Synergistic Effects of Physicochemical Parameters on Bio-Fabrication of Mint Silver Nanoparticles: Structural Evaluation and Action Against HCT116 Colon Cancer Cells

Introduction

Plant body act as a repository of diverse secondary metabolites that are not only responsible for various environmental, social and defensive responses of plants but also provide many benefits to humans.¹ Plants have natural mechanisms to entrap metallic constituents found in their vicinity by their absorption from the soil solution and their transport to different plant organs to convert them into nanometals that later assimilate into their bodies and prevent plants from the toxic effects of excessive metals into their habitat.^2,3 The top-bottom approach to carve the bulk materials into their nano-forms by using the reducing and stabilizing abilities of plant secondary metabolites depends greatly on reaction conditions that can be harnessed by physicochemical parameters and influence the final size, shape, and capping of nanomaterials.^4–6

Physicochemical parameters provide a toolbox to carve nanoparticles and have different effects. Temperature plays a vital role by not only providing the activation energy that is usually required for the inception of a chemical reaction but also favors by increasing the molecular collision that enhances the possibility of the reactants to collide and convert into their resultant product. Different pH ranges have different influences on the reaction kinetics and molecular dynamics. pH contributes greatly to increase or decrease the number of H⁺ ions in the reaction mixture.⁷ Lower the pH value results in increasing the concentration of H⁺. pH does not directly affect the conformational changes of proteins and enzymes but the change in the concentration of H⁺ ions can shape and alter the electronegative properties of the substrate that can affect their binding with the enzymatic active site.^2,8,9 The ratio of reactants, their proportion and conjunction with catalyst act in a synergistic fashion along with temperature and pH. Modulation of physicochemical switches have effects on the morphological and biochemical basis of nanostructures that contribute toward their biocompatibility and make them suitable to treat various diseases.^10,11

Cancer is reported as a leading cause of death with around more than 10 million cases every year and is caused by clonally selected mutations in key tumor-suppressor genes and oncogenes.¹² Conventional treatment of cancer involves the surgical removal of cancer sites, chemotherapeutic and radioactive killing of the cancer cells but these treatments often lead to the deterioration of the patient’s body and development of resistance in cancer cells against treatment that negatively affect the treatment success rate.^13–15 Colorectal cancer is the third most common cancer and makes 10% of all reported cases worldwide. Conventional oncological medicines against colorectal cancer results in the damage of many healthy cells and vital organs of patients owing to a decrease in quality of life. The route of administration of cancer chemotherapeutics involves the circulation through the bloodstream to the cancer site and does not have any selectivity. Radioactive treatment of colorectal cancer results in extreme diarrhea, abdominal pain, difficulty to urinate and pain during defecation which make routine medicines very unsuitable for patients. Tumor cells have biology different than normal cells such as the rapid proliferation of blood vessels that is called angiogenesis, poor permeability of vessels and lymphatic drainage. This varied behavior of cancer cells from normal cells has used as an opportunity by nanotechnologists to design functional nanodrugs to target cancer cells with utmost selectivity and precision.^16–18

Plant-mediated green synthesis provides an advantage to synthesize nanoparticles of biocompatible nature without adding additional capping or stabilizing agents.¹⁹ The plant body has many different functional groups that cap the metallic core of the Ag and prevent them from agglomeration.²⁰ There are many reports available about phytosynthesis of nanoparticles but the detailed studies explaining the role of different physicochemical parameters and their synergic effects on the synthesis of AgNPs are limited. The present study was devised to use Mentha arvensis (mint) from the Lamiaceae family well renowned for the presence of antioxidants,²¹ to tailor AgNPs and study the effects of different reactions conditions on reaction kinetics, molecular mechanics and the yield of nanoparticles. Herein we report the (schematic overview is represented in Scheme 1) synergistic effects of various reaction parameters on bio-fabrication of AgNPs, their detailed structural evaluation and abilities to induce apoptosis and cell cycle suspension.

Scheme 1 Schematic representation of the work layout. Step 1 and 2 explain the effects of different physicochemical reaction parameters to optimize the synthesis of AgNPs. Step 3 is representing the spectrophotometric results of various reaction conditions. Step 4 is highlighting the characterization of nanostructures. Step 5 and 6 is showing the biological applications of bio-fabricated AgNPs. Note: Red triangle and circle represent the shape of nanoparticles.

