Green synthesis and chemical characterization of copper nanoparticles using Allium saralicum leaves and assessment of their cytotoxicity,antioxidant, antimicrobial,and cutaneous wound healing properties

In recent decades, nanotechnology is growing rapidly owing to its widespread application in science and industry. The aim of the experiment was the green synthesis of copper nanoparticles using Allium saralicum R.M. Fritsch aqueous extract and assessment of their cytotoxicity, antioxidant, antibacterial, antifungal, and cutaneous wound healing effects under in vitro and in vivo conditions. These nanoparticles were characterized by Fourier transformed infrared spectroscopy (FT‐IR), UV–visible spectroscopy, field emission scanning electron microscopy (FE‐SEM), transmission electron microscopy (TEM), and atomic force microscopy (AFM). DPPH free radical scavenging test was done to assess the antioxidant properties, which indicated similar antioxidant potentials for CuNPs@Allium and butylated hydroxytoluene. Minimum Inhibitory Concentration (MIC), Minimum Bactericidal Concentration (MBC), and Minimum Fungicidal Concentration (MFC) were specified by macro‐broth dilution assay. CuNPs@Allium indicated higher antibacterial and antifungal effects than all standard antibiotics (p ≤ 0.01). Also, CuNPs@Allium inhibited the growth of all bacteria at 1–8 mg/ml concentrations and removed them at 2–8 mg/ml concentrations (p ≤ 0.01). In the case of antifungal properties of CuNPs@Allium, they prevented the growth of all fungi at 1–4 mg/ml concentrations and destroyed them at 2–8 mg/ml concentrations (p ≤ 0.01). In vivo experiment, after creating the cutaneous wound, the rats were randomly divided into six groups (n = 10): untreated control, treatment with Eucerin basal ointment, treatment with 3% tetracycline ointment, treatment with 0.2% CuSO₄ ointment, treatment with 0.2% A. saralicum ointment, and treatment with 0.2% CuNPs@Allium ointment. Use of CuNPs@Allium ointment in the treatment groups substantially reduced (p ≤ 0.01) the wound area, total cells, neutrophil, macrophage, and lymphocyte and remarkably raised (p ≤ 0.01) the wound contracture, hydroxyl proline, hexosamine, hexuronic acid, fibrocyte, and fibrocytes/fibroblast rate compared to other groups. The synthesized CuNPs@Allium had high cell viability dose‐dependently (Investigating the effect of the plant on HUVEC cell line) and revealed this method was nontoxic. The results revealed the useful non‐cytotoxic, antioxidant, antibacterial, antifungal, and cutaneous wound healing effects of CuNPs@Allium.     

In vitro and in vivo evaluation of cytotoxicity,antioxidant, antibacterial,antifungal, and cutaneous wound healing properties of gold nanoparticles produced via a green chemistry synthesis using Gundelia tournefortii L. as a capping and reducing agent

The exploitation of various plant materials for the biosynthesis of nanoparticles is considered a green technology because it does not involve any harmful chemicals. The aim of the experiment was chemical characterization and evaluation of cytotoxicity, antioxidant, antibacterial, antifungal, and cutaneous wound healing activities of gold nanoparticles using aqueous extract of Gundelia tournefortii L. leaves (AuNPs@GT). These nanoparticles were characterized by fourier transformed infrared spectroscopy (FT‐IR), field emission scanning electron microscopy (FE‐SEM), energy dispersive X‐ray spectroscopy (EDS), and UV–visible spectroscopy. DPPH free radical scavenging test was done to assess the antioxidant properties, which indicated similar antioxidant potentials for AuNPs@GT and butylated hydroxytoluene. Agar diffusion tests were applied to determine the antibacterial and antifungal characteristics. Minimum Inhibitory Concentration (MIC), Minimum Bactericidal Concentration (MBC), and Minimum Fungicidal Concentration (MFC) were specified by macro‐broth dilution assay. AuNPs@GT indicated higher antibacterial and antifungal effects than all standard antibiotics (p ≤ 0.01). Also, AuNPs@GT inhibited the growth of all bacteria and fungi and removed them at 2‐4 mg/mL concentrations (p ≤ 0.01). In vivo experiment, after creating the cutaneous wound, the rats were randomly divided into six groups: untreated control, treatment with Eucerin basal ointment, treatment with 3% tetracycline ointment, treatment with 0.2% HAuCl₄ ointment, treatment with 0.2% G. tournefortii ointment, and treatment with 0.2% AuNPs@GT ointment. These groups were treated for 10 days. For histopathological and biochemical analysis of the healing trend, a 3 × 3 cm section was prepared from all dermal thicknesses at day 10. Use of AuNPs@GT ointment in the treatment groups substantially reduced (p ≤ 0.01) the wound area, total cells, neutrophil, and lymphocyte and remarkably raised (p ≤ 0.01) the wound contracture, hydroxyl proline, hexosamine, hexuronic acid, fibrocyte, fibroblast, and fibrocytes/fibroblast rate compared to other groups. The synthesized AuNPs@GT had great cell viability dose‐dependently (Investigating the effect of the plant on HUVEC cell line) and revealed this method was nontoxic. The results showed that the leave aqueous extract of G. tournefortii is very good bioreductant in the synthesis of gold nanoparticles for treatment of bacterial, fungal, and skin diseases.     

