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Review

Bioactive Compounds from Cocoa Husk: Extraction, Analysis and Applications in Food Production Chain

1
Department of Drug Science and Technology, University of Turin, Via P. Giuria 9, 10125 Turin, Italy
2
GREEN Extraction Team, INRAE, UMR 408, Avignon University, F-84000 Avignon, France
3
Research Group for Advanced Materials & Sustainable Catalysis (AMSC), State Key Laboratory Breeding Base of Green Chemistry-Synthesis Technology, College of Chemical Engineering, Zhejiang University of Technology, Hangzhou 310014, China
4
Amity Institute of Food Technology, Amity University, Noida 201303, India
5
World-Class Research Center “Digital Biodesign and Personalized Healthcare”, Sechenov First Moscow State Medical University, 119146 Moscow, Russia
*
Author to whom correspondence should be addressed.
Foods 2022, 11(6), 798; https://doi.org/10.3390/foods11060798
Submission received: 6 February 2022 / Revised: 28 February 2022 / Accepted: 8 March 2022 / Published: 10 March 2022

Abstract

:
Cocoa husk is considered a waste product after cocoa processing and creates environmental issues. These waste products are rich in polyphenols, methylxanthine, dietary fibers, and phytosterols, which can be extracted and utilized in various food and health products. Cocoa beans represent only 32–34% of fruit weight. Various extraction methods were implemented for the preparation of extracts and/or the recovery of bioactive compounds. Besides conventional extraction methods, various studies have been conducted using advanced extraction methods, including microwave-assisted extraction (MAE), ultrasonic-assisted extraction (UAE), subcritical water extraction (SWE), supercritical fluid extraction (SFE), and pressurized liquid extraction (PLE). To include cocoa husk waste products or extracts in different food products, various functional foods such as bakery products, jam, chocolate, beverage, and sausage were prepared. This review mainly focused on the composition and functional characteristics of cocoa husk waste products and their utilization in different food products. Moreover, recommendations were made for the complete utilization of these waste products and their involvement in the circular economy.

Graphical Abstract

1. Introduction

Cocoa is one of the most utilized plant products in chocolates, snacks, and beverages. The annual production of cocoa was about 4.72 million tons in the year 2020, with an expected sale of around USD 20 billion in 2021 [1]. By the year 2025, the cocoa market is expected to grow at a compound annual growth rate (CAGR) of 7.33%. During cocoa processing, various byproducts including cocoa bean husk, cocoa shell, and pulp are generated, which is estimated to be 85% of the cocoa production [2]. If left behind, these waste products create pollution and economical losses [3]. The environmental impact of cocoa pod waste is related to methane and carbon dioxide generation by bacterial degradation; moreover, disposed of by-products can propagate diseases causing significant crop losses. The cocoa industry produces waste which causes environmental and ecological issues and which poses challenges for its proper utilization into the circular economy [4]. Unfortunately, considering the growing demand and utilization of cocoa products, this waste is generated at a larger proportion.
The cocoa waste products have been investigated and found to contain various bioactive compounds, including dietary fiber, polyphenols, pectin, methylxanthine, fat, and phytosterols [5]. The cocoa waste extract/fractions were tested and found effective in mitigating several disease conditions, including diabetes, hypercholesterolemia, hypertension, and inflammation [6]. To improve the extract quality, various advanced extraction methods were carried out in the last decades. These mainly include, ultrasonics, supercritical CO2, microwaves, pressurized liquid extraction, and subcritical water extraction. Moreover, efforts have been made to create greener processes by replacing organic solvents with green solvents (deep eutectic solvents, water, CO2). The cocoa waste extract/powder was also utilized to add value to various food products (cake, chocolate, beverages, etc.) and improve their physicochemical and functional properties. To utilize these cocoa waste products in a green circular economy concept, a greener processing strategy is expected. The development of greener technology allows for the recovery of valuable compounds from these wastes in a green and sustainable manner, thereby providing a direct way to utilize them in food products.
Over the last decade, several investigations have been conducted to extract all the bioactive compounds to be applied in food products [4]. The present review will discuss the recent advances in the extraction of bioactive compounds and their utilization in the food production chain. Moreover, the recommendations were made on the complete utilization of cocoa waste (as a raw material and after processing), which could be adopted for the circular economy concept.

2. Bioactive Compounds Extraction from Cocoa Bean Husk

Waste material generated during production includes cocoa pod husk, pulp, and cocoa bean shells. Dietary fiber, polyphenols, methylxanthines, phytosterols are some of the major compounds extracted from cocoa pod husks or cocoa shells (Figure 1). In recent decades, these compounds have been extracted using advanced/green extraction technologies and tested for their application in food products (Table 1).
Pectins are natural polymers used for a variety of applications, including emulsifiers, gelling agents, thickeners, stabilizers, and fat or sugar replacers [30]. In a study, pectin from cocoa pod husk was analyzed to determine its physicochemical and antimicrobial activity [7]. The pectin was extracted using aqueous citric acid (4% w/v) followed by precipitation of extract using ethanol. A pectin yield of 23.3% was obtained with a degree of esterification of 26.8% and showed good physicochemical properties. The pectin was characterized as highly acetylated low-methoxy pectin having rich mineral contents. The obtained product also showed high antimicrobial activity against E. coli and S. aureus. In another study, the effect of extraction conditions on pectin yield from cocoa husk was investigated [8]. Various solvents including water, citric acid (pH 2.5, 4), and hydrochloric acid (pH 2.5, 4) were investigated. It was found that temperature, time, and sample-to-solvent ratio affected the pectin yield. As such, the highest yield of pectin (7.62%) was obtained using citric acid (pH 2.5) as a solvent, an extraction temperature of 95 °C for 3 h, and a sample-to-solvent ratio of 1:25.
Citric acid is mostly used for extracting pectin. However, the use of nitric acid, oxalic acid, and ascorbic acid-based extraction of pectin from cocoa pod husk has also been reported. As such, using nitric acid-based extraction of pectin from cocoa pod husk, it was found that increasing the temperature increased the extraction yield [9]. The optimum extraction condition was a pH of 1.5, extraction temperature of 100 °C, and extraction time of 30 min. Oxalic acid-based extraction under microwave radiation conditions was intended to separate pectin from cocoa pod husk. It was found that a higher oxalic acid concentration, lower pH, and irradiation time increased pectin yield. Moreover, under microwave conditions, the extraction time was shorter than the conventional extraction [10]. Ascorbic acid-based extraction of pectin from cocoa pod husk was carried out. The optimum condition was pH 2.5, 95 °C, for 45 min of extraction time [11].

