Biosynthesis and Characterizations of Silver Nanoparticles from Annona squamosa Leaf and Fruit Extracts for Size-Dependent Biomedical Applications

Abstract

Green synthesis differs in the way that the plant produces chemicals that act as reducing and stabilizing agents, and by adopting this green synthesis, we have synthesized silver nanoparticles (AgNPs) from the leaf and fruit extracts of Annona squamosa (also known as Sharifa), where these extracts have played an important role as reducing and capping agents. The nanoparticles were synthesized as the consequence of a reduction that happened between plant extracts and the precursor solution. The prepared AgNPs were then characterized using scanning electron microscopy, UV-Visible spectroscopy, and X-ray diffraction to study their morphology, optical response, and crystallinity. A single distinctive absorption peak of colloidal AgNPs samples was observed at 430 nm and 410 nm for leaf and fruit extract samples, having an optical bandgap of 2.97 eV and 2.88 eV, respectively, with a spherical shape having a diameter in the range of 35–90 nm and 15–50 nm, respectively, whilst XRD studies supported the FCC cubic structure of the mediated AgNPs. These green synthesized AgNPs have a wide variety of uses, particularly in the biomedical domain, where they have the potential to treat numerous diseases and are reported to be efficient against antibacterial, anti-cancer, and anti-diabetic activities.

1. Introduction

The most significant feature of nanotechnology is to develop more reliable processes for the synthesis of nanomaterials with a wide variety of sizes, good mono-dispersity, and chemical compositions [1]. Nanomaterials of various shapes and sizes ranging from 1 nm to 100 nm are being synthesized on a large scale in laboratories because of their wide-ranging and practical uses in a variety of industries. In addition to various chemical methods, two approaches, top-down and bottom-up, are widely employed for nanoparticle synthesis [2]. However, the usage of lethal and toxic chemicals was their stumbling block [3]. During the last decade, nanotechnologists have proposed a very profitable and efficient method to synthesize nanoparticles (NPs), which is also known for its user-friendly and non-toxic nature, as well as the fact that there are no complex instruments involved in employing the green synthesis method, which also minimizes ecotoxicity [4]. The biosynthesized metallic NPs have a broad spectrum of applications in science and technology, including medicine, biotechnology, physics, chemistry, and material sciences.

In contrast to other methods that require the usage of costly and harmful chemicals as reducing, capping, and some stabilizing agents for the synthesis of NPs, green synthesis utilizes the plant itself to produce such chemicals that work as natural reducing and stabilizing agents [5]. Magnetic NPs have been reported to be biosynthesized using various plants [6,7], with plant parts, such as leaves [8], flowers [9], stem bark [10], and seeds [11] being used as nanoparticles factories. Silver nanoparticles (AgNPs) mediated by Moringa oleifera leaves [12], ZnO NPs mediated by Capsicum annuum fruit extract [13], platinum NPs mediated by date extracts [14], and many more have been reported so far [15,16,17]. Biological waste and byproducts, such as peels [16] and Annona squamosa leaves [17], have also been reported to be employed in the green synthesis of AgNPs, anticipating the potential of AgNPs for a number of applications and prompting researchers to further examine AgNPs synthesized by plants to investigate their potential in healthcare.