Materials and Methods

Processing of Plant Material and Aqueous Extract Preparation

M. arvensis has purchased from the local farmer’s market Sialkot (32.485272° N 74.543575° E) Pakistan. Samples were washed, dried to remove the moisture, chopped into small pieces and pulverized in the kitchen grinding machine to make a fine powder. For the preparation of aqueous extracts, 1 to 10 ratio of plant material and distilled water was prepared, respectively, and heated on a hot plate at 45–65 °C for 10–20 min. After the boiling, the aqueous extract was filtered and used immediately as fresh for the reduction of silver salt.²⁰

Chemical Reagents

All chemical reagents purchased for the synthesis and biological applications of silver nanoparticles were of analytical grade and used as received without any further purification.

Phytosynthesis of AgNPs

Silver nitrate solution of a specific concentration was mixed with freshly prepared plant extract in a ratio of 1 to 9 of plant extract and silver nitrate solution, respectively. The reaction was carried out at a defined pH, temperature and reaction mixture was stirred continuously. An aliquot was taken out from the flask and the absorbance was measured by using crystalline quartz cuvettes with the help of UV-Visible spectrophotometer (Shimadzu 1601, Japan) in the range of 200–900 nm of light wavelength. Absorbance was measured after a specified interval of time to observe the reaction kinetically and to determine the synthesis of AgNPs. After the completion, the reaction was quenched by removing the flask from the hot plate and diluted with a small amount of distilled water. The reaction mixture was centrifuged at 1000× g (Sorvall RT 7 Plus) for 1 hour, thrice to separate the AgNPs from reaction mixture.²²

Optimization of Physicochemical Parameters for the Synthesis of AgNPs

The multifactorial experimental design was used to arrange reaction parameters. Physicochemical conditions such as pH, temperature, the concentration of AgNO₃, incubation period and plant extract ratio in the reaction mixture were optimized in a way that one parameter was changed while the rest of the parameters were kept constant. Different combinations of reaction conditions were devised to study their synergistic and individual effects. The effects of different reaction conditions on the synthesis of AgNPs were studied by using UV-Visible spectrophotometer.²³

Determination of Suitable Ratio of Reactants for the Synthesis of AgNPs

For the determination of the optimum mixing ratio of reactants, a 2 mM solution of AgNO₃ was prepared. 100 μL of plant extract was mixed with 900 μL of AgNO₃ and the concentration of plant extract increased gradually from 100 μL to 900 μL and the concentration of the silver salt solution was decreased subsequently from 900 μL to 100 μL, to record the effects of different mixing concentrations over the synthesis of AgNPs. Mixtures were incubated in an oven at 60 °C for 24 hours. At the end of the incubation, period absorbance was recorded in the range of 200–900 nm of light wavelength.²⁴

Morphological and Optical Characterization of AgNPs

Physical characterization of synthesized silver nanoparticles was performed by using different material characterization techniques to explore their structural morphologies. Nanoparticles synthesis was observed initially by observing a change in the color of the reaction mixture. UV-Visible Spectrophotometer (Shimadzu 1601, Japan) was used for the optical characterization and the aliquot of the colloidal AgNPs was observed between 200–900 nm of light wavelength. Scanning Electron Microscope (SEM) JEOL 7500F HRSEM was used to measure the size and shape of nanoparticles by preparation of the samples on copper grids by a drop coating method and observed by using different voltages and laser powers. The elemental composition of AgNPs was determined by Energy Dispersive X-Ray Analysis (EDX) that involves using detectors associated with JEOL 7500F HRSEM. Atomic Force Microscopy (AFM) images were collected on an Agilent 5500 AFM and the sample was placed on a silicon wafer and was prepared on a spin coater (Laurell WS-650Mz-23NPP) machine to spread nanoparticles on a silicon wafer. The hydrodynamic diameter of nanoparticles was measured by preparing colloidal sample solution of nanoparticles into 1× PBS at 25 °C by using Dynamic Light Scattering (DLS) machine of Malvern Instruments particle sizer, Zetasizer Nano S, Malvern Instruments, UK and rest of the parameters were adjusted by using automatic machine settings.^25–28

IC₅₀ Measurement of AgNPs (Sulforhodamine B Assay (SRB))

