Review

Introduction

The utilization of nanotechnology for constructing nanoscale products in research and development divisions is growing [1]. Nanotechnology can be used to produce a broad range of products applicable to an equally broad array of scientific sectors. “Creation,” “exploitation,” and “synthesis” are terms associated with nanotechnology, which generally considers materials that measure less than 1 mm. “Nano” is derived from the Greek word “nanos”, meaning “dwarf, tiny, or very small” [2]. Nanotechnologies are generally classified as wet, dry, and computational. Wet nanotechnology is associated with living organisms such as enzymes, tissues, membranes, and other cellular components. Dry nanotechnology is associated with physical chemistry and the production of inorganic items, such as silicon and carbon. Computational nanotechnology is associated with simulations of nanometer-sized structures [3]. These three dimensions (wet, dry, and computational) depend on each other for optimal functionality, represented in Fig. 1. Nanotechnology supports diverse unique industries, such as electronics, pesticides, medicine, and parasitology, and thus provides a platform for collaboration [4]. Nanobiotechnology provides one such example, wherein the study and development combine multiple scientific sectors, including nanotechnology, biotechnology, material science, physics, and chemistry [2, 5].

Fig. 1
figure 1

Different types of nanotechnology

Biologically synthesized nanoparticles with antimicrobial, antioxidant, and anticancer properties are possible through the collaboration of different natural science sectors. These nanotechnologies may provide novel resources for the evaluation and development of newer, safer, and effective drug formulations [6].

Different Modes of Nanoparticle Synthesis

Nanoparticles, which have unique properties due to their size, distribution, and morphology, are critical components of any nanotechnology. In the late 1970s, R.O. Becker et al. used silver particles to treat infections caused by microorganisms during the treatment of orthopedic diseases, resulting in faster bone recovery [7]. At present, varied physical, chemical, biological, and hybrid methods (Fig. 2) are utilized to synthesize distinct nanoparticles [8, 9]. The synthesis of nanoparticles has traditionally relied on two approaches, physical and chemical. These approaches include ion sputtering, solvothermal synthesis, reduction, and sol-gel techniques. Nanoparticle synthesis methods can also be classified as bottom-up and top-down. Chemical methods involve the reduction of chemicals [10], electrochemical procedures [11], and reduction of photochemicals [12]. Plant-based synthesis of nanoparticles is in contrast faster, safer and lighter; works at low temperatures; and requires only modest and environmentally safe components [13]. Plant-based nanoparticles have attracted more attention due to growing interest in environmentally conscious products. In addition, the synthesis of nanoparticles using plants offers other advantages, such as the utilization of safer solvents, decreased use of dangerous reagents, milder response conditions, feasibility, and their adaptability in use for medicinal, surgical, and pharmaceutical applications. [14]. Furthermore, physical requirements for their synthesis, including pressure, energy, temperature, and constituent materials, are trivial.

Fig. 2
figure 2

Methods involved in nanoparticle synthesis

Nanoparticles made of noble metals have also received attention over the last few years, as they can be used in medicine, biology, material science, physics, and chemistry [15]. Among the several noble metal nanoparticles, silver nanoparticles (AgNPs) have attracted special attention due to their distinct properties, which include favorable electrical conductivity, chemical stability, and catalytic and antibacterial activity [12]. Silver at the nanoscale also has different properties from bulk silver. Synthesis of AgNPs is an emerging area and is much sought after [16]. The green synthesis of AgNPs has been accomplished using plants, microorganisms, and other biopolymers [12]. Wet chemical synthesis can be robustly scaled for the large-scale synthesis of AgNPs of tunable shape and size through optimization of synthesis conditions. However, wet chemical methods use toxic chemicals, which are hazardous for the environment and usually result in the adsorption of toxic chemicals on to the surface of synthesized AgNPs, making them unsuitable for biomedical applications. In contrast, physical methods are expensive and cumbersome for the large-scale production of nanoparticles. Therefore, the development of environmentally conscious, energy-efficient, facile, and rapid green synthesis methods that avoid toxic and hazardous chemicals has attracted significant interest [17]. In addition, due to their potent antimicrobial activity, AgNPs have also been used in clothing [18], foods [19], sunscreens, and cosmetics [20, 21].

