  22. Gao, Q.; Wu, C.; Yu, J.; Wang, M.; Ma, Y.; Li, C. Textural Characteristic, Antioxidant Activity, Sugar, Organic Acid, and Phenolic Profiles of 10 Promising Jujube (Ziziphus jujuba Mill.) Selections. J. Food Sci. 2012, 77, C1218–C1225. [Google Scholar] [CrossRef] [PubMed]
  23. Shi, Q.; Zhang, Z.; Su, J.; Zhou, J.; Li, X. Comparative Analysis of Pigments, Phenolics, and Antioxidant Activity of Chinese Jujube (Ziziphus jujuba Mill.) during Fruit Development. Molecules 2018, 23, 1917. [Google Scholar] [CrossRef]
  24. Cheng, G.; Bai, Y.; Zhao, Y.; Tao, J.; Lü, Y.; Tu, G.; Ma, L.; Liao, N.; Xu, X. Flavonoids from Ziziphus jujuba Mill var. spinosa. Tetrahedron 2000, 56, 8915–8920. [Google Scholar] [CrossRef]
  25. Chang, S.C.; Hsu, B.; Chen, B.H. Structural characterization of polysaccharides from Zizyphus jujuba and evaluation of antioxidant activity. Int. J. Biol. Macromol. 2010, 47, 445–453. [Google Scholar] [CrossRef]
  26. Choi, S.H.; Ahn, J.B.; Kozukue, N.; Levin, C.E.; Friedman, M. Distribution of Free Amino Acids, Flavonoids, Total Phenolics, and Antioxidative Activities of Jujube (Ziziphus jujuba) Fruits and Seeds Harvested from Plants Grown in Korea. J. Agric. Food Chem. 2011, 59, 6594–6604. [Google Scholar] [CrossRef]
  27. Li, J.; Liu, Y.; Fan, L.; Ai, L.; Liang, S. Antioxidant activities of polysaccharides from the fruiting bodies of Zizyphus Jujuba cv. Jinsixiaozao. Carbohydr. Polym. 2011, 84, 390–394. [Google Scholar] [CrossRef]
  28. Kim, H. Effects of the Zizyphus jujuba Seed Extract on the Lipid Components in Hyperlipidemic Rats. J. Food Sci. Nutr. 2002, 7, 72–77. [Google Scholar] [CrossRef]
  29. Parveen, S.; Bukhari, N.I.; Shehzadi, N.; Qamar, S.; Ali, E.; Naheed, S.; Latif, A.; Yuchi, A.; Hussain, K. Chemical and pharmacological comparison of modern and traditional dosage forms of Joshanda. Nat. Product. Res. 2017, 33, 858–861. [Google Scholar] [CrossRef] [PubMed]
  30. Ji, X.; Zhang, F.; Zhang, R.; Liu, F.; Peng, Q.; Wang, M. An acidic polysaccharide from Ziziphus jujuba cv. Muzao: Purification and structural characterization. Food Chem. 2019, 274, 494–499. [Google Scholar] [CrossRef]
  31. Zhao, L.; Liu, F.; Ge, J.; Li-Li, M.; Wu, L.; Xue, X. Changes in eleven pesticide residues in jujube (Ziziphus jujuba Mill.) during drying processing. Dry. Technol. 2017, 36, 965–972. [Google Scholar] [CrossRef]
  32. Shams Najafabadi, N.; Sahari, M.A.; Barzegar, M.; Esfahani, Z.H. Effects of concentration method and storage time on some bioactive compounds and color of jujube (Ziziphus jujuba var vulgaris) concentrate. J. Food Sci. Technol. 2017, 54, 2947–2955. [Google Scholar] [CrossRef]
  33. Ziyaev, R.; Irgashev, T.; Israilov, I.A.; Abdullaev, N.D.; Yunusov, M.S.; Yunusov, S.Y. Alkaloids of Ziziphus jujuba the structure of juziphine and juzirine. Chem. Nat. Compd. 1977, 13, 204–207. [Google Scholar] [CrossRef]
  34. Komoto, T.T.; Bernardes, T.M.; Mesquita, T.B.; Bortolotto, L.F.B.; Silva, G.; Bitencourt, T.A.; Baek, S.J.; Marins, M.; Fachin, A.L. Chalcones Repressed the AURKA and MDR Proteins Involved in Metastasis and Multiple Drug Resistance in Breast Cancer Cell Lines. Molecules 2018, 23, 2018. [Google Scholar] [CrossRef]
  35. Sun, Y.; Liang, Z.; Shan, C.; Viernstein, H.; Unger, F.M. Comprehensive evaluation of natural antioxidants and antioxidant potentials in Ziziphus jujuba Mill. var. spinosa (Bunge) Hu ex H. F. Chou fruits based on geographical origin by TOPSIS method. Food Chem. 2011, 124, 1612–1619. [Google Scholar] [CrossRef]
  36. Chen, K.; Fan, D.; Fu, B.; Zhou, J.; Li, H. Comparison of physical and chemical composition of three chinese jujube (Ziziphus jujuba Mill.) cultivars cultivated in four districts of Xinjiang region in China. Food Sci. Technol. 2018, 39, 912–921. [Google Scholar] [CrossRef]
  37. Hernández, F.; Noguera-Artiaga, L.; Burló, F.; Wojdyło, A.; Carbonell-Barrachina, Á.A.; Legua, P. Physico-chemical, nutritional, and volatile composition and sensory profile of Spanish jujube (Ziziphus jujuba Mill.) fruits. J. Sci. Food Agric. 2016, 6, 2682–2691. [Google Scholar] [CrossRef]
