Plasma treated fabrics coated with naturally derived Ag‐NPs for biomedical application

Ethnic value of many known plants are underexploited for medicinal application besides their proven traditional qualities. One such plant known for wound healing is Tridax procumbens. This plant has wound healing property and is commercially unexploited. Silver nanoparticle (Ag‐NP) were synthesized using this plant extracts using different solvents (methanol, ethyl acetate and aqueous), which exhibit resonance at 426, 424 and 418 nm, respectively. This plant‐mediated Ag‐NPs have strong anti‐bactericidal activity against Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa, Streptococcus pyogenes, Klebsiella pneumonia, Serratia marcescens and Bacillus subtilis with methanol extract. Further instance, elemental composition was confirmed by energy dispersive X‐ray analysis and particle size ranges were observed at 80–200 nm with spherical shape nanoparticles by scanning electron microscopy and transmission electron microscopy analysis. The biocompatibility of Ag‐NPs was assessed using fibroblast cell line (L929) by MTT assay with 109.35 µg IC₅₀ value. The oxygen plasma treated and non‐treated bamboo spunlaced nonwoven fabrics were coated with the Ag‐NPs by exhaust method. Contact angle and water retention revealed significant difference in absorption ability of plasma treated fabric. Field emission scanning electron microscopy revealed the presence of Ag‐NPs in plasma coated fabrics. The fabricated cloth was studied for anti‐microbial and microbial penetration ability.Inspec keywords: solvents (industrial), organic compounds, woven composites, field emission scanning electron microscopy, plasma materials processing, contact angle, transmission electron microscopy, X‐ray diffraction, fabrics, biomedical materials, wounds, silver, nanoparticles, particle size, nanofabrication, thermal analysis, antibacterial activity, microorganisms, X‐ray chemical analysisOther keywords: biomedical application, ethnic value, medicinal application, wound healing property, silver nanoparticle synthesis, methanol, ethyl acetate, Escherichia coli, Pseudomonas aeruginosa, Streptococcus pyogenes, Klebsiella pneumonia, nonwoven fabrics, field emission scanning electron microscopy, plasma coated fabrics, fabricated cloth, solvents, antibactericidal activity, Staphylococcus aureus, particle size, transmission electron microscopy, oxygen plasma treatment, bamboo material, Tridax procumbens extracts, Serratia marcescens, Bacillus subtilis, elemental composition, energy dispersive X‐ray analysis, scanning electron microscopy, material biocompatibility, fibroblast cell line, exhaust method, contact angle, water retention, absorption ability, antimicrobial property, microbial penetration ability, size 424.0 nm, size 418.0 nm, size 80.0 nm to 200.0 nm, size 426.0 nm, Ag     

Facile synthesis of silver nanoparticles mediated by polyacrylamide‐reduction approach to antibacterial application

The current time increase in the prevalence of antibiotic resistant ‘super‐bugs’ and the risks associated with food safety have become global issues. Therefore, further research is warranted to identify new and effective antimicrobial substances. Silver nanoparticles (Ag‐NPs) were synthesized by autoclaving technique using, different concentrations of Ag salt (AgNO₃) solution (1, 5, 10, and 25 mM). Their presence was confirmed by a surface plasmon resonance band at ∼435 nm using UV–Vis absorption spectra. The morphology of the synthesized Ag‐NPs stabilized by polyacrylamide (PAM) was examined by TEM, SAED, and EDS. TEM images revealed that the synthesized Ag‐NPs had an average diameter of 2.98±0.08 nm and SAED and EDS results confirmed the formation of Ag‐NPs. In addition, FT‐IR spectroscopy revealed that a PAM polymer matrix stabilized the Ag‐NPs. The well diffusion method, was used to test, Gram positive and Gram negative bacteria were examined. Also the minimal inhibitory concentration (MIC) and minimal bactericidal concentration (MBC) were studied against Ag‐NPs. The Ag‐NPs exhibited strong inhibitory activity, MIC and MBC against the tested clinical bacterial isolates. These results suggest that Ag‐NPs stabilized in PAM are highly effective against clinical bacterial isolates can be applied in medical fields.Inspec keywords: antibacterial activity, silver, nanoparticles, nanomedicine, surface plasmon resonance, X‐ray chemical analysis, transmission electron microscopy, electron diffraction, Fourier transform infrared spectroscopy, microorganisms, ultraviolet spectra, visible spectraOther keywords: Ag‐NP facile synthesis, PAM‐reduction approach, antibacterial application, antibiotic resistant super‐bugs, food safety, antimicrobial agents, antibiotics, antimicrobial substances, Ag salt solution concentration, ultraviolet‐visible absorption spectra, polyacrylamide, transmission electron microscopy, electron diffraction, energy dispersive X‐ray spectroscopy, TEM images, Fourier transform infrared spectroscopy, PAM polymer matrix, diffusion method, Gram positive bacteria, Gram negative bacteria, clinical bacterial isolates, Ag     