2.1. Microwave-Assisted Extraction

The use of microwave technology for extracting bioactive compounds has been tremendously increased due to its commercial applications and advances [31]. As such, the use of microwave technology for extracting bioactive compounds from cocoa husk pods has also been investigated over the last two decades. In another study, microwave-assisted extraction (MAE) of the cocoa bean shell was carried out to obtain polyphenol and polysaccharide fractions which were used to produce pectin-based films [19]. The film was prepared using pectin and cocoa bean shells, and ZnO/Zn nanoparticles were added to improve the thermal, barrier, structural, morphological, and optical properties of the film. The obtained biofilm prepared by the pectin–cocoa bean shell extract–ZnO/Zn nanoparticles showed greater UV and oxygen barrier properties and thus can be used for active packaging for increasing the shelf-life of food products.
Anthocyanins are polyphenolic compounds known for their color properties and health effects [32]. Anthocyanin was extracted from cocoa peel using MAE and factors such as extraction time, microwave power, particle size, and sample-to-solvent ratio were investigated using response surface methodology [20]. The highest yield of anthocyanin obtained from MAE was 1.435 mM under the optimum condition of particle size (60 mesh), sample-to-solvent ratio (0.0625 w/v), extraction time (10 min), and microwave power (450 W).
Phytosterols play an important role in maintaining health and mitigating several disease conditions [33]. As such, their extraction from plants has been largely focused on obtaining and utilizing them for various health products [34]. In an attempt, the optimum extraction conditions for β-sitosterol (a phytosterol) from cocoa shells were determined under MAE conditions using absolute ethanol [21]. The effect of temperature, microwave power, and radiation time was determined, and the optimum extraction condition was recorded as 70 °C, 500 W, and 10 min, respectively. The β-sitosterol yield under optimum extraction conditions was recoded as 3546.1 mg/100 g, which was 13% higher than the yield obtained using the conventional maceration. Catechin was also extracted from cocoa husk waste using MAE [17]. The MAE temperature was set at 70 °C, and the cocoa waste was extracted with ethanol at a ratio of 3:100 g/mL under varying extraction times (4, 6, 8, and 10 min). It was found that a longer extraction time of 8 and 10 min produces a higher extraction yield of total phenolic content and total catechin content.
The phenolic antioxidant compounds extracted under MAE conditions showed high antioxidant activity [19]. The optimum extraction condition was an extraction time of 5 min, pH of 12, a temperature of 97 °C, and a sample-to-solvent ratio of 0.04 g/L. Moreover, pH played an important role and an alkaline pH promoted the extraction of compounds. At a high pH value, the extract was rich in protein, polysaccharides, and polyphenols, and had high antioxidant activity.

2.2. Water Extraction

Green extraction technology with minimum utilization of energy, time, resources, and free from organic solvents is considered an environmentally friendly and sustainable solution [35]. Green extraction of phenolics from cocoa husk powder using water as a solvent was carried out using heat-assisted extraction [16]. Factors such as extraction temperature, time, acidity, and sample-to-solvent ratio were optimized. The highest extraction yield for total phenolic compounds, total flavonoids, total flavanols, total phenolic acids, total proanthocyanidins, total ortho-diphenols, and antioxidant activity was recorded at 100 °C, 90 min, 0% citric acid, and 0.02 g cocoa shell/mL of water. The compounds reported in the extract are hydroxybenzoic acid, hydroxycinnamic acid, mandelic acid, phenylacetic acid, flavan-3-ols (monomers/dimers), flavonols. Moreover, the water extract was compared with the organic extract, and it was found that most of the compounds were extracted in the water. As such, quercetin 3-O galactoside, quercetin 3-O-glucoside, procyanidin B2, procyanidin B1, (+)- catechin, and (−)-epicatechin were recorded in higher concentrations. In addition, compounds such as mandelic acid, 3,4-dihydroxyphenylacetic acid, and 4-hydroxyphenylacetic acid were recorded only in the water extract.

2.3. Extraction in Supercritical CO2

Fat and methylxanthines (theobromine and caffeine) were extracted from cocoa shells using supercritical CO2 [23]. Pressure (2000–6000 psi), temperature (313–333 K), and time (30–90 min) were varied to obtain the optimum extraction condition. It was found that the fat yield is around 94.73% (which is the most effective extraction), while for caffeine the extraction yield is about 90%; however, theobromine could not be extracted under optimum supercritical CO2 extraction conditions (6000 psi, 313 K, 90 min) due to low solubility.
Dietary fiber plays an important role in human health and metabolism [36] and was extracted from cocoa shells using high voltage electric discharge conditions [24]. It was found that the high-voltage electrical discharge condition had a significant impact on the physical properties of the dietary fiber. Furthermore, it increased the fiber content, grinding ability, and water-binding capacity. It was also observed that the tannin content changed during the high voltage discharge treatment, which had a significant impact on the fiber pretreatment and resulted in a more undigested sample. Supercritical fluid extraction was conducted to extract polyphenols from the cocoa husk. The particle size, extraction temperature, time, pressure, and ethanol concentration were optimized. The results showed a particle size of less than 0.26 mm, extraction time of 147 min, extraction temperature of 308.15 K, and pressure of 20 MPa; moreover, 20% of ethanol increased TPC, total flavon-3-oles, and total carotenoids content [13]. Supercritical CO2 extraction was found to increase the phenolic compounds’ extraction and antioxidant activity using ethanol as a co-solvent under the optimal extraction condition of 60 °C, 299 bar, and 13.7% ethanol concentration [37]. The combined effect of supercritical fluid extraction and pressurized liquid extraction (using ethanol) on the antioxidant compounds’ extraction from cocoa bean hulls was investigated. It was found that a higher phenolic content and antioxidant activity were recorded under the combined extraction process compared to the individual extraction process [29].

2.4. Subcritical Water Extraction

Subcritical water extraction is one of the recent advances in extraction technologies and is considered green [38]. It changes the properties of water by varying the temperature and pressure, thereby affecting solubility, mass transfer, and extraction capacity. Various factors, such as temperature, time, and sample to solvent ratio were varied from 120–220 °C, 15–75 min, and 1:10–1:30 g/mL to obtain very high-end products [25]. Various compounds were detected under optimum extraction conditions (temperature 170 °C, time 75 min, sample to solvent ratio 1:20). These include theobromine, caffeine, theophylline, gallic acid, epicatechin, catechin, chlorogenic acid, and total phenols. Moreover, other chemical molecules, such as mannose, glucose, xylose, arabinose, rhamnose, and fructose, and 5-hydroxy methylfurfural, furfural, levulinic acid, and formic acid were detected. In another study, phenolics from cocoa bean shell was extracted using subcritical water and then encapsulated with maltodextrin and whey protein using a spray drying technique [26]. The SWE was carried out at a temperature of 150 °C with an extraction pressure of 30 bar for 15 min. It was found that whey protein protects the phenolic content resulting in a higher content of gallic acid, caffeine, and theobromine as compared to maltodextrin. Using subcritical water extraction technology, pectin was extracted from cocoa pod husk at a higher yield as compared to citric acid-based extraction [15].

2.5. Ultrasound-Assisted Extraction

Ultrasound-assisted extraction of flavonoids from cocoa shells was introduced to determine the optimum extraction conditions [22]. Ethanol concentration (70–90%), temperature (45–65 °C), and irradiation time (30–60 min) were optimized. The highest total flavonoid yield was obtained as 7.47 mg RE/g dw at 80% ethanol, 55 °C, and 45 min of time.
The pressurized liquid extraction method was used to obtain the ethanolic extract of cocoa bean shells containing flavonoids and alkaloids. With variation in temperature and extraction time, the extraction yield of the compounds was affected. As such, by increasing the extraction temperature and time, the flavonoid and alkaloid extraction increased, while the procyanidins B2 degraded. It was interesting to note that the lyophilized extract showed higher flavonoids (catechin, epicatechin, procyanidin B2) and alkaloid (theobromine, caffeine) content as compared to the dried cocoa shell powder extract [18].