Green synthesis and chemical characterization of silver nanoparticles from aqueous extract of Falcaria vulgaris leaves and assessment of their cytotoxicity and antioxidant,antibacterial, antifungal and cutaneous wound healing properties

Nanotechnology encompasses the understanding of the fundamental physics, biology, chemistry and technology of nanometre‐scale objects. In recent decades, nanotechnology has grown rapidly owing to its widespread application in science and industry. The aim of the work reported was the green synthesis and chemical characterization of silver nanoparticles from aqueous extract of Falcaria vulgaris leaves (AgNPs@Falcaria) and evaluation of their cytotoxicity and antioxidant, antibacterial, antifungal and cutaneous wound healing effects under in vitro and in vivo conditions. These nanoparticles were characterized using Fourier transform infrared and UV–visible spectroscopies, scanning and transmission electron microscopies and atomic force microscopy. 2,2‐Diphenyl‐1‐picrylhydrazyl free radical scavenging experiments were conducted to evaluate the antioxidant potential, which indicated similar antioxidant potentials for AgNPs@Falcaria and butylated hydroxytoluene. The synthesized AgNPs@Falcaria had great cell viability dose‐dependently, indicating their non‐toxicity. Minimum inhibitory, minimum bactericidal and minimum fungicidal concentrations were determined by macro‐broth dilution assay. The data were analysed using SPSS software (Duncan post hoc test). AgNPs@Falcaria revealed higher antibacterial and antifungal activities than many standard antibiotics (p ≤ 0.01). Also, AgNPs@Falcaria prevented the growth of all bacteria at 2–8 mg ml^?1 concentrations and removed them at 4–16 mg ml^?1 concentrations (p ≤ 0.01). AgNPs@Falcaria inhibited the growth of all fungi at 2–4 mg ml^?1 concentrations and destroyed them at 4–8 mg ml^?1 concentrations (p ≤ 0.01). For in vivo experiments, after creating a cutaneous wound, rats were randomly divided into six groups: untreated control, treatment with eucerin basal ointment, treatment with 3% tetracycline ointment, treatment with 0.2% AgNO₃ ointment, treatment with 0.2% F. vulgaris ointment and treatment with 0.2% AgNPs@Falcaria ointment. Use of AgNPs@Falcaria ointment in the treatment groups substantially decreased (p ≤ 0.01) the wound area, total cells, neutrophils and lymphocytes and markedly raised (p ≤ 0.01) wound contracture, hydroxyproline, hexosamine, hexuronic acid, fibrocytes and fibrocyte/fibroblast ratio compared to the other groups. In summary, the synthesized AgNPs@Falcaria revealed non‐cytotoxicity and antioxidant, antibacterial, antifungal and cutaneous wound healing activities in a dose‐dependent manner.     

Preparation,characterization, and evaluation of cytotoxicity,antioxidant, cutaneous wound healing,antibacterial, and antifungal effects of gold nanoparticles using the aqueous extract of Falcaria vulgaris leaves

The new age drugs are nanoparticles of metals, which can combat conditions like wounds and fight human pathogens like bacteria. The aim of the experiment was preparation, characterization, and assessment of cytotoxicity, antioxidant, cutaneous wound healing, antibacterial, and antifungal potentials of gold nanoparticles using the aqueous extract of Falcaria vulgaris leaves (AuNPs@F. vulgaris) under in vitro and in vivo condition. These nanoparticles were characterized by FT‐IR, UV, XRD, FE‐SEM, TEM, and AFM. The synthesized AuNPs@F. vulgaris had great cell viability dose‐dependently (Investigating the effect of the nanoparticles on HUVEC cell line) and indicated these nanoparticles were nontoxic. DPPH free radical scavenging test was done to evaluate the antioxidant potentials, which showed similar antioxidant potentials for AuNPs@F. vulgaris and butylated hydroxytoluene. In part of cutaneous wound healing effect of F. vulgaris, after creating the cutaneous wound, the rats were randomly divided into six groups: untreated control, treatment with Eucerin basal ointment, treatment with 3% tetracycline ointment, treatment with 0.2% HAuCl₄ × H₂O ointment, treatment with 0.2% F. vulgaris ointment, and treatment with 0.2% AuNPs@F. vulgaris ointment. These groups were treated for 10 days. Use of AuNPs@F. vulgaris ointment in the treatment groups substantially decreased (p ≤ 0.01) the wound area, total cells, neutrophil, and lymphocyte and remarkably raised (p ≤ 0.01) the wound contracture, hydroxyl proline, hexuronic acid, fibrocyte, and fibrocytes/fibroblast rate compared to other groups. In antimicrobial part, MIC, MBC, and MFC were specified by macro‐broth dilution assay. AuNPs@F. vulgaris revealed higher antibacterial and antifungal properties than many standard antibiotics (p ≤ 0.01). Also, AuNPs@F. vulgaris prevented the growth of all bacteria at 2‐8 mg/ml concentrations and removed them at 2‐16 mg/ml concentrations (p ≤ 0.01). In case of antifungal potentials of AuNPs@F. vulgaris, they inhibited the growth of all fungi at 2‐4 mg/ml concentrations and destroyed them at 2‐8 mg/ml concentrations (p ≤ 0.01). In conclusion, synthesized AuNPs@F. vulgaris revealed non‐cytotoxicity, antioxidant, cutaneous wound healing, antibacterial, and antifungal activities.     