Encapsulation of the reductase component of p ‐hydroxyphenylacetate hydroxylase in poly(lactide‐co ‐glycolide) nanoparticles by three different emulsification techniques

p ‐Hydroxyphenylacetate 3‐hydroxylase component 1 (C ₁) is a useful enzyme for generating reduced flavin and NAD⁺ intermediates. In this study, poly(lactide‐co‐glycolide) (PLGA) nanoparticles (NPs) were used to encapsulate the C ₁ (PLGA‐C ₁ NPs). Enzymatic activity, stability, and reusability of PLGA‐C ₁ NPs prepared using three different methods [oil in water (o/w), water in oil in water (w/o/w), and solid in oil in water (s/o/w)] were compared. The s/o/w provided the optimal conditions for encapsulation of C ₁ (PLGA‐C _1,s NPs), giving the highest enzyme activity, stability, and reusability. The s/o/w method improves enzyme activity ∼11 and 9‐fold compared to w/o/w (PLGA‐C _1,w NPs) and o/w (PLGA‐C _1,o NPs). In addition, s/o/w prepared PLGA‐C _1,s NPs could be reused 14 times with nearly 50% activity remaining, a much higher reusability compared to PLGA‐C _1,o NPs and PLGA‐C _1,w NPs. These nanovesicles were successfully utilised to generate reduced flavin mononucleotide (FMN) and supply this cofactor to a hydroxylase enzyme that has application for synthesising anti‐inflammatory compounds. Therefore, this recycling biocatalyst prepared using the s/o/w method is effective and has the potential for use in combination with other enzymes that require reduced FMN. Application of PLGA‐C _1,s NPs may be possible in additional biocatalytic processes for chemical or biochemical production.Inspec keywords: nanoparticles, enzymes, biotechnology, biochemistry, recycling, catalysts, nanofabrication, encapsulationOther keywords: reductase component, poly(lactide‐co‐glycolide) nanoparticles, emulsification techniques, p‐hydroxyphenylacetate 3‐hydroxylase component, NAD⁺ intermediates, PLGA, enzymatic activity, PLGA‐C₁ reusability, water in oil in water methods, solid in oil in water methods, oil in water methods, optimal conditions, encapsulation, enzyme stability, enzyme reusability, s/o/w method, reduced flavin mononucleotide, hydroxylase enzyme, anti‐inflammatory compounds, recycling biocatalyst, FMN, biocatalytic processes, biochemical production, chemical production     

Biogenic synthesis of biopolymer‐based Ag–Au bimetallic nanoparticle constructs and their anti‐proliferative assessment

This study reports an eco‐friendly‐based method for the preparation of biopolymer Ag–Au nanoparticles (NPs) by using gum kondagogu (GK; Cochlospermum gossypium), as both reducing and protecting agent. The formation of GK‐(Ag–Au) NPs was confirmed by UV‐absorption, fourier transformed infrared (FTIR), atomic force microscopy (AFM), scanning electron microscope (SEM) and transmission electron microscope (TEM). The GK‐(Ag–Au) NPs were of 1–12 nm in size. The anti‐proliferative activity of nanoparticle constructs was assessed by MTT assay, confocal microscopy, flow cytometry and quantitative real‐time polymerase chain reaction (PCR) techniques. Expression studies revealed up‐regulation of p53, caspase‐3, caspase‐9, peroxisome proliferator‐activated receptors (PPAR) PPARa and PPARb, genes and down‐regulation of Bcl‐2 and Bcl‐x(K) genes, in B16F10 cells treated with GK‐(Ag–Au) NPs confirming the anti‐proliferative properties of the nanoparticles.Inspec keywords: nanomedicine, transmission electron microscopy, genetics, cellular biophysics, molecular biophysics, enzymes, nanofabrication, gold, silver, scanning electron microscopy, nanoparticles, Fourier transform infrared spectra, atomic force microscopy, biomedical materialsOther keywords: size 1.0 nm to 12.0 nm, Ag‐Au, anti‐proliferative assessment, eco‐friendly‐based method, anti‐proliferative activity, anti‐proliferative properties, biopolymer‐based Ag–Au bimetallic nanoparticle, Cochlospermum gossypium, gum kondagogu, biopolymer preparation, biogenic synthesis, UV‐absorption, Fourier transform infrared spectroscopy, scanning electron microscopy, transmission electron microscopy, atomic force microscopy, MTT assay, confocal microscopy, flow cytometry, caspase‐3, caspase‐9, peroxisome proliferator‐activated receptors, Bcl‐2 gene, Bcl‐x(K) gene, B16F10 cells     

Bio‐green synthesis ZnO‐NPs in Brassica napus pollen extract: biosynthesis,antioxidant, cytotoxicity and pro‐apoptotic properties

The bio‐green methods of synthesis nanoparticles (NPs) have advantages over chemo‐physical procedures due to cost‐effective and ecofriendly products. The goal of current investigation is biosynthesis of zinc oxide NPs (ZnO‐NPs) and evaluation of their biological assessment. Water extract of Brassica napus pollen [rapeseed (RP)] prepared and used for the synthesis of ZnO‐NPs and synthesised ZnO‐NP characterised using ultraviolet–visible, X‐ray diffraction, Fourier‐transform infrared spectroscopy, field emission scanning electron microscope and transmission electron microscope. Antioxidant properties of ZnO‐NPs, cytotoxic and pro‐apoptotic potentials of NPs were also evaluated. The results showed that ZnO‐NPs have a hexagonal shape with 26 nm size. ZnO‐NPs synthesised in RP (RP/ZnO‐NPs) exhibited the good antioxidant potential compared with the butylated hydroxyanisole as a positive control. These NPs showed the cytotoxic effects against breast cancer cells (M.D. Anderson‐Metastasis Breast cancer (MDA‐MB)) with IC₅₀ about 1, 6 and 6 μg/ml after 24, 48 and 72 h of exposure, respectively. RP/ZnO‐NPs were found effective in increasing the expression of catalase enzyme, the enzyme involved in antioxidants properties of the cells. Bio‐green synthesised RP/ZnO‐NPs showed antioxidant and cytotoxic properties. The results of the present study support the advantages of using the bio‐green procedure for the synthesis of NPs as an antioxidant and as anti‐cancer agents.Inspec keywords: II‐VI semiconductors, wide band gap semiconductors, ultraviolet spectra, toxicology, X‐ray diffraction, biochemistry, zinc compounds, nanomedicine, enzymes, biomedical materials, particle size, antibacterial activity, transmission electron microscopy, molecular biophysics, visible spectra, nanofabrication, cellular biophysics, nanoparticles, cancer, field emission scanning electron microscopy, Fourier transform infrared spectra, semiconductor growthOther keywords: bio‐green synthesis ZnO‐NPs, zinc oxide NPs, synthesised ZnO‐NP, field emission scanning electron microscope, transmission electron microscope, antioxidant properties, bio‐green synthesised RP‐ZnO‐NPs, Fourier‐transform infrared spectroscopy, X‐ray diffraction, breast cancer cells MDA‐MB, pro‐apoptotic potentials, cytotoxic effects, catalase enzyme, bio‐green procedure, time 48.0 hour, time 72.0 hour, size 26.0 nm, time 24.0 hour, ZnO     