2.6. Conditions and Solvents Optimization

The particle size of a plant sample for extraction is usually ignored. In one study, the impact of cocoa bean shell particle size was tested on the physicochemical, bioactive compounds, and antioxidant activity [28]. Three particle sizes were considered, i.e., high (Dp > 701 um), intermediate (417 um< Dp < 701 um), and lowest (Dp < 417 um). It was found that as the particle size reduced, the extraction efficiency for dietary fiber (65.58 g/100 g), polyphenolic compounds (epicatechin, 6.33 mg/g; catechin, 4.58 mg/g), and methylxanthine (theobromine, 12.77 mg/g; caffeine, 6.13 mg/g) was increased.
The effect of solvents on the extraction of bioactive compounds from cocoa waste was also studied [12]. In an attempt, the theobromine-rich extract was prepared by varying the solvents (water, chloroform, and 70% ethanol), extraction time (30, 60, and 90 min), and the number of extraction cycles (1 or 2). The optimal extraction condition for the maximum theobromine yield (6.79 mg/100 g) was found as 70% ethanol, extraction time of 90 min, temperature of 80 °C, and 1 cycle of extraction. Alcoholic solvents under atmospheric pressure were used to extract the bioactive compounds and fat content. Two solvents, ethanol and isopropanol, were used at 75 °C and 90 °C, respectively. The fat content was obtained in the range of 3–70% with absolute solvents. Hydrated alcohol was found to be suitable for extracting bioactive compounds, especially for alkaloids (73% yield) [39]. In another study, the different phytochemicals from the cocoa husk and cocoa bean were analyzed [40]. In the cocoa husk, a high content of phenolic acid was recorded, while in the cocoa bean, a high content of flavonoids was recorded. A total of 49 compounds were detected.
Deep eutectic solvent (DES) is a new class of green, non-flammable solvents typically formed by mixing choline chloride with hydrogen bond donors [41]. Deep eutectic solvents (DESs) have been used to extract bioactive compounds from cocoa shells. In one study, MAE was performed using DES for extracting bioactive compounds from cocoa shells [27]. The yield of the compounds in DES was lower than DES/MAE. For instance, the yield of theobromine was 2.5–5.0 mg/g under DES/MAE, while under DES it was 2.1 to 4.6 mg/g. Similarly, for caffeine, it was 0.778–1.599 mg/g in DES/MAE, while it was 0.68–1.52 mg/g under DES; however, the DPPH antioxidant activity was lower in DES/MAE compared to DES. It was found that the water content in different choline chloride-based DES influences the oxidation, while the extraction time and temperature showed no significant impact. Heat-stirring assisted extraction (HSE) or ultrasound probe-assisted extraction was used along with deep eutectic solvents for preparing extracts rich in phenolics and alkaloids [14]. It was found that ultrasound (3 min, 200 W) DES (lactic acid:ChCl) was superior in extracting the compounds (chlorogenic acid, caffeine, and theobromine) compared to HSE.

3. Functional Food Containing Cocoa Husk Powder/Extract

Being a rich source of bioactive compounds, the cocoa husk powder/extract has been tested and used as an additive in various food products for improving the physical, chemical, and biological properties of the products [42]. These bioactive compounds showed remarkable biological activities, which could provide functionality to food products (Figure 2).
The dietary fiber from cocoa bean husk was found effective against various disease conditions. As such, soluble dietary fiber, insoluble dietary fiber, and total dietary fiber were produced from cocoa bean shells and tested for hypoglycemic and cholesterol-lowering effects. Among all, soluble dietary fiber showed higher glucose adsorption capacity, α- amylase inhibition activity, cholesterol, and sodium cholate binding capacity [43]. Moreover, cocoa shell flour was found to prevent hyperlipidemia in HepG2 cells [44]. Due to the presence of a high quantity of dietary fiber, cocoa bean husk was used in several food formulations. Chocolate, as such, is considered as having nutritional and caloric value; however, the addition of fiber further improved the nutritional properties, while decreasing the polyphenolic content. In one study, cocoa shell (as a source of dietary fiber) was added to dark and milk chocolate and improved the dietary fiber content without any major impact on the polyphenolic content, and hence could be considered for its use. The quality of the prepared chocolate was comparable to commercial chocolate [45]. Cocoa hull phenolic extract was prepared and encapsulated using spray drying, incorporated in biscuits preparation, and tested for its stability during the baking process. Polyphenols were extracted using ethanol under ambient temperature for 30 min. The spray-dried powder was used to produce biscuits containing wheat flour (55.2%), sugar (13.7%), shortening (29.5%), and cocoa spray-dried powder (0.32%). Microencapsulation improves the stability of polyphenolic compounds in biscuits [46]. In a similar study, high-fiber functional biscuits were prepared using cocoa bean shells and tested for their consumption by diabetic patients. The biscuits showed α-glucosidase inhibitory activity [47]. In a cake formation, vegetable oil was substituted with cocoa bean hull by 30, 40, and 50%, and was found to effectively improve the physical, chemical, and sensory properties. It was found that the cocoa hull cake increased dietary fiber, phenolic compounds, and antioxidant activity [48]. The dietary fiber properties of cocoa husk were tested for their influence on physicochemical and sensory properties of emulsion-type pork sausages at different concentrations of cocoa powder (0.25–2%). It was found that cocoa powder increased the stability of the emulsion, increased flavor acceptability, and overall product acceptability. Furthermore, it significantly inhibited lipid peroxidation in the sausages during storage (refrigerated) [49].
The polyphenols and methylxanthine compounds in cocoa bean shell extract exerted various biological activities. As such, the antioxidant and apoptotic activity of cocoa husk extract was reported when tested on prostate cancer cells. The fraction (ethylacetate and butanol) of the extract was found to contain catechin, epicatechin, and procyanidin B. It was found that the extract showed antioxidant and apoptotic activity in PC3 and DU145 cells [50]. In another study, the anti-hypertensive and anti-hyperuricemia effects of cocoa pod husk extract were reported by inhibiting xanthine oxidase and angiotensin-1-converting enzyme and scavenging free radicals [51]. In one study, the skin whitening effect of a cocoa pod extract was determined based on a tyrosinase assay and sun-screening effect (UV 200–400 nm). It showed inhibition of the tyrosine enzyme and exhibited a UV-B sunscreen effect, thereby exerting anti-wrinkle skin whitening and sunscreen effects [52]. Some studies also suggested the effect of cocoa husk extract in the treatment of oral cavities and related symptoms. As such, in one study, a cocoa bean husk extract was tested for its mouth rinse activity in children (10 mL of 0.1%) and was found to inhibit the Streptococcus mutans count in saliva; the results were comparable with chlorhexidine (commercial product) [53]. Root canal treatment failure is mostly due to the presence of Enterococcus faecalis. Cocoa pod husk extract was found effective against E. faecalis at an extract concentration of 3.12% [54]. Moreover, it was found that cocoa bean shell extract (with concentrated epicatechin and tannin) counteracted oxysterol-induced inflammation in vitro [55].
Due to the presence of polyphenols and methylxanthine content in cocoa bean husk extract, it has been tested in various food products for improving product functionality. As such, cocoa bean shell extract containing polyphenols and methylxanthine was added to a flavored beverage after in vitro digestion for improving its functionality and consumer acceptance. It was found that the bioaccessibility of methylxanthine was 100%, while for polyphenols (B procyanidins and epicatechin) it was 50%. An increased α-glucosidase inhibition activity of the value-added beverage was also recorded with high acceptability of the product by the consumer [56]. In another study, the utilization of cocoa bean husk extract (obtained by the thermal treatment at 170 °C for 30 min) into a virgin olive oil jam in freeze-dried form or encapsulated form was investigated. It was found that the cocoa extract provided stability to the product and contained value-added phenolics, theobromine, and epicatechin. In addition, it was found that in food rich in fat/oil, the lyophilized form of the cocoa extract was suitable, while for aqueous food products the encapsulated cocoa extract was more effective [57].
To increase in the bioactivity of the natural products the fermentation technology has been effectively used in recent years. As such, a solid-state fermentation was used to increase the bioactivity of cocoa pod husk using Pleurotus ostreatus or Calocybe indica. It was found that the obtained extract after fermentation showed higher antimicrobial activity against bacteria (Bacillus cereus, Methicillin Resistant Staphylococcus aureus, Salmonella paratyphi, Pseudomonas aeruginosa, Escherichia coli, and Klebsiella pneumoniae) and fungi (Candida albicans, Aspergillus niger, A. favus, and Trichophyton rubrum) as compared to non-fermented extract. The obtained phytochemicals in the extract included polyphenolics, glycerine, pimelic ketone, D-ribonic acid, methyl myristate, palmitic acid methyl ester, oleic acid ethyl ester, lauramide, oleic acid amide, 1,2-cyclododecanediol, resorcinol, phytol, and others [58]. In another solid-state fermentation study [59], the cocoa shell was used as a raw material and utilized by Penicillium roqueforti for its conversion into valuable products. It was found that after the fermentation, a significant increase in the phenolic compounds and total carotenoid concentration was recorded, while the concentrations of anthocyanins and flavonoids did not change significantly. Moreover, saponin concentration and antioxidant potential along with oleic, denoleic, linolenic, and saturated fatty acids were increased after the cocoa shell fermentation.