The most essential and distinctive aspect of NPs is their increased surface-area-to-volume ratio, which explains the reason behind their potential for size-dependent applications. The most efficiently explored NPs, recently, are those formed of noble metals, namely Ag, Pt, Au, and Pd, whereas AgNPs, among the four stated above, play an essential role in biology and medicine. The synthesis of AgNPs by reducing aqueous silver nitrate (AgNO₃) with aqueous Annona squamosa leaf and fruit extracts provide innovative, non-toxic, environmentally friendly, as well as cost-effective reducing agents for bio-reduction of AgNO₃, and are used in folklore medicine for the treatment of various ailments. The phytochemicals, mainly flavones, terpenoids, sugars, ketones, aldehydes, carboxylic acids, and amides, are the primary ingredients found in plants that are involved in the bio-reduction of nanoparticles [18]. Flavonoids have a variety of functional groups that boost their capacity to reduce metal ions because of the tautomeric reactions in flavonoids that transform the enol-form into the keto-form and release the reactive hydrogen atom, resulting in the conversion of metal ions into stable atoms, which then nucleate under continual heating and stirring to synthesize nanoparticles [19]. Sugars found in plant extracts, such as glucose and fructose, may also have a role in the creation of metallic nanoparticles. Glucose has the ability to play a role in the size and shape of distributed nanoparticles, whereas fructose is responsible for monodispersed silver nanoparticles [20]. The protein present in plant extracts with a functional amino group (NH₂) also participates in reducing metal ions to stable metallic atoms [21]. Functional groups found in phytochemicals, such as flavones, alkaloids, phenols, and anthracenes (such as –C–O–C–, –C–O–, and –C=C–) can play an important role in the formation of metallic nanoparticles via metallic atom agglomeration followed by metallic ion reduction. The natural chemical compounds are present in significant quantities in Annona squamosa, such as flavonoids, alkaloids, potassium, ascorbic acid, amino acids, riboflavin, and acetogenins. The leaf study revealed the presence of caryophyllene, cadinol, muurolene, and isoquinoline alkaloids. Annoreticuin and isoannoreticuin are acetogenins discovered in leaves that are cytotoxic to human tumor cells [22], whereas samoquasine, benzylisoquinoline, and tertahydroisoquinoline are alkaloids identified in plant fruit extract. Further, the root and bark include liriodenine and oxoanalobine, and the bark extract has a single acetogenin, solamin, distinct bullatacinone, and two triterpenoids, making it appropriate for antisecticidal applications [23]. Quercetin, a biomolecule comprised of three rings and five OH groups, is the major biomolecule found in Annona squamosa extracts with the formula C₁₅H₁₀O₇ [24]. Owing to the presence of these functional groups, Annona squamosa showed peculiarly different antimicrobial and cytotoxic accomplishments. The AgNPs derived from Annona squamosa plant leaf extract are of high therapeutic interest due to their efficacy against a variety of bacterial infections and are chosen over other metal NPs due to their extremely small size, improved physio-chemical characteristics, nontoxicity to human cells, and inexpensive production cost [25]. They are also well-known for their excellent antibacterial activity, despite their small size [26].

This innovative study is aimed at exploring the synthesis of AgNPs using a green synthesis method from the leaf and fruit extracts of Annona squamosa in order to identify their potential for biological and biomedical applications. As per our understanding, it is the first-ever study that explores Annona squamosa fruit extracts’ potential for being used as antibacterial treatments and provides a comparison of leaf and fruit extracts for size-dependent biomedical applications. This work revealed efficient antibacterial effects without the use of any chemical entities by maintaining the purity of the green-produced AgNPs, which is a significant advantage over prior studies [16,17]. For the first time, the antibacterial activity of various concentrations of synthesized AgNPs (25 µg/mL, 50 µg/mL, and 100 µg/mL) was investigated, as well as a comparison of their extract activities. The mechanism of bacterial cell death has also been demonstrated in detail.

2. Materials and Methods

Materials: Fresh Annona squamosa (sweet apple) fruit and leaves were obtained from the Botanical Garden (University of the Punjab, Lahore, Pakistan), and were then washed, dried (in the case of pulp fruit), and crushed into a fine powder (in the case of leaves).

Chemicals and Equipment: The only chemical, silver nitrate solution (Sigma Aldrich Inc., Lahore, Pakistan) having 99.95% purity, was used. The deionized water used was synthesized in the lab at the Centre of Excellence in Solid State Physics, at the University of the Punjab, Lahore, Pakistan. A hot plate, beakers, an electronic weight balance, a vernier caliper, Petri dishes, and magnetic bits were among the instruments used, with all the experiments taking place at room temperature.

Methods: The synthesis of AgNPs was performed by following the methods outlined below:

• Leaf and fruit extract preparation;
• Precursor solution preparation;
• Nanoparticle synthesis.

Leaf Extract Preparation: The collected Annona squamosa leaves were washed 2–3 times with fresh water to eliminate any discrepancies in results, then thoroughly dried before being crushed into powder form, and 5 g of this powder was weighed, which was then mixed with 100 mL of deionized water in a beaker containing 5 g of leaves powder. The beaker was placed on the hot plate and the solution was boiled and stirred for 25–30 min at boiling temperature before being filtered by Whatman filter paper no.1. Figure 1a–d depicts the step-by-step synthesis of the leaf extract.

Fruit Extract Preparation: The Annona squamosa fruit was peeled, cut, rinsed 2–3 times with fresh water to avoid any discrepancy, and then soaked for 24 h in 100 mL of deionized water. After 24 h, the beaker was placed on a hot plate, and the solution was boiled and stirred for 35–40 min at a boiling temperature before being filtered by Whatman filter paper no.1. Figure 1e–h depicts the step-by-step preparation of the fruit (pulp) extract.