  38. Fukalova, F.T.; García-Martínez, M.D.; Esteve Ciudad, P.; Raigón Jiménez, M.D. The Effects of Low-Input (Wild and Organic Farming) Conditions on the Nutritional profile of Ziziphus jujuba Mill. Fruits from the Valencian Mediterranean. Sustainability 2023, 15, 14587. [Google Scholar] [CrossRef]
  39. Danthu, P.; Soloviev, P.; Totté, A.; Tine, E.; Ayessou, N.; Gaye, A.; Fall, M. Caractères physico-chimiques et organoleptiques comparés de jujubes sauvages et des fruits de la variété Gola introduite au Sénégal. Fruits 2002, 57, 173–182. [Google Scholar] [CrossRef]
  40. Višnjevec, M.A.; Arbeiter, A.B.; Hladnik, M.; Ota, A.; Skrt, M.; Butinar, B.; Bandelj, D. An Integrated Characterization of Jujube (Ziziphus jujuba Mill.) Grown in the North Adriatic Region. Food Technol. Biotechnol. 2019, 57, 17–28. [Google Scholar] [CrossRef] [PubMed]
  41. Chiti, S.; Basiri, S.; Mortazavi, A.; Sharifi, A. Evaluation on Physicochemical Properties and Antioxidant Capacity of Two Iranian Jujube (Ziziphus jujuba Mill.) Cultivars. J. Med. Plants By-Prod. 2019, 8, 85–93. [Google Scholar]
  42. San, B.; Yildirim, A.N. Phenolic, alpha-tocopherol, beta-carotene and fatty acid composition of four promising jujube (Ziziphus jujuba Miller) selections. J. Food Compos. Anal. 2010, 23, 706–710. [Google Scholar] [CrossRef]
  43. Wu, L.; Li, L.; Zhang, G.; Jiang, N.; Ouyang, X.; Wang, M. Geographical and Varietal Traceability of Chinese Jujubes Based on Physical and Nutritional Characteristics. Foods 2021, 10, 2270. [Google Scholar] [CrossRef]
  44. Reche, J.; Almansa, M.S.; Hernández, F.; Amorós, A.; Legua, P. Physicochemical and Antioxidant Capacity of Jujube (Ziziphus jujube Mill.) at Different Maturation Stages. Agronomy 2021, 11, 132. [Google Scholar] [CrossRef]
  45. Ivanišová, E.; Grygorieva, O.; Abrahamova, V.; Schubertova, Z.; Terentjeva, M.; Brindza, J. Characterization of morphological parameters and biological activity of jujube fruit (Ziziphus jujuba Mill.). J. Berry Res. 2017, 7, 249–260. [Google Scholar] [CrossRef]
  46. Al-Reza, S.M.; Bajpai, V.K.; Kang, S.C. Antioxidant and antilisterial effect of seed essential oil and organic extracts from Zizyphus Jujuba. Food Chem. Toxicol. 2009, 47, 2374–2380. [Google Scholar] [CrossRef]
  47. Al-Reza, S.M.; Rahman, A.; Lee, J.; Kang, S.C. Potential roles of essential oil and organic extracts of Zizyphus jujuba in inhibiting food-borne pathogens. Food Chem. 2010, 119, 981–986. [Google Scholar] [CrossRef]
  48. Alhakmani, F.; Khan, S.A.; Ahmad, A. Determination of total phenol, in-vitro antioxidant and anti-inflammatory activity of seeds and fruits of Zizyphus spina-christi grown in Oman. Asian Pac. J. Trop. Biomed. 2014, 4, S656–S660. [Google Scholar] [CrossRef]
  49. Kamiloglu, Ö.; Ercisli, S.; Sengül, M.; Toplu, C.; Serçe, S. Total phenolics and antioxidant activity of jujube (Zizyphus jujube Mill.) genotypes selected from Turkey. Afr. J. Biotechnol. 2009, 8, 303–307. [Google Scholar]
  50. Li, J.; Liang, S.; Liu, Y.; Fan, L.; Ai, L. Screening of a functional polysaccharide from Zizyphus jujuba cv. Jinsixiaozao and its property. Int. J. Biol. Macromol. 2011, 49, 255–259. [Google Scholar] [CrossRef]
  51. Zhang, H.; Jiang, L.; Shu, Y.; Ye, Y.; Ren, F. Systematic evaluation of antioxidant capacities of the ethanolic extract of different tissues of jujube (Ziziphus jujuba Mill.) from China. Food Chem. Toxicol. 2010, 48, 1461–1465. [Google Scholar] [CrossRef]
  52. Yue, Y.; Wu, S.; Zhang, H.; Zhang, X.; Niu, Y.; Cao, X.; Huang, F.; Ding, H. Characterization and hepatoprotective effect of polysaccharides from Ziziphus jujuba Mill. var. spinosa (Bunge) Hu ex H. F. Chou sarcocarp. Food Chem. Toxicol. 2014, 74, 76–84. [Google Scholar] [CrossRef]
  53. Chen, C.F.; Lee, J.F.; Wang, D.; Shen, C.Y.; Shen, K.-P.; Lin, M. Water extract of Zizyphus jujube attenuates Ischemia/Reperfusion–Induced liver injury in rats (PP106). Transplant. Proc. 2010, 42, 741–743. [Google Scholar] [CrossRef]
  54. Shen, X.; Tang, Y.; Yang, R.; Yu, L.; Tai-Hui, F.; Duan, J.-A. The protective effect of Zizyphus jujube fruit on carbon tetrachloride-induced hepatic injury in mice by anti-oxidative activities. J. Ethnopharmacol. 2009, 122, 555–560. [Google Scholar] [CrossRef]