Synthesis of Ag‐NPs impregnated cellulose composite material: its possible role in wound healing and photocatalysis

Cellulose is the natural biopolymer normally used as supporting agent with enhanced applicability and properties. In present study, cellulose isolated from citrus waste is used for silver nanoparticles (Ag‐NPs) impregnation by a simple and reproducible method. The Ag‐NPs fabricated cellulose (Ag‐Cel) was characterised by powder X‐rays diffraction, Fortier transform infrared spectroscopy and scanning electron microscopy. The thermal stability was studied by thermo‐gravimetric analysis. The antibacterial activity performed by disc diffusion assay reveals good zone of inhibition against Staphylococcus aureus and Escherichia coli by Ag‐Cel as compared Ag‐NPs. The discs also displayed more than 90% reduction of S. aureus culture in broth within 150 min. The Ag‐Cel discs also demonstrated minor 2,2‐diphenyl 1‐picryl‐hydrazyl radical scavenging activity and total reducing power ability while moderate total antioxidant potential was observed. Ag‐Cel effectively degrades methylene‐blue dye up to 63.16% under sunlight irradiation in limited exposure time of 60 min. The Ag‐NPs impregnated cellulose can be effectively used in wound dressing to prevent bacterial attack and scavenger of free radicals at wound site, and also as filters for bioremediation and wastewater purification.Inspec keywords: silver, nanoparticles, particle reinforced composites, nanocomposites, filled polymers, wounds, nanomedicine, biomedical materials, photochemistry, catalysis, X‐ray diffraction, Fourier transform infrared spectra, scanning electron microscopy, thermal stability, thermal analysis, antibacterial activity, dyes, wastewater treatment, contaminated site remediation, nanofabricationOther keywords: silver nanoparticles, impregnated cellulose composite, wound healing, photocatalysis, natural biopolymer, citrus waste, powder X‐ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy, thermal stability, thermo‐gravimetric analysis, antibacterial activity, disc diffusion assay, Staphylococcus aureus, Escherichia coli, inhibition zone, broth, 2,2‐diphenyl 1‐picryl‐hydrazyl radical scavenging activity, total reducing power ability, total antioxidant potential, methylene‐blue dye, sunlight irradiation, wound dressing, bacterial attack, free radical scavenger, wastewater purification, bioremediation filters, wound site, time 60 min, Ag     

Synthesis,characterisation and bactericidal effect of ZnO nanoparticles via chemical and bio‐assisted (Silybum marianum in vitro plantlets and callus extract) methods: a comparative study

Currently, the evolution of green chemistry in the synthesis of nanoparticles (NPs) with the usage of plants has captivated a great response. In this study, in vitro plantlets and callus of Silybum marianum were exploited as a stabilising agent for the synthesis of zinc oxide (ZnO) NPs using zinc acetate and sodium hydroxide as a substitute for chemical method. The contemporary investigation defines the synthesis of ZnO NPs prepared by chemical and bio‐extract‐assisted methods. Characterisation techniques such as X‐ray diffraction, scanning electron microscopy, Fourier transform infrared spectroscopy and energy dispersive X‐ray were used to confirm the synthesis. Although chemical and bio‐assisted methods are suitable choices for NPs synthesis, the bio‐assisted green assembly is advantageous due to superior stability. Moreover, this report describes the antibacterial activity of the synthesised NPs against standard strains of Klebsiella pneumonia and Bacillus subtilis.Inspec keywords: zinc compounds, II‐VI semiconductors, wide band gap semiconductors, nanoparticles, nanofabrication, semiconductor growth, antibacterial activity, X‐ray diffraction, X‐ray chemical analysis, scanning electron microscopy, Fourier transform infrared spectra, nanobiotechnologyOther keywords: chemical methods, bio‐assisted methods, Silybum marianum in vitro plantlets methods, Silybum marianum in vitro callus extract methods, green chemistry, zinc oxide nanoparticles, sodium hydroxide, zinc acetate, X‐ray diffraction, scanning electron microscopy, Fourier transform infrared spectroscopy, energy dispersive X‐ray analysis, bio‐assisted green assembly, antibacterial activity, Klebsiella pneumonia, Bacillus subtilis, ZnO     

Biogenic synthesis of Au,Ag and Au–Ag alloy nanoparticles using Cannabis sativa leaf extract