Synthesis of AgNPs

The use of plants for nanoparticle synthesis offers a wide range of benefits over other biological synthesis methods because it does not require the maintenance of cell cultures and incorporates support for the large-scale synthesis of nanoparticles [22]. Extracellular nanoparticle synthesis, which utilizes extracts from individual leafs rather than entire plants, may prove to be more inexpensive due to easier downstream processing (Fig. 3). Sastry and his group are responsible for pioneering nanoparticle synthesis using plant extracts [2227].

Green synthesis of AgNPs using plant extracts containing phytochemical agents has attracted considerable interest (Table 1). This environmentally friendly approach is more biocompatible and cost-efficient and includes the capability of supporting larger synthesis [28, 29]. The synthesis of AgNPs via different “green” chemico-physical conditions, as well as by numerous microorganisms, has been heavily investigated. When AgNPs are chemically synthesized, three main components are required: (1) silver salt (e.g., AgNO3), (2) a reducing agent (e.g., NaBH4), and (3) a stabilizing or capping agent (e.g., polyvinyl alcohol) for controlling the size of nanoparticles and preventing their aggregation [30]. AgNPs have applications in wound-healing, eye disease therapy, DNA processing, and pharmaceuticals in addition to other relevant mainstream applications: electronics, optics, catalysis, and Raman scattering [3135]. Lokini et al. [36] showed that AgNPs could destabilize the outer membrane and rupture the plasma membrane, thereby depleting intracellular ATP. Silver has a greater affinity to react with sulfur or phosphorus-containing biomolecules in the cell; therefore, sulfur-containing proteins in the membrane or inside cells and phosphorus-containing elements like DNA are likely to be preferential sites for binding AgNPs. The advantages of using plants for the synthesis of nanoparticles include their availability, safety in handling, and presence of a variability of metabolites that may aid in reducing silver. The time required to reduce 90 % of silver ions is approximately 2 to 4 h [27]. Gericke and Pinches [37] reported that the size of particles that form intracellularly could be controlled by altering key factors such as pH, temperature, substrate concentration, and time of exposure to the substrate.

Table 1 Green synthesis of silver nanoparticles using different plant extracts

The biochemical and molecular mechanisms of AgNP biosynthesis remain poorly characterized and should be investigated to further optimize the process. For instance, characterization of biochemical mechanisms underscored the importance of phytochemicals, which may mediate biosynthesis. Improvements in chemical composition, size, shape, and dispersity of nanoparticles would permit the use of nanobiotechnology in a variety of other applications [38]. Plant crude extracts contain novel secondary metabolites such as phenolic acid, flavonoids, alkaloids, and terpenoids, which are mainly responsible for the reduction of ionic metal into bulk metallic nanoparticles [39]. Primary and secondary metabolites are constantly involved in redox reactions required to synthesize eco-friendly nanoparticles. Biosynthesis reactions can be modulated to transform the shape and size of nanoparticles by using different metal concentrations and amounts of plant extract in the reaction medium [27, 40].

Capsicum annuum leaf extracts contain a number of biomolecules, such as proteins, enzymes, polysaccharides, amino acids, and vitamins, which could act as bioreductants for metal ions or as scaffolds to direct the formation of AgNPs in solution. In detail, the mechanism underlying the bioreduction of silver was hypothesized to first involve trapping of silver ions on the surface of proteins in the extract via electrostatic interactions (i.e., recognition process). Silver ions are then reduced by proteins, leading to changes in their secondary structure and the formation of silver nuclei. Silver nuclei subsequently grow by the further reduction of silver ions and their accumulation at nuclei [41]. Callicarpa maingayi stem methanolic extracts were used for the synthesis of AgNPs, leading to the formation of [Ag (Callicarpa maingayi)]+ complex. Plant extracts contain aldehyde groups, which are responsible for the reduction of silver ions into metallic AgNPs. The different functional group, –C = 0, C = N, indicates amide I of polypeptides that are responsible for the capping of ionic substances into metallic nanoparticles. Molecular studies on the biosynthesis of silver crystals have revealed a complex process, which is not fully understood yet [42].

