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Summary: In present research, photocatalytic degradation of textile wastewater was investigated through the combined effect of ozonation and photocatalysis processes. Catalytic acids in the nano-particle form under moderate reaction conditions were used for the successful disintegration of contaminants in textile wastewater which in turn increases the process efficiency. Moreover, the combined effect of the photocatalytic-ozonation process after secondary treatment of textile wastewater on discharge requirements of zero discharge hazardous chemicals (ZDHC) by Road to Zero was also studied. Different parameters were optimized like ozone flowrate, catalytic concentration, UV light intensity, and reaction time. Results revealed that overall process efficiency is influenced by ozone and reaction time. In contrast, an increased rate of degradation is attributed to the synthesized TiO2 (anatase) in nanoparticle form. The combined ozone-assisted photo-catalytic process showed the COD, BOD, and TSS removal efficiencies of 91.5%, 94%, and 86% at 25 °C temperature and pH 7-9. The results were attained at optimum conditions like reaction time (140 min), Ozone concentration (2 g/hr), TiO2 concentration (2g/L), and UV energy (88 W), respectively. The study demonstrated the efficiency of an integrated process for the degradation of real textile wastewater. Thus, combined photocatalytic and ozonation processes are known to exhibit better responses than individual processes for pollutants removal from textile wastewater. [ABSTRACT FROM AUTHOR]

A simple, rapid, precise, accurate high performance liquid chromatography method has been developed and subsequently validated for determination of valsartan in rabbit plasma. The method was developed employing mixture of mobile phase consisting of 0.02 M potassium dihydrogen phosphate buffer and acetonitrile (45:55), pH was adjusted to 2.7 using 50% orthophosphoric acid and pumped thorough chromatographic system at a flow rate of 1 ml/min. An isocratic elution mode was carried out at HPLC system (Agilent Technologies, 1200 series, USA) fitted with variable wavelength detector and data processing software ChemStation. For sample analysis, 20µl sample was injected and eluate was monitored at 225nm wavelength. Pharmacokinetic evaluation was performed in rabbits after the oral administration of valsartan loaded PVA-copoly(AA) hydrogels. The mean Cmax of valsartan was 408.439ng/ml, Tmax was 12h and half life (t1/2) was 8.812h. The extraction procedure was simple with good response even at very low drug concentration, thereby making this method suitable for pharmacokinetic application. It is concluded that developed method is simple, fast, cost effective, and reproducible for the analysis of pharmacokinetic parameters in the rabbit plasma. [ABSTRACT FROM AUTHOR]

Objective of the study was to synthesize a chemically cross-linked poly(hydroxyethylmethacrylate-co-methacrylic acid) hydrogel [p(HEMA-co-MAA hydrogel)] for pH-responsive, controlled drug delivery of Flurbiprofen. pH-sensitive hydrogel drug delivery system was synthesized with the help of poly hydroxyethyl methacrylate (HEMA) and methacrylic acid (MAA) by using ethylene glycol dimethacrylate (EGDMA) as crosslinker. The monomers (HEMA and MAA) were successfully cross linked through free radical polymerization process, initiated by benzoyl peroxide in an aqueous medium. All formulations were loaded with Flurbiprofen as a model drug and evaluated at pH 1.2 and pH 7.4 to investigate pH-responsive nature of the system. Fourier transform infrared spectroscopy (FTIR) was performed to confirm the cross-linking of copolymer while thermo gravimetric analysis (TGA) and differential scanning calorimetry (DSC) were performed to evaluate the thermal stability of the system. Swelling studies and in-vitro release studies were carried out to evaluate pH-responsive nature of the hydrogels. FTIR confirmed that monomers were successfully cross-linked to form a copolymer. Hydrogel system showed less swelling at lower pH while at higher pH, it showed higher swelling, releasing drug in the same fashion. It was concluded that a stable hydrogel network was chemically cross-linked showing pH-responsive nature and thus, synthesized p(HEMA-co-MAA) hydrogels can be successfully employed as potential candidate for controlled drug delivery. [ABSTRACT FROM AUTHOR]