Precursor Solution Preparation: A 100 mL solution of 10 mM AgNO₃ was prepared by dissolving 0.169 g of AgNO₃ in 100 mL of deionized water and was employed as a precursor for both the leaf and fruits’ extract of Annona squamosa mediated AgNPs. The prepared solution is shown in Figure 2a.

Annona squamosa leaf mediated AgNPs: To make Annona squamosa leaf extract-mediated AgNPs, 45 mL of AgNO₃ precursor solution was heated in a beaker, and 5 mL of Annona squamosa leaves extract was added dropwise into this boiling solution, which was then boiled for a further 25–30 min. Because of a surface plasmon resonance effect [27], the color changed from light yellow to light brown and then dark brown, indicating that a pH change happened, hinting at the formation of dark brown colored nano-sized AgNPs, as shown in Figure 2c, which were then stored at 4 °C for further characterizations.

Annona squamosa fruit-mediated AgNPs: For the synthesis of Annona squamosa fruit extract-mediated AgNPs, 45 mL of AgNO₃ precursor solution in a beaker was boiled, and 5 mL of Annona squamosa fruit extract was added dropwise into this boiling solution, which was then boiled further for 30–35 min at 80 °C, after which the color changed from transparent to light yellow and then to light brown. This action was caused by the surface plasmon resonance effect [27], which suggested that a pH change occurred, indicating the creation of light brown colored nano-sized silver particles, as seen in Figure 2e, which were preserved at 4 °C for subsequent characterizations.

Figure 2a–e depicts the final solution colors in the stepwise synthesis of NPs, and these synthesized AgNPs from leaf and fruit extracts were then analyzed using characterization techniques, such as scanning electron microscopy (SEM, S3400N, Hitachi Analysis Machine, Tokyo, Japan), X-ray diffraction (Diffractometer: Bruker D8 Advance Diffractometer, Bremen, Germany), and UV-Vis spectroscopy (Shimadzu UV-1800, Shimadzu Corp., Kyoto, Japan).

Protocols for Antibacterial Activity: The antibacterial potency of Annona squamosa leaf and fruit extracts, along with their mediated AgNPs, were analyzed against Gram-negative bacteria; Escherichia coli and Pseudomonas aeruginosa were provided by the Institute of Molecular Biology and Biotechnology, University of Lahore, Lahore Pakistan. The Muller Hinton Agar was prepared and poured in Petri dishes until it gains a jelly-like texture, then the bacterial strains were sub-cultured in this solution by the disk diffusion method to evaluate antibacterial activity. The five wells of 10 mm diameter each were created to pore solutions in them, such as deionized water, Annona squamosa leaf, as well as fruit extracts and AgNPs synthesized from both extracts with varying concentrations (25 µg/mL, 50 µg/mL, and 100 µg/mL) in each well 1 to 5, respectively. These dishes were then incubated at 37 °C for 24 h to analyze the zone of inhibition (ZOI) of each extract and AgNPs, with the help of a vernier caliper to measure the bacterial growth inside the respective well.

3. Results and Discussions

3.1. Synthesis of Nanoparticles (NPs)

This study focused on the synthesis of AgNPs, which are more advantageous owing to their small size and nontoxicity to human cells but toxic to microorganisms, such as bacteria [28]. Because of these characteristics, AgNPs have special physical, chemical, and optical properties that are important in bio-nanotechnology [29]. Green synthesis provides another source for the synthesis of NPs, such as AgNPs [30], in which the plant and fruit extract itself are employed as a reducing agent, converting metal ions into stable metal NPs [31].

A reduction process occurred when fruit and leaf extracts were added to the precursor solution, resulting in the creation of AgNPs [32]. Figure 3 depicts a schematic mechanism of AgNPs synthesis in which AgNO₃ was dissolved in deionized water with no color, boiled, and stirred on a hot plate at a boiling temperature prior to the addition of Annona squamosa leaf/fruit extract into the beaker. After the addition of the extract solution, it acted as a reducing and stabilizing agent, converting Ag⁺¹ ions to Ag⁰ particles on continuous heating and stirring, which is the basis of silver nuclei formation, and could also be visualized by the solution color changing. Following the start of the nucleation process, additional heating and stirring contributed to the nucleation and growth processes, which resulted in the synthesis of the required AgNPs, as indicated by the golden brown and light brown colors of the final solution treated with leaf and fruit extracts, respectively. Herein, phenol and other reducing agents found in citrus extracts were the primary sources of reducing Ag⁺¹ ions to Ag⁰ particles, and hence the observed color transformation was attributed to a reduction mechanism [33]. By manipulating the concentrations of extracts and precursor solutions, the ultimate size of the produced AgNPs may be adjusted [34]. Recent research has shown the shapes, size ranges, and structures of AgNPs as described by several methods [35].