Physical Requisites for the Synthesis of AgNPs

Easier, more reliable, and environmentally friendly methods to synthesize nanoparticles accelerate their widespread adoption, which would benefit humans and the environment [43]. Silver disassembles into particles following the addition of plant extract, which may lead to a color change. Solutions of AgNPs appear dark, yellow-brown in color because of the surface plasmon resonance phenomenon [44]. Gardea-Torresdey et al. [45] determined the influence of pH on the mass of nanoparticles when using alfalfa biomass in the biosynthesis of colloidal gold. Mock et al. [46] reached a similar conclusion that the unique pH conditions of different extracts affect nanoparticle size and shape. Two extracts from the same host plant may have a different pH, thus highlighting the need for better synthesis methods for nanoparticles. Large nanoparticles are most often formed only at lower pH values, instead of higher pH values, as has been previously reported [47, 48]. Dwivedi and Gopal [49], utilizing extracts of Chenopodium album, observed trivial variations in zeta potentials of nanoparticles in pH conditions ranging from 2 to 10 and determined that nanoparticles were more stable when exposed to higher pH conditions. Veerasamy et al. [50] demonstrated that mangosteen extracts induced the nucleation of a cluster of AgNPs at pH values over 4. Furthermore, nanoparticles grew rapidly, with their pH values ranging from basic to neutral. These results demonstrate the significant impact of pH on parameters of nanoparticles. The formation and growth of nanoparticles is retarded by acidic conditions, whereas basic conditions promote nanoparticle assembly. Larger nanoparticles are formed in lower pH conditions (pH 4), whereas significantly smaller nanoparticles are formed in higher pH conditions (pH 8). Our results indicate that the size of nanoparticles decreases when pH increases. pH values in the range of 2–14 play an important role in the synthesis of AgNPs. In plants, AgNP synthesis occurs at various pH values depending on the plant species [50]. However, previous studies have indicated that neutral pH is optimal for AgNP synthesis. At this pH, little or no assembly of AgNPs into particles of suitable size and shape occurs [51].

Newly synthesized AgNPs, formed within 60 min of incubation with leaf extracts of Eucalyptus chapmaniana, exhibited a UV-Vis peak at 413 nm [52]. The UV-Vis spectra of AgNPs, synthesized with leaf extracts of Desmodium gangeticum for an optimum incubation time of 90 min, exhibited a peak at 450 nm [53]. Vilchis-Nestor et al. [54] demonstrated a UV-Vis peak at 436 nm for AgNPs formed within 4 h of incubation with Camellia sinensis extracts. Chandran et al. [27] synthesized AgNPs with leaf extracts of Aloe vera incubated for 24 h, which exhibited a UV-Vis peak at 410 nm. UV-Vis absorption spectra reach a maximum when the synthesis of nanoparticles (NPs) is complete, which requires sufficient time for the nucleation and subsequent stabilization of nanoparticles. Song and colleagues synthesized stable AgNPs extracellularly, with average particle sizes ranging from 15 to 500 nm, with Pinus densiflora, Diospyros kaki, Ginkgo biloba, Magnolia kobus, and Platanus orientalis leaf extracts. The rate of synthesis and final conversion to AgNPs was faster with higher reaction temperatures. However, average particle sizes of nanoparticles produced with D. kaki leaf extracts decreased from 50 to 16 nm when the temperature of synthesis was increased from 25 to 95 °C [16]. Ocimum sanctum leaf extracts could reduce silver ions into crystalline AgNPs (4–30 nm) within 8 min of the reaction. These nanoparticles were likely stable due to the presence of proteins, which may act as capping agents. O. sanctum leaves contain ascorbic acid which was likely important for the reduction of silver ions into metallic AgNPs [55].

Monodisperse spherical AgNPs (~3 nm) were also synthesized using gum kondagogu (nontoxic polysaccharide derived as an exudate from the bark of Cochlospermum gossypium) [56].

Characterization of Synthesized AgNPs

The synthesis of AgNPs using a 5:1 ratio of fruit extracts of Piper longum was evident by a change in the color of 1 mM AgNO3 solution from colorless to brownish-yellow, which resulted in a peak at 430 nm in UV-Vis spectra [57]. Aqueous leaf extracts of Manilkara zapota were used to synthesize AgNPs, which exhibited XRD with 2θ values of 38.06°, 44.37°, 64.51°, and 77.31° sets of lattice planes, which may be indexed to the (111), (200), (220), and (311) face-centered cubic (fcc) structure of silver, respectively [58].