For determining the IC₅₀ of nanoparticles, 2000 HCT116 colon cancer cells were seeded in 100 μL of DMEM complete medium in a 96 well plate. The next day, cells were treated with different concentrations made by serial dilutions of nanoparticles. After 3 days, cells were fixed by adding 41 μL of 10% TCA directly to the wells. The plate was incubated overnight at 4 °C, washed 4 times with tap water and allowed to dry at 37 °C for 15 minutes. Cells were stained by adding 100 μL of 0.06% SRB to the wells and incubated for 30 minutes at room temperature. Washing was performed 4 times using 1% acetic acid in tap water and the plates were allowed to dry for 15 minutes at room temperature. Dye was eluted using 100 μL of 10 mM Tris and incubated at room temperature on a shaker at 300 rpm for 5 minutes. Finally, the absorbance was collected at 490 nm and IC₅₀ was measured by using GraphPad Prism^® software.²⁹

Measurement of Apoptotic Colon Cancer Cells Treated with Plant Aqueous Extract and AgNPs (Annexin V Apoptosis Assay)

Cells were harvested after the incubation period and washed in ice-cold 1× PBS solution. After that, the cells were resuspended again in ice-cold 1× PBS and re-centrifuged at 300× g for 5–10 min at 4 °C. The supernatant was discarded and the cells were resuspended in 1× annexin binding buffer (ice cold). The cell density was maintained at 1× 10⁶ cells/mL in 1× annexin binding buffer. 100 μL of cell suspension (resuspended in 1× Annexin binding buffer) was taken into a new Eppendorf tube and 5 μL of Fluorescein isothiocyanate (FITC) or Alexa fluor 488 labeled Annexin V was added to each 100 μL cell suspension. Followed by the addition of 1 μL of propidium iodide (100 μg/mL) to each 100 μL cell suspension. Incubated for 15 min at room temperature in the dark. At the end of incubation, 400 μL of ice-cold annexin binding buffer was added, mixed gently and the samples were incubated on ice and data was acquired on flow cytometer as soon as possible.³⁰

Cell Cycle Analysis of AgNPs-Treated HCT116 Colon Cancer Cells

The ability of the Propodium iodide to bind with the DNA stoichiometrically provides an advantage to determine the percentage of the cells into different cell phases that was measured by using cell cycle analysis.³¹ For cell cycle analysis, cells were cultured in a 6-well plate at a density of 1 million. After treatment for 72 hours, cells were collected by trypsinization, washed and fixed with 70% freshly prepared ethanol for 1 hour on ice. Cells were centrifuged, washed with PBS and resuspended again in 1mL PBS supplemented with 5 μL of RNAse A and 10 μL of Propidium iodide. Incubation was carried out in the dark at 37 °C for 1 hour and finally, cells were acquired by fluorescence-activated cell sorting (FACS) using FL-2 for the detection of Propidium iodide.³⁰

Data Analysis

Graphs were plotted using the Origin Lab Pro^® and Microsoft MS Excel^® Program. GraphPad Prism^® software was used for the determination of IC₅₀.

Results and Discussion

Synergistic Effects of Different Physicochemical Reaction Conditions on the Synthesis of AgNPs (Spectrophotometric Analysis)

Physicochemical parameters provide an only opportunity to act as a toolbox to control the top-bottom carving and fabrication of biogenic materials. pH, temperature, concentration and the proportion of reactants play a vital role to control the chemical kinetics, catalysis and reaction dynamics.^7,32,33

Effects of Different Concentrations of AgNO₃ and Temperature on the Synthesis of AgNPs

Different physicochemical conditions have different effects on the reaction kinetics, yield, morphological features and on the biochemical attributes of AgNPs.⁷ The concentration of AgNO₃ plays a key role to act as a source of the Ag⁺ ions in the reaction mixture. A meager concentration of Ag may decrease the rate of chemical reaction and excess of Ag may result in the synthesis of large size nanoparticles or clumps or it may suppress synthesis.³⁴ Change in the color of the reaction mixture from clear brown to dark brown was indicated as an initial sign of AgNP synthesis. There was no observable change in the color of the reaction mixture when 1 mM of AgNO₃ was used as reactants (Figure 1A). It can be because of the presence of less Ag⁺ ions in the reaction mixture that does not function to initiate the process of synthesis. Change in the color of the reaction mixture is a response of the interaction of nanoparticles of different sizes and shapes to different electromagnetic light waves.³⁵

Figure 1 UV-Visible spectrum representing AgNP synthesis under different physicochemical conditions. (A) Temperature 30 °C, 1 mM; (B) temperature 30 °C, 3 mM; (C) temperature 30 °C, 5 mM; (D) temperature 60 °C, 1 mM; (E) temperature 60 °C, 3 mM; (F) temperature 60 °C, 5 mM.