  55. Chen, J.; Li, Z.; Maiwulanjiang, M.; Zhang, W.L.; Zhan, J.Y.; Lam, C.; Zhu, K.Y.; Yao, P.; Choi, R.C.Y.; Lau, D.T.-W.; et al. Chemical and Biological Assessment of Ziziphus jujuba Fruits from China: Different Geographical Sources and Developmental Stages. J. Agric. Food Chem. 2013, 61, 7315–7324. [Google Scholar] [CrossRef]
  56. Yoo, K.; Li, H.; Hwang, I.K.; Choi, J.H.; Lee, C.H.; Kwon, D.Y.; Ryu, S.Y.; Kim, Y.S.; Kang, I.; Shin, H.-C.; et al. Zizyphus attenuates ischemic damage in the gerbil hippocampus via its antioxidant effect. J. Med. Food 2010, 13, 557–563. [Google Scholar] [CrossRef]
  57. Yu, L.; Jiang, B.; Luo, D.; Shen, X.; Guo, S.; Duan, J.-A.; Tang, Y. Bioactive components in the fruits of Ziziphus jujuba Mill. against the inflammatory irritant action of Euphorbia plants. Phytomedicine 2012, 19, 239–244. [Google Scholar] [CrossRef]
  58. Beg, M.A.; Teotia, U.; Farooq, S. In vitro antibacterial and anticancer activity of Ziziphus. J. Med. Plants Stud. 2016, 4, 230–233. [Google Scholar]
  59. Daneshmand, F.; Zare-Zardini, H.; Ebrahimi, L. Investigation of the antimicrobial activities of Snakin-Z, a new cationic peptide derived from Zizyphus jujuba fruits. Nat. Product. Res. 2013, 27, 2292–2296. [Google Scholar] [CrossRef]
  60. Hong, E.H.; Song, J.; Kang, K.B.; Sung, S.H.; Ko, H.; Yang, H. Anti-Influenza Activity of Betulinic Acid from Zizyphus jujuba on Influenza A/PR/8 Virus. Biomol. Ther. 2015, 23, 345–349. [Google Scholar] [CrossRef] [PubMed]
  61. Kaeidi, A.; Taati, M.; Hajializadeh, Z.; Jahandari, F.; Rashidipour, M. Aqueous extract of Zizyphus jujuba fruit attenuates glucose induced neurotoxicity in an in vitro model of diabetic neuropathy. PubMed 2015, 18, 301–306. [Google Scholar]
  62. Taati, M.; Alirezaei, M.; Moshkatalsadat, M.H.; Rasoulian, B.; Moghadasi, M.; Sheikhzadeh, F.; Sokhtezari, A. Protective effects of Ziziphus jujuba fruit extract against ethanol-induced hippocampal oxidative stress and spatial memory impairment in rats. J. Med. Plants Res. 2011, 5, 915–921. [Google Scholar]
  63. Chen, J.; Yan, A.L.; Lam, K.Y.C.; Lam, C.; Li, N.; Yao, P.; Xiong, A.; Dong, T.; Tsim, K.W.K. A Chemically Standardized Extract of Ziziphus jujuba Fruit (Jujube) Stimulates Expressions of Neurotrophic Factors and Anti-oxidant Enzymes in Cultured Astrocytes. Phytother. Res. 2014, 28, 1727–1730. [Google Scholar] [CrossRef]
  64. Chen, J.; Maiwulanjiang, M.; Lam, K.Y.C.; Zhang, W.L.; Zhan, J.Y.; Lam, C.; Xu, S.L.; Zhu, K.Y.; Yao, P.; Lau, D.T.-W.; et al. A Standardized Extract of the Fruit of Ziziphus jujuba (Jujube) Induces Neuronal Differentiation of Cultured PC12 Cells: A Signaling Mediated by Protein Kinase A. J. Agric. Food Chem. 2014, 62, 1890–1897. [Google Scholar] [CrossRef]
  65. Heo, H.J.; Park, Y.; Suh, Y.-M.; Choi, S.-J.; Kim, M.-J.; Cho, H.-Y.; Chang, Y.-J.; Hong, B.; Kim, H.-K.; Kim, E.; et al. Effects of oleamide on choline acetyltransferase and cognitive activities. Biosci. Biotechnol. Biochem. 2003, 67, 1284–1291. [Google Scholar] [CrossRef]
  66. Zare-Zardini, H.; Tolueinia, B.; Hashemi, A.; Ebrahimi, L.; Fesahat, F. Antioxidant and Cholinesterase Inhibitory Activity of a New Peptide From Ziziphus jujuba Fruits. Am. J. Alzheimer’s Dis. Other Dement. 2013, 28, 702–709. [Google Scholar] [CrossRef]
  67. Pahuja, M.; Mehla, J.; Reeta, K.H.; Joshi, S.; Gupta, Y.K. Hydroalcoholic extract of Zizyphus jujuba ameliorates seizures, oxidative stress, and cognitive impairment in experimental models of epilepsy in rats. Epilepsy Behav. 2011, 21, 356–363. [Google Scholar] [CrossRef]
  68. Pahuja, M.; Kleekal, T.; Reeta, K.H.; Tripathi, M.; Gupta, Y.K. Interaction profile of Zizyphus jujuba with phenytoin, phenobarbitone, and carbamazepine in maximal electroshock-induced seizures in rats. Epilepsy Behav. 2012, 25, 368–373. [Google Scholar] [CrossRef]
  69. Yeung, W.; Chung, K.F.; Poon, M.M.K.; Ho, F.Y.; Zhang, S.P.; Zhang, Z.J.; Ziea, E.; Taam, V.W. Prescription of Chinese Herbal Medicine and Selection of acupoints in Pattern-Based Traditional Chinese Medicine Treatment for Insomnia: A Systematic Review. Evid.-Based Complement. Altern. Med. 2012, 2012, 902578. [Google Scholar] [CrossRef]
