Prediction of HC5s for phthalate esters by use of the QSAR-ICE model and ecological risk assessment in Chinese surface waters.

Due to their endocrine-disrupting effects and the risks posed in surface waters, in particular by chronic low-dose exposure to aquatic organisms, phthalate esters (PAEs) have received significant attention. However, most assessments of risks posed by PAEs were performed at a selection level, and thus limited by empirical data on toxic effects and potencies. A quantitative structure activity relationship (QSAR) and interspecies correlation estimation (ICE) model was constructed to estimate hazardous concentrations (HCs) of selected PAEs to aquatic organisms, then they were used to conduct a multiple-level environmental risk assessment for PAEs in surface waters of China. Values of hazardous concentration for 5% of species (HC5s), based on acute lethality, estimated by use of the QSAR-ICE model were within 1.25-fold of HC5 values derived from empirical data on toxic potency, indicating that the QSAR-ICE model predicts the toxicity of these three PAEs with sufficient accuracy. The five selected PAEs may be commonly measured in China surface waters at concentrations between ng/L and µg/L. Risk quotients according to median concentrations of the five PAEs ranged from 3.24 for di(2-ethylhexhyl) phthalate (DEHP) to 4.10 × 10-3 for dimethyl phthalate (DMP). DEHP and dibutyl phthalate (DBP) had risks to the most vulnerable aquatic biota, with the frequency of exceedances of the predicted no-effect concentration (PNECs) of 75.5% and 38.0%, respectively. DEHP and DBP were identified as having "high" or "moderate" risks. Results of the joint probability curves (JPC) method indicated DEHP posed "intermediate" risk to freshwater species with a maximum risk product of 5.98%. The multiple level system introduced in this study can be used to prioritize chemicals and other new pollutant in the aquatic ecological.

Intimate coupling of gC3N4/CdS semiconductor on eco-friendly biocarrier loofah sponge for enhanced detoxification of ciprofloxacin.

Ciprofloxacin is one of the antibiotics predominantly used to treat bacterial infections, however excess usage, and release of antibiotic from various sources to the environment can cause severe risks to human health since it was considered as emerging pollutant. This study deals with the intimately coupled photocatalysis and biodegradation (ICPB) of ciprofloxacin using gC3N4/CdS photocatalytic semiconductor and eco-friendly renewable loofah sponge as biocarrier in the ICPB. The photocatalyst gC3N4/CdS was prepared and their synergistic photocatalytic degradation of ciprofloxacin were assessed and the results shows that gC3N4/CdS (20%) exhibit 79% degradation efficiency in 36 h. Further ICPB exhibited enhanced ciprofloxacin degradation 95% at 36 h. The 62.4% and 81.1% of chemical oxygen demand (COD) removal was obtained in the photocatalysis and ICPB respectively. Enhanced degradation of ciprofloxacin and COD removal was due to the synergetic photoelectrons generated from the gC3N4/CdS (20%) transferred to the bacterial communities which intensely mineralize the degradation products produced from the photocatalysis process. Furthermore, production of hydroxyl •OH and superoxide radical anion O2• were identified actively involved in the degradation of ciprofloxacin. The biocarrier loofah sponge provided favourable environment to the bacterial communities for the formation of biofilm and production of extracellular polymeric substances (EPS). Excess quantity of EPS production in the ICPB helps in the prevention of toxicity of photocatalyst to bacterial communities as well as facilitate the extracellular electron transfer process. This work provides a novel path for enhanced degradation of ciprofloxacin using eco-friendly, low cost and renewable biocarrier loofah sponge in the ICPB system.

Sunlight-driven intimately coupled photocatalysis and biodegradation (SDICPB): A sustainable approach for enhanced detoxification of triclosan.