Green synthesis of silver nanoparticles using aqueous extract of Stachys lavandulifolia flower,and their cytotoxicity,antioxidant, antibacterial and cutaneous wound‐healing properties

In a biological process where the herbal tea (Stachys lavandulifolia) aqueous extract was applied as a capping and reducing agent, nanoparticles (NPs) of silver (Ag) were synthesized. These AgNPs were characterized using Fourier transform‐infrared spectroscopy, field emission‐scanning electron microscopy, energy‐dispersive X‐ray spectroscopy, transmission electron microscopy and ultraviolet–visible spectroscopy. The synthesized AgNPs had great cell viability dose‐dependently [investigating the effect of the plant on human umbilical vein endothelial cell line] and indicated this method was non‐toxic. In this study, the 2,2‐diphenyl‐1‐picrylhydrazyl (DPPH) free radical scavenging test was carried out to examine antioxidant properties, which revealed similar antioxidant properties for AgNPs and butylated hydroxytoluene. Agar diffusion tests were applied to determine the antibacterial characteristics. The macro‐broth tube test was run to determine minimum inhibitory concentration. All data of antibacterial and cutaneous wound‐healing examinations were analyzed by SPSS 21 software (Duncan post hoc test). AgNPs showed higher antibacterial property than all standard antibiotics (p ≤ 0.01). Also, AgNPs prevented the growth of all bacteria at 2–8 mg/ml concentrations and destroyed them at 2–16 mg/ml concentrations (p ≤ 0.01). For the in vivo experiment, after creating the cutaneous wound, the rats were randomly divided into six groups: untreated control; treatment with Eucerin basal ointment; treatment with 3% tetracycline ointment; treatment with 0.2% AgNO₃ ointment; treatment with 0.2% S. lavandulifolia ointment; and treatment with 0.2% AgNPs ointment. These groups were treated for 10 days. For histopathological and biochemical analysis of the healing trend, a 3 × 3‐cm section was prepared from all dermal thicknesses at day 10. Use of AgNPs ointment in the treatment groups substantially reduced (p ≤ 0.01) the wound area, total cells, neutrophil, macrophage and lymphocyte, and remarkably raised (p ≤ 0.01) the wound contracture, hydroxyl proline, hexosamine, hexuronic acid, fibrocyte and fibrocytes/fibroblast rate compared with other groups. Seemingly, AgNPs can be used as a medical supplement owing to their non‐cytotoxic, antioxidant, antibacterial and cutaneous wound‐healing properties.     

Green synthesis of silver nanoparticles from aqueous extract of Ziziphora clinopodioides Lam and evaluation of their bio-activities under in vitro and in vivo conditions

The purpose of this experiment was the green synthesis of silver nanoparticles from aqueous extracts of Ziziphora clinopodioides Lam (AgNPs@Ziziphora) and assessment of their cytotoxicity, antioxidant, antibacterial, antifungal, and cutaneous wound-healing effects. These nanoparticles were characterized using ultraviolet–visible spectroscopy (UV–Vis), X-ray diffraction (XRD), field emission scanning electron microscopy with energy-dispersive X-ray spectroscopy (FESEM-EDX), atomic force microscopy (AFM), and transmission electron microscopy (TEM). UV–Vis, TEM, and FESEM analyses indicated that the size of Ag nanoparticles (AgNPs) depended on Z. clinopodioides and AgNO₃ concentrations. In vitro biological experiments indicated that AgNPs@Ziziphora has excellent antioxidant potential against DPPH, antifungal effects against Candida guilliermondii, Candida krusei, Candida glabrata, and Candida albicans, and antibacterial activities against Staphylococcus aureus, Bacillus subtilis, Streptococcus pneumonia, Salmonella typhimurium, Pseudomonas aeruginosa, and Escherichia coli O157:H7. Also, these nanoparticles did not exhibit cytotoxicity property against human umbilical vein endothelial cells (HUVECs). An in vivo biological test revealed that AgNPs@Ziziphora ointment significantly (p ≤ 0.01) increased the levels of wound contracture, blood vessels, hydroxyl proline, hexuronic acid, hexosamine, fibrocytes, fibroblasts, and fibrocyte/fibroblast ratio and significantly (p ≤ 0.01) decreased the wound area, and levels of total cells, neutrophils, and lymphocytes than other groups in rats. The results of UV–Vis, XRD, FESEM-EDX, AFM, and TEM confirmed that the aqueous extract of Z. clinopodioides can be used to produce silver nanoparticles with significant antioxidant, antimicrobial, and cutaneous wound-healing properties without any cytotoxicity.     

Ethnomedicinal plant-extract-assisted green synthesis of iron nanoparticles using Allium saralicum extract,and their antioxidant,cytotoxicity, antibacterial,antifungal and cutaneous wound-healing activities

