Adsorption coupled photocatalytic degradation of dichlorvos using LaNiMnO6 perovskite nanoparticles supported on polypropylene filter cloth and carboxymethyl cellulose microspheres

Increasing pesticide application and improper wastewater disposal methods contaminate water resources and severely affect the ecology as well as environment. The present study is focused on the adsorption coupled photocatalytic degradation of dichlorvos using UV light in presence of LaNiMnO6 perovskite nanoparticles (Prv) supported on polypropylene filter cloth (PPPrv) and carboxymethyl cellulose (CMCPrv) microspheres. The synthesized LaNiMnO6 perovskite nanoparticles were characterized by XRD, FT-IR, SEM and EDX. The adsorption percentage of DCV followed the order: CMCPrv (62.7%) > PPPrv (46.1%) > Prv (32.6%). Equilibrium studies suggested the heterogenous mode of adsorption. Pseudo-first order exhibited the good linearity indicating the involvement of physical forces. Thermodynamics showed an endothermic and spontaneous nature of adsorption. The influences of various photocatalytic parameters viz., pH, irradiation time, initial DCV concentration, Prv loading and catalyst dosage on DCV degradation were investigated. Ex situ studies conducted for 8 h of sunlight exposure showed complete degradation of DCV present in industrial wastewater which was confirmed by GC-MS analysis. The advantage of CMCPrv as supported catalyst is the easy separation and reuse for four cycles. The present work is the first report that signifies the potential efficacy of CMCPrv to serve as an effective remedial agent for DCV removal from contaminated water

Antibody-Oligonucleotide Conjugates: A Twist to Antibody-Drug Conjugates

A summary of the key technological advancements in the preparation of antibody–oligonucleotide conjugates (AOCs) and the distinct advantages and disadvantages of AOCs as novel therapeutics are presented. The merits and demerits of the different approaches to conjugating oligonucleotides to antibodies, antibody fragments or other proteins, mainly from the perspective of AOC purification and analytical characterizations, are assessed. The lessons learned from in vitro and in vivo studies, especially the findings related to silencing, trafficking, and cytotoxicity of the conjugates, are also summarized

Synthesis of optically active seven-membered 1,5-anhydrocarbasugars and 1,4,5-tribenzoyloxy-2-ethoxy cycloheptanes via [5+2] cycloaddition

[5+2] Cycloaddition followed by asymmetric dihydroxylation procedure have been utilized to prepare novel cyclitols. Accordingly, rac-2 alpha-hydroxy-6 alpha-ethoxy-1,5-anhydro cyclohept-3-ene, 10 derived from [5+2] cycloaddition of 3-oxidopyrylium ylide and vinyl ether has been recognized as a seven-membered carbasugar equivalent and elaborated to 1,4,5-tribenzoyloxy-2-ethoxy cycloheptanes through a flexible, regio- and stereoselective strategy involving Sharpless asymmetric dihydroxylation conditions to resolve the compounds obtained. The structures and relative configurations of newly synthesized (+)-2 alpha-acetoxy-6 alpha-ethoxy-3 beta,4 beta-dihydroxy-1,5-anhydro cycloheptane ((+)-12)); (-)-1 beta,4 beta,5 beta-tribenzoyloxy-6 alpha-ethoxy cycloheptane ((-)-17) and (+)-1 alpha,4 alpha,5 alpha-tribenzoyloxy-6 beta-ethoxy cycloheptane ((+)-17) are unambiguously established by single crystal X-ray analysis and duly supported by H-1 and C-13 NMR spectroscopy data. (C) 2012 Elsevier Ltd. All rights reserved