  70. Li, M.; Wang, Y. Phamarcological comparison of two Ziziphus jujuba cultivars. J. Chin. Med. Mater. 1993, 16, 35–37. [Google Scholar]
  71. Peng, W.-H.; Hsieh, Μ.-T.; Lee, Y.-S.; Lin, Y.-C.; Liao, J. Anxiolytic effect of seed of Ziziphus jujuba in mouse models of anxiety. J. Ethnopharmacol. 2000, 72, 435–441. [Google Scholar] [CrossRef]
  72. Jiang, J.; Huang, X.; Chen, J.; Lin, Q. Comparison of the sedative and hypnotic effects of flavonoids, saponins, and polysaccharides extracted from Semen Ziziphus jujube. Nat. Product. Res. 2007, 21, 310–320. [Google Scholar] [CrossRef] [PubMed]
  73. Li, B.; Wang, L.; Liu, Y.; Chen, Y.; Zhang, Z.; Zhang, J. Jujube promotes learning and memory in a rat model by increasing estrogen levels in the blood and nitric oxide and acetylcholine levels in the brain. Exp. Ther. Med. 2013, 5, 1755–1759. [Google Scholar] [CrossRef]
  74. Zhang, Y.; Qiao, L.; Song, M.; Wang, L.; Xie, J.; Feng, H. Hplc-ESI-MS/MS analysis of the water-soluble extract from Ziziphi spinosae semen and its ameliorating effect of learning and memory performance in mice. Pharmacogn. Mag. 2014, 10, 509. [Google Scholar] [CrossRef]
  75. Wang, C.; Cheng, D.; Cao, J.; Jiang, W. Antioxidant capacity and chemical constituents of Chinese jujube (Ziziphus jujuba Mill.) at different ripening stages. Food Sci. Biotechnol. 2013, 22, 639–644. [Google Scholar] [CrossRef]
  76. Tanideh, N.; Jamshidzadeh, A.; Saghesloo, A.G.; Rahmanifar, F.; Mokhtari, M.; Koohi-Hosseinabadi, O.; Omidi, M.; Najibi, A. Effects of hydroalcoholic extract of Ziziphus jujuba on acetic acid induced ulcerative colitis in male rat (Rattus norvegicus). J. Coloproctology 2016, 36, 189–195. [Google Scholar] [CrossRef]
  77. Naftali, T.; Feingelernt, H.; Lesin, Y.; Rauchwarger, A.; Konikoff, F.M. Ziziphus jujuba Extract for the Treatment of Chronic Idiopathic Constipation: A Controlled Clinical Trial. Digestion 2008, 78, 224–228. [Google Scholar] [CrossRef]
  78. Periasamy, S.; Liu, C.T.; Wu, W.H.; Chien, S.; Liu, M.Y. Dietary Ziziphus jujuba Fruit Influence on Aberrant Crypt Formation and Blood Cells in Colitis-Associated Colorectal Cancer Mice. Asian Pac. J. Cancer Prev. 2015, 16, 7561–7566. [Google Scholar] [CrossRef]
  79. Yang, Y.J.; Kim, M.J.; Lee, H.J.; Lee, W.; Yang, J.; Kim, H.H.; Shim, M.S.; Heo, J.W.; Son, J.D.; Kim, W.H.; et al. Ziziphus jujuba Miller Ethanol Extract Restores Disrupted Intestinal Barrier Function via Tight Junc-tion Recovery and Reduces Inflammation. Antioxidants 2024, 13, 575. [Google Scholar] [CrossRef]
  80. Ninave, P.B.; Patil, S.D. Antiasthmatic potential of Zizyphus jujuba Mill and Jujuboside B.—Possible role in the treatment of asthma. Respir. Physiol. Neurobiol. 2019, 260, 28–36. [Google Scholar] [CrossRef]
  81. Naik, S.R.; Bhagat, S.; Shah, P.D.; Tare, A.A.; Ingawale, D.K.; Wadekar, R. Evaluation of anti-allergic and anti-anaphylactic activity of ethanolic extract of Zizyphus jujuba fruits in rodents. Rev. Bras. Farmacogn. 2013, 23, 811–818. [Google Scholar] [CrossRef]
  82. Vafaei, F.; Abdollahzadeh, F. Investigating the effects of Hydroalcoholic extract of jujube fruit (Zizyphus vulgaris L.) on second degree burn wound healing in Balb/c mice. PubMed J. Med. Life 2015, 8, 117–120. [Google Scholar]
  83. Pourahmadi, M.; Fathi, M.; Rahimipour, M.; Shaterian, N.; Kargar Jahromi, H. Hydroalcoholic Extract of Ziziphus jujuba Leaf to Prevent Ethylene Glycol and Ammonium Chloride-Induced Kidney Stones in Male Rat: Is it Effective? Urol. J. 2023, 20, 397–402. [Google Scholar] [CrossRef]
  84. Hoshyar, R.; Mohaghegh, Z.; Torabi, N.; Abolghasemi, A. Antitumor activity of aqueous extract of Ziziphus jujube fruit in breast cancer: An in vitro and in vivo study. Asian Pac. J. Reprod. 2015, 4, 116–122. [Google Scholar] [CrossRef]
  85. Hoseinifar, S.H.; Zou, H.K.; Van Doan, H.; Harikrishnan, R.; Yousefi, M.; Paknejad, H.; Ahmadifar, E. Can dietary jujube (Ziziphus jujuba Mill.) fruit extract alter cutaneous mucosal immunity, immune related genes expression in skin and growth performance of common carp (Cyprinus carpio)? Fish. Shellfish. Immunol. 2019, 94, 705–710. [Google Scholar] [CrossRef]