The aim of the experiment was the evaluation of antioxidant, cytotoxicity, antibacterial, antifungal and cutaneous wound-healing activities of green synthesized iron nanoparticles using Allium saralicum R.M. Fritsch leaves (FeNPs@AS). These nanoparticles were spherical with a size range of 40–45 nm, and were characterized using various analysis techniques including ultraviolet–visible spectroscopy to determine the presence of FeNPs@AS in the solution. We studied functional groups of A. saralicum extract in the reduction and capping process of FeNPs@AS by Fourier transform-infrared spectroscopy; crystallinity and FCC planes by X-ray diffraction pattern; and surface morphology, shapes and size of FeNPs@AS by scanning electron microscopy and transmission electron microscopy. Agar diffusion tests were done to determine the antibacterial and antifungal characteristics. FeNPs@AS prevented the growth of all bacteria and removed them at 2–8 mg/ml concentrations (P ≤ 0.01). In the case of antifungal potentials of FeNPs@AS, they inhibited the growth of all fungi and destroyed them at 2–4 mg/ml concentrations (P ≤ 0.01). The 2,2-diphenyl-1-picrylhydrazyl test revealed similar antioxidant potentials for FeNPs@AS and butylated hydroxytoluene. The synthesized FeNPs@AS had great cell viability dose-dependently and indicated this method was non-toxic. For the in vivo experiment, after creating the cutaneous wound, the rats were randomly divided into six groups: treatment with 0.2% FeNPs@AS ointment; treatment with 0.2% A. saralicum ointment; treatment with 0.2% FeCl₃·6H₂O ointment; treatment with 3% tetracycline ointment; treatment with Eucerin basal ointment; and untreated control. These groups were treated for 10 days. Use of FeNPs@AS ointment in the treatment groups significantly decreased (P ≤ 0.01) the wound area, total cells, neutrophils and lymphocytes, and significantly raised (P ≤ 0.01) the wound contracture, hydroxyl proline, hexosamine, hexuronic acid, fibrocyte and fibrocytes/fibroblast rate compared with other groups. These results show that the inclusion of A. saralicum extracts improves the therapeutical properties of FeNPs, which led to a significant enhancement in the antioxidant, non-cytotoxicity, antibacterial, antifungal and cutaneous wound-healing activities of the nanoparticles.     

Ziziphora clinopodioides Lam leaves aqueous extract mediated synthesis of zinc nanoparticles and their antibacterial,antifungal, cytotoxicity,antioxidant, and cutaneous wound healing properties under in vitro and in vivo conditions

LamZiziphora clinopodioides Biosynthesis of metal nanoparticles using plant medicine is under exploration is due to wide biomedica applications and research interest in nanotechnology, the recent study was assessing green synthesis of zinc nanoparticle using ), the use of plant material Ziziphoraleaves extract (ZnNPs@ not only makes the process eco‐friendly but also the abundance makes it more economical. Also, in this study, Vis. and– were characterized using different techniques including UVZiziphora were synthesized in aqueous medium using the plant extract as stabilizing and reducing agents. The synthesized ZnNPs@Ziziphora conditions. ZnNPs@in vivo and in vitro under Ziziphorawe investigated the therapeutical properties of ZnNPs@ FT‐IR spectroscopy, . SEM images exhibited a uniform spherical morphology in size of 32.34 Thermal Gravimetric Analysis (TGA)ray diffraction (XRD), scanning electron microscopy (SEM), and Energy Dispersive X‐ray Spectrometry (EDS), and‐X Escherichia coli, and Pseudomonas aeruginosa, Salmonella typhimurium part of this study, these nanoparticles indicated excellent antibacterial properties against Gram‐negative bacteria (in vitronm for the biosynthesized nanoparticles. In the biological , andCandida krusei, Candida albicans, Candida glabrata), antifungal potentials against Bacillus subtilis, andStaphylococcus aureus, Streptococcus pneumoniaO157:H7) and Gram‐positive bacteria ( leaves aqueous extract can be used to yield zinc nanoparticles with a significant amount of antibacterial, antifungal, antioxidant, and cutaneous wound healing properties without any cytotoxicity.Z. clinopodioides ointment ameliorated the cutaneous wounds with increasing the levels of wound contracture, vessel, hydroxyl proline, hexosamine, hexuronic acid, fibrocyte, and fibrocytes/fibroblast rate and decreeing the wound area, total cells, and lymphocyte compared to other groups in rats. The results of UV, FT‐IR, XRD, FE‐SEM, EDS, and TGA confirm that the Ziziphora part of our experiment, ZnNPs@in vivo, non‐cytotoxicity effect against human umbilical vein endothelial cells, and antioxidant activity against DPPH. In the biological Candida guilliermondii     

Falcaria vulgaris leaf aqueous extract mediated synthesis of iron nanoparticles and their therapeutic potentials under in vitro and in vivo condition

In recent years, researchers have used bionanotechnology techniques as cost‐effective and eco‐friendly routes to fabricate nanoparticles. The present study confirms the ability of aqueous extract of Falcaria vulgaris for the biosynthesis of iron nanoparticles (FeNPs@F. vulgaris). Also, in this study, we showed the antioxidant, cytotoxicity, cutaneous wound healing, antibacterial, and antifungal activities of these nanoparticles. FeNPs@F. vulgaris were characterized by UV, FT‐IR, XRD, FE‐SEM, and TEM analysis. According to the XRD analysis, 25.3 nm was measured for the crystal size of nanoparticles. FE‐SEM and TEM images exhibited a uniform spherical morphology and average diameters of 25 nm for the biosynthesized nanoparticles. FTIR results offered protein and polysaccharides in F. vulgaris were the sources of reducing power, reducing iron ions to FeNPs@F. vulgaris. In vivo design, FeNPs@F. vulgaris ointment remarkably reduced (p ≤ 0.01) the wound area, total cells, neutrophil, and lymphocyte and substantially increased (p ≤ 0.01) the wound contracture, vessel, hydroxyl proline, hexosamine, hexuronic acid, fibrocyte, and fibrocytes/fibroblast rate compared to other groups in rats. Also, FeNPs@F. vulgaris indicated potential antioxidant activity against DPPH, antifungal potentials against Candida glabrata, Candida albicans, Candida krusei, and Candida guilliermondii, antibacterial properties against Gram‐positive bacteria (Streptococcus pneumonia, Staphylococcus aureus, and Bacillus subtilis) and Gram‐negative bacteria (Salmonella typhimurium, Pseudomonas aeruginosa, and Escherichia coli O157:H7) without any cytotoxicity effect against human umbilical vein endothelial cells. Finally, the results showed the useful antioxidant, non‐cytotoxic, cutaneous wound healing, antifungal, and antibacterial effects of FeNPs@F. vulgaris.     

