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3篇 您的检索式:作者名="M.V.N."
    题名 作者 年代 出处 被引量
1Measurements and numerical simulations of the degree of activity and vegetation cover on parabolic dunes in north-eastern Brazil显示文摘O. Duran M.V.N. Silva L.J.C. Bezerra H.J. Herrmann L.P. Maia 2008Geomorphology2008,,3:1
2Separation of stereoisomers of sertraline and its related enantiomeric impurities on a dimethylated β-cyclodextrin stationary phase by HPLC显示文摘R. Nageswara Rao M.V.N. Kumar Talluri Pawan K. Maurya 2009Journal of Pharmaceutical and Biomedical Analysis2009,,3:1
3Selective separation, detection of zotepine and mass spectral characterization of degradants by LC–MS/MS/QTOF显示文摘A simple, precise, accurate stability-indicating gradient reversed-phase high-performance liquid chromatographic(RP–HPLC) method was developed for the quantitative determination of zotepine(ZTP) in bulk and pharmaceutical dosage forms in the presence of its degradation products(DPs). The method was developed using Phenomenex C18column(250 mm 4.6 mm i.d., 5 mm) with a mobile phase containing a gradient mixture of solvents, A(0.05% trifluoroacetic acid(TFA), pH?3.0) and B(acetonitrile). The eluted compounds were monitored at 254 nm; the run time was within 20.0 min, in which ZTP and its DPs were well separated, with a resolution of 41.5. The stress testing of ZTP was carried out under acidic, alkaline, neutral hydrolysis, oxidative, photolytic and thermal stress conditions. ZTP was found to degrade significantly in acidic, photolytic, thermal and oxidative stress conditions and remain stable in basic and neutral conditions.The developed method was validated with respect to specificity, linearity, limit of detection, limit of quantification, accuracy, precision and robustness as per ICH guidelines. This method was also suitable for the assay determination of ZTP in pharmaceutical dosage forms. The DPs were characterized by LC–MS/MS and their fragmentation pathways were proposed.M.V.N. Kumar Talluri Naveen Reddy Kandimalla Raju Bandu Divya Chundi Ramesh Marupaka Ragampeta Srinivas 2014Journal of Pharmaceutical Analysis2014,4,2:0
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