Fourier transform infrared (FTIR) spectroscopy, which is used to evaluate chemical bonds in surface atoms and functional atoms on the surface of nanoparticles, can be used to characterize physical properties of nanomaterials and their functions [59, 60]. Certain proteins and metabolites, such as terpenoids or flavonoids that are present in leaf extracts of Prosopis juliflora, may be responsible for the decay and pause of AgNPs synthesis [61]. The FTIR spectra of AgNPs synthesized using either fresh or dried Codium capitatum extracts exhibited a strong transmission band at 1535 cm−1 corresponding to the bending vibration of secondary amines of proteins. The FTIR peak at 1637 cm−1 for AgNPs synthesized using Andrographis paniculata extracts can be attributed to the carbonyl stretch of amides and could be related to proteins that potentially cap AgNPs [62]. In C. annuum extracts, the formation of AgNPs is mediated by amine groups or the secondary structure of proteins [63].

The hydroxyl and carbonyl groups present in carbohydrates, flavonoids, terpenoids, and phenolic compounds are powerful reducing agents that may be responsible for the bioreduction of Ag+ ions necessary for AgNP synthesis. FTIR studies confirm that the carbonyl groups of amino acids and peptides of proteins have a strong affinity to bind metal ions, and they may encapsulate nanoparticles, forming a protective coat-like shell that prevents their further aggregation and leading to their stabilization in the medium [64].

A single-step method (biogenic) for the synthesis of AgNPs utilizes Ziziphus jujuba leaf extract as a reducing and stabilizing agent at room temperature. TEM images revealed nanoparticles featuring differing shapes and sizes, averaging 25 nm. These results were confirmed by DLS analysis, which revealed a hydrodynamic radius of 28 nm [65]. Environmentally friendly synthesis of AgNPs, which utilized Argemone mexicana leaf extracts and were 20 nm in size, had antimicrobial and antifungal activity against multiple bacterial and fungal pathogens [66]. Extracts from the Cycas leaf were utilized to prepare AgNPs measuring 2–6 nm [67]. AgNPs, measuring 14 nm and synthesized using Solanum torvum extracts, exhibited a peak at 434 nm in UV-Vis spectra. Using EDX analysis, Arunachalam et al. [28] showed that AgNPs were crystalline in nature and observed strong signal energy peaks for silver atoms in the range of 2–4 keV with weaker signals for carbon, oxygen, and chloride, which are prevalent biomolecules in Memecylon umbellatum. The size, shape, and size distribution of nanoparticles were observed by TEM and selected area electron diffraction (SAED) patterns of TEM images [68]. The crystalline nature of AgNPs was determined by SAED, which revealed fcc silver.

A facile biosynthesis method utilizing methanolic extracts of Vitex negundo, which can be performed at room temperature, was used to successfully synthesize spherical colloidal AgNPs of different sizes, although it required different reaction times. The sizes of colloidal AgNPs prepared for 6, 24, and 48 h averaged 10.11 ± 3.98, 12.80 ± 4.97, and 18.23 ± 8.85 nm, respectively [69]. The morphology and size of AgNPs synthesized using Pulicaria glutinosa extracts were examined by TEM, which revealed monodisperse spherical nanoparticles between 40 and 60 nm [70]. AgNPs synthesized using seed extracts of Artocarpus heterophyllus exhibited variance in their size, ranging from 3 to 25 nm with an average of 10.78 nm [71]. AgNPs fabricated using Boerhaavia diffusa leaf extracts as the nontoxic reducing agent and examined by TEM revealed AgNPs that were fcc structures of spherical shape and an average particle size of 25 nm [72].