Synthesis of titanium nanoparticles using Allium eriophyllum Boiss aqueous extract by green synthesis method and evaluation of their remedial properties

The application of nanotechnologies to medicine, or nanomedicine, which has already demonstrated its tremendous impact on the pharmaceutical and biotechnology industries, is rapidly becoming a major driving force behind ongoing developments in the antimicrobial and wound healing fields. This study confirms the potential of Allium eriophyllum Boiss aqueous extract for the green synthesis of titanium nanoparticles (TiNPs). Also, we reveal the antioxidant, cytotoxicity, cutaneous wound healing, antifungal and antibacterial properties of TiNPs. These nanoparticles were characterized using Fourier transform infrared (FT‐IR) and UV–visible spectroscopies, X‐ray diffraction (XRD), transmission electron microscopy (TEM) and field emission scanning electron microscopy (SEM). FT‐IR findings suggested molecular interactions of compounds in the plant were the sources of reducing power, reducing titanium ions to TiNPs. In XRD analysis, 22.8 nm was measured for the crystal size of the nanoparticles. SEM and TEM images indicated a uniform spherical morphology and average diameters of 22 nm. 2,2‐Diphenyl‐1‐picrylhydrazyl experiments were conducted to assess the antioxidant activities, which indicated similar antioxidant potentials for TiNPs and butylated hydroxytoluene. In the antimicrobial part of this study, agar diffusion experiments were done to determine the antibacterial and antifungal characteristics. TiNPs had antifungal activities against Candida guilliermondii, C. krusei, C. albicans and C. glabrata and antibacterial potentials against Gram‐negative bacteria (Pseudomonas aeruginosa, Salmonella typhimurium and Escherichia coli O157:H7) and Gram‐positive bacteria (Staphylococcus aureus, Streptococcus pneumoniae and Bacillus subtilis). Also, these nanoparticles did not have any cytotoxicity against human umbilical vein endothelial cells. In in vivo experiments, TiNP ointment significantly decreased (p ≤ 0.01) wound area, total cells, macrophages, neutrophils and lymphocytes and notably increased (p ≤ 0.01) wound contracture, vessels, hydroxyproline, hexosamine, hexuronic acid, fibrocytes and fibrocyte/fibroblast ratio in rats. The results of FT‐IR, UV, XRD, TEM and SEM analyses confirm that aqueous extract of A. eriophyllum leaves can be used to yield TiNPs with notable antioxidant, antibacterial, antifungal and cutaneous wound healing potentials without any cytotoxicity. Further clinical trials are necessary for confirmation of these remedial properties of TiNPs in humans.     

Assessment of antioxidant,cytotoxicity, antibacterial,antifungal, and cutaneous wound healing activities of green synthesized manganese nanoparticles using Ziziphora clinopodioides Lam leaves under in vitro and in vivo condition

In recent decades, nanotechnology is growing rapidly owing to its widespread application in medical science. The aim of the experiment was the evaluation of cytotoxicity, antioxidant, antibacterial, antifungal, and cutaneous wound healing activities of green synthesized manganese nanoparticles using Ziziphora clinopodioides Lam leaves (MnNPs@ZC). The synthesized MnNPs@ZC were characterized using different techniques including UV–Vis., FT-IR spectroscopy, X-ray diffraction (XRD), scanning electron microscopy (SEM), and energy dispersive X-ray spectrometry (EDS). According to the XRD analysis, 48.10 nm was measured for the crystal size of nanoparticles. SEM images exhibited a uniform spherical morphology and size in the range of 47.58 to 70.26 nm for the biosynthesized nanoparticles. MnNPs@ZC revealed excellent non-cytotoxicity effect against human umbilical vein endothelial cells, antioxidant activity against DPPH, antibacterial properties against Gram-negative bacteria (Salmonella typhimurium, Pseudomonas aeruginosa, and Escherichia coli O157:H7) and Gram-positive bacteria (Streptococcus pneumonia, Staphylococcus aureus, and Bacillus subtilis), and antifungal potentials against Candida glabrata, Candida albicans, Candida guilliermondii, and Candida krusei. Also, use of MnNPs@ZC ointment decreased significantly (p ≤ 0.01) the wound area, total cells, neutrophil, and lymphocyte and raised significantly (p ≤ 0.01) the wound contracture, hydroxyl proline, hexosamine, hexuronic acid, fibrocyte, and fibrocytes/fibroblast rate compared to other groups in experimental animals. In conclusion, synthesized MnNPs@ZC indicated antibacterial, antifungal, non-cytotoxicity, antioxidant, and cutaneous wound healing effects in a dose-depended manner. After confirming in the clinical trials, these nanoparticles can be used in human for the treatment of cutaneous and infectious diseases.     