An increase in the concentration of AgNO₃ resulted in increasing the ionic concentration of Ag that may function to affect the enzymatic conformations and electronegative states of reactants resulted in the change of the color of the reaction mixture (very light brown). Surface plasmon resonance (SPR) band which is a result of the vibration of free electrons of AgNPs in coordination with the metal lattice in resonance and the oscillating electromagnetic field of light waves, was observed³⁶ (Figure 1B). Increasing the concentration of the Ag ions (5 mM AgNO₃) resulted in decreasing the synthesis and no SPR band was observed (Figure 1C). It was confirmed that 30 °C is not a suitable temperature to initiate the redox chemical reactions to reduce the Ag. Even an increase in the concentration of Ag did not affect the reaction kinetics.

Temperature plays a very important role in reaction dynamics by providing activation and kinetic energy. It affects the conformation of many biomolecules and also contributes toward the increase in the kinetic motion of atoms that enhance the process of ionization.⁸ The characteristic SPR band of AgNPs was observed at 3 mM and 5 mM of AgNO₃ at 60 °C (Figure 1E and F), while the reaction proceeded very slow when 1 mM of silver salt was used (Figure 1D). The reaction was completed early (3 h) when 5 mM of AgNO₃ was used in comparison to 3 mM (4 h & 30 mins) which is represented by the height of the SPR band. According to the Beer Lambert’s Law peak height of the SPR band is directly proportional to the concentration of the reacting species. Higher the concentration of the AgNPs higher the SPR band and vice versa.¹² It was confirmed that the temperature is not only the factor to design the nanoparticles but the concentration of the metallic salt also contributes toward the synthesis along with the incubation period. It was also observed that the SPR band was shifted gradually toward the longer wavelength with an increase in the incubation period (Redshift). According to Mie’s scattering theory,³⁷ small molecules absorb light at a shorter wavelength while the large molecules absorb light at a longer wavelength. Redshift is expressing an increase in the size of the nanoparticles with an increasing incubation period.

The increasing temperature at 120 °C was found futile for the synthesis of AgNPs by using M. arvensis aqueous extract (Figure 2A–C). Temperature up to the optimum threshold can denature plant metabolites, alter their functional conformations and breakdown secondary molecules that hinder synthesis.

Figure 2 UV-Visible spectrum representing AgNP synthesis under different physicochemical conditions. (A) Temperature 120 °C, 1 mM; (B) temperature 120 °C, 3 mM; (C) temperature 120 °C, 5 mM; (D) temperature 60 °C, 1 mM, pH 5; (E) temperature 60 °C, 1 mM, pH 7; (F) temperature 60 °C, 1 mM, pH 9.

Effects of Different pH Conditions Along with the Concentrations of AgNO₃ on the Synthesis of AgNPs

pH plays a very important role in the synthesis of AgNPs by increasing or decreasing the concentration of H⁺ ions that alter the electronegative state of the reactants.^11,34 A set of different pH conditions acidic, neutral and basic were maintained by adjusting pH at 5, 7 and 9 respectively. 1 mM of the AgNO₃ did not report any change in color of the reaction mixture at acidic and basic pH (Figure 2D and F) but there was a slight increase in the SPR band height at neutral pH (Figure 2E).

A very broad asymmetrical peak was observed at acidic pH when 3 mM of AgNO₃ was used (Figure 3A). SPR band was also broad at neutral pH (Figure 3B) but it was very meager at basic pH (Figure 3C). According to the spectroscopic peak analysis broad peak represents the anisotropic, large size or big clumps of polydisperse nanoparticles. SPR band is a response of morphology, dielectric environment of the synthesized nanoparticles and their composition influence.¹²

Figure 3 UV-Visible spectrum representing AgNP synthesis under different physicochemical conditions. (A) Temperature 60 °C, 3 mM, pH 5; (B) temperature 60 °C, 3 mM, pH 7; (C) temperature 60 °C, 3 mM, pH 9; (D) temperature 60 °C, 5 mM, pH 5; (E) temperature 60 °C, 5 mM, pH 7; (F) temperature 60 °C, 5 mM, pH 9.