Biogenic synthesis of gold (Au), silver (Ag) and bimetallic alloy Au–Ag nanoparticles (NPs) from aqueous solutions using Cannabis sativa as reducing and stabilising agent has been presented in this report. Formation of NPs was monitored using UV–visible spectroscopy. Morphology of the synthesised metallic and bimetallic NPs was investigated using X‐ray diffraction and scanning electron microscopy. Elemental composition and the surface chemical state of NPs were confirmed by energy dispersive X‐ray spectroscopy analysis. Fourier transform‐infrared spectroscopy was utilised to identify the possible biomolecules responsible for the reduction and stabilisation of the NPs. Biological applicability of biosynthesised NPs was tested against five bacterial strains namely Klebsiella pneumonia, Bacillus subtilis (B. subtilis), Escherichia coli, Staphylococcus aureus and Pseudomonas aeruginosa (P. aeruginosa) and Leishmania major promastigotes. The results showed considerable antibacterial and anti‐leishmanial activity. The Au–Ag bimetallic NPs showed improved antibacterial activity against B. subtilis and P. aeruginosa as compared to Au and Ag alone, while maximum anti‐leishmanial activity was observed at 250 μg ml⁻¹ NP concentration. These results suggest that biosynthesised NPs can be used as potent antibiotic and anti‐leishmanial agents.Inspec keywords: silver, silver alloys, gold, gold alloys, nanoparticles, nanofabrication, reduction (chemical), ultraviolet spectra, visible spectra, X‐ray diffraction, scanning electron microscopy, X‐ray chemical analysis, Fourier transform infrared spectra, microorganisms, antibacterial activityOther keywords: biogenic synthesis, Cannabis sativa leaf extract, bimetallic alloy Au–Ag nanoparticles, aqueous solutions, reducing agent, stabilising agent, UV–visible spectroscopy, X‐ray diffraction, scanning electron microscopy, elemental composition, surface chemical state, energy dispersive X‐ray spectroscopy analysis, Fourier transform‐infrared spectroscopy, biomolecules, bacterial strains, Klebsiella pneumonia, Bacillus subtilis, Escherichia coli, Staphylococcus aureus, Pseudomonas aeruginosa, Leishmania major promastigotes, antibacterial activity, anti‐leishmanial activity, Ag, Au, AuAg     

Effect of Ag‐NPs synthesised by Chamaemelum nobile extract on the inflammation and oxidative stress induced by carrageenan in mice paw

An environmentally friendly and rapid procedure was developed to synthesise silver nanoparticles (Ag‐NPs) by Chamaemelum nobile extract and to evaluate its in vivo anti‐inflammatory and antioxidant activities. The ultraviolet–visible absorption spectrum of the synthesised Ag‐NPs showed an absorbance peak at 422. The average size of spherical nanoparticles was 24 nm as revealed by transmission electron microscopy. Fourier transform infra‐red spectroscopy analysis supported the presence of biological active compounds involved in the reduction of Ag ion and X‐ray diffraction confirmed the crystalline structure of the metallic Ag. The anti‐inflammatory and antioxidant activity of the Ag‐NPs was investigated against carrageenan‐induced paw oedema in mice. The levels of malondialdehyde (MDA) and antioxidant enzymes superoxide dismutase, catalase, glutathione peroxidase and inflammatory cytokines tumour necrosis factor (TNF‐α), interferon gamma and interleukin (IL)‐6, IL‐1β were assessed in this respect. The results demonstrated that anti‐inflammatory activity of the Ag‐NPs might be due to the ability of the nanoparticles to reduce IL‐1β, IL‐6 and TNF‐α. Moreover, reduction of antioxidant enzymes along with an increase in MDA level shows that the anti‐inflammatory activity of the synthesised Ag‐NPs by C. nobile is attributed to its ameliorating effect on the oxidative damage.Inspec keywords: silver, nanoparticles, nanofabrication, ultraviolet spectra, visible spectra, particle size, transmission electron microscopy, Fourier transform infrared spectra, X‐ray diffraction, crystal structure, enzymes, molecular biophysics, tumours, biomedical materials, nanomedicineOther keywords: Chamaemelum nobile extract, oxidative stress, mice paw, silver nanoparticles, antiinflammatory activity, antioxidant activity, ultraviolet‐visible absorption spectrum, spherical nanoparticle size, transmission electron microscopy, Fourier transform infrared spectroscopy, biological active compounds, X‐ray diffraction, crystalline structure, carrageenan‐induced paw oedema, malondialdehyde, antioxidant enzymes, superoxide dismutase, catalase, glutathione peroxidase, inflammatory cytokines, tumour necrosis factor, interferon gamma, interleukin, IL‐1β, IL‐6, TNF‐α, MDA level, Ag     

Sialic acid‐conjugated PLGA nanoparticles enhance the protective effect of lycopene in chemotherapeutic drug‐induced kidney injury