3.2. Characterizations

3.2.1. X-ray Diffraction (XRD) Analysis

The structural analysis of synthesized AgNPs was performed by XRD to investigate a material’s purity, crystal structure, crystal phase identification, lattice parameter, crystallite size, and crystal defects [36,37]. It is a nondestructive technique that is based on the coherent scattering mechanism, where the sample is collimated and electrons penetrate the inner transition, producing X-rays that are then thrown over the sample, rotated at different angles, and hence the intensity of reflected X-rays is recorded at these different angles. When the X-rays satisfy Bragg’s equation, an intensity peak is obtained [38], which is further investigated to explore structural parameters. The XRD pattern of AgNPs was recorded by an X-ray Powder Diffractometer (Bruker D8 Advance Diffractometer, Bremen, Germany).

The XRD data were collected by a Bruker D8 advanced with Cu-kα radiation as an X-ray source, having a wavelength of 1.5406 Å. The pattern was obtained in the range of 20° and 80° of 2θ values with a step width of 2θ = 0.04, as shown in Figure 4. As we can see, peaks appear in the pattern at different 2θ values, which confirmed the presence of AgNPs demonstrating the hkl values of (111), (200), (220), and (311) at 2θ values of 37.55°, 45.15°, 65.7° and 77.75°, respectively, in the case of leaf mediated AgNO₃, as shown in Figure 4a, while the same planes were observed in fruit-mediated AgNPs, as shown in Figure 4b, with a slight change in 2θ values as 38.27°, 44.5°, 64.7° and 77.7°, respectively. These results confirm that the green synthesized AgNPs are face-centered cubical, indicating that they are crystalline in nature [39], and when these patterns were compared to JCPDS ID No. 04-0783, it was discovered that they were silver, and more specifically, AgNPs.

Stress and strain have an effect on the crystal lattice, and instrumental modifications can influence peak width, whereas full-width half maxima (FWHM), which is denoted by β was calculated using the major peak of the 111 plane in the XRD pattern and calculated to be 0.0069 and 0.0197 for leaf and fruit extracts mediated AgNPs, respectively. The Bragg’s law [40] was used to calculate the lattice parameter, while the Debye–Scherrer equation [41] was used to measure the crystallite size of the synthesized AgNPs as given below.

$$\mathrm{D}=\frac{\delta \lambda }{\beta Cos\theta }$$

(1)

Table 1. Lattice parameter and crystallite size of synthesized AgNPs.

Sample	Two Theta (2θ) (Degrees)	FWHM β (Rad)	Miller INDICES	Lattice Constant (nm)	Crystallite Size (nm)
Annona squamosa leaf extract mediated AgNPs	37.5°	0.0069	(111)	1.34	21.4
Annona squamosa fruit extract mediated AgNPs	38.2°	0.0197	(111)	0.539	8.0

shows the measured structural parameters, with the calculated crystallite size of Annona squamosa mediated AgNPs being 21.4 nm for leaf extract and 8.0 nm for fruit extract, respectively, indicating a good affinity with our estimated UV-Vis results.

3.2.2. UV-Vis Spectroscopy Analysis

UV-Vis spectroscopy is a frequent and successful approach for studying the optical responses of colloidal NPs due to the narrow bandgap between the valance and conduction bands of metallic NPs such as AgNPs, where electrons can freely move between them. Surface plasmon resonance (SPR) is a resonant oscillation of conduction electrons caused by electrons on the surface of AgNPs in response to incoming light. Colloidal NPs produce a variety of colors as a result of SPR absorption, depending on various factors, such as size, shape, and the surrounding medium [38]. A Shimadzu UV-1800 (Japan) UV-Vis spectroscopy model was employed, which provided us with graphical data shown in relation to wavelength (along the x-axis) and absorbance (along the y-axis). This analysis was used to confirm whether or not we have synthesized the required particles by providing information about the absorption peaks [32]. AgNPs differ from other NPs in that they exhibit a surface plasmon resonance effect [42], which occurs when light interacts with conduction electrons present on the exposed metal surface, resulting in collective electronic oscillations in response to specific light wavelengths [43].