The shape of the SPR band determines the shape of the nanoparticles. Symmetrical and narrow SPR band represents the small, spherical and monodisperse nanoparticles.³⁸ A very symmetrical and narrow SPR band was observed at acidic pH when 5 mM of AgNO₃ was used (Figure 3D) and the synthesis of NPs at basic and neutral pH was very meager (Figure 3E and F). So 5 mM with acidic pH was selected as the optimum condition for the phytosynthesis of AgNPs by using M. arvensis aqueous extract as the reducing agent. It can be explained that pH contributes greatly to increase or decrease the number of H⁺ ions in the reaction mixture that alters the electronegative state of reactants. Lower the pH value results in increasing the concentration of H⁺ ions that subsequently increase the collision of the reactants and have a direct influence on the reaction kinetics. pH does not directly affect the conformational changes of proteins and enzymes but the change in the concentration of H⁺ ions can shape and alter the morphological properties of the substrate by changing electronegativity that can affect their binding with the enzymatic active site.^39,40

Effects of Different Ratios of AgNO₃ and Plant Extract on the Synthesis of AgNPs

Different ratios of the mixture of the plant extract and AgNO₃ have different impacts on the synthesis of the AgNPs²⁴ (Figure 4A). Analysis of the UV-Vis spectrum manifested that the 1 to 9 ratio of the plant extract and silver nitrate, respectively, as the only proportion to report the synthesis of AgNPs. A specific concentration of Ag ions and plant biomolecules act synergistically to reduce and stabilize the bulk silver. An increase in the concentration of plant extract resulted in an increasing concentration of phytometabolites that suppressed the process of reduction. Ali et al²⁴ studied the effects of different concentrations of plant extracts and AgNO₃ that are in favor of our reported results.

Figure 4 (A) UV-Visible spectrum representing the effects of different ratios of reactants on AgNP synthesis; (B) synthesis under optimized physicochemical conditions. Notes: Red arrow shows redshift in absorbance peak. An increase in the incubation period resulted in increasing the absorbance at a higher wavelength of light.

Synthesis of AgNPs Under Optimized Physicochemical Conditions

UV-spectrums were observed critically while the location, absorption unit (a.u.) and the SPR band shift was considered to find out the most suitable conditions for the synthesis of AgNPs (Figure 4B). The peak location of the UV-spectrum depends on particle size, shape, temperature and dielectric constant of the sample medium.⁸ It was found when 5 mM solution of the AgNO₃ was mixed with the plant extract in 1 to 9 ratio of the plant extract and silver salt, respectively, and the reaction temperature was maintained at the 60 °C resulted in the synthesis of AgNPs after the interval of 3 h and pH of the reaction mixture measured before synthesis was acidic.

Physical Characterization of AgNPs

The structural evaluation of AgNPs phytosynthesized and stabilized by the eco-friendly method was performed mainly by using SEM and AFM. SEM micrographs revealed that NPs are anisotropic, nearly spherical, triangular and cubical (Figure 5A and B). The size of the triangular nanoprisms was observed in the range of 90–150 nm (Figure 5A). SEM analysis also reported nanoparticles of various different shapes and sizes (Figure 5C and D). AFM images reported NPs of very small sizes and most of the NPs were found to be in a range of ~7–30 nm as some large size nanoparticles lost in the air during the process of preparation of the sample. AFM images further confirmed that the NPs are anisotropic and nearly spherical (Figure 6A and B).

Figure 5 SEM images of AgNPs. (A) Red triangle highlights nanoprisms; (B) red circle represents a small spherical nanoparticle; (C and D) NPs of different shapes and sizes.

Figure 6 AFM images of AgNPs. (A and B) Red circles highlight the NPs of different shapes and sizes.