Biomedical Applications of AgNPs

Antimicrobial Activity of AgNPs

The threat posed by the potential outbreak of antibiotic-resistant microbes is growing globally and demands the introduction and production of novel more advanced platforms for the study and development of more potent antimicrobial agents against multidrug-resistant strains [73]. The antimicrobial activity of AgNPs is widely recognized, though their activity can change with physical characteristics of the nanoparticle, such as its shape, mass, size, and composition, and conditions of its synthesis, such as by pH, ions, and macromolecules [74]. Their shapes can be relevant to their antibacterial activity [75]. Compared to larger AgNPs, smaller AgNPs have a greater binding surface and show more bactericidal activity [76]. Variation in the thickness and molecular composition of the membrane structures of gram-positive and gram-negative bacteria account for the difference in their sensitivities to AgNPs [77]. Bactericidal activity is presumably due to changes in the structure of the bacterial cell wall as a result of interactions with embedded AgNPs, leading to increased membrane permeability and consequently death [78]. AgNPs also interact with sulfur- and phosphorus-rich biomaterials, which include intracellular components, such as proteins or DNA, and extracellular components such as membrane proteins. These components influence the respiration, division, and ultimately survival of cells [79]. Upon compromising the bacterial cell wall, silver ions (as part of AgNPs) can enter into cells, leading to the accumulation of damaged DNA and effect on protein synthesis [80].

AgNPs synthesized with Skimmia laureola leaf extracts have antibacterial activity, with maximum growth inhibition activity against Staphylococcus aureus (14.67 mM), followed by Klebsiella pneumoniae, Pseudomonas aeruginosa (14.33 mM), and Escherichia coli (11.67 mM) [81]. AgNPs synthesized with mangrove plant Avicennia marina extracts exhibited highest inhibition activity against E. coli (18.40 ± 0.97 mM) and lowest against S. aureus (10.87 ± 1.33 mM). Its minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) were 0.25 and 50.0 μg/mL, respectively, against select bacteria [82]. Sankar et al. [83] synthesized AgNPs with extracts of oregano (Origanum vulgare), which exhibited antimicrobial activity against human pathogens, including Escherichia coli, Aeromonas hydrophila, Salmonella spp., Shigella dysenteriae, Salmonella paratyphi, and Shigella sonnei. Furthermore, AgNPs were cytotoxic to human lung cancer lines (A549 cells), which killed 50 % of cells at 100 μg/mL. Sathishkumar et al. [84] evaluated the bactericidal activity of AgNPs synthesized with Morinda citrifolia leaf extracts against a wide range of human pathogens, such as Escherichia coli, Pseudomonas aeruginosa, Klebsiella pneumoniae, Enterobacter aerogenes (gram-negative), Bacillus cereus, and Enterococcus sp. (gram-positive). The antibacterial activity of AgNPs synthesized with Rosmarinus officinalis extracts was tested against gram-positive bacteria, and the maximum zones of inhibition at dosages of 20, 40, and 80 mg/disk were 21.52, 30, and 31.2 mm, respectively, against S. aureus and 13.4, 15.63, and 16.21 mm, respectively, against Bacillus subtilis [85]. The antimicrobial activity of the medicinal plant Onosma dichroantha and antimicrobial activity of silver chloride nanoparticles suggest a novel approach to the development of bactericides applicable to a wide range of applications, such as the treatment of burn wounds and injuries [86].

AgNPs synthesized with Prunus yedoensis leaf extracts exhibited significant antibacterial activity against two skin pathogens, Propionibacterium acnes and Staphylococcus epidermidis. Exhibited zone of inhibition (ZOI) sustained greater levels of AgNPs (30 μg) after 48 h of inhibition against two gram-positive bacteria; furthermore, tetracycline sulfate at volume of 100 μg/mL was evaluated [87]. AgNPs synthesized with O. vulgare leaf extracts have broad-spectrum antibacterial activity against nine different human pathogens. Greater than 10-mm zones of inhibition were observed against Escherichia coli (enteropathogenic, EP), Aeromonas hydrophila, Salmonella paratyphi, Salmonella sp., Shigella dysenteriae, and Shigella sonnei. This level of antibacterial activity was comparable to the standard antibiotic chloramphenicol [83]. Saxena et al. [88] synthesized AgNPs using Ficus benghalensis leaf extracts, and its bactericidal activity against E. coli was evaluated by the broth microdilution method. The bactericidal activity of AgNPs synthesized with B. diffusa plant extracts was evaluated against three fish bacterial pathogens, Aeromonas hydrophila, Pseudomonas fluorescens, and Flavobacterium branchiophilum. Of these, F. branchiophilum was more sensitive to AgNPs, and the other two pathogens were equally sensitive [72]. Tripathi et al. [89] evaluated bactericidal activity of silver nanoballs at a concentration of 40 μg/mL against Escherichia coli, Salmonella typhimurium, Bacillus subtilis, and Pseudomonas aeruginosa by measuring colony-forming units (CFU). Silver nanoballs prevented the growth of bacteria and induced toxicity.