Green synthesis and chemical characterization of silver nanoparticles obtained using Allium saralicum aqueous extract and survey of in vitro antioxidant,cytotoxic, antibacterial and antifungal properties

Allium saralicum R.M. Fritsch has been used in Iranian traditional medicine as a remedial supplement for microbial diseases. This paper reports the green synthesis, chemical characterization and antioxidant, cytotoxic, antibacterial and antifungal properties of silver nanoparticles obtained using aqueous extract of A. saralicum leaves. In this synthesis, no surfactants or stabilizers were used. For characterization, UV–visible spectroscopy, transmission electron microscopy, X‐ray diffraction, energy‐dispersive X‐ray spectroscopy and field emission scanning electron microscopy were used. 2,2‐Diphenyl‐1‐picrylhydrazyl was used in experiments to assess the antioxidant potential of the silver nanoparticles, which revealed an impressive prevention in comparison with butylated hydroxytoluene. The synthesized silver nanoparticles at low doses (1–250 μg dl^?1) did not show marked cytotoxic activity (against cervical cancer cells (Hela), breast cancer cells (MCF‐7) and human embryonic kidney cells (HEK‐293)). Agar diffusion tests were applied to determine the antibacterial and antifungal characteristics. Compared with all standard antimicrobials, the silver nanoparticles showed higher antibacterial and antifungal activities (p ≤ 0.01). Also, the silver nanoparticles inhibited the growth of all bacteria and fungi at concentrations of 31–250 μg ml^?1, and destroyed them at concentrations of 31–500 μg ml^?1 (p ≤ 0.01). Because the silver nanoparticles obtained using aqueous extract of A. saralicum leaves have antioxidant, non‐cytotoxic, antifungal and antibacterial potentials, they can be used as a medical supplement or drug.     

Pongamia pinnata seed extract‐mediated green synthesis of silver nanoparticles: Preparation,formulation and evaluation of bactericidal and wound healing potential

Pongamia pinnata – a plant used since olden times in Ayurvedic treatment – is reported to have diverse functions including antibacterial, antidiabetic, antineurodegenerative, antiepileptic, antiulcer, etc. In this study, our objective was to prepare silver nanoparticles (AgNPs) by green synthesis mediated by methanolic seed extract of P. pinnata and to determine their antimicrobial and antioxidant potential and wound healing activity. AgNPs were characterized for particle size and shape and for antioxidant potential. Further, the AgNPs were incorporated in a gel. The wound healing activity was investigated using an excision wound healing model in Wistar rats. The AgNP‐loaded gel was applied topically to the wounded rats daily for 30 days. The wound contraction was calculated and histopathological studies of the healed tissues were conducted. Karanjin content of the extract was found to be 349 ± 2.16 mg g^?1. Formation of AgNPs was confirmed using transmission and scanning electron microscopies and X‐ray diffraction. AgNPs showed good antioxidant potential and were active against Staphylococcus aureus, Escherichia coli, Bacillus subtilis and Pseudomonas aeruginosa. Significant wound healing activity (p < 0.05) was shown by the AgNP gel as compared to 5% Betadine ointment. Thus, the prepared AgNPs have antimicrobial and wound healing effects that may be useful in treatment of topical infections especially in wounds.     

Application of titanium nanoparticles containing natural compounds in cutaneous wound healing

The aim of the study was the rapid green synthesis of titanium nanoparticles using the aqueous extract of Falcaria vulgaris leaves (TiNPs@FV) and exploring their antioxidant, cytotoxicity, antifungal, antibacterial, and cutaneous wound healing activities under in vitro and in vivo condition. These nanoparticles were characterized by UV-Vis, Fourier transform-infrared(FT-IR), X-ray diffraction XRD), field emission-scanning electron microscopy FE-SEM), and transmission electron microscopy TEM) analyses. The synthesized TiNPs@FV had great cell viability on human umbilical vein endothelial cells and indicted this method was nontoxic. DPPH (2,2-diphenyl-1-picrylhydrazyl) test revealed similar antioxidant potentials for F. vulgaris, TiNPs@FV, and butylated hydroxytoluene. All data of antibacterial, antifungal, and cutaneous wound healing tests were analyzed by SPSS 22 software. In the antimicrobial part of this study, TiNPs@FV indicated higher antifungal and antibacterial effects than all standard antibiotics (p ≤ 0.01). Minimal inhibitory concentration (MIC) and minimal fungicidal concentration of TiNPs@FV against all fungi were at 2–4 mg/mL and 2-8 mg/mL ranges, respectively. But, MIC and minimal bactericidal concentration of TiNPs@FV against all bacteria were at 2-8 mg/mL and 2-16 mg/mL ranges, respectively. In the part of cutaneous wound healing, use of TiNPs@FV ointment significantly (p ≤ 0.01) raised the wound contracture, vessel, hydroxyl proline, hexuronic acid, hexosamine, fibrocyte, and fibrocytes/fibroblast rate and significantly (p ≤ 0.01) decreased the wound area, total cells, neutrophil, and lymphocyte compared to other groups in rats. The results of FT-IR, UV-Vis, XRD, TEM, and FE-SEM confirm that the aqueous extract of F. vulgaris leaves can be used to yield titanium nanoparticles with a notable amount of remedial effects.     