4. The Cocoa Pod Husk/Shell Solid Waste after Extraction: Circular Economy Concept?

The emerging new green extraction technologies (subcritical water extraction, supercritical fluid extraction) have provided an eco-friendly sustainable means of preparing and extracting the compounds from cocoa bean husk and cocoa shells. These green extraction processes utilize natural products without affecting the environment and make the process more efficient; however, in most cases, the solid residue remaining after the extraction process creates environmental problems. To meet the demands of the circular economy, not only does the food waste/byproducts utilization need to be conducted but the waste processing (e.g., solid residue after extraction) also needs to be utilized in a sustainable manner (Figure 3).
In the case of cocoa pod husk or cocoa shell extraction, the solid residue was left behind. These are mainly discarded as waste and cannot fully justify the circular economy concept. To date, only some research has been conducted utilizing this solid waste after extraction (SWE). Moreover, some research has been conducted to utilize the cocoa pod husk for preparing compost [60] and biochar [61,62], which was further used as a plant nutrient/fertilizer [63,64] and for the bioremediation of toxic chemicals from an aqueous medium [65,66]. In line with this, the SWE residues remaining after the extraction could be treated to remove chemical entities and then processed to form compost and biochar products for their complete utilization in a circular economy approach. Efficient industrial exploitation of the residual fibers is clearly expected; however, capital investment strongly depends on biomass fractions upgrading (lignin cellulose and hemicellulose). Despite the high content of lignin in cocoa bean shells and pod husks (15–39%) [4], its recovery from the product stream with high purity still remains a challenging task. Highly efficient processes for biomass fractionation and lignin depolymerization should be rapidly implemented in industrial biorefineries for the preparation of new materials from lignin monomers [67]. The relevant advances in circular economy strategies have prompted new business models supported by enabling technologies and operative skills that could reduce the costs of cocoa husk extracts. Purified extracts enriched in flavanols, flavonols, and other polyphenols showed impressive nutraceutical properties and value compared to the traditional management of cocoa husk as agricultural composting and mulching are one order of magnitude higher.

5. Conclusions

The present review highlighted advanced protocols and enabling technologies for extracting bioactive compounds from cocoa bean husk and cocoa shells over the last decade. The applications of cocoa by-products extract in different food products for improving physicochemical and functional properties were also reviewed.
Research on the extraction of bioactive compounds strongly suggests the use of advanced green extraction technologies for the recovery of pectin, dietary fibers, polyphenols, methylxanthine, and phytosterols. The use of microwave and supercritical CO2 are seen in a larger context, provided the application of these high-end technologies. Moreover, research on green extract preparation is gaining pace using subcritical water extraction and by replacing organic solvents with deep eutectic solvents. The extract has been used in various food products, including cake, chocolates, sausages, biscuits, jam, and beverages, and was found to improve physicochemical and functional properties. To utilize the growing cocoa waste production, the greener process is preferably used to not only limit the environmental runoff of hazardous chemicals but to also provide more economical, less laborious, and process-efficient products. The focus should also be on the zero waste/complete utilization of cocoa waste in food products and solid waste after extraction to biochar and compost for the circular economy and sustainability.

Author Contributions

Conceptualization, T.B., F.C. and G.C.; writing—original draft preparation, T.B., S.R. and C.C.; writing—review and editing, M.T. and G.C.; supervision, F.C. and G.C.; project administration, G.C. All authors have read and agreed to the published version of the manuscript.

Funding

This work was financially supported by the University of Turin and the Ministry of Science and Higher Education of the Russian Federation (World-Class Research Centers agreement № 075-15-2020-926).

Data Availability Statement

Not applicable.