Triclosan is considered as recalcitrant contaminant difficult to degrade from the contaminated wastewater. Thus, promising, and sustainable treatment method is necessary to remove triclosan from the wastewater. Intimately coupled photocatalysis and biodegradation (ICPB) is an emerging, low-cost, efficient, and eco-friendly method for the removal of recalcitrant pollutants. In this study BiOI photocatalyst coated bacterial biofilm developed at carbon felt for efficient degradation and mineralization of triclosan was studied. Based on the characterization of BiOI prepared using methanol had lower band gap 1.85 eV which favors lower recombination of electron-hole pair and higher charge separation which ascribed to enhanced photocatalytic activity. ICPB exhibits 89% of triclosan degradation under direct sunlight exposure. The results showed that production of reactive oxygen species hydroxyl radical and superoxide radical anion played crucial role in the degradation of triclosan into biodegradable metabolites further the bacterial communities mineralized the biodegradable metabolites into water and carbon dioxide. The confocal laser scanning electron microscope results emphasized that interior of the biocarrier shows a large number of live bacterial cells existing in the photocatalyst-coated carrier, where the little toxic effect on bacterial biofilm occurred on the exterior of the carrier. The extracellular polymeric substances characterization result remarkable confirms that which could act as sacrificial agent of photoholes further helped by preventing the toxicity to the bacterial biofilm from the reactive oxygen species and triclosan. Hence, this promising approach can be a possible alternative method for the wastewater treatment polluted with triclosan.

Enhanced sulfamethazine detoxification by a novel BiOCl (110)/NrGO/BiVO4 heterojunction.

The emerging contaminants removal from the environment has recently been raised concerns due to their presence in higher concentrations. Over usage of emerging contaminant such as sulfamethazine poses serious threat to the aquatic and human health as well. This study deals with rationally structured a novel BiOCl (110)/NrGO/BiVO4 heterojunction which is used to detoxify sulfamethazine (SMZ) antibiotic efficiently. The synthesised composite was well characterized and the morphological analysis evidenced the formation of heterojunction consisted of nanoplates BiOCl with dominant exposed (110) facets and leaf like BiVO4 on NrGO layers. Further results revealed that the addition of BiVO4 and NrGO tremendously increased the photocatalytic degradation efficiency of BiOCl with the rate of 96.9% (k = 0.01783 min-1) towards SMZ within 60 min of visible light irradiation. Furthermore, heterojunction energy-band theory was employed to determine the degradation mechanism of SMX in this study. The larger surface area of BiOCl and NrGO layers are believed to be the reason for higher activity which facilitates the excellent charge transfer and improved light absorption. In addition, SMZ degradation products identification was carried out by LC-ESI/MS/MS to determine the pathway of degradation. The toxicity assessment was studied using E. coli as a model microorganism through colony forming unit assay (CFU), and the results indicated a significant reduction in biotoxicity was observed in 60 min of degradation process. Thus, our work gives new methods in developing various materials that effectively treat emerging contaminants from the aqueous environment.

A novel magnetic AgVO3/rGO/CuFe2O4 hybrid catalyst for efficient hydrogen evolution and photocatalytic degradation.

A superior semiconductor material with efficient charge separation and easy reuse could be a promising route for efficient photocatalytic hydrogen evolution and pollutant degradation. AgVO3 is one of the best visible light active materials which has attracted much attention for several biological and environmental applications. In the aim of enhancing its stability and recyclability a novel AgVO3/rGO/CuFe2O4 heterojunction was prepared by hydrothermal method for hydrogen generation (H2) and 4-nitrophenol (4-NP) degradation as well. The composite was well characterized by XRD, SEM, HR-TEM, XPS and VSM. The morphological images suggested the rod shaped AgVO3 and irregular shaped CuFe2O4 are unevenly distributed on reduced graphene oxide (rGO) layers. The hydrogen evolution results indicated that the composite showed around 8.937 mmol g-1h-1 of H2 generation which was ∼2.3 times and ∼9.2 times higher than pure AgVO3 (3.895 mmol g-1h-1) and CuFe2O4 (0.96 mmol g-1h-1) respectively. The 4-NP degradation efficiency of the prepared composite was observed as 94.7% (k = 0.01841 min-1) which is much higher than the AgVO3 (66.3%) and CuFe2O4 (38.2%) after 4 h of irradiation. The higher efficiency could be attributed to the heterojunction formation and faster charge separation. The radical trapping results indicated that the •OH, O2•- and photogenerated h+ are the main species responsible for efficient activity. The AgVO3/rGO/CuFe2O4 heterojunction showed 49.6 emu/g of saturation magnetization and confirms that it could be easily separated with an external magnet, and showed 85.3% of degradation efficiency even after 6 recycles which indicated its higher stability and recyclability. Thus, our study provides new insight into hydrogen generation and phenol degradation using AgVO3 based recyclable composites.

