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161.
Kinetics of in situ degradation bis-(2-chloroethyl) sulphide (sulphur mustard, HD) on polyoxometalate impregnated carbon systems such as 11-molybdo-1-vanadophosphoric acid (V1/C), phosphotungstic acid (PTA/C), sodium phosphotungstic acid (PTANa/C), phosphomolybdic acid (PMoA/C), sodium phosphomolybdic acid (PMoANa/C) and silicotungstic acid (SiTA/C) have been studied. These carbons were characterized for micropore volume and surface area by N2 Brunauer, Emmett and Teller (BET) equation. For degradation studies the solution of HD in chloroform was prepared and taken for the uniform adsorption on the carbon systems using incipient volume. Degradation kinetics was monitored by gas chromatograph equipped with flame ionization detector (GC/FID) and found to be following the pseudo first order kinetics. The values of kinetic rate constant and half-life were calculated. V1/C system showed the fastest degradation of HD. Hemimustard, thiodiglycol, 1,4-oxathiane, sulphoxide and vinyl-2-chloroethyl sulphide were found to be the degradation products with V1/C system which indicated the oxidative, hydrolytic and dehydrohalogenation reactions, responsible for HD degradation. Effect of moisture was also studied on most reactive system, i.e., V1/C. The study indicated that V1/C can be used as a promising adsorbent system for the degradation of HD. 相似文献
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In this work, a two-dimensional potential distribution formulation is presented for multi-material gate poly-crystalline silicon thin film transistors. The developed formulation incorporates the effects due to traps and grain-boundaries. In short-channel devices, short-channel effects and drain-induced barrier lowering (DIBL) effect exists, and are accounted for in the analysis. The work aims at the reduction of DIBL effect and grain-boundary effects i.e. to reduce the potential barriers generated in the channel by employing gate-engineered structures. A study of work-functions and electrode lengths of multi-material gate electrode is done to suppress the potential barriers, hot electron effect and to improve the carrier transport efficiency. Green's function approach is adopted for the two-dimensional potential solution. The results obtained show a good agreement with simulated results, thus, demonstrating the validity of our model. 相似文献
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The prenatal administration of indomethacin in obstetric management has been implicated as a cause of neonatal cardio-pulmonary, gastrointestinal and renal complications. The present report describes two cases of twin pregnancy resulting in premature delivery at the 33rd and 30th week following prolonged maternal indomethacin treatment for 9 and 4 weeks respectively. Neonatal cardiovascular and renal complications were observed and an unusual severe ischemia of a lower limb occured in each of the first twins following insertion of an umbilical arterial line. It is suggested that prolonged antenatal exposure to the drug may increase the systemic arterial constrictive reactivity in some newborn infants and that special caution should be exercised during arterial catheterization of susceptible cases. 相似文献
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Ishwor Poudel Manjusha Annaji Fajar Setyo Wibowo Robert D. Arnold Oladiran Fasina Brian Via Vijaya Rangari Maria Soledad Peresin Forrest Smith Muralikrishnan Dhanasekaran Amit K. Tiwari R. Jayachandra Babu 《International journal of molecular sciences》2022,23(22)
Hispolon, a phenolic pigment isolated from the mushroom species Phellinus linteus, has been investigated for anti-inflammatory, antioxidant, and anticancer properties; however, low solubility and poor bioavailability have limited its potential clinical translation. In this study, the inclusion complex of hispolon with Sulfobutylether-β-cyclodextrin (SBEβCD) was characterized, and the Hispolon-SBEβCD Complex (HSC) was included within the sterically stabilized liposomes (SL) to further investigate its anticancer activity against melanoma cell lines. The HSC-trapped-Liposome (HSC-SL) formulation was investigated for its sustained drug delivery and enhanced cytotoxicity. The inclusion complex in the solid=state was confirmed by a Job’s plot analysis, molecular modeling, differential scanning calorimetry (DSC), Fourier transform infrared spectroscopy (FTIR), Proton nuclear magnetic resonance (NMR) spectroscopy, and scanning electron microscopy (SEM). The HSC-SL showed no appreciable deviation in size (<150 nm) and polydispersity index (<0.2) and improved drug encapsulation efficiency (>90%) as compared to control hispolon liposomes. Individually incorporated hispolon and SBEβCD in the liposomes (H-CD-SL) was not significant in loading the drug in the liposomes, compared to HSC-SL, as a substantial amount of free drug was separated during dialysis. The HSC-SL formulation showed a sustained release compared to hispolon liposomes (H-SLs) and Hispolon-SBEβCD liposomes (H-CD-SLs). The anticancer activity on melanoma cell lines (B16BL6) of HSC and HSC-SL was higher than in H-CD-SL and hispolon solution. These findings suggest that HSC inclusion in the HSC-SL liposomes stands out as a potential formulation approach for enhancing drug loading, encapsulation, and chemotherapeutic efficiency of hispolon and similar water insoluble drug molecules. 相似文献