Acknowledgments

The University of Turin and the Ministry of Science and Higher Education of the Russian Federation are acknowledged for the financial support.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Statista. Cocoa Production Worldwide from 1980/81 to 2020/21. 2021. Available online: https://www.statista.com/statistics/262620/global-cocoa-production/ (accessed on 12 December 2021).
  2. Handojo, L.; Triharyogi, H.; Indarto, A. Cocoa bean shell waste as potential raw material for dietary fiber powder. Int. J. Recycl. Org. Waste Agric. 2019, 8, 485–491. [Google Scholar] [CrossRef] [Green Version]
  3. Vásquez, Z.S.; de Carvalho Neto, D.P.; Pereira, G.V.; Vandenberghe, L.P.; de Oliveira, P.Z.; Tiburcio, P.B.; Rogez, H.L.; Neto, A.G.; Soccol, C.R. Biotechnological approaches for cocoa waste management: A review. Waste Manag. 2019, 90, 72–83. [Google Scholar] [CrossRef] [PubMed]
  4. Mariatti, F.; Gunjević, V.; Boffa, L.; Cravotto, G. Process intensification technologies for the recovery of valuable compounds from cocoa by-products. Innov. Food Sci. Emerg. Technol. 2021, 68, 102601. [Google Scholar] [CrossRef]
  5. Loullis, A.; Pinakoulaki, E. Carob as cocoa substitute: A review on composition, health benefits and food applications. Eur. Food Res. Technol. 2018, 244, 959–977. [Google Scholar] [CrossRef]
  6. Panak Balentić, J.; Ačkar, Đ.; Jokić, S.; Jozinović, A.; Babić, J.; Miličević, B.; Šubarić, D.; Pavlović, N. Cocoa shell: A by-product with great potential for wide application. Molecules 2018, 23, 1404. [Google Scholar] [CrossRef] [Green Version]
  7. Adi-Dako, O.; Ofori-Kwakye, K.; Manso, S.F.; Boakye-Gyasi, M.E.; Sasu, C.; Pobee, M. Physicochemical and antimicrobial properties of cocoa pod husk pectin intended as a versatile pharmaceutical excipient and nutraceutical. J. Pharm. 2016, 2016, 1–12. [Google Scholar] [CrossRef] [Green Version]
  8. Chan, S.Y.; Choo, W.S. Effect of extraction conditions on the yield and chemical properties of pectin from cocoa husks. Food Chem. 2013, 141, 3752–3758. [Google Scholar] [CrossRef]
  9. Vriesmann, L.C.; Teófilo, R.F.; de Oliveira Petkowicz, C.L. Optimization of nitric acid-mediated extraction of pectin from cacao pod husks (Theobroma cacao L.) using response surface methodology. Carbohydr. Polym. 2011, 84, 1230–1236. [Google Scholar] [CrossRef] [Green Version]
  10. Pangestu, R.; Amanah, S.; Juanssilfero, A.B.; Perwitasari, U. Response surface methodology for microwave-assisted extraction of pectin from cocoa pod husk (Theobroma cacao) mediated by oxalic acid. J. Food Meas. Charact. 2020, 14, 2126–2133. [Google Scholar] [CrossRef]
  11. Priyangini, F.; Walde, S.G.; Chidambaram, R. Extraction optimization of pectin from cocoa pod husks (Theobroma cacao L.) with ascorbic acid using response surface methodology. Carbohydr. Polym. 2018, 202, 497–503. [Google Scholar] [CrossRef]
  12. Nguyen, V.T.; Nguyen, N.H. Proximate composition, extraction, and purification of theobromine from cacao pod husk (Theobroma cacao L.). Inf. Technol. J. 2017, 5, 14. [Google Scholar] [CrossRef]
  13. Pico Hernández, S.M.; Jaimes Estévez, J.; López Giraldo, L.J.; Murillo Méndez, C.J. Supercritical extraction of bioactive compounds from cocoa husk: Study of the main parameters. Rev. Fac. Ing. Univ. Antioq. 2019, 91, 95–105. [Google Scholar] [CrossRef] [Green Version]
  14. Ruesgas-Ramón, M.; Suárez-Quiroz, M.L.; González-Ríos, O.; Baréa, B.; Cazals, G.; Figueroa-Espinoza, M.C.; Durand, E. Biomolecules extraction from coffee and cocoa by-and co-products using deep eutectic solvents. J. Sci. Food Agric. 2020, 100, 81–91. [Google Scholar] [CrossRef] [PubMed]
  15. Muñoz-Almagro, N.; Valadez-Carmona, L.; Mendiola, J.A.; Ibáñez, E.; Villamiel, M. Structural characterisation of pectin obtained from cacao pod husk. Comparison of conventional and subcritical water extraction. Carbohydr. Polym. 2019, 217, 69–78. [Google Scholar] [CrossRef] [Green Version]
  16. Rebollo-Hernanz, M.; Cañas, S.; Taladrid, D.; Segovia, Á.; Bartolomé, B.; Aguilera, Y.; Martín-Cabrejas, M.A. Extraction of phenolic compounds from cocoa shell: Modeling using response surface methodology and artificial neural networks. Sep. Purif. Technol. 2021, 270, 118779. [Google Scholar] [CrossRef]
  17. Rosyidi, D.; Thohari, I. Characteristics of catechin extracted from cocoa husks using microwave assisted extraction (MAE). Biodiversitas 2019, 20, 3626–3631. [Google Scholar]
  18. Okiyama, D.C.; Soares, I.D.; Cuevas, M.S.; Crevelin, E.J.; Moraes, L.A.; Melo, M.P.; Oliveira, A.L.; Rodrigues, C.E. Pressurized liquid extraction of flavanols and alkaloids from cocoa bean shell using ethanol as solvent. Food Res. Int. 2018, 114, 20–29. [Google Scholar] [CrossRef]
  19. Mellinas, A.C.; Jiménez, A.; Garrigós, M.C. Pectin-Based Films with Cocoa Bean Shell Waste Extract and ZnO/Zn-NPs with Enhanced Oxygen Barrier, Ultraviolet Screen and Photocatalytic Properties. Foods 2020, 9, 1572. [Google Scholar] [CrossRef]
  20. Rahmawati, I.; Fachri, B.A.; Manurung, Y.H.; Reza, M. Application of response surface methodology in optimization condition of anthocyanin extraction process of cocoa peel waste with Microwave Assisted Extraction Method (MAE). In IOP Conference Series: Earth and Environmental Science; IOP Publishing: East Java, Indonesia, 2020; Volume 743, p. 01209. [Google Scholar]
  21. Ibrahim, N.H.; Mahmud, M.S.; Nurdin, S. Microwave-assisted extraction of β-sitosterol from cocoa shell waste. In IOP Conference Series: Materials Science and Engineering; IOP Publishing: Kuala Lumpur, Malaysia, 2020; Volume 991, p. 012106. [Google Scholar]
  22. Yusof, A.H.; Abd Gani, S.S.; Zaidan, U.H.; Halmi, M.I.E.; Zainudin, B.H. Optimization of an ultrasound-assisted extraction condition for flavonoid compounds from cocoa shells (Theobroma cacao) using response surface methodology. Molecules 2019, 24, 711. [Google Scholar] [CrossRef] [Green Version]
  23. González-Alejo, F.A.; Barajas-Fernández, J.; Olán-Acosta, M.D.L.Á.; Lagunes-Gálvez, L.M.; García-Alamilla, P. Supercritical Fluid Extraction of Fat and Caffeine with Theobromine Retention in the Cocoa Shell. Processes 2019, 7, 385. [Google Scholar] [CrossRef] [Green Version]