Facile fabrication of AgVO3/rGO/BiVO4 hetero junction for efficient degradation and detoxification of norfloxacin.

In the recent past, the development of efficient materials for degradation and detoxification of antibiotics has gained more attention in wastewater treatment process. As a visible light active material AgVO3 has attracted much concern in environmental remediation. To improve its efficiency and stability, a novel heterojunction was prepared by combining AgVO3 with rGO and BiVO4 through a hydrothermal method. The prepared AgVO3/rGO/BiVO4 composite was further utilized for effective detoxification of Norfloxacin (NFC) antibiotic. The morphological analysis revealed the clear rod shaped AgVO3 and leaf like BiVO4 that are evenly distributed on reduced graphene oxide (rGO) layers. The visible light absorbance and the catalytic activity of AgVO3/rGO/BiVO4 was dramatically improved compared to pure AgVO3 and BiVO4. From the results it showed that the degradation efficiency of AgVO3/rGO/BiVO4 (∼96.1%, k = 0.01782 min-1) was 2.5 times higher than pure AgVO3 and 3.4 times higher than the pure BiVO4 respectively towards NFC after 90 min. The higher efficiency could be attributed to the heterojunction formation and faster charge separation. The radical trapping experiments results indicated that the •OH, and O2•- are the main species responsible for degradation. The degradation products of NFC were analysed through ESI-LC/MS and pathway was proposed. Furthermore, the toxicity assessment of pure NFC and its degradation products was studied using E. coli as the model bacteria through colony forming unit assay and the results indicated the efficient detoxification was attained during the degradation process. Thus, our study provides new insight into detoxification of antibiotics using AgVO3 based composites.

Fabrication of novel BiPO4/Ag3PO4@rGO hybrid composite for effective detoxification of tetracycline.

A practical photocatalytic method using efficient and nontoxic is crucial for wastewater treatment technology. The present study deals with the preparation of BiPO4/Ag3PO4@rGO heterojunction through hydrothermal process and utilized it for efficient degradation and detoxification of Tetracycline (TCL) antibiotic. The prepared composite was characterized by X-ray diffraction, UV-vis DRS spectroscopy, Scanning electron microscope (SEM), Transmission electron microscope (TEM) and XPS (X-ray photoelectron spectroscopy). From our study, it was evident that the addition of Ag3PO4 extensively improved the photocatalytic efficiency of BiPO4 with a degradation of the rate of 94.6% (k = 0.01783 min-1) towards TCL under visible light within 90 min irradiation. The heterojunction energy-band theory has been adopted to understand the mechanism of degradation. The improved efficiency was ascribed to the excellent charge transfer between the interface of p-n heterojunction and the improvement in the absorption of light. Furthermore, LC/ESI-MS/MS (liquid chromatography-electrospray ionization tandem mass spectrometry) carried out TCL degradation product identification to propose the degradation pathway. The biotoxicity assessment studies revealed that effective detoxification was observed during degradation. Thus, this work extends new methods for developing new BiPO4-based heterojunction composites to meet the requirements for remediation of a contaminated aqueous environment.

A novel BiOCl (110)/rGO/Ag3PO4 (111) heterostructure for efficient detoxification of 2,4-dichlorophenol.