Lycopene (LYC) is known to protect cells from oxidative damage caused by free radicals in human tissues. In the present study, the authors designed a LYC‐loaded sialic acid (SA)‐conjugated poly(D,L‐lactide‐co‐glycolide) (PLGA) nanoparticle (LYC‐NP) to enhance the therapeutic efficacy of LYC in acute kidney injury. The characteristics of the LYC‐NPs were defined according to particle size, morphology, and in vitro drug release. The LYC‐NPs exhibited a controlled release of LYC over 48 h. Confocal laser scanning microscopy clearly highlighted the targeting potential of SA. Enhanced green fluorescence was observed for the LYC‐NPs in H₂ O₂ ‐treated human umbilical vein endothelial cells, indicating enhanced internalisation of NPs. The LYC‐NPs showed significantly greater cell viability than H₂ O₂ ‐treated cells. In addition, the LYC‐NPs remarkably reduced proinflammatory cytokine levels, attributable mainly to the increased cellular internalisation of the SA‐based carrier delivery system. Furthermore, protein levels of caspase‐3 and ‐9 were significantly down‐regulated after treatment with the LYC‐NPs. Overall, they have demonstrated that SA‐conjugated PLGA‐NPs containing LYC could be used to treat kidney injury.Inspec keywords: fluorescence, biomedical materials, biological tissues, cellular biophysics, drugs, proteins, molecular biophysics, injuries, drug delivery systems, kidney, nanomedicine, biochemistry, optical microscopy, nanoparticles, nanofabrication, cancer, toxicology, blood vessels, particle sizeOther keywords: sialic acid‐conjugated PLGA nanoparticles, chemotherapeutic drug‐induced kidney injury, LYC‐NP, LYC‐loaded sialic acid‐conjugated poly(D,L‐lactide‐co‐glycolide) nanoparticle, SA‐conjugated PLGA‐NP, protective effect, lycopene, human tissues, particle size, in vitro drug release, confocal laser scanning microscopy, green fluorescence, human umbilical vein endothelial cells, cell viability, proinflammatory cytokine levels, cellular internalisation, SA‐based carrier delivery system, time 48.0 hour     

Hypnea musciformis‐mediated Ag/AgCl‐NPs inhibit pathogenic bacteria,HCT‐116 and MCF‐7 cells’ growth in vitro and Ehrlich ascites carcinoma cells in vivo in mice

In the present study, Ag/AgCl‐NPs were biosynthesised using Hypnea musciformis seaweed extract; NPs synthesis was confirmed by a change of colour and observation of a razor‐sharp peak at 424 nm by UV–visible spectroscopy. Synthesised nanoparticles were characterised by transmission electron microscopy, energy‐dispersive X‐ray spectroscopy, X‐ray powder diffraction and Fourier transform infrared spectroscopy. Bacterial cell growth inhibition proves that the Ag/AgCl‐NPs have strong antibacterial activity and cell morphological alteration was observed in treated bacterial cells using propidium iodide (PI). Ag/AgCl‐NPs inhibited Ehrlich ascites carcinoma (EAC) cells, colorectal cancer (HCT‐116) and breast cancer (MCF‐7) cell line in vitro with the IC₅₀ values of 40.45, 24.08 and 36.95 μg/ml, respectively. Initiation of apoptosis in HCT‐116 and MCF‐7 cells was confirmed using PI, FITC‐annexin V and Hoechst 33342 dye. No reaction oxygen species generation was observed in both treated and untreated cell lines. A significant increase of ATG‐5 gene expression indicates the possibility of autophagy cell death besides apoptosis in MCF‐7 cells. The initiation of apoptosis in EAC cells was confirmed by observing caspase‐3 protein expression. Ag/AgCl‐NPs inhibited 22.83% and 51% of the EAC cell growth in vivo in mice when administered 1.5 and 3.0 mg/kg/day (i.p.), respectively, for 5 consequent days.     

Synergistic evaluation of AgO2 nanoparticles with ceftriaxone against CTXM and blaSHV genes positive ESBL producing clinical strains of Uro‐pathogenic E. coli

The silver oxide nanoparticles (AgO₂ ‐NPs) were synthesised using silver foil as a new precursor in wet chemical method. X‐ray diffraction analysis shows crystallographic structures of AgO₂ ‐NPs with crystallite size of 35.54 nm well‐matched with standard cubic structure. Scanning electron microscopy analysis clearly shows the random distribution of spherical‐shaped nanoparticles. Energy dispersive X‐ray analysis confirmed the purity of the samples as it shows no impurity element. Fourier transforms infra‐red analysis confirmed the formation of AgO₂ ‐NPs with the presence of Ag‐O‐Ag stretching bond. All the techniques also confirmed the loading of ceftriaxone drug on the surface of AgO₂ ‐NPs. This study also described the effect of AgO₂ ‐NPs having synergistic activity with β lactam antibiotic i.e. ceftriaxone against ESBL generating Escherichia coli (E. coli). Among isolated strains of E. coli, 60.0% were found to be ESBL producer. The synergistic activities of AgO₂ ‐NPs with ceftriaxone suggest that these combinations are effective against MDR‐ESBL E. coli strains as evident by increase in zone sizes. The present study observed rise in MDR‐ESBL E. coli with polymorphism of blaCTXM and blaSHV causing UTI infections in Pakistani population. The antibiotic and AgO₂ ‐NPs synergistic effect can be used as an efficient approach to combat uro‐pathogenic infections.Inspec keywords: antibacterial activity, nanofabrication, nanomedicine, drugs, nanoparticles, microorganisms, crystallites, scanning electron microscopy, silver compounds, X‐ray diffraction, X‐ray chemical analysis, Fourier transform infrared spectra, organic compounds, geneticsOther keywords: synergistic evaluation, clinical strains, silver oxide nanoparticles, silver foil, wet chemical method, X‐ray diffraction analysis, crystallographic structures, standard cubic structure, spherical‐shaped nanoparticles, energy dispersive X‐ray analysis, ceftriaxone drug, synergistic activity, ESBL producer, scanning electron microscopy, Fourier transform infrared analysis, Escherichia coli, blaSHV gene positive ESBL, crystallite size, random distribution, β lactam antibiotics, MDR‐ESBL E. coli strains, polymorphism, blaCTXM, uro‐pathogenic infections, uro‐pathogenic E. coli, AgO₂      