AgNPs, which are filled with polyphenolic compounds, disrupt the cell walls of bacteria, which make gram-negative bacteria specifically sensitive. Polyphenolic compounds generate free radicals and other oxygen-based reactive species, which can induce considerable damage and toxicity [75]. Other damages may result as membranes become disrupted, including the widespread loss of K+ ions, leading to a decrease in membrane potential. Significant membrane disruption results in cytoplasmic leakage, which includes the discharge of proteins and lipopolysaccharide molecules. The outer membrane of bacteria is composed of lipopolysaccharides and is fundamentally asymmetric, while the inner membrane comprises tight chains of phospholipids, which are semi-permeable [75]. The exact mechanism of interaction between AgNPs and bacteria is not fully understood. AgNPs may attach to the cell wall and thus disrupt membrane permeability and ultimately cell respiration. AgNPs can also directly penetrate into cells since they may bind to cell wall proteins that contain sulfur and phosphorus-containing biomolecules such as DNA [90, 91]. Thus, they can easily bind to constituents of the bacterial cell and disturb normal functions of the cell. Another possible mechanism is the release of Ag cations, which are antibacterial, from AgNPs [92].

AgNPs in Cancer Control

AgNPs perform well as cancer therapeutics because they can disrupt the mitochondrial respiratory chain, which induces the generation of reactive oxygen species (ROS), and ATP synthesis, which can induce DNA damage [93, 94]. AgNPs synthesized with Sesbania grandiflora leaf extracts were demonstrated to be cytotoxic to MCF-7 cancer cells. Morphological characteristics, including the disruption of membrane integrity, decreased cell growth, cytoplasmic condensation, and cell clumping, were observed in MCF-7 cells treated with AgNPs, whereas control cells remained active. In addition, apoptotic features, such as cell shrinkage and nuclear condensation and fragmentation, were also observed in MCF-7 tumor cells 48 h after treatment with 20 μg/mL of AgNPs. AgNPs synthesized with S. grandiflora extracts induced the generation of free radicals, which resulted in oxidative damage and caspase-mediated apoptosis [95].

AgNPs synthesized with Guignardia mangiferae extracts exhibited potent antifungal activity against plant pathogenic fungi. IC50 values of AgNPs were 63.37, 27.54, and 23.84 μg/mL against normal African monkey kidney (Vero), HeLa (cervical), and MCF-7 (breast) cells, respectively, after a 24-h incubation period. Thus, AgNPs synthesized with G. mangiferae extracts are highly biocompatible, have potentially wider applicability, and should be explored as promising candidates for a variety of biomedical/pharmaceutical and agricultural applications [96]. AgNPs were synthesized using extracts from different plant origins: Cucurbita maxima (petals), Moringa oleifera (leaves), and Acorus calamus (rhizome). Among the three synthesized nanoparticles, AgNPs synthesized with A. calamus rhizome extracts had enhanced antimicrobial and anticancer activity, which were evaluated through MTT assays against epidermoid A431 carcinoma cells. AgNPs synthesized with A. calamus rhizome extracts were superior to AgNPs generated with petal and leaf extracts in their antimicrobial and anticancer activities [97]. Both treated (synthesized) and untreated AgNPs induced DNA fragmentation at all concentrations [98]. Compared to untreated cells, cells treated with AgNPs synthesized using Phytolacca decandra, Hydrastis canadensis, Gelsemium sempervirens, and Thuja occidentalis extracts exhibited DNA laddering, confirming the apoptotic effects of nanoparticles. Specifically, AgNPs synthesized using P. decandra and G. sempervirens extracts effectively induced DNA laddering compared to AgNPs synthesized using H. canadensis and T. occidentalis extracts [98].