The elemental composition of AgNPs was obtained by using EDX analysis (Figure 7). The characteristic peak of Ag was observed at 3 KeV and the intensity of the Ag signal was ~ 80%. EDX analysis also reported a very small amount of C, Cl, Mg, and Si which maybe because of the stabilization of AgNPs with phytometabolites while the presence of Cu is maybe because of the involvement of the signals from the copper grid. Figure 7, inset represents the percentage of different elements present in the AgNPs colloidal solution. Some previous studies determined the phytochemical composition of M. arvensis and they showed the presence of Chlorine-containing sesquiterpenes and monoterpene which may be responsible for the presence of Cl containing AgNP.^41,42

Figure 7 Energy dispersive X-ray analysis to represent the elemental composition of colloidal AgNPs. (inset: Bar chart shows the percentage intensity of different elements).

Particles Size Analysis of AgNPs

The hydrodynamic particle size distribution of AgNPs in Brownian motion was measured by using a dynamic light scattering technique. The sample was prepared into a 1× PBS solution to screen the effects of the charge on the surface of nanoparticles. Opposite charge ions from buffer condense around the particles and help in screening long-distance electrostatic interactions.⁴³ Very dilute colloidal solution of AgNPs was prepared and sonicated before to reduce the aggregation of clusters of nanoparticles. Figure 8 shows the hydrodynamic diameter of AgNPs and It was measured between ~17–400 nm. Hydrodynamic diameter is always greater than reported SEM and AFM size as it collectively represents the size of the metallic core and the biological corona that consists of functional groups originally belong to plant secondary metabolites. Size distribution by number (Inset Figure 8) represents the average size of most of the nanoparticles in the colloidal sample that was observed between 12–40 nm while the average hydrodynamic diameter of a single nanoparticle was reported 21.08 nm. Polydispersity index was measured at 0.209 which signifies that the nanoparticles are moderately dispersed and well suited to be used in biomedical therapies.

Figure 8 Particle size analysis of biosynthesized AgNPs by using a dynamic light scattering technique. Hydrodynamic diameter of AgNPs was measured between ~17 and 400 nm, while the average size of most of the nanoparticles was reported 12–40 nm (inset represents particle size distribution of AgNPs by number).

Cytotoxicity of Plant Aqueous Extract and AgNPs Against Colon Cancer Cells

Colon or colorectal cancer is the third most common cancer and is a leading cause of death due to its sever action and mechanisms to resist chemotherapeutic drugs. Multiple drug resistance (MDR) to the chemotherapeutic drugs became a global concern as it negatively affects the success rate of the disease.⁴⁴

Sulforhodamine B (SRB) assay (Figure 9) results showed that the AgNPs expressed cell death and the IC₅₀ (half-maximum inhibitory concentration) was recorded at 1.7 μg/mL. IC₅₀ is a quantitative measurement of the molar concentration of a material or a drug to inhibit or halt a particular biological process or its components such as enzymes, receptors or any signaling mechanism. Lower IC₅₀ (1.7 μg/mL) represents the great potency of the drug and is a universal indicator to measure the efficacy of a drug.

Figure 9 IC50 measurement of biosynthesized AgNPs against HCT116 colon cancer cells. Water was used as negative control, while AgNO3 was used as a positive control.

Annexin V apoptosis assay (Figure 10) results showed that the plant aqueous extracts are not effective to induce cell death against human colon cancer cells and only 3.67% of the total number of the cells expressed cell death which shows that the plant aqueous extracts are not effective against colon cancer cells. It can be explained that the aqueous extract is not embellished with the phytochemicals to exhibit cytotoxicity against cancer cells.

Figure 10 Fluorescence-activated cell sorting (FACS) plot to represent the cytotoxicity of plant aqueous extract against HCT116 colon cancer cells. (A) AgNO3 and; (B) M. arvensis aqueous extract reported 2.22% and 3.67% cytotoxic activity, respectively.

The dose-responsive activity of bio-fabricated AgNPs was reported by using an Annexin V apoptosis assay (Figure 11) and it was found that the increase in the concentration of AgNPs dose resulted in increasing cytotoxicity against HCT116 colon cancer cells. 131 µg/mL of AgNPs expressed 10.05% killing of cancer cells while the toxicity increased to 30% at 262 µg/mL. Though the exact mechanism which is responsible to evade colon cancer cells is still unknown.

Figure 11 Fluorescence-activated cell sorting (FACS) plot to represent the cytotoxicity of different doses of AgNPs against HCT116 colon cancer cells. (A) Control AgNO3 131 µg/mL; (B) AgNPs 131 µg/mL and (C) AgNPs 262 µg/mL.