Evaluation of antibacterial property of hydroxyapatite and zirconium oxide‐modificated magnetic nanoparticles against Staphylococcus aureus and Escherichia coli

In the first section of this research, superparamagnetic nanoparticles (NPs) (Fe₃ O₄) modified with hydroxyapatite (HAP) and zirconium oxide (ZrO₂) and thereby Fe₃ O₄ /HAP and Fe₃ O₄ /ZrO₂ NPs were synthesised through co‐precipitation method. Then Fe₃ O₄ /HAP and Fe₃ O₄ /ZrO₂ NPs characterised with various techniques such as X‐ray photoelectron spectroscopy, X‐ray diffraction, scanning electron microscopy, energy dispersive X‐ray analysis, Brunauer–Emmett–Teller, Fourier transform infrared, and vibrating sample magnetometer. Observed results confirmed the successful synthesis of desired NPs. In the second section, the antibacterial activity of synthesised magnetic NPs (MNPs) was investigated. This investigation performed with multiple microbial cultivations on the two bacteria; Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli). Obtained results proved that although both MNPs have good antibacterial properties, however, Fe₃ O₄ /HAP NP has greater antibacterial performance than the other. Based on minimum inhibitory concentration and minimum bactericidal concentration evaluations, S. aureus bacteria are more sensitive to both NPs. These nanocomposites combine the advantages of MNP and antibacterial effects, with distinctive merits including easy preparation, high inactivation capacity, and easy isolation from sample solutions by the application of an external magnetic field.Inspec keywords: nanocomposites, X‐ray chemical analysis, microorganisms, magnetic particles, scanning electron microscopy, precipitation (physical chemistry), nanomagnetics, X‐ray diffraction, X‐ray photoelectron spectra, nanoparticles, superparamagnetism, iron compounds, antibacterial activity, biomedical materials, nanomedicine, calcium compounds, nanofabrication, Fourier transform infrared spectra, magnetometers, zirconium compoundsOther keywords: antibacterial effects, antibacterial property, superparamagnetic nanoparticles, X‐ray photoelectron spectroscopy, X‐ray diffraction, X‐ray analysis, antibacterial activity, bactericidal concentration, S. aureus bacteria, Staphylococcus aureus, Escherichia coli, hydroxyapatite, coprecipitation method, scanning electron microscopy, energy dispersive X‐ray analysis, Brunauer‐Emmett‐Teller method, Fourier transform infrared spectroscopy, vibrating sample magnetometer, microbial cultivations, nanocomposites     

Metabolomic profiling of ZrO2 nanoparticles in MC3T3‐E1 cells

The authors'' previous study showed that zirconium oxide nanoparticles (ZrO₂ NPs) induce toxic effects in MC3T3‐E1 cells; however, its toxicological mechanism is still unclear. Liquid chromatography–mass spectrometry/time‐of‐flight mass spectrometry was used to reveal the metabolite profile and toxicological mechanism of MC3T3‐E1 cells in response to ZrO₂ NPs. The results demonstrated that MC3T3‐E1 cells treated with ZrO₂ NPs for 24 and 48 h presented different metabolic characteristics. Following ZrO₂ NP treatment for 24 h, 96 upregulated and 129 downregulated metabolites in the positive ion mode, as well as 91 upregulated and 326 downregulated metabolites in the negative ion mode were identified. Following ZrO₂ NP treatment for 48 h, 33 upregulated and 174 downregulated metabolites were identified in the positive ion mode, whereas 37 upregulated and 302 downregulated metabolites were confirmed in the negative ion mode. Among them, 42 differential metabolites were recognised as potential metabolites contributing to the induced toxic effects of ZrO₂ NPs in MC3T3‐E1 cells. Most of the differential metabolites were lysophosphatidylcholine and lysophosphatidylethanolamide, indicating that exposure to ZrO₂ NPs may have a profound impact on human cellular function by impairing the membrane system. The results also provide new clues for the toxicological mechanism of ZrO₂ NP dental materials.     

Targeting microbial biofilms: by Arctium lappa l. synthesised biocompatible CeO2 ‐NPs encapsulated in nano‐chitosan

This study is planned to synthesise new biocompatible, nano antimicrobial formulation against biofilm producing strains. Aqueous root extract of Arctium lappa l. was used to synthesise ceria nanoparticles (CeO₂ ‐NPs). The synthesised nanoparticles were encapsulated with nano‐chitosan by sol–gel method and characterised using standard techniques. Gas chromatography‐mass spectrometer of Arctium lappa l. revealed the presence of ethanol, acetone, 1‐ propanol, 2‐methylethane, 1,1‐di‐ethoxy, 1‐Butanol, and oleic acid acted as reducing and surface stabilising agents for tailoring morphology of CeO₂ ‐NPs. Erythrocyte integrity after treatment with synthesised nanomaterials was evaluated by spectrophotometer measurement of haemoglobin release having biocompatibility. Scanning electron microscopy revealed the formation of mono dispersed beads shaped particles with mean particle size of 26.2 nm. X‐ray diffractometry revealed cubic crystalline structure having size of 28.0 nm. After encapsulation by nano‐chitosan, the size of CeO₂ ‐NPs enhances to 48.8 nm making average coverage of about 22.6 nm. The synthesised nanomaterials were found effective to disrupt biofilm of S. aureus and P. aeruginosa. Interestingly, encapsulated CeO₂ ‐NPs revealed powerful antibacterial and biofilm disruption activity examined by fluorescent live/dead staining using confocal laser scanning microscopy. The superior antibacterial activities exposed by encapsulated CeO₂ ‐NPs lead to the conclusion that they could be useful for controlling biofilm producing multidrug resistance pathogens.Inspec keywords: particle size, microorganisms, organic compounds, nanomedicine, sol‐gel processing, cellular biophysics, scanning electron microscopy, optical microscopy, nanoparticles, antibacterial activity, fluorescence, biomedical materials, nanofabrication, X‐ray diffraction, chromatography, filled polymers, cerium compoundsOther keywords: microbial biofilms, aqueous root extract, sol–gel method, gas chromatography‐mass spectrometer, 1‐di‐ethoxy, 1‐Butanol, nanomaterial synthesis, mean particle size, antibacterial activities, ethanol, acetone, 1‐ propanol, biocompatible ceria‐nanoparticle encapsulation, nano‐chitosan, Arctium lappa l., oleic acid, erythrocyte integrity, spectrophotometer measurement, haemoglobin release, mono dispersed beads shaped particle formation, X‐ray diffractometry, cubic crystalline structure, fluorescent live/dead staining, confocal laser scanning microscopy, multidrug resistance pathogens, size 26.2 nm, size 28.0 nm, size 48.8 nm, size 22.6 nm, CeO₂      