The IC50 values of AgNPs synthesized using Potentilla fulgens extracts were 4.91 and 8.23 μg/mL in MCF-7 and U-87 cell lines, respectively. Furthermore, the cytotoxic effects of nanoparticles were evaluated against cancerous and normal cells using trypan blue assay and flow cytometric analysis. In contrast to their effect on normal cells, nanoparticles are capable of impairing or killing cancerous cells [29]. AgNPs synthesized with Coleus amboinicus extracts were cytotoxic to EAC cell lines. AgNPs induced 50 and 70 % cytotoxicity at 30 and 50 μg/mL, respectively, indicating concentration-dependent cytotoxicity [99]. AgNPs synthesized with alcoholic flower extracts of Nyctanthes arbor-tristis can be used for molecular imaging and drug delivery. Even at the highest concentration tested (250 μg/mL), AgNPs were only marginally toxic to L929 cells [100]. The anticancer activity of AgNPs synthesized with unripe fruits of Solanum trilobatum against a human breast cancer cell line (MCF-7) was evaluated in vitro using MTT assays, nuclear morphological characteristics, and RT-PCR and western blot analyses. MCF-7 cells treated with either AgNPs or cisplatin exhibited decreased Bcl-2 expression and increased Bax expression, indicating the involvement of mitochondria in the mechanism of death induced by AgNPs [101].

Mitochondria function as critical centers of signaling; their integrity can be compromised by various regulators of apoptosis [102, 103]. The generation of ROS by AgNPs may also require mitochondria, which may initiate intrinsic caspase-dependent apoptotic pathways leading to cell death. Nanoparticles synthesized with Rosa indica extracts have the potential to be used in a wide range of therapeutic anticancer applications. AgNPs synthesized with green petals of R. indica act as radical scavengers and induce apoptosis in HCT-15 cells and the generation of ROS [104].

Antioxidant Activity of AgNPs

AgNPs synthesized using Leptadenia reticulata leaf extracts, at a concentration of 500 μg/mL, have the highest recorded radical scavenging activity of 64.81 % [105]. Plant extracts promote DPPH radical scavenging activity of AgNPs, which is dose dependent. The ability of antioxidants to scavenge DPPH radicals is likely due to their ability to donate hydrogens and easily incorporate electrons; the latter is possible due to the presence of host lipophilic radicals. A change of color from purple to yellow was observed at 517 nm [106]. The DPPH radical scavenging activity of HAuCl4 and AgNO3 was trivial compared to nanoparticles, which may be due to salt conditions or weaker solubility of metal oxides [107].

A sophisticated reaction can be observed between phenolic compounds and phosphotungstic and phosphomolybdic acids in Folin-Ciocalteu reagents [108]. Phenolic compounds present in plant extracts exhibited high antioxidant and reduction activities, which are important for the synthesis of AgNPs [109]. The higher total phenolic content of Eclipta prostrata leaf extracts supports the assembly of silver ions into smaller AgNPs, because of the donation of electrons by these compounds [110].

Antidiabetic Activity of AgNPs

The ability of AgNPs synthesized using stem extracts of Tephrosia tinctoria to control blood sugar levels was evaluated. AgNPs scavenged free radicals, decreased levels of enzymes that catalyze the hydrolysis of complex carbohydrates (α-glucosidase and α-amylase), and increased the consumption rate of glucose [111]. Due to the adverse effects of methylene blue (MB) on the environment, the removal of MB from wastewater is an important area of research and a key challenge for researchers. AgNPs synthesized with aqueous stem extracts of Salvadora persica were able to degrade MB in a light-dependent manner; by converting hazardous materials into nonhazardous ones, AgNPs potentially have significant applications in water purification [112]. MB exhibits characteristic absorption peaks at 663 and 614 nm, which were used to monitor the photo-degradation of MB. Higher concentrations induce the aggregation of AgNPs, leading to an increase in particle size and a decrease in specific surface area and surface active sites of particles [113]. The most effective concentration of AgNPs for the photo-degradation of MB was 8 mg.