  86. As’adi, N.; Kariman, N. Herbal prevention and treatment of nipple trauma and/or pain in Iranian studies: A systematic review. J. HerbMed Pharmacol. 2018, 7, 168–175. [Google Scholar] [CrossRef]
  87. Miwa, T.K. Structural determination and uses of jujube oil. J. Am. Oil Chem. Soc. 1984, 61, 407–410. [Google Scholar] [CrossRef]
  88. Pazyar, N.; Yaghoobi, R.; Mr, G.; Kazerouni, A.; Rafeie, E.; Jamshydian, N. Jujube in dermatology: A succinct review. PubMed 2013, 148, 687–691. [Google Scholar]
  89. Wunderlin, R.P. Guide to the vascular plants of central Florida. Brittonia 1983, 35, 308. [Google Scholar] [CrossRef]
  90. Ashour, M.L.; Ayoub, N.; Singab, A.N.B.; Azizi, M.M.A. Simmondsia chinensis (Jujube): A Comprehensive Pharmacognostic Study. J. Pharmacogn. Phytochem. 2013, 2, 97–120. [Google Scholar]
  91. Schwarz, J.S.; Weisspapir, M.R.; Shani, A.; Amselem, S. Enhanced antiinflammatory activity of diclofenac in jojoba oil submicron emulsion cream. J. Appl. Cosmetol. 1996, 14, 19–24. [Google Scholar]
  92. Archana, C.; Amaldoss, M.J.N. Synthesis and Characterization of Valacyclovir HCl Hybrid Solid Lipid Nanoparticles by Using Natural Oils. Recent. Pat. Drug Deliv. Formul. 2019, 13, 46–61. [Google Scholar] [CrossRef]
  93. Nasr, M.; Abdel-Hamid, S.; Mofath, N.H.; Fadel, M.; Alyoussef, A.A. Jojoba Oil Soft Colloidal Nanocarrier of a Synthetic Retinoid: Preparation, Characterization and Clinical Efficacy in Psoriatic Patients. Curr. Drug Deliv. 2017, 14, 426–432. [Google Scholar] [CrossRef] [PubMed]
  94. Lee, N.K.; Shin, H.J.; Kim, W.-S.; In, G.; Han, C.K. Studies on the Chemical Constituents from the Seeds of Zizyphus jujuba var. inermis. Nat. Product. Sci. 2017, 23, 258–264. [Google Scholar] [CrossRef]
  95. Elaloui, M.; Laamouri, A.; Albouchi, A.; Cerny, M.; Mathieu, C.; Vilarem, G.; Hasnaoui, B. Chemical compositions of the Tunisian Ziziphus jujuba oil. Emir. J. Food Agric. 2014, 26, 602–608. [Google Scholar] [CrossRef]
  96. Abd-Alrahman, S.H.; Salem-Bekhit, M.M.; Elhalwagy, M.E. Chemical composition and an-timicrobial activity of Ziziphus jujuba seeds extract. J. Pure Appl. Microbiol. 2013, 7, 379–385. [Google Scholar]
  97. Krška, B.; Mishra, S. Sensory evaluation of different products of Ziziphus jujuba Mill. Acta Hortic. 2009, 840, 557–562. [Google Scholar] [CrossRef]
  98. Rashwan, A.K.; Karim, N.; Shishir, M.R.I.; Bao, T.; Yang, L.; Chen, W. Jujube fruit: A potential nutritious fruit for the development of functional food products. J. Funct. Foods 2020, 75, 104205. [Google Scholar] [CrossRef]
  99. Djilali, A.B.; Mohamed, N.; Gelicus, A.; Salem, B.; Allaf, K. Evaluation of Physical-Chemical, pharmacodynamic and pharmacological attributes of hot air dried and swell dried jujube powders. J. Food Process Eng. 2016, 40, e12364. [Google Scholar] [CrossRef]
  100. Jeong, O.; Kim, H. Dietary chokeberry and dried jujube fruit attenuates high-fat and high-fructose diet-induced dyslipidemia and insulin resistance via activation of the IRS-1/PI3K/Akt pathway in C57BL/6 J mice. Nutr. Metab. 2019, 16, 38. [Google Scholar] [CrossRef]
  101. Najjaa, H.; Ben Arfa, A.; Elfalleh, W.; Zouari, N.; Neffati, M. Jujube (Zizyphus lotus L.): Benefits and its effects on functional and sensory properties of sponge cake. Indian. Agric. Res. Inst. 2020, 15, e0227996. [Google Scholar] [CrossRef]
  102. Wang, L.; Jing, N.; Liu, X.; Jiang, G.; Liu, Z. Nurturing and modulating gut microbiota with jujube powder to enhance anti-PD-1 efficiency against murine colon cancer. J. Funct. Foods 2020, 64, 103647. [Google Scholar] [CrossRef]
  103. Entani, E.; Asai, M.; Tsujihata, S.; Tsukamoto, Y.; Ohta, M. Antibacterial Action of Vinegar against Food-Borne Pathogenic Bacteria Including Escherichia coliO157:H7. J. Food Prot. 1998, 61, 953–959. [Google Scholar] [CrossRef] [PubMed]
  104. Hua, Z.; Lu, Y.; Lu, Z.; Cao, M. Changes of main components and antioxidant properties during jujube vinegar fermentation. J. Chin. Inst. Food Sci. Technol. 2013, 13, 248–253. [Google Scholar]
  105. Vithlani, V.A.; Patel, H.V. Production of functional vinegar from Indian jujube (Zizyphus mauritiana) and its antioxidant properties. J. Food Technol. 2010, 8, 143–149. [Google Scholar]