An effective method using nontoxic and efficient photocatalysts are crucial for wastewater treatment. Bismuth oxychloride (BiOCl) is considered as one of the valuable photocatalysts due to its unique layered plate like structure, however higher recombination and unsatisfied visible light absorption efficiency seriously affecting its applications. Addition of tetrahedral silver phosphate (Ag3PO4) which is known for its superior photocatalytic efficiency under visible light is believed to be the solution for the issue. Upon further adding of reduced graphene oxide (rGO) could form a bridging structure and enhance the activity. Considering the merits of these materials the BiOCl (110)/rGO/Ag3PO4 (111) heterojunction has been successfully constructed for 2,4-dichlorophenol (DCP) enhanced detoxification. The efficiency in degradation was found to be 94.8% by BiOCl/rGO/Ag3PO4 (k = 0.01879 min-1) that was greater to that of pure Ag3PO4 (∼1.9 times; k = 0.00818 min-1) and pure BiOCl (∼2.8 times; k = 0.00642 min-1) after 60 min of visible light irradiation. The mechanism of degradation was explained through the principle of heterojunction energy-band theory. Furthermore, 2,4-dichlorophenol (2,4-DCP) degradation products identification was carried out by ESI/LC-MS to propose the degradation pathway. Furthermore, the phytotoxicity of the intermediate products was investigated by estimating the germination index (GI) values on Phaseolus vulgaris (P. vulgaris) at different time intervals and the GI values were found to be 10.79% and 80.17% before and after degradation respectively. Thus, our results revealed that efficient and significant toxicity reduction was observed in this photodegradation.

Novel assembly of BiVO4@N-Biochar nanocomposite for efficient detoxification of triclosan.

The wide spread of antibacterial and antifungal agents demands in growing multifunctional materials to completely eliminate these organic contaminants in water. BiVO4 (Bismuth vanadate) is a superior catalyst under visible light but suffers with high photoelectron-hole pair recombination rate and poor adsorption capacity which limits its efficiency. Addition of N-doped Biochar (N-Biochar) to BiVO4 with large specific surface area and high conductivity are anticipated to overcome the problem and promote the catalytic performance. Thus, the present study developed a simple hydrothermal method to prepare BiVO4@N-Biochar catalyst for efficient detoxification of Triclosan (TCS). The morphological analysis results suggested that BiVO4 particles were evenly distributed on carbon surface amongst the N-Biochar matrix. Within 60 min of visible light irradiation, nearly 94.6% TCS degradation efficiency was attained by BiVO4@N-Biochar (k = 0.02154 min-1) while only 56.7% was attained with pure BiVO4 (k = 0.00637 min-1). In addition, LC-MS/MS technique was utilized to determine the TCS degradation products generation in the photodegradation process and pathway was proposed. Furthermore, the E. coli (Escherichia coli) colony forming unit assay was used to determine the biotoxicity of the degradation products in which 72.3 ± 2.6% of detoxification efficiency was achieved and suggested a substantial reduction in biotoxicity during the photodegradation.

Novel magnetically separable tetrahedral Ag3PO4/NrGO/CuFe2O4 photocatalyst for efficient detoxification of 2,4-dichlorophenol.