  24. Barišić, V.; Flanjak, I.; Kopjar, M.; Benšić, M.; Jozinović, A.; Babić, J.; Šubarić, D.; Miličević, B.; Doko, K.; Jašić, M.; et al. Does High Voltage Electrical Discharge Treatment Induce Changes in Tannin and Fiber Properties of Cocoa Shell? Foods 2020, 9, 810. [Google Scholar] [CrossRef] [PubMed]
  25. Jokić, S.; Gagić, T.; Knez, Ž.; Šubarić, D.; Škerget, M. Separation of active compounds from food by-product (cocoa shell) using subcritical water extraction. Molecules 2018, 23, 1408. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  26. Jokić, S.; Nastić, N.; Vidović, S.; Flanjak, I.; Aladić, K.; Vladić, J. An approach to value cocoa bean by-product based on subcritical water extraction and spray drying using different carriers. Sustainability 2020, 12, 2174. [Google Scholar] [CrossRef] [Green Version]
  27. Pavlović, N.; Jokić, S.; Jakovljević, M.; Blažić, M.; Molnar, M. Green Extraction Methods for Active Compounds from Food Waste—Cocoa Bean Shell. Foods 2020, 9, 140. [Google Scholar] [CrossRef] [Green Version]
  28. Botella-Martínez, C.; Lucas-Gonzalez, R.; Ballester-Costa, C.; Pérez-Álvarez, J.Á.; Fernández-López, J.; Delgado-Ospina, J.; Chaves-López, C.; Viuda-Martos, M. Ghanaian Cocoa (Theobroma cacao L.) Bean Shells Coproducts: Effect of Particle Size on Chemical Composition, Bioactive Compound Content and Antioxidant Activity. Agronomy 2021, 11, 401. [Google Scholar] [CrossRef]
  29. Mazzutti, S.; Rodrigues, L.G.G.; Mezzomo, N.; Venturi, V.; Ferreira, S.R.S. Integrated green-based processes using supercritical CO2 and pressurized ethanol applied to recover antioxidant compouds from cocoa (Theobroma cacao) bean hulls. J. Supercrit. Fluids 2018, 135, 52–59. [Google Scholar] [CrossRef]
  30. Vanitha, T.; Khan, M. Role of pectin in food processing and food packaging. In Pectins-Extraction, Purification, Characterization and Applications; Masuelli, M., Ed.; Intech Open: London, UK, 2019. [Google Scholar]
  31. Cintas, P.; Calcio Gaudino, E.; Cravotto, G. Pharmaceutical and nutraceutical compounds from natural matrices. In Microwave-Assisted Extraction for Bioactive Compounds: Theory and Practice; Chemat, F., Cravotto, G., XII, Eds.; Series: Food Engineering Series; Springer Nature: New York, NY, USA, 2013; Volume 4, pp. 181–206. [Google Scholar]
  32. Khoo, H.E.; Azlan, A.; Tang, S.T.; Lim, S.M. Anthocyanidins and anthocyanins: Colored pigments as food, pharmaceutical ingredients, and the potential health benefits. Food Nutr. Res. 2017, 61, 1361779. [Google Scholar] [CrossRef] [Green Version]
  33. Feng, S.; Belwal, T.; Li, L.; Limwachiranon, J.; Liu, X.; Luo, Z. Phytosterols and their derivatives: Potential health-promoting uses against lipid metabolism and associated diseases, mechanism, and safety issues. Compr. Rev. Food Sci. Food Saf. 2020, 19, 1243–1267. [Google Scholar] [CrossRef]
  34. Moreau, R.A.; Whitaker, B.D.; Hicks, K.B. Phytosterols, phytostanols, and their conjugates in foods: Structural diversity, quantitative analysis, and health-promoting uses. Prog. Lipid Res. 2002, 41, 457–500. [Google Scholar] [CrossRef]
  35. Chemat, F.; Vian, M.A.; Cravotto, G. Green extraction of natural products: Concept and principles. Int. J. Mol. Sci 2012, 13, 8615–8627. [Google Scholar] [CrossRef] [Green Version]
  36. Lattimer, J.M.; Haub, M.D. Effects of dietary fiber and its components on metabolic health. Nutrients 2010, 2, 1266–1289. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  37. Valadez-Carmona, L.; Ortiz-Moreno, A.; Ceballos-Reyes, G.; Mendiola, J.A.; Ibáñez, E. Valorization of cacao pod husk through supercritical fluid extraction of phenolic compounds. J. Supercrit. Fluids 2018, 131, 99–105. [Google Scholar] [CrossRef]
  38. Cheng, Y.; Xue, F.; Yu, S.; Du, S.; Yang, Y. Subcritical water extraction of natural products. Molecules 2021, 26, 4004. [Google Scholar] [CrossRef] [PubMed]
  39. Soares, I.D.; Okiyama, D.C.G.; da Costa Rodrigues, C.E. Simultaneous green extraction of fat and bioactive compounds of cocoa shell and protein fraction functionalities evaluation. Food Res. Int. 2020, 137, 109622. [Google Scholar] [CrossRef] [PubMed]
  40. Cádiz-Gurrea, M.D.L.L.; Fernández-Ochoa, Á.; Leyva-Jiménez, F.J.; Guerrero-Muñoz, N.; Villegas-Aguilar, M.D.C.; Pimentel-Moral, S.; Ramos-Escudero, F.; Segura-Carretero, A. LC-MS and spectrophotometric approaches for evaluation of bioactive compounds from Peru cocoa by-products for commercial applications. Molecules 2020, 25, 3177. [Google Scholar] [CrossRef]
  41. Smith, E.L.; Abbott, A.P.; Ryder, K.S. Deep eutectic solvents (DESs) and their applications. Chem. Rev. 2014, 114, 11060–11082. [Google Scholar] [CrossRef] [Green Version]
  42. Campos-Vega, R.; Nieto-Figueroa, K.H.; Oomah, B.D. Cocoa (Theobroma cacao L.) pod husk: Renewable source of bioactive compounds. Trends Food Sci. Technol. 2018, 81, 172–184. [Google Scholar] [CrossRef]
  43. Nsor-Atindana, J.; Zhong, F.; Mothibe, K.J.; Bangoura, M.L.; Lagnika, C. Quantification of total polyphenolic content and antimicrobial activity of cocoa (Theobroma cacao L.) bean shells. Pak. J. Nutr 2012, 11, 672–677. [Google Scholar] [CrossRef] [Green Version]
  44. Braojos, C.; Benitez, V.; Rebollo-Hernanz, M.; Cañas, S.; Aguilera, Y.; Arribas, S.M.; Martin-Cabrejas, M.A. Evaluation of the Hypolipidemic Properties of Cocoa Shell after Simulated Digestion Using In Vitro Techniques and a Cell Culture Model of Non-Alcoholic Fatty Liver Disease. Proceedings 2021, 70, 58. [Google Scholar] [CrossRef]
  45. Barišić, V.; Stokanović, M.C.; Flanjak, I.; Doko, K.; Jozinović, A.; Babić, J.; Šubarić, D.; Miličević, B.; Cindrić, I.; Ačkar, Đ. Cocoa Shell as a Step Forward to Functional Chocolates—Bioactive Components in Chocolates with Different Composition. Molecules 2020, 25, 5470. [Google Scholar] [CrossRef]
  46. Papillo, V.A.; Locatelli, M.; Travaglia, F.; Bordiga, M.; Garino, C.; Coïsson, J.D.; Arlorio, M. Cocoa hulls polyphenols stabilized by microencapsulation as functional ingredient for bakery applications. Food Res. Int. 2019, 115, 511–518. [Google Scholar] [CrossRef] [PubMed]