  106. Cai, H.; Zhang, Q.; Shen, L.; Luo, J.; Zhu, R.; Mao, J.; Zhao, M.; Cai, C. Phenolic profile and antioxidant activity of Chinese rice wine fermented with different rice materials and starters. LWT 2019, 111, 226–234. [Google Scholar] [CrossRef]
  107. Jin, Z.; Sun, H.; Sun, T.; Wang, Q.; Yao, Y. Modifications of ‘Gold Finger’ Grape Berry Quality as Affected by the Different Rootstocks. J. Agric. Food Chem. 2016, 64, 4189–4197. [Google Scholar] [CrossRef]
  108. Xu, K.; Xu, K. Quality evaluation of Chinese red wine based on cloud model. J. Food Biochem. 2019, 43, e12787. [Google Scholar] [CrossRef]
  109. Zhao, M.-N.; Zhang, F.; Zhang, L.; Liu, B.-J.; Meng, X.-H. Mixed fermentation of jujube juice (Ziziphus jujuba Mill.) with L. rhamnosus GG and L. plantarum-1: Effects on the quality and stability. Inst. Food Sci. Technol. 2019, 54, 2624–2631. [Google Scholar] [CrossRef]
  110. Zhang, W.; Zhang, L.; Xu, C. Chemical and volatile composition of jujube wines fermented by Saccharomyces cerevisiae with and without pulp contact and protease treatment. Food Sci. Technol. 2016, 36, 204–209. [Google Scholar] [CrossRef]
  111. Zhao, Z.; Li, S.J.; Zhao, J.; Dai, L.; Liu, P.; Liu, M.J. Selection of Chinese jujube cultivars for juice processing based on theory of satisfaction and multidimensional matrix. Acta Hortic. 2016, 1116, 61–64. [Google Scholar] [CrossRef]
  112. Zozio, S.; Servent, A.; Cazal, G.; MbéguiéAMbéguié, D.; Ravion, S.; Pallet, D.; Hiol, A. Changes in antioxidant activity during the ripening of jujube (Ziziphus mauritiana Lamk). Food Chem. 2014, 150, 448–456. [Google Scholar] [CrossRef] [PubMed]
  113. Shin, Y.U.; Yun, Y.; Kim, T.C.; Kim, Y.S.; Lee, K.K. A study on the processing suitability of pear and Chinese jujube cultivars. Res. Rep. Rural. Dev. Adm. Farm. Manag. Agric. Eng. Seric. Farm. Prod. Util. 1992, 34, 58–65. [Google Scholar]
  114. Uddin, M.B.; Hussain, I. Development of Diversified Technology for Jujube (Ziziphus jujuba L.) Processing and Preservation. World J. Dairy. Food Sci. 2012, 7, 74–78. [Google Scholar]
  115. Wang, R.; Ding, S.; Zhao, D.; Wang, Z.; Wu, J.; Hu, X. Effect of dehydration methods on antioxidant activities, phenolic contents, cyclic nucleotides, and volatiles of jujube fruits. Food Sci. Biotechnol. 2016, 25, 137–143. [Google Scholar] [CrossRef]
  116. Wojdyło, A.; Figiel, A.; Legua, P.; Lech, K.; Carbonell-Barrachina, Á.A.; Hernández, F. Chemical composition, antioxidant capacity, and sensory quality of dried jujube fruits as affected by cultivar and drying method. Food Chem. 2016, 207, 170–179. [Google Scholar] [CrossRef]
  117. Wojdyło, A.; Lech, K.; Nowicka, P.; Hernández, F.; Figiel, A.; Carbonell-Barrachina, Á.A. Influence of Different Drying Techniques on Phenolic Compounds, Antioxidant Capacity and Colour of Ziziphus jujube Mill. Fruits. Molecules 2019, 24, 2361. [Google Scholar] [CrossRef] [PubMed]
  118. Liu, Y.H.; Zhao, Q.X. Studies on the fermentation technics of dry wild jujube wine. Adv. Mater. Res. 2011, 236–238, 2951–2956. [Google Scholar] [CrossRef]
  119. Zhao, Z.Y.; Jams, J. Jellyproducts. In Specialty Foods: Processing Technology, Quality, and Safety, 1st ed.; Zhao, Y., Ed.; CRC Press LLC; Taylor & Francis Group: Boca Raton, FL, USA, 2012; pp. 135–156. [Google Scholar]
  120. Fazio, A.; La Torre, C.; Caroleo, M.C.; Caputo, P.; Cannataro, R.; Plastina, P.; Cione, E. Effect of Addition of Pectins from Jujubes (Ziziphus jujuba Mill.) on Vitamin C Production during Heterolactic Fermentation. Molecules 2020, 25, 2706. [Google Scholar] [CrossRef] [PubMed]
  121. Rashidi, H.; Azarpazhooh, E.; Shagholi, R. The potential of jujube in the production of functional food products. Technol. Med. Aromat. Plants Iran. 2024, 5, 13–24. [Google Scholar] [CrossRef]
  122. Song, J.; Liu, J.; Wang, K.; Gao, L.; Wang, X.; Peng, J.; Wang, N. Effect of jujube powder addition on the aroma profile of quinoa snacks (QS). Food Sci. Nutr. 2024, 12, 4810–4818. [Google Scholar] [CrossRef] [PubMed]