An effective as well as eco-friendly photodegradation methods by atoxic and easily reusable photocatalysts are essential for wastewater treatment. Silver phosphate (Ag3PO4) specifically in tetrahedral shape is one of the superior catalysts under visible light but its photocorrosion, poor electron transfer ability and low surface adsorption properties limits its applications. Combination of Ag3PO4 and nitrogen doped reduced graphene oxide (NrGO) having higher in surface area, ample functional groups and hetero atom doping is expected to get over the problem. Further addition of a spinel ferrite (CuFe2O4) could enhance the visible light response activity and helps in easy separation of catalyst for reuse. Given the merits of Ag3PO4, NrGO and CuFe2O4 we rationally integrated a novel magnetically separable stable Ag3PO4/NrGO/CuFe2O4 photocatalyst for efficient detoxification of 2,4-dichlorophenol (2,4-DCP). About 95.3% degradation efficiency was achieved by Ag3PO4/NrGO/CuFe2O4 (k = 0.01978 min-1) which was ~2.6 times higher than pure Ag3PO4 (k = 0.00747 min-1) in 60 min of visible light irradiation. The Ag3PO4/NrGO/CuFe2O4 heterojunction was able to separate and recycle easily using an external magnetic field due to its strong magnetism, and after 5 recycles it showed 88.6% of degradation efficiency revealed its higher stability and recyclability. The photocatalytic mechanism of Ag3PO4/NrGO/CuFe2O4 was explained by heterojunction energy-band theory. In addition, the plausible intermediate products of 2,4-dichlorophenol were analyzed by ESI/LC-MS and proposed the pathway. Moreover, the phytotoxicity was also studied on V. radiata in which GI (germination index) was found to be 11.97% before degradation, while 80.31% of GI was observed in 60 min of degradation which revealed that more significant reduction in toxicity was attained on this photodegradation.

Facile synthesis of ZnO nanoparticles by Actinidia deliciosa fruit peel extract: Bactericidal, anticancer and detoxification properties.

Synthesis of nanoparticles by eco-friendly method pulled an extensive concern worldwide due its biocompatibility and wide range of applications as catalysts, microbicidal agents, cancer treatment, sensors etc. Though different chemical methods available for preparation of ZnO nanoparticles, synthesis by utilizing plant material is an excellent substitute and green method as well. The present study describes preparation of ZnO nanoparticles by low-cost green synthetic way using Actinidia deliciosa (kiwi) fruit peel extract and its excellent biological and catalytic properties. The synthesized nanoparticles were well characterized by UV visible spectroscopy, X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), Scanning electron microscopy (SEM), Transmission electron microscopy (TEM) and Energy-dispersive X-ray spectroscopy (EDAX). The bactericidal activity of the ZnO nanoparticles was determined by using Staphylococcus aureus (S. aureus), while mechanism of cell death was studied by SEM images. Superior anticancer activity was also observed in inhibiting the colon cancer cells (HCT116) by the ZnO nanoparticles. In addition, ZnO nanoparticles showed efficient photocatalytic activity towards degradation of p-bromophenol, about 96.3% within 120 min. Furthermore, phytotoxicity of the intermediate products was analyzed using Vigna radiata (V. radiata) as a model plant. About 8.0% of germination index (GI) was observed in pure p-BP while it increased to 82.3%, and exhibited that the detoxification of p-BP was attained after 120 min of degradation. Thus, the present study demonstrates ZnO nanoparticles prepared from simple, rapid, inexpensive, eco-friendly and efficient green method gives alternative root for biomedicine and wastewater treatment technologies.

A mediator-free whole-cell electrochemical biosensing system for sensitive assessment of heavy metal toxicity in water.

A bioelectrochemical sensing system (BES) based on electroactive bacteria (EAB) has been used as a new and promising tool for water toxicity assessment. However, most EAB can reduce heavy metals, which usually results in low toxicity response. Herein, a starvation pre-incubation strategy was developed which successfully avoided the metal reduction during the toxicity sensing period. By integrating this starvation pre-incubation procedure with the amperometric BES, a sensitive, robust and mediator-free biosensing method for heavy metal toxicity assessment was developed. Under the optimized conditions, the IC50 (half maximal inhibitory concentration) values for Cu2+, Ni2+, Cd2+, and Cr6+ obtained were 0.35, 3.49, 6.52, 2.48 mg L-1, respectively. The measurement with real water samples also suggested this method was reliable for practical application. This work demonstrates that it is feasible to use EAB for heavy metal toxicity assessment and provides a new tool for water toxicity warning.

Enhanced detoxification of p-bromophenol by novel Zr/Ag-TiO2@rGO ternary composite: Degradation kinetics and phytotoxicity evolution studies.