  47. Rojo-Poveda, O.; Barbosa-Pereira, L.; El Khattabi, C.; Youl, E.N.; Bertolino, M.; Delporte, C.; Pochet, S.; Stévigny, C. Polyphenolic and methylxanthine bioaccessibility of cocoa bean shell functional biscuits: Metabolomics approach and intestinal permeability through caco-2 cell models. Antioxidants 2020, 9, 1164. [Google Scholar] [CrossRef] [PubMed]
  48. Öztürk, E.; Ova, G. Evaluation of cocoa bean hulls as a fat replacer on functional cake production. Turk. J. Agric.-Food Sci. Technol. 2018, 6, 1043–1050. [Google Scholar] [CrossRef] [Green Version]
  49. Choi, J.; Kim, N.; Choi, H.Y.; Han, Y.S. Effect of cacao bean husk powder on the quality properties of pork sausages. Food Sci. Anim. Resour. 2019, 39, 742. [Google Scholar] [CrossRef]
  50. Choi, J.; Yang, C.; Lim, W.; Song, G.; Choi, H. Antioxidant and apoptotic activity of cocoa bean husk extract on prostate cancer cells. Mol. Cell Toxicol. 2021, 17, 1–11. [Google Scholar] [CrossRef]
  51. Irondi, A.E.; Olawuyi, A.D.; Lawal, B.S.; Boligon, A.A.; Olasupo, F.; Olalekan, S.I. Comparative inhibitory effects of cocoa bean and cocoa pod husk extracts on enzymes associated with hyperuricemia and hypertension in vitro. Int. Food Res. J. 2019, 26, 557–564. [Google Scholar]
  52. Karim, A.A.; Azlan, A.; Ismail, A.; Hashim, P.; Abd Gani, S.S.; Zainudin, B.H.; Abdullah, N.A. Phenolic composition, antioxidant, anti-wrinkles and tyrosinase inhibitory activities of cocoa pod extract. BMC Complement Altern. Med. 2014, 14, 1–13. [Google Scholar]
  53. Babu, N.V.; Vivek, D.K.; Ambika, G. Comparative evaluation of chlorhexidine mouthrinse versus cacao bean husk extract mouthrinse as antimicrobial agents in children. Eur. Arch. Paediatr. Dent. 2011, 12, 245–249. [Google Scholar] [CrossRef]
  54. Yuanita, T.; Oktavianti, R.A.; Suryani, D.F.; Rukmo, M.; Kunarti, S.; Kusuma, A.H. The Inhibitory Ability of Cocoa Pod Husk Extract on Enterococcus faecalis Glucosyltransferase Enzyme Activity. J. Contemp. Dent. 2020, 21, 271–276. [Google Scholar] [CrossRef]
  55. Rossin, D.; Barbosa-Pereira, L.; Iaia, N.; Testa, G.; Sottero, B.; Poli, G.; Zeppa, G.; Biasi, F. A dietary mixture of oxysterols induces in vitro intestinal inflammation through TLR2/4 activation: The protective effect of cocoa bean shells. Antioxidants 2019, 8, 151. [Google Scholar] [CrossRef] [Green Version]
  56. Cantele, C.; Rojo-Poveda, O.; Bertolino, M.; Ghirardello, D.; Cardenia, V.; Barbosa-Pereira, L.; Zeppa, G. In vitro bioaccessibility and functional properties of phenolic compounds from enriched beverages based on cocoa bean shell. Foods 2020, 9, 715. [Google Scholar] [CrossRef] [PubMed]
  57. Hernández-Hernández, C.; Morales-Sillero, A.; Fernández-Prior, M.Á.; Fernández-Bolaños, J.; de la Paz Aguilera-Herrera, M.; Rodríguez-Gutiérrez, G. Extra virgin olive oil jam enriched with cocoa bean husk extract rich in theobromine and phenols. LWT 2019, 111, 278–283. [Google Scholar] [CrossRef]
  58. Ogidi, C.O.; Abioye, S.A.; Akinyemi, D.D.; Fadairo, F.B.; Bolaniran, T.; Akinyele, B.J. Bioactivity assessment of ethanolic extracts from Theobroma cacao and Cola spp. wastes after solid state fermentation by Pleurotus ostreatus and Calocybe indica. Adv. Tradit. Med. 2021, 21, 1–13. [Google Scholar] [CrossRef]
  59. Lessa, O.A.; dos Santos Reis, N.; Leite, S.G.F.; Gutarra, M.L.E.; Souza, A.O.; Gualberto, S.A.; de Oliveira, J.R.; Aguiar-Oliveira, E.; Franco, M. Effect of the solid-state fermentation of cocoa shell on the secondary metabolites, antioxidant activity, and fatty acids. Food Sci. Biotechnol. 2018, 27, 107–113. [Google Scholar] [CrossRef]
  60. Munongo, M.E.; Nkeng, G.E.; Njukeng, J.N. Production and characterization of compost manure and biochar from cocoa pod husks. Int. J. Adv. Sci. Res. Manag. 2017, 2, 26–31. [Google Scholar]
  61. Tsai, C.H.; Tsai, W.T.; Liu, S.C.; Lin, Y.Q. Thermochemical characterization of biochar from cocoa pod husk prepared at low pyrolysis temperature. Biomass Convers. Biorefin. 2018, 8, 237–243. [Google Scholar] [CrossRef]
  62. Tsai, W.T.; Hsu, C.H.; Lin, Y.Q.; Tsai, C.H.; Chen, W.S.; Chang, Y.T. Enhancing the pore properties and adsorption performance of cocoa pod husk (CPH)-Derived biochars via post-acid treatment. Processes 2020, 8, 144. [Google Scholar] [CrossRef] [Green Version]
  63. Kayode, C.O.; Adeoye, G.O.; Ezekiel-Adewoyin, D.T.; AyanfeOluwa, O.E.; Ogunleti, D.O.; Adekunle, A.F. Influence of cocoa pod husk-based compost on nutrient uptake of okra (Abelmoschus esculentus (L.) MOENCH) and soil properties on an Alfisol. Commun. Soil Sci. Plant Anal. 2018, 49, 2113–2122. [Google Scholar] [CrossRef]
  64. Bahrun, A.; Fahimuddin, M.Y.; Rakian, T.C. Cocoa Pod Husk Biochar Reduce Watering Frequency and Increase Cocoa Seedlings Growth. Int. J. Agric. Environ. Biotechnol. 2018, 3, 1635–1639. [Google Scholar] [CrossRef]
  65. Córdova, B.M.; Santa Cruz, J.P.; Huamani-Palomino, R.G.; Baena-Moncada, A.M. Simultaneous adsorption of a ternary mixture of brilliant green, rhodamine B and methyl orange as artificial wastewater onto biochar from cocoa pod husk waste. Quantification of dyes using the derivative spectrophotometry method. New J. Chem. 2020, 44, 8303–8316. [Google Scholar] [CrossRef]
  66. Yong, S.K.; Leyom, J.; Tay, C.C.; Talib, S.A. Sorption of lead from aqueous system using cocoa pod husk biochar: Kinetic and isotherm studies. Int. J. Eng. Technol. 2018, 7, 241–244. [Google Scholar] [CrossRef]
  67. Acciardo, E.; Tabasso, S.; Cravotto, G.; Bensaid, S. Process intensification for lignin valorization. Chem. Eng. Proc. Process Intensif. 2022, 171, 108732. [Google Scholar] [CrossRef]
Figure 1. Major bioactive compounds extracted from cocoa bean husk and cocoa shell.
Figure 1. Major bioactive compounds extracted from cocoa bean husk and cocoa shell.
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Figure 2. Valorization of food products with cocoa bean husk or cocoa shell extract.
Figure 2. Valorization of food products with cocoa bean husk or cocoa shell extract.
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Figure 3. Circular economy concept for cocoa bean husk products. For the circular economy, the cocoa shell husk processed waste products (e.g., residue left after extraction of compounds) could be recycled/reused (e.g., biochar, compost) to provide a complete waste valorization solution with potential sustainable benefits.