Microbicidal activity of TiO2 nanoparticles synthesised by sol–gel method

In this study, the authors investigated antimicrobial activity of TiO₂ nanoparticles (NPs) synthesised by sol–gel method. As synthesised TiO₂ NPs were characterised by X‐ray diffraction, scanning electron microscopy and ultraviolet‐visible absorption spectroscopy. The antimicrobial activity of calcined TiO₂ nanoparticle samples was examined in day light on Gram positive bacteria (Staphylococcus aureus, Streptococcus pneumonia and Bacillus subtilis), Gram negative bacteria (Proteus vulgaris, Pseudomonas aeruginosa and Escherichia coli) and fungal test pathogen Candida albicans. The synthesised TiO₂ NPs were found to be effective in visible light against Streptococcus pneumonia, Staphylococcus aureus, Proteus vulgaris, Pseudomonas aeruginosa and Candida albicans.Inspec keywords: titanium compounds, microorganisms, nanomedicine, biomedical materials, nanofabrication, sol‐gel processing, ultraviolet spectra, visible spectra, X‐ray diffraction, scanning electron microscopy, nanoparticles, antibacterial activityOther keywords: microbicidal activity, titanium dioxide nanoparticle, sol‐gel method, antimicrobial activity, X‐ray diffraction, scanning electron microscopy, ultraviolet‐visible absorption spectroscopy, Gram positive bacteria, Staphylococcus aureus, Streptococcus pneumonia, Bacillus subtilis, TiO₂ , Candida albicans, fungal test pathogen, Escherichia coli, Pseudomonas aeruginosa, Proteus vulgaris, Gram negative bacteria     

Nutratherapeutics approach against cancer: tomato‐mediated synthesised gold nanoparticles

In this study, an eco‐friendly biosynthesis of stable gold nanoparticles (T‐GNPs) was carried out using different concentrations of tomato juice (nutraceuticals) as a reducing agent and tetrachloroauric acid as a metal precursor to explore their potential application in cancer therapeutics. The synthesis of T‐GNPs was monitored by UV‐visible absorption spectroscopy, which unveiled their formation by exhibiting the typical surface plasmon absorption maxima at 522 nm. The size of T‐GNPs was found to be 10.86 ± 0.6 nm. T‐GNPs were characterised by dynamic light scattering, zeta potential, transmission electron microscopy analysis and Fourier transform infrared spectroscopy. T‐GNPs were further investigated for their anti‐cancer activity against human lung carcinoma cell line (A ₅₄₉) and human cervical cancer cell line wherein the IC₅₀ values were found to be 0.286 and 0.200 mM, respectively. T‐GNPs inhibited the growth of cancer cells by generating ROS and inducing apoptosis. T‐GNPs were found highly effective by virtue of their size, metallic property and capping molecules. Thus, this study opens up the prospects of using nutraceutical (tomato juice) as nutratherapeutic agent (T‐GNPs) against critical diseases like lung cancer and cervical cancer.Inspec keywords: gold, nanoparticles, particle size, cancer, ultraviolet spectra, visible spectra, electrokinetic effects, transmission electron microscopy, Fourier transform infrared spectra, cellular biophysics, spectrochemical analysis, nanomedicine, nanofabricationOther keywords: tomato‐mediated synthesised gold nanoparticles, tomato juice, reducing agent, tetrachloroauric acid, cancer therapeutics, UV‐visible absorption spectroscopy, surface plasmon absorption, dynamic light scattering, zeta potential, transmission electron microscopy analysis, Fourier transform infrared spectroscopy, human lung carcinoma cell line, anticancer activity, human cervical cancer cell line, nutratherapeutic agent, lung cancer, Au     

Green preparation of seaweed‐based silver nano‐liquid for cotton pathogenic fungi management