Different Field Applications of AgNPs

Nanotechnology applications are highly suited for biological molecules because of their unique properties. Nanotechnology is a growing area of research in the fields of material science and biological science [114]. Silver nanoparticles have attracted the attention of researchers because of their broad applications in diverse areas, such as integrated circuits [115], sensors [116], biolabeling, filters, antimicrobial deodorant fibers [117], cell electrodes [43], low-cost paper batteries (silver nano-wires) [118], and antimicrobials [119]. AgNPs have been used extensively as antimicrobial agents in the health industry, food storage, textile coatings, and a number of environmental applications [120], few of which are shown in Fig. 4. Antimicrobial properties of AgNPs are beneficial for different fields of medicine, various industries, animal husbandry, packaging, accessories, cosmetics, health, and the military. In general, therapeutic effects of silver particles (in suspension) depend on different parameters, including particle size (surface area and energy), particle shape (catalytic activity), particle concentration (therapeutic index), and particle charge (oligodynamic quality) [121].

Fig. 3
figure 3

Plant-mediated synthesis of silver nanoparticles: their characteristic properties and therapeutic applications

The viability of A549 cells treated for 6 h with 10 and 50 μg/mL of AgNPs synthesized with Albizia adianthifolia leaf extracts was 21 and 73 %, respectively, and that of normal peripheral lymphocytes was 117 and 109 %, respectively, indicating that AgNPs are nontoxic to normal PLs cells [122]. AgNPs synthesized with Indigofera aspalathoides extracts were tested in wound-healing applications following excision in animal models [28]. AgNPs synthesized with Chrysanthemum morifolium extracts were added to clinical ultrasound gels, which are used with an ultrasound probe, and were found to have bactericidal activity, contributing to the sterility of the instrument [123]. AgNPs synthesized with M. zapota leaf extracts exhibited acaricidal activity against Rhipicephalus (Boophilus) microplus (LC50 = 3.44 mg/L) [58]. The IC50 values of AgNPs synthesized using aqueous extracts of Ashoka or neem leaves against Plasmodium falciparum were 8 and 30 μg/mL, respectively [124]. Appreciable larvicidal activity of AgNPs synthesized with aqueous extracts of E. prostrata was observed against Anopheles subpictus and Culex tritaeniorhynchus [125]. The population of bacteria decreased after 6 h when 10 mg of AgNPs synthesized using P. juliflora leaf extracts was used to treat 100 mL of sewage and increased over time [56]. AgNPs synthesized with Acacia nilotica pod extracts were used to treat glassy carbon electrodes, which exhibited greater catalytic activity in reducing benzyl chloride than glassy carbon and metallic Ag electrodes [126]. AgNPs synthesized using Gloriosa superba extracts act through the electron relay effect and influence the degradation of MB after 30 min [127].

Fig. 4
figure 4

Different applications of synthesized silver nanoparticles

Conclusions

In summary, silver nanoparticles (AgNPs) exhibit remarkable physical, mixture, optical, and natural properties compared to other biomedical nanomaterials, which make them ideal in various stages of diverse biomedical applications. Nanoparticles synthesized with plant concentrates have yielded promising results in biomedical applications. Comprehensive examination further contemplated that repercussions of nanoparticles give essentially the same number of preferences and purposes of enthusiasm for remedial applications in examination to standard medicines and antidotes to poisons. The use of AgNPs in medicinal transport systems may also be utilized in the future in the field of arrangement. AgNPs have the potential to function as therapeutics with diverse clinical and pharmacological properties. They may be used in broad applications, including as anticancer agents or bactericidal agents during surgery or recovery. In this way, the green synthesis of AgNPs as novel remedial authorities will be significant in various biomedical applications. Notwithstanding their potential in restorative applications, the impact of AgNPs on human welfare (both positive and negative) should be completely considered before their widespread use. The adaptability of manufacturing techniques for AgNPs and their easy reconstitution into distinct media have prompted further research into the hypothetical impact of nanoparticles as antimicrobial, antiviral, and mitigating agents. The shape, size, and size distribution of AgNPs can be controlled by modifying synthesis conditions, such as with specialists, stabilizers, or distinct engineering techniques. The productive translation of silver into nanotechnology applications requires safe, creative, and eco-conscious strategies and greater control over their biodistribution and pharmacokinetics in clinical applications.