The toxicity and persistence of the halogenated aromatics, particularly brominated phenolic compounds have drawn serious concerns to the environment, emphasizing the potential effects on human health and ecosystems balance. Advanced oxidation process (AOP) has received much attention as an alternative for the conventional wastewater treatment methods to treat water contaminated with toxic pollutants. This study investigated the degradation and detoxification of p-bromophenol (p-BP) by a novel Zr/Ag-TiO2@rGO photocatalyst under visible light. Upon 3 h of visible light irradiation over Zr/Ag-TiO2@rGO, more than 95% of p-BP (15 mg/L) degradation was achieved at a rate of 0.23 min-1. The degradation products were identified by GC-MS and possible degradation pathway was proposed. The phytotoxicity evolution of the degraded products was assessed on Vigna radiata (V. radiata), in which seeds treated with pure p-BP showed less germination (40%) compared to degradation products (100%). Furthermore, the germination index (GI) of p-BP was found to be 11.1% before degradation while it increased to 80.5% after 3 h of degradation indicated that this photodegradation process achieved detoxification of p-BP. Thus, this study demonstrated that p-BP elimination and detoxification could be simply achieved with Zr/Ag-TiO2@rGO nanocomposite under visible light irradiation, which provides new solution for wastewater treatment and water reuse in crop irrigation.

Efficient detoxification of triclosan by a S-Ag/TiO2@g-C3N4 hybrid photocatalyst: process optimization and bio-toxicity assessment.

Owing to their persistency and toxicity, development of an effective strategy to eliminate antibiotic residues from the aquatic system has become a major environmental concern. Doping TiO2 with hetero atoms and forming a hybrid structure with g-C3N4 could serve as an efficient visible light active photocatalytic candidate. In this study, a novel S-Ag/TiO2@g-C3N4 hybrid catalyst was prepared for visible light degradation and detoxification of triclosan (TS) antibiotic. The effect of various operational parameters towards the photocatalytic degradation was systematically evaluated through response surface methodology (RSM) based on central composite design (CCD). The highest TS degradation (92.3%) was observed under optimal conditions (TS concentration = 10 mg L-1, pH = 7.8, and catalyst weight = 0.20 g L-1) after 60 min. Efficient charge separation resulted from the doped nanoparticles (silver and sulphur), the existing integrated electric field of the heterojunction and the overlying light response of hybridized TiO2 and g-C3N4, thus the S-Ag/TiO2@g-C3N4 composite showed impressively higher activity. The main degradation products of TS were identified by LC/ESI-MS analysis. In addition, the toxicity of the degradation products was investigated through an Escherichia coli (E. coli) colony forming unit assay and the results revealed that under optimal conditions a significant reduction in biotoxicity was noticed.

Photocatalytic mineralization and degradation kinetics of sulphamethoxazole and reactive red 194 over silver-zirconium co-doped titanium dioxide: Reaction mechanisms and phytotoxicity assessment.

The photodegradation and phytotoxicity of the pharmaceutical antibiotic, sulphamethoxazole (SMX) and the azo-dye reactive-red-194 (RR194) under visible-light irradiation of TiO2 nanoparticles modified by silver and zirconium was investigated. The results indicated that sulphamethoxazole and its toxic degradation by product, 3-amino-5-methylisoxazole and RR-194 could be degraded efficiently by the co-doped Zr/Ag-TiO2 catalyst. PL studies and ROS generation results suggested that the effective charge separation was carried out while irradiation of the modified TiO2 nanoparticles. Phytotoxicity tests demonstrated lower percentage of germination in P. vulgaris (40%), V. radiata (30%) and P. lunatus (30%) of the seeds treated with 50 ppm of SMX, compared to the seeds treated with the degradation products (100%). The results with 50 ppm of RR-194 also showed lower percentage of germination in P. vulgaris (40%), V. radiata (50%) and P. lunatus (30%) compared to the degradation products (100%). Furthermore, significant increase in root and shoot development was observed in the seeds treated with the degraded products when compared with SMX and RR-194. Overall, this study contributes to further understanding the photodegradation mechanisms, degradation products and environmental fate of SMX and RR-194 in water which helps in the evaluation and mitigation of the environmental risk of SMX and RR-194 for water reuse and crop irrigation.