As shown in Figure 5a,b, the UV-Vis analysis displays a graph of leaf and fruit-mediated AgNPs, with the wavelength along the x-axis and absorbance along the y-axis, where the AgNO₃ precursor solution and leaf/fruit extract did not show any absorption peaks; however, a peak at 430 nm and 410 nm indicated the presence of AgNPs in the sample solution due to the surface plasmon resonance effects. According to the literature, AgNPs often have UV-Vis peaks in the 400–500 nm wavelength range, depending on their size [44]. Furthermore, the presence of a single absorption peak suggested the development of spherical-shaped AgNPs, which were investigated further using morphological SEM analysis [45]. Moreover, the optical bandgap of leaf and fruit-mediated AgNPs was computed by Tauc’s plot [46] using the relation:

$$\alpha h\vartheta =A {(h\vartheta -E_g)}^n$$

(2)

where α represents the absorption coefficient, hν is the photon energy, A is a constant, and E_g is the optical bandgap energy, respectively, while n depends on electron transitions, and n = 2 corresponds to direct electron transitions with a direct optical bandgap. The graph between (αhν)² and E_g, as shown in Figure 5c,d, estimates the optical bandgap energy of synthesized AgNPs as 2.97 eV and 2.88 eV using leaf (Figure 5c) and fruit extracts (Figure 5d), respectively, which are comparable with existing literature at 2.9 eV [47], and 3.4 eV [48]. These results are more significant, and minor variations in the optical bandgap may be attributable to quantum confinement effects [49].

3.2.3. Scanning Electron Microscope (SEM) Analysis

SEM is a popular and widely used technique for evaluating the shape, size distribution, surface morphology, and elemental composition of nanomaterials. The AgNPs samples were prepared for SEM analysis by cleaning the Si wafer slides with IPA and ethanol first, then placing drops of the sample on the slides and allowing them to dry. The samples were then mounted on double carbon tape to provide a conductive medium for SEM imaging, while the crystallite size was measured using the Debye–Scherrer formula. SEM analysis was utilized to explore the shape of the leaf and fruit extract-mediated AgNPs by evaluating micrographs at 500 nm and 200 nm scales, as shown in Figure 6a–d. The leaf extract and fruit extract-mediated AgNPs yielded micrographs that display the particle size distribution as well as the shape [50], and offer a histogram by physically counting the particles or using specialist software [51]. The analysis of Annona squamosa leaf extract-mediated AgNPs revealed that the particle size of silver was in the range of 35–90 nm, whereas fruit extract-mediated AgNPs exhibited a range of 15–50 nm and demonstrated their spherical shape, which generally depends on various factors, such as pH level, temperature, reaction time, extract, and precursor solution concentrations, which, as a whole, identifies the reason for the different sizes of AgNPs [52]. The size distribution of silver nanoparticles can be minimized by adjusting the operational parameters prior to syntheses, such as temperature, reaction time, precursor concentration, and extract quantity.

Small spherical-shaped silver particles, like bright tiny spots, can be seen on the extract’s larger bio-particles in the case of AgNPs generated by leaf extract, while the agglomeration of a few smaller particles into small clusters can also be seen in Figure 6a. Smaller NPs have high surface energy and agglomerate into larger-sized particles to lower their surface energy [53]. The size distribution range of these spherical AgNPs was determined to be 35–90 nm, as seen in Figure 6b’s magnified view of the 200 nm scale and graphically displayed in Figure 7a of particle size histogram. The fruit extract-mediated AgNPs also exhibited a spherical shape but with tiny bright spots, with a bit less agglomeration effect compared to leaf extract-mediated AgNPs (Figure 6c), whereas a magnified view with a scale of 200 nm is demonstrated in Figure 6d. The smaller size of particles confirmed the low surface energy and hence, high throughput with a size distribution of 15–50 nm, as presented in the histogram in Figure 7b.