Figure 3. Circular economy concept for cocoa bean husk products. For the circular economy, the cocoa shell husk processed waste products (e.g., residue left after extraction of compounds) could be recycled/reused (e.g., biochar, compost) to provide a complete waste valorization solution with potential sustainable benefits.
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Table 1. Extraction methods used for obtaining bioactive compounds from cocoa pod husk or cocoa shell in the last decade.
Table 1. Extraction methods used for obtaining bioactive compounds from cocoa pod husk or cocoa shell in the last decade.
CompoundsExtraction MethodYield (w/w)References
Cocoa pod husk
PectinAqueous citric acid (4% w/v) followed by precipitation of extract using ethanol23.3%[7]
PectinWater, citric acid (2.5, 4 pH), and hydrochloric acid (2.5, 4 pH)7.62%[8]
PectinNitric acid, pH 1.5, 100 °C of extraction temperature, and 30 min of extraction time9.0%[9]
PectinOxalic acid + microwave radiation condition at pH 1.16, L/S = 25.0 and 15 min. of irradiation time9.64%[10]
PectinAscorbic acid-based extraction, pH 2.5, 95 °C, for 45 min4.2%[11]
Theobromine rich extract70% ethanol, extraction time of 90 min, temperature of 80 °C, and 1 cycle of extractionTheobromine yield (6.79 mg/100 g)[12]
TPC, total flavon-3-oles, and total carotenoids contentSupercritical fluid extraction, particle size less than 0.26 mm, extraction time of 147 min, extraction temperature of 308.15 K, pressure of 20 MPa, and 20% ethanolTPC (35.11 EAG mg/g), a total flavan-3-oles content (12.89 EEP mg/g) and total carotenoids content (64.35 EBC mg/g)[13]
phenolics and alkaloidsHeat-stirring assisted extraction (HSE) or ultrasound probe assisted extraction was used along with deep eutectic solventsultrasound (3 min, 200 W) Des (lactic acid:ChCl) was found superior in extracting the compounds (chlorogenic acid, caffeine, and theobromine) compared to HSE[14]
PectinSubcritical water extraction121 °C, 103.4 bar, and 30 min[15]
Total phenolic compounds, total flavonoids, total flavanols, total phenolic acids, total proanthrocyanidins, total ortho-diphenols, and antioxidant activityHeat-assisted extraction, 100 °C, 90 min, 0% citric acid, and 0.02 g cocoa shell/mL of waterUPLC-ESI-MS/MS revealed the presence of 15 phenolic compounds, being protocatechuic acid, procyanidin B2, (−)-epicatechin, and (+)-catechin, the major ones[16]
Total phenolic content and total catechin contentMAE, absolute ethanol, 70 °C, 3:100 g/mL, 8 and 10 minTotal phenol content (TPC) and total catechin content (TCC)[17]
Cocoa bean shell
Flavonoids and alkaloidsPressurized liquid extractionLyophilized extract showed higher flavonoids (catechin, epicatechin, procyanidin B2) and alkaloid (theobromine, caffeine) content as compared to the dried cocoa shell powder extract[18]
Polyphenols and polysaccharides- pectin-based filmsMicrowave-assisted extraction (MAE)obtained biofilm prepared by pectin-cocoa bean shell extract-ZnO/Zn nanoparticle showed greater UV and oxygen barrier properties[19]
AnthocyaninMAE, particle size (60 mesh), sample to solvent ratio (0.0625 w/v), extraction time (10 min), and microwave power (450 W)1.435 mM[20]
β-sitosterolMAE, absolute ethanol, 70 °C, 500 W, and 10 min3546.1 mg/100 g[21]
FlavonoidsUltrasound-assisted extraction under 80% ethanol, 55 °C, for 45 minTFC = 7.47 mg RE/g dw[22]
Protein, polysaccharide, and polyphenolsMAE, 5 min of extraction time, pH of 12, 97 °C of temperature, and sample to solvent ratio of 0.04 g/LPectin-based films[19]
Fat and methylxanthines (theobromine and caffeine)Supercritical CO2, 6000 psi, 313 K, 90 min94.73% (which is most effective extraction), while for caffeine the extraction yield is about 90%[23]
Dietary fiberHigh-voltage electric dischargeIncreased fiber content[24]
Polyphenols and methylxanthinesSubcritical water extraction, temperature 170 °C, time 75 min, sample to solvent ratio 1:20theobromine, caffeine, theophylline, gallic acid, epicatechin, catechin, chlorogenic acid, and total phenols[25]
Polyphenols and methylxanthinesSubcritical water extraction, 150 °C with extraction pressure of 30 bar for 15 minthat whey protein protects the phenolic content resulted in higher content of gallic acid, caffeine, and theobromine as compared to maltodextrin[26]
AlkaloidsMAE was performed using DESTheobromine (2.502–5.004 mg/g) and caffeine (0.778–1.599 mg/g)[27]
Dietary fiber, polyphenolic compounds, and methylxanthineParticle sizes were considered, i.e., high (Dp > 701 um), intermediate (417 um < Dp < 701 um) and lowest (Dp < 417 um)Dietary fiber (65.58 g/100 g), polyphenolic compounds (epicatechin, 6.33 mg/g; catechin, 4.58 mg/g), and methylxanthine (theobromine, 12.77 mg/g; caffeine, 6.13 mg/g)[28]
PhenolicsCombined effect of supercritical fluid extraction and pressurized liquid extractionTPC values from 35 to 51 mg GAE/g and EC50 values from 115 to 177 µg/mL[29]
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Belwal, T.; Cravotto, C.; Ramola, S.; Thakur, M.; Chemat, F.; Cravotto, G. Bioactive Compounds from Cocoa Husk: Extraction, Analysis and Applications in Food Production Chain. Foods 2022, 11, 798. https://doi.org/10.3390/foods11060798

AMA Style

Belwal T, Cravotto C, Ramola S, Thakur M, Chemat F, Cravotto G. Bioactive Compounds from Cocoa Husk: Extraction, Analysis and Applications in Food Production Chain. Foods. 2022; 11(6):798. https://doi.org/10.3390/foods11060798

Chicago/Turabian Style

Belwal, Tarun, Christian Cravotto, Sudipta Ramola, Monika Thakur, Farid Chemat, and Giancarlo Cravotto. 2022. "Bioactive Compounds from Cocoa Husk: Extraction, Analysis and Applications in Food Production Chain" Foods 11, no. 6: 798. https://doi.org/10.3390/foods11060798

APA Style

Belwal, T., Cravotto, C., Ramola, S., Thakur, M., Chemat, F., & Cravotto, G. (2022). Bioactive Compounds from Cocoa Husk: Extraction, Analysis and Applications in Food Production Chain. Foods, 11(6), 798. https://doi.org/10.3390/foods11060798

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