Preliminary investigation of catalytic, antioxidant, anticancer and bactericidal activity of green synthesized silver and gold nanoparticles using Actinidia deliciosa.

Herein we report a rapid low cost one step green synthetic method using Actinidia deliciosa fruit extract for preparation of stable and multifunctional silver and gold nanoparticles. The synthesized nanoparticles were successfully used as green catalysts for the reduction of 4-nitrophenol (4-NP) and methylene blue (MB). The enhanced biological activity of the prepared nanoparticles was investigated based on its highly stable antioxidant, anticancer and bactericidal effects. TEM micrographs showed that the silver nanoparticles (AgNPs) formed were predominantly spherical in shape having diameters ranging from 25 to 40nm, while gold nanoparticles (AuNPs) shown particle size ranges from 7 to 20nm. EDAX (energy-dispersive X-ray spectroscopy) and XPS (X-ray photoelectron spectroscopy) results confirmed the presence of elemental silver and gold. X-ray diffraction (XRD) pattern revealed the formation of face-centered cubic structure for AgNPs and AuNPs. The Fourier-transform infrared (FTIR) spectrum indicated the presence of possible functional groups in the biomolecule responsible for capping the nanoparticles. The AgNPs treated HCT116 cells showed 78% viability at highest concentration (350µg/mL), while AuNPs showed 71% viability at highest concentration (350µg/mL) using MTT assay, which provides promising approach for alternative nano-drug development. The antimicrobial activity of the nanoparticles was investigated using Pseudomonas aeruginosa (P.aeruginosa) in which damaging the cell membrane was observed by TEM images. Our results revealed that the green synthesis method is easy, rapid, inexpensive, eco-friendly and efficient in developing multifunctional nanoparticles in near future in the field of biomedicine, water treatment and nanobiotechnology.

Visible-light-driven photocatalytic inactivation of MS2 by metal-free g-C3N4: Virucidal performance and mechanism.

The challenge to achieve effective water disinfection of pathogens, especially viruses, with minimized harmful disinfection byproducts calls for a cost-effective and environmentally benign technology. Here, polymeric graphitic carbon nitride (g-C3N4), as a metal-free robust photocatalyst, was explored for the first time for its ability to inactivate viruses under visible light irradiation. MS2 with an initial concentration of 1 × 108 PFU/mL was completely inactivated by g-C3N4 with a loading of 150 mg/L under visible light irradiation of 360 min. g-C3N4 was a robust photocatalyst, and no decrease in its virucidal performance was observed over five cycles of sequential MS2 photocatalytic inactivation. The reactive oxygen species (ROSs) were measured by a range of scavengers, and photo-generated electrons and its derived ROSs (O- 2) were found to be the leading contributor for viral inactivation. TEM images indicated that the viral particle shape was distorted and the capsid shell was ruptured after photocatalysis. Viral surface proteins, particularly replicase proteins and maturation proteins, were damaged by photocatalytic oxidation. The loss of proteins would result in the leakage and rapid destruction of interior components (four main types of RNA genes), finally leading to viral death without regrowth. Our work opens a new avenue for the exploration and applications of a low-cost, high-efficient, and robust metal-free photocatalyst for green/sustainable viral disinfection.

Amelioration of excision wounds by topical application of green synthesized, formulated silver and gold nanoparticles in albino Wistar rats.