Formulation and characterization of a novel cutaneous wound healing ointment by silver nanoparticles containing Citrus lemon leaf: A chemobiological study

IntroductionFormulating new wound-healing ointments by natural compounds is the first research priority in the developing and developed countries. This study was intended to provide green formulation of Ag-NP ointment containing Citrus lemon leaf aqueous extract and examine its capability of healing cutaneous wounds and its antioxidant and cytotoxicity activities under in vitro and in vivo conditions.Materials and methodsDifferent techniques, including UV–Vis and FT-IR spectroscopy, were used to characterize Ag-NPs. MTT assay was used to investigate cytotoxicity property of Ag-NPs. Antioxidant activity of Ag-NPs were examined by DPPH in the presence of butylated hydroxytoluene as positive control. Parameters of cutaneous wound healing were measured both histopathologically and biochemically.ResultsClear peak at 429 nm shown by UV–Vis spectroscopy indicated formation of Ag-NPs. In FT-IR spectroscopy, presence of many antioxidant compounds provided an excellent condition to reduce silver in Ag-NPs. FE-SEM and TEM images showed spherical Ag-NPs with an average size of 25.1 nm. The synthesized silver nanoparticles had excellent cell viability on the HUVECs line and indicated this method was nontoxic. Application of Ag-NP ointment improved wound healing parameters significantly (P ≤ 0.01). Ag-NPs reduced wound areas, total cells, neutrophils and lymphocytes significantly (P ≤ 0.01) and increased wound contracture, vessels, hexosamines, hydroxyl proline, hexuronic acid, fibrocytes, fibroblasts and fibrocyte/ fibroblast ratios significantly (P ≤ 0.01).ConclusionsOnce our results are verified by clinically experimental studies, Ag-NP ointment can be used as a modern one to treat several types of wounds, especially cutaneous ones, in humans.     

Green synthesis of silver nanoparticles using Thymus kotschyanus extract and evaluation of their antioxidant,antibacterial and cytotoxic effects

Present study used ecofriendly, cost efficient and easy method for synthesis of silver nanoparticles (Ag NPs) at the room temperature by Thymus Kotschyanus extract as reducing and capping agent. Various analytical technique including UV–Vis absorption spectroscopy determined presence of Ag NPs in the solution, the functional groups of Thymus Kotschyanus extract in the reduction and capping process of Ag NPs are approved by FT‐IR, crystallinity with the fcc plane approved from the X‐ray diffraction (XRD) pattern, energy dispersive spectroscopy (EDS) determined existence of elements in the sample, surface morphology, diverse shapes and size of present Ag NPs were showed by using scanning electron microscopy (SEM), atomic force microscopy (AFM) and high resolution transmission electron microscopy (HRTEM). Beginning and end destroy temperature of present silver nanoparticles were determined by thermal gravimetric spectroscopy (TGA). In addition, antibacterial, antioxidant and cytotoxicity properties of Ag NPs were studied. Agar disk and agar well diffusion are the methods to determined antibacterial properties of synthesized Ag NPs. Also MIC (Minimum Inhibitory Concentration) and MBC (Minimum Bactericidal Concentration) were recognized by macro broth dilution assay. DPPH free radical scavenging assay was used for antioxidant property and compare to butylated hydroxytoluene (BHT) as standard antioxidant that showed high antioxidant activity more than BHT. Synthesized Ag NPs have great cell viability in a dose depended manner and demonstrate that this method for synthesis silver nanoparticles provided nontoxic. The average diameter of synthesized Ag NPs was about 50–60 nm.     

Chemical characterization and evaluation of antimicrobial and cutaneous wound healing potentials of gold nanoparticles using Allium saralicum R.M. Fritsch

The use of herbal medicines dates back a long way in history. Herbal medicines have been widely used all over the world since ancient times and have been recognized by physicians and patients for their good therapeutic value as they have fewer adverse effects than modern medicines. Recently, researchers have used gold nanoparticles synthesized by plants in the prevention, control, and treatment of infectious disorders and cutaneous wounds. The aims of this study were to synthesize gold nanoparticles from aqueous extract of Allium saralicum R.M. Fritsch (AuNPs) and assess their therapeutic capacities. The nanoparticles were characterized by UV–visible spectroscopy (UV–Vis), Fourier-transform infrared (FT-IR) spectroscopy, X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM) and transmission electron microscopy (TEM). FT-IR results offered polysaccharides and protein in A. saralicum were the sources of reducing power, reducing gold ions to AuNPs. According to XRD analysis, the crystal size of the nanoparticles was 41.6 nm. TEM and FE-SEM images exhibited average diameters of 45 nm for the biosynthesized nanoparticles. The synthesized AuNPs had great cell viability on HUVECs line and showed this method was nontoxic. The 2,2-diphenyl-1-picrylhydrazyl free radical scavenging test indicated similar antioxidant potentials for A. saralicum, AuNPs, and butylated hydroxytoluene. To determine the antifungal and antibacterial properties of HAuCl₄, A. saralicum, and AuNPs, agar diffusion tests were used. The aim of the application both HAuCl₄ and A. saralicum in microbial tests was to investigate the synergism effects between them. The minimum inhibitory concentration (MIC), minimum bactericidal concentration (MBC), and minimum fungicidal concentration (MFC) were specified by macro-broth dilution assay. AuNPs exhibited higher antifungal and antibacterial effects than all standard antibiotics (p ≤ 0.01). The MIC and MBC of AuNPs against all bacteria were in the ranges 1–4 mg/ml and 2–8 mg/ml, respectively. The MIC and MFC of AuNPs against all fungi were in the ranges 1–4 mg/ml and 2–4 mg/ml, respectively. In vivo part, AuNPs ointment group raised significantly (p ≤ 0.01) the wound contracture, vessel, hydroxyl proline, hexuronic acid, fibrocyte, fibroblast, and fibrocytes/fibroblast rate and decreased significantly (p ≤ 0.01) the wound area, total cells, and lymphocyte compared to other groups in rats. The results of FT-IR, UV–Vis, XRD, TEM, and FE-SEM analyses confirm that the aqueous extract of A. saralicum leaves can be used to yield gold nanoparticles with a notable amount of remedial effects without any cytotoxicity against HUVECs.     