  123. Bae, G.Y.; Ahn, Y.; Hong, K.B.; Jung, E.J.; Suh, H.J.; Jo, K. Sleep-enhancing effect of water extract from jujube (Zizyphus jujuba Mill.) seeds fermented by Lactobacillus brevis L32. Foods 2023, 12, 2864. [Google Scholar] [CrossRef] [PubMed]
  124. Feng, C.; Wang, B.; Zhao, A.; Wei, L.; Shao, Y.; Wang, Y. Quality characteristics and antioxidant activities of goat milk yogurt with added jujube pulp. Food Chem. 2019, 277, 238–245. [Google Scholar] [CrossRef] [PubMed]
  125. Wang, W.; Jia, R.; Hui, Y.; Zhang, F.; Zhang, L.; Liu, Y. Utilization of two plant polysaccharides to improve fresh goat milk cheese: Texture, rheological properties, and microstructure characterization. J. Dairy. Sci. 2023, 106, 3900–3917. [Google Scholar] [CrossRef] [PubMed]
  126. Song, W.; Liu, L.L.; Ren, Y.J.; Wei, S.D.; Yang, H.B. Inhibitory effects and molecular mechanism on mushroom tyrosinase by condensed tannins isolation from the fruit of Ziziphus jujuba Mill. var. Spinosa (Bunge) Hu ex H. F. Chow. Int. J. Biol. Macromol. 2020, 165, 1813–1821. [Google Scholar] [CrossRef] [PubMed]
  127. Gavahian, M.; Chu, Y.-H.; Farahnaky, A. Effects of ohmic and microwave cooking on textural softening and physical properties of rice. J. Food Eng. 2019, 243, 114–124. [Google Scholar] [CrossRef]
  128. Gavahian, M.; Mathad, G.N.; Pandiselvam, R.; Lin, J.; Sun, D.W. Emerging technologies to obtain pectin from food processing by-products: A strategy for enhancing resource efficiency. Trends Food Sci. Technol. 2021, 115, 42–54. [Google Scholar] [CrossRef]
  129. Guediri, A.; Bouguettoucha, A.; Tahraoui, H.; Chebli, D.; Zhang, J.; Amrane, A.; Khezami, L.; Assadi, A.A. The Enhanced Adsorption Capacity of Ziziphus jujuba Stones Modified with Ortho-Phosphoric Acid for Organic Dye Removal: A Gaussian Process Regression Approach. Water 2024, 16, 1208. [Google Scholar] [CrossRef]
  130. Qin, N.; Li, Y.; Zhang, L.; Guo, L.; Zhang, W.; Li, G.; Bai, J. Effects of mixed enzymolysis alone or combined with acetylation or carboxymethylation on the role of jujube kernel fibre as a biosorbent for wastewater treatment. RSC Adv. 2024, 14, 23037–23047. [Google Scholar] [CrossRef]
  131. Gavade, N.; Kadam, A.; Suwarnkar, M.; Ghodake, V.; Garadkar, K. Biogenic synthesis of multi-applicative silver nanoparticles by using Ziziphus jujuba leaf ex-tract. Spectrochim. Acta Part. A Mol. Biomol. Spectrosc. 2015, 136, 953–960. [Google Scholar] [CrossRef]
  132. Kandavalli, S.; Sundramurthy, V.; Krishnasamy, V.; Prasad, G.; Kasi, U.; Rajesh, S.; Rajesh Kumar, B.; Selvaraju, M.; Kadaikunnan, S.; Khaled, J. Bioresin based hybrid green composite preparation using Holoptelea integrifolia fibers reinforced by Ziziphus jujube seed particles: A fuzzy logic assisted optimization of mechanical behaviour. Z. Für Phys. Chem. 2024. [Google Scholar] [CrossRef]
  133. Kandasamy, S.K.; Ramyea, R.; Chandrasekaran, A.; Sruthi, V.; Sudharsan, M.; Sugan Raj, R.; Monika, M. Highly Carbonized, Porous Activated Carbon Derived from Ziziphus jujuba for Energy Storage. In Advances in Clean. Energy and Sustainability. ICAER 2022. Green. Energy and Technology; Doolla, S., Rather, Z.H., Ra-madesigan, V., Eds.; Springer: Singapore, 2022. [Google Scholar] [CrossRef]
  134. Eroglu, M.; Ciftci, M.; Simsek, U.G.; Akarsu, S.; Arslan, S.; Hames, M.A.; Mutlu, M. Effect of dietary supplementation of jujube fruit (Ziziphus jujuba) powder on performance, some biochemical parameters, and egg quality in quails (Coturnix coturnix japonica). Pol. J. Vet. Sci. 2024, 27, 211–220. [Google Scholar] [CrossRef]
Figure 1. Main chemical compounds in different parts of Z. jujuba [17,21,30,31,32,33,34,35].
Figure 1. Main chemical compounds in different parts of Z. jujuba [17,21,30,31,32,33,34,35].
Plants 13 02724 g001
Figure 2. Structural formulas of the main chemical components in Z. jujuba applications in pharmacology.
Figure 2. Structural formulas of the main chemical components in Z. jujuba applications in pharmacology.
Plants 13 02724 g002aPlants 13 02724 g002bPlants 13 02724 g002c
Figure 3. Pharmaceutical forms containing jujube oil [91,92,93].
Figure 3. Pharmaceutical forms containing jujube oil [91,92,93].
Plants 13 02724 g003
Table 1. Sugar content of fruits from Ziziphus jujuba from different parts of the world.