Wound healing, a complex biological process, has attained a lot of attention as dermatologists are primarily interested in stimulated wound closure without formation of scar or a faint scar. The recent upsurgence of nanotechnology has provided novel therapeutic materials in the form of silver and gold nanoparticles which accelerate the wound healing process. The effect of formulated nanoparticles using Coleus forskohlii root extract (green synthesized) has been tried out for ameliorating full thickness excision wounds in albino Wistar male rats. The evaluation of in vivo activity of nanoparticles in wound healing was carried out on open wounds made by excision on the dorsal sides of albino Wistar rats under anesthesia, and the healing of the wounds was assessed. Histological aspects of the healing process were studied by a HE (Hematoxylin and Eosin) staining method to assess various degrees of re-epithelialization and the linear alignment of the granulation tissue whereas Van Gieson's histochemical staining was performed to observe collagen fibers. The healing action shown by the formulated nanoparticles was remarkable during the early stages of wound healing, which resulted in the substantial reduction of the whole healing period. Topical application of formulated gold nanoparticles was found to be more effective in suppressing inflammation and stimulating re-epithelialization compared to silver nanoparticles during the healing process. The results throw light on the amelioration of excision wounds using nanoparticles which could be a novel therapeutic way of improving wound healing in clinical practice. The mechanism of advanced healing action of both types of nanoparticles could be due to their antimicrobial, antioxidant and anti-inflammatory properties.

Enhanced photo-catalytic activity of Sr and Ag co-doped TiO2 nanoparticles for the degradation of Direct Green-6 and Reactive Blue-160 under UV & visible light.

This work is focused on sol-gel synthesis of silver and strontium co-doped TiO2 nanoparticles and their utilization as photo-catalysts in degradation of two textile dyes. Effect of pH, intensity of light, amount of photo-catalyst, concentration of dye, sensitizers, etc., were studied to optimize conditions for obtaining enhanced photo-catalytic activity of synthesized nanoparticles. XRD, BET, HR-TEM, EDAX and UV-Vis (diffused reflectance mode) techniques were used to characterize the nanoparticles. Interestingly, band gap of Sr and Ag co-doped TiO2 nanoparticles showed considerable narrowing (2.6 eV) when compared to Ag doped TiO2 (2.7 eV) and undoped TiO2 (3.17 eV) nanoparticles. Incorporation of Ag and Sr in the lattice of TiO2 could bring isolated energy levels near conduction and valence bands thus narrowing band gap. The XRD analysis shows that both Ag and Sr nanoparticles are finely dispersed on the surface of titania framework, without disturbing its crystalline structure. TEM images indicate that representative grain sizes of Ag-doped TiO2 & Sr and Ag co-doped TiO2 nanoparticles are in the range of 8-20 nm and 11-25 nm, respectively. Effective degradation of Direct Green-6 (DG-6) and Reactive Blue-160 (RB-160) under UV and visible light has been achieved using the photo-catalysts. Sr and Ag co-doped TiO2 photo-catalysts showed higher catalytic activity during degradation process in visible region when compared to Ag-doped and undoped TiO2 nanoparticles which could be attributed to the interactive effect caused by band gap narrowing and enhancement in charge separation. For confirming degradation of the dyes, total organic carbon (TOC) content was monitored periodically.

Zirconium and silver co-doped TiO2 nanoparticles as visible light catalyst for reduction of 4-nitrophenol, degradation of methyl orange and methylene blue.

Catalytic activity of Zr and Ag co-doped TiO2 nanoparticles on the reduction of 4-nitrophenol, degradation of methylene blue and methyl orange was studied using sodium borohydride as reducing agent. The nanoparticles were characterized using X-ray diffraction, energy dispersive X-ray, high resolution transmission electron microscopy, selected area electron diffraction and UV-Vis spectroscopy. The rate of the reduction/degradation was found to increase with increasing amount of the photocatalyst which could be attributed to higher dispersity and small size of the nanoparticles. The catalytic activity of Zr and Ag co-doped TiO2 nanoparticles showed no significant difference even after recycling the catalyst four times indicating a promising potential for industrial application of the prepared photocatalyst.