Unusual coordination mode of aroyl/acyl thiourea ligands and their π‐arene ruthenium (II) piano‐stool complexes: Synthesis,molecular geometry,theoretical studies and biological applications

Two mononuclear ruthenium complexes ( 1 and 2 ) with aroyl/acylthiourea as an ancillary ligand of type, [(η⁶‐p‐cymene)RuCl(L‐N,S)], where [ L1  = 2,4‐dichloro‐N‐(o‐tolylcarbamothioyl)benzamide] and L2  = N‐(phenylcarbamothioyl)cyclohexanecarboxamide] were synthesized and well characterized. The single crystal X‐ray diffraction studies revealed the coordination mode and the geometry of the complexes. The two complexes adopted general piano‐stool (three‐legged) geometry with a novel coordination mode of aroyl/acylthiourea through amide N (anionic) and thiocarbonyl S (neutral). This type of monobasic bidentate coordination of the aroyl/acylthiourea ligand was witnessed the first time around the metal ion. The coordination of the complexes was well explained through geometric parameters and frontier molecular orbital parameter values computed at the B3LYP/SDD level. The synthesized complexes were also screened for their antibacterial, antifungal, antioxidant and in vitro antiproliferative activities. Complexes exhibited good antimicrobial agents against various pathogens. The antioxidant activity of the complex 2 has shown most potent activity with IC₅₀ value of 48.55 ± 1.7 μM compared to the reference drug. In addition, the in vitro antiproliferative activity of the complex 2 showed excellent activity against HepG‐2 cell line with the IC₅₀ value of 24.30 ± 1.20 μM which is close to Doxorubicin standard drug.     

Design,Synthesis, and Bioassay of Novel Compounds of Isolongifolenone Oxime Derivatives

A succession of new isolongifolenone oxime derivatives have been designed and synthesized. The structures of these compounds were identified by IR, ¹H‐NMR, ¹³C‐NMR, mass spectra, and elemental analysis. The bioassays of antibacterial, antifungal, and insecticidal activity were carried out. The in vitro antibacterial and antifungal activities were evaluated by the disk diffusion method, and the minimum inhibitory concentration was determined by the microdilution method, while the insecticidal activity was tested by the spraying method or the straw impregnation method. The results of bioassays showed that compound 3f was more active in resisting all the tested bacterial and fungal organisms when compared to the standard drug amoxicillin at the lowest concentration of 31.3 μg/ml. Compound 4 , synthesized by Beckmann rearrangement reaction of isolongifone oxime, exerted moderate insecticidal activity against soybean aphid. Furthermore, compound 3m exhibited more activity in killing armyworms than the standard drug flucycloxuron at the concentration of 0.5 mg/l.     

Polarity-guided phytochemical extraction,polyphenolic characterization,and multimode biological evaluation of Seriphidium kurramense (Qazilb.) Y. R. Ling

Purpose of studyThe undertaken study aims to assess the polyphenolic profile, and antioxidant, antimicrobial, antiviral, antidiabetic, and cytotoxic potential of Seriphidium kurramense (Qazilb.) Y. R. Ling extracts.MethodsExtracts of aerial parts were prepared by successive extraction (n-hexane {Sk-nH}, ethyl acetate {Sk-EA}, methanol {Sk-M} and aqueous {Sk-Aq}). Chromogenic assays determined the antioxidant profile while HPLC quantified several polyphenols. Agar well diffusion was employed for antimicrobial potential while brine shrimp and hemolytic assays established the biosafety profile.ResultsThe results have shown that maximum extract recovery (17.49% w/w), total phenolics content (24.44 ± 0.15 μg GAE/mgE), and total flavonoids content (6.87 ± 0.25 μg QE/mgE) were recorded in Sk-Aq. RP-HPLC quantified a significant amount of syringic acid (1.43 ± 0.05 µg/mgE), caffeic acid (0.48 ± 0.02 µg/mgE), gentisic acid (6.44 ± 0.01 µg/mgE), and quercetin (4.39 ± 0.01 µg/mgE) in Sk-Aq, while maximum amounts of thymoquinone (0.21 ± 0.02 µg/mgE) and luteolin (3.90 ± 0.03 µg/mgE) along with apigenin (3.72 ± 0.03 µg/mgE) existed in Sk-M and highest quantities of ferulic acid (2.98 ± 0.01 µg/mgE), myricetin (1.04 ± 0.02 µg/mgE) and kaempferol (1.23 ± 0.01 µg/mgE) were found to be present in Sk-EA. A substantial free radical scavenging (85.87 ± 1.00%), total reducing power (211.93 ± 0.97 µg AAE/mgE), and urease inhibition activity (87.99 ± 0.19% at 500 µg/ml) were also recorded in the Sk-Aq. The highest antioxidant capacity (243.5 ± 1.12 µg AAE/mgE), antibacterial, antifungal, and antiviral activity (100% reduction in plaque formation at 400 µg/ml) were observed for Sk-EA. Maximum antibacterial and antifungal activities were revealed against Klebsiella pneumoniae (MIC = 25 ± 0.37 µg/ml), and Candida albicans (MIC = 50 ± 0.19 µg/ml) respectively. The prominent antidiabetic potential was displayed by Sk-nH in terms of α-amylase and α-glucosidase inhibition.ConclusionThe results reported, herein suggest that S. kurramense can be a promising candidate for antioxidant, antibacterial, antifungal, antiviral, and antidiabetic secondary metabolites.