The selective activity of AgNPs against colon cells can be because of the presence of chlorides in colloidal AgNPs that was observed in EDX analysis (Figure 7). Previous studies on phytochemical evaluation of M. arvensis confirmed the presence of Chlorine-containing sesquiterpenes and monoterpene that are mainly responsible for the presence of Cl.^41,42 Some studies reported the cytotoxic potential of Cl^45–47 and the presence of high chlorine contents in M. arvensis fabricated AgNPs can be one reason for their selective anticancer activities. It was confirmed in our previous study that M. arvensis fabricated AgNPs are biocompatible and a very high dose of nanoparticles is required to cause lysis of Red blood cells or erythrocytes. Chloride ions contribute to exchange bicarbonates (HCO₃⁻) across the plasma cell membrane of the RBCs and help to maintain ionic balance which is termed as chloride shift. It is mainly responsible for the selective cytotoxic potential of AgNPs against colon cancer cells.⁴⁸ Biocompatibility of mint fabricated AgNPs against RBCs and their selective cytotoxic potential against colon cancer cells can help to manage the limitations of conventional treatments of colon cancer.

The other possible reason for the selective anticancer activity of AgNPs is their small size that let these NPs to internalize the cells by crossing the plasma membrane barrier and disruption of the cell metabolic process or the entrapment of the mitochondria to take control of the power-house of the cell. Cytotoxic potential of AgNPs against HCT116 colon cancer cells can also be attributed to the interaction of nanoparticles with DNA, RNA, and proteins which can result in altering their conformational changes and fragmentation of their active structure. Another possible reason can be the positive charge of ionic Ag that helps to get it attached with the plasma cell membrane that has negatively charged proteins which eventually break the cell membrane and lead to cell death. It is also speculated that Ag⁺ bind with the thiol group (-SH group) of the enzymes and form the stable complexes such as Ag-S which results in the change of enzymatic configuration and blockage of activity site.^1,8,39,49

Cell Cycle Analysis of AgNPs-Treated HCT116 Colon Cancer Cells

Cell cycle analysis contributes greatly to determine cells in different phases of the cell cycle. Cell cycle analysis showed (Figure 12) that the bio-fabricated AgNPs have promising abelites to suspend/arrest the cell cycle. Increasing the dose of the AgNPs resulted in the entrapment of the greater number of cells in the Sub-G1 (M1) phase which shows a subsequent decrease in DNA content of cells. The peak representing the G1 (M2) decreased gradually which manifested that the less number of cells are entering the cell cycle. 26% of cells were reported separately into Sub G1/G₀ and G1 phase when AgNPs-treated cells were used while only 4% of cells were in the G1/G₀ phase and 39% of cells were in the G1 phase in the respective control (AgNO₃). These results greatly suggest that the AgNPs bio-fabricated from M. arvensis aqueous extract are highly effective to halt the growth of colon cancer cells (HCT116) by arresting the cell cycle and most of the cells in the sample population attained death. Our results are in favor of previously reported work.³⁰

Figure 12 Effects of biosynthesized AgNP on cell cycle of colon cancer cells. (A–C) Effect of different doses of the AgNO3; (D–F) effect of different doses of AgNPs on the cell cycle of colon cancer cells. Notes: M1, Sub-G1 phase; M2, G1 phase; M3, S phase; M4, G2 phase.

Conclusion

Herein we explain the influence of different physicochemical conditions eg temperature, pH, the concentration of AgNO₃ and the proportion of different reactants on the synthesis of AgNPs bio-fabricated from M. arvensis (mint) aqueous extract. It was observed that the mild-acidic conditions are better for the synthesis of AgNPs at moderate temperature. Different physicochemical conditions play a vital role to carve the physical and biological attributes of the nano-moieties by altering the reaction kinetics, molecular dynamics, and catalysis. Biological applications of silver nanoparticles implicated in this study found that the NPs are highly efficacious against HCT116 human colon cancer cells. Cell cycle analysis against HCT116 cancer cells unraveled that the silver nanoparticles suspended cell division in the Sub-G1 phase which shows that the AgNPs are not only affecting the cell life but also hampering the further proliferation. The results from this study provide the experimental evidence to understand the synergistic impact of physicochemical reaction parameters on nanoparticles synthesis and their abilities to suppress the growth of cancer cells may lead to the development of highly efficacious anticancer drugs to overcome the limitations of conventional treatment of colon cancer.