Table 1. Sugar content of fruits from Ziziphus jujuba from different parts of the world.
CountryType of SugarValueReference
ChinaFructose(3.24–8.66), g/100 g fw[36]
Glucose(2.97–8.44), g/100 g fw[36]
Sucrose(16.39–25.8), g/100 g fw[36]
SpainFructose(4.8–5.7), g/100 mL[37]
Glucose(3.0–3.9), g/100 mL[37]
Sucrose(1.6–9.4), g/100 mL[37]
ItalyFructose* (0.43–0.63), g/100 g fw[38]
** 0.81, g/100 g fw
Glucose* (2.35–3.35), g/100 g fw[38]
** 3.28, g/100 g fw
Sucrose* (0.97–1.38), g/100 g fw[38]
** 0.22, g/100 g fw
* Organic Crop System; ** Wild System.
Table 2. Nutritional composition of fruits from Ziziphus jujuba from different parts of the world.
Table 2. Nutritional composition of fruits from Ziziphus jujuba from different parts of the world.
Type of NutrientCountryValueReference
LipidsSenegal(1.3–2.5), g/100 g[39]
Slovenia2.5 g/100 g[40]
Iran(0.40–0.72), g/100 g[41]
Turkey(0.05–0.1) g/100 g[42]
Italy(0.02–0.04), g/100 g *[38]
0.03 g/100 g/100 g **
ProteinsIran(3.24–3.92), g/100 g[41]
China(1.87–3.97), g/100 g[36]
Senegal(1.7–6.9), g/100 g[39]
Italy(0.29–0.40), g/100 g *[38]
0.26 g/100 g **
CarbohydratesItaly* (21.55–31.74), g/100 g fw[38]
** 24.79, g/100 g fw
** 0.22, g/100 g fw
* Organic Crop System; ** Wild System.
Table 3. Elements composition of fruits from Ziziphus jujuba from different parts of the world.
Table 3. Elements composition of fruits from Ziziphus jujuba from different parts of the world.
Type of NutrientCountryValueReference
CalciumSenegal(0.76–4.88), g/kg[39]
Slovenia1.77 g/kg[40]
Spain(0.23–0.72), g/kg[37]
Italy(0.056–0.27), g/kg *[38]
0.065 g/ kg **
PotassiumItaly(0.90–2.26), g/kg *[38]
1.20 g/ kg **
China(2.066–7.183) g/kg[43]
Slovenia8.29, g/kg[40]
Spain(11.9–13.8), g/100 g *[37]
SodiumItaly(0.0392–0.0962), g/kg *[38]
0.043 g/ kg **
China(0.00378–0.375), g/kg[43]
Slovenia1.77, g/kg[40]
Spain(0.11–0.43), g/kg *[37]
MagnesiumChina(0.147–0.400), g/kg[43]
Senegal(0.21–1.37), g/ kg[39]
Italy(0.0811–0.197), g/ k *[40]
0.0748 g/kg **
* Organic Crop System; ** Wild System.
Table 4. Bioactive components of the jujube fruits.
Table 4. Bioactive components of the jujube fruits.
CountryType of Bioactive ComponentsValueReference
SpainCitric acid(0.3–0.77), g/100 mL[37]
Ascorbic acid(0.41–0.64), g/100 mL[37]
Carotenoids(0.22–0.39), mg/100 g fw[44]
Total Chlorophyl(0.29–0.51), mg/100 g fw[44]
Total antioxidant activity ABTS(31.30–51.07), mM Trolox/kg fw[44]
Total antioxidant activity DPPH(199.81–322.15), mM Trolox/kg fw[44]
Total antioxidant activity FRAP(52.21–109.87), mM Trolox/kg fw[44]
UkraineCarotenoids(1.53–14.31), μg/g[45]
Total Polyphenol content(8.76–21.61), mg GAE/g[45]
Total Flavonoids content(1.49–11.59), μg QE/g[45]
Total antioxidant activity DPPH(11.18–16.82), mg TEAC/g[45]
TurkeyBeta-carotene(7.00–35.00), μg/100 g[42]
ItalyTotal antioxidant capacity* (213.74–241.31), μM ET/100 g fw[38]
** 243.14, μM ET/100 g fw
Total Polyphenols* (480,83–630,81), mg EGA/100 g fw[38]
** 520.71, mg EGA/100 g fw
Ascorbic acid* (288.10–441.13), mg/100 g fw[38]
** 303.06, mg/100 g fw
** 0.22, g/100 g fw
* Organic Crop System; ** Wild System.
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Popstoyanova, D.; Gerasimova, A.; Gentscheva, G.; Nikolova, S.; Gavrilova, A.; Nikolova, K. Ziziphus jujuba: Applications in the Pharmacy and Food Industry. Plants 2024, 13, 2724. https://doi.org/10.3390/plants13192724

AMA Style

Popstoyanova D, Gerasimova A, Gentscheva G, Nikolova S, Gavrilova A, Nikolova K. Ziziphus jujuba: Applications in the Pharmacy and Food Industry. Plants. 2024; 13(19):2724. https://doi.org/10.3390/plants13192724

Chicago/Turabian Style

Popstoyanova, Desislava, Anelia Gerasimova, Galia Gentscheva, Stoyanka Nikolova, Anna Gavrilova, and Krastena Nikolova. 2024. "Ziziphus jujuba: Applications in the Pharmacy and Food Industry" Plants 13, no. 19: 2724. https://doi.org/10.3390/plants13192724

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Article metric data becomes available approximately 24 hours after publication online.
Back to TopTop