4. Antibacterial Activity

The AgNPs produced from A. indica and C. colocynphis extracts have been found to be effective for larvicidal activity (anti-dengue) with size ranges of 11–21 nm and 21–31 nm, respectively [54]. As the present study explored distinct extracts, it discovered a size range of 35–90 nm and 15–50 nm, with the larger size showing the agglomeration effect caused by various factors, such as extract concentration, pH value, temperature, time, and so on, while the smaller size range shows a significant structure with less surface energy, and thus particles with a small size can be more effective for anti-cancer, antibacterial, and anti-larvicidal applications [54]. Additionally, the antibacterial activity of different leaf extract-mediated AgNPs with sizes ranging from 3–15 nm has been established [29], indicating a large potential for future prospects in biomedical applications. Moreover, Malachra Capitata leaf extract was also reported to synthesize spherical polydisperse AgNPs with sizes ranging from 5–70 nm, and the presence of natural functional chemicals was confirmed by FTIR analysis, demonstrating its potential for further antimicrobial properties [50]. This technology is potentially exciting for the large-scale synthesis of various inorganic materials due to the applications of such environmentally friendly NPs in antibacterial, wound healing, and other medical applications, and toxicity studies on human pathogens by AgNPs pave the way for a new class of antibacterial medicines.

4.1. Antibacterial Activity Results

The antibacterial evaluation of employed Annona squamosa leaf and fruit extracts along with their mediated AgNPs is described in

Table 2. Antibacterial activity of Annona squamosa leaf and fruit extract-mediated silver nanoparticles by forming ZOI.

Samples	Concentration of Nanoparticles	Zone of Inhibition (ZOI)
		E. coli	P. aeruginosa
Annona squamosa leaf extract-mediated Silver Nanoparticles	100 µg/mL	19.3 mm	18.8 mm
	50 µg/mL	16.5 mm	16.1 mm
	25 µg/mL	15.7 mm	14.6 mm
Annona squamosa fruit extract-mediated Silver Nanoparticles	100 µg/mL	16.2 mm	16.8 mm
	50 µg/mL	15.4 mm	16.0 mm
	25 µg/mL	13.6 mm	14.8 mm

and illustrated in Figure 8. The results revealed that plant extracts and their mediated AgNPs were both efficacious against bacterial growth, with high concentrations of AgNPs being more appealing to both bacterial strains than their counterparts.

4.2. Antibacterial Mechanism

Silver is a widely used antibacterial agent that can kill over 650 distinct microorganisms, including gram-negative and gram-positive bacteria, fungi, and viruses, demonstrating medicinal effects for about 2000 years [55]. Silver is commonly employed in the nitrate form to generate antimicrobial effects; however, silver nanoparticles have a significant exposed surface area for microorganisms’ interaction. Silver must be in ionized form to have an antibacterial capability where it shows inert properties, and upon interacting with moisture/target, it releases silver ions [56]. AgNPs can attack bacteria in various ways, such as the electrostatic interaction between Ag⁺¹ and negatively charged bacterial cell plasma membranes, causing cell death [57]. This interaction is due to oxidative stress produced by reactive oxygen species (ROS) in the bacterial cell membrane [58]. Furthermore, when AgNPs impregnate the bacterial cell membrane by disrupting the respiratory chains, they then seep into the organelles and react with DNA, ribosomes, and enzymes where the released Ag⁺¹ ions can form complex compounds with nucleic acids and primarily interact with nucleosides rather than phosphate groups, causing denaturation of the genetic material and apoptosis after binding with their components. The AgNPs also accumulate in the bacterial membranes of E. coli and P. aeruginosa cells, causing enhanced permeability and cell death. This schematic mechanism is illustrated in Figure 9.

5. Conclusions

In this study, we have summarized the impact of Annona squamosa as a reducing and capping agent that helps to reduce metal NPs such as silver and successfully synthesized AgNPs using leaf and fruit extracts by adopting a green synthesis method, which is an eco-friendly, cost-effective, non-hazardous, and speedy method. Flavonoids, phenolic compounds, quercetin, alkaloids, acetogenins, carotenoids, and other phytochemicals found in Annona squamosa extracts are responsible for their reducing behavior, as well as their biological applications. The size ranges of AgNPs mediated by leaf and fruit extracts were found to be 35–90 nm and 15–50 nm, respectively, with both displaying an FCC crystal structure. The findings demonstrate that both extracts and their mediated AgNPs were effective against bacterial growth, with high concentrations of AgNPs being more appealing to both bacterial strains than their counterparts, predicting a large potential for industrial applications, such as antibacterial rugs, wound healing, anti-cancer activity against various cell lines, textiles, paints, implantable medical devices, and many more, based on their size and shape.