Silver nanoparticles (Ag NPs) were synthesised using the crude ethyl acetate extracts of Ulva lactuca and evaluated their bioefficacy against two crop‐damaging pathogens. The sets of lattice planes in the XRD spectrum for the Ag NPs were indexed to the 111, 200, 220 and 311 orientations and support the crystalline nature of the Ag NPs. The 3414 and 2968 cm⁻¹ peaks were observed in crude algal thallus extract and they were characteristic of terpenoids. Further, a peak at 1389 cm⁻¹ was observed as fatty acids. The marine macroalgae terpenoids and palmitic acid acted as reducing agent and stabiliser, respectively. The size (3 and 50 nm) and shape (spherical) of Ag NPs were recorded. The energy‐dispersive X‐ray spectroscopy analysis exemplified the presence of silver in its elemental nature. Moreover, U. lactuca Ag NPs were effective against two cotton phytopathogens namely Fusarium oxysporum f.sp. vasinfectum (FOV) and Xanthomonas campestris pv. malvacearum (XAM). The minimum inhibitory concentration was found to be 80.0 and 43.33 μg ml⁻¹ against FOV and XAM, respectively. Results confirmed the anti‐microbial activity of green nanoparticles against select pathogens and suggest their possible usage in developing antifungal agents for controlling destructive pathogens in a cotton agroecosystem.Inspec keywords: nanoparticles, biotechnology, antibacterial activity, silver, microorganisms, X‐ray chemical analysis, crops, X‐ray diffraction, cottonOther keywords: crude ethyl acetate extracts, crop‐damaging pathogens, lattice planes, XRD spectrum, crystalline nature, crude algal thallus, fatty acids, marine macroalgae terpenoids, palmitic acid, energy‐dispersive X‐ray spectroscopy analysis, elemental nature, cotton phytopathogens, green nanoparticles, destructive pathogens, cotton agroecosystem, green preparation, seaweed‐based silver nanoliquid, cotton pathogenic fungi management, silver nanoparticles, Ag NP, Ag     

Green synthesis of silver nanoparticles using bovine skin gelatin and its antibacterial effect on clinical bacterial isolates

Nanoparticles are being increasingly used in day‐to‐day life. Therefore, concerns have been raised regarding their interactions with the surrounding environment. This study focused on a simple green method for synthesizing silver nanoparticles (Ag‐NPs) in an autoclave at 15 psi (103 kPa) and 121°C. An aqueous solution of AgNO₃ as a precursor of Ag‐NPs and gelatin (type B) reducing and/or stabilizing (capping) agent were used. The effect of various AgNO₃ concentrations of certain gelatin concentration and various gelatin concentrations at constant AgNO₃ concentration, and autoclaving time, was studied. UV‐Vis spectra ascribed that the presence of localized surface plasmon resonance (SPR) of the synthesized Ag‐NPs. TEM images and the selected area of electron diffraction confirmed, the formation of Ag‐NPs with a diameter of approximately 5 ±0.35 nm. Furthermore, FT‐IR revealed that a gelatin polymer matrix stabilized the synthesized Ag‐NPs. The Well diffusion assay was used to test the effect of Ag‐NPs on six clinical bacterial isolates, where Gram positive bacteria were more susceptible to Ag‐NPs than Gram negative bacteria. Therefore, Ag‐NPs capped by gelatin have remarkable potential effect as an antibacterial agent, and they not only have various medical applications but can also be used in biological, pharmaceutical and industrial fields.Inspec keywords: silver, nanoparticles, nanomedicine, antibacterial activity, microorganisms, nanofabrication, skin, gelatin, ultraviolet spectra, visible spectra, surface plasmon resonance, transmission electron microscopy, electron diffraction, Fourier transform infrared spectra, polymers, biomedical materialsOther keywords: green synthesis, silver nanoparticles, bovine skin gelatin, antibacterial effect, clinical bacterial isolates, autoclave, reducing agent, stabilising agent, ultraviolet‐visible spectra, localised surface plasmon resonance, transmissions electron microscope images, electron diffraction, Fourier transform infrared spectroscopy, gelatin polymer matrix, well diffusion assay, gram negative bacteria, Escherichia coli, Pseudomonas aeruginosa, Klebsiella pneumoniae, gram positive bacteria, Bacillus megaterium, Streptococcus pyogenes, Staphylococcus aureus, temperature 121 degC, Ag     

Label‐free and dynamic monitoring of cytotoxicity to the blood–brain barrier cells treated with nanometre copper oxide

A cytotoxicity study was conducted with a primary culture of the nervous system cells, including brain microvascular endothelial cells (BMECs) and astrocytes, which are important components of the blood–brain barrier. The real‐time cell analysis (RTCA) was used to determine the cytotoxicity of copper‐oxide nanoparticles (CuO NPs). The IC₅₀ values of CuO NPs in astrocytes and BMECs were determined by the RTCA at different exposure times and were used as base values for further research. DNA damage after exposure to CuO NPs for 3 and 24 h was assessed using comet assay at the IC₅₀ obtained from RTCA. The onset time of cytotoxicity induced by CuO NPs was 2 and 2–4 h post‐exposure in BMECs and astrocytes, respectively. Furthermore, the degree of cytotoxicity induced by exposure to CuO NPs for 24–48 h in the BMECs and astrocytes was similar. Treatment with CuO NPs at 1/2*IC₅₀ and 1/5*IC₅₀ for 3 h induced genotoxicity in both cells as assessed by a measurement of DNA damage, although no cytotoxicity was observed. However, significant DNA damage was observed at all concentrations of CuO NPs used in this study, when the treatment time was 24 h.Inspec keywords: biochemistry, blood, brain, cellular biophysics, copper compounds, DNA, molecular biophysics, nanoparticles, toxicologyOther keywords: label‐free cytotoxicity monitoring, dynamic cytotoxicity monitoring, blood‐brain barrier cells, nervous system cells, brain microvascular endothelial cells, astrocytes, real‐time cell analysis, copper‐oxide nanoparticles, comet assay, genotoxicity, DNA damage measurement, time 24 h to 48 h, time 2 h to 4 h, CuO