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      JPA Prize in 2014

      2015-11-17 01:24:02
      Journal of Pharmaceutical Analysis 2015年4期

      JPA Prize in 2014

      The outstanding editor awarded the 2014 JPA Prize was as follows:

      Bart De Spiegeleer

      Department of Pharmaceutical Analysis

      Drug Quality & Registration group

      Ghent University

      Belgium

      The two excellent referees awarded the 2014 JPA Prize were as follows:

      1. Stacy Brown

      Pharmaceutical Sciences

      East Tennessee State University

      United States of America

      2. Satyanarayanaraju Sagi

      School of Pharmacy

      National Center for Natural Products Research

      University of Mississippi

      United States of America

      The three top cited papers awarded the 2014 JPA Prize were as follows:

      1. Joseph J. Kirkland, Stephanie A. Schuster*, William L. Johnson, Barry E. Boyes. Fused-core particle technology in high-performance liquid chromatography: An overview. Journal of Pharmaceutical Analysis, 2013, 3(5): 303-312.

      2. Srinivasa Rao Polagani, Nageswara Rao Pilli,Ramakrishna Gajula, Venkateswarlu Gandu*.

      Simultaneous determination of atorvastatin, metformin and glimepiride in human plasma by LC-MS/MS and its application to a human pharmacokinetic study. Journal of Pharmaceutical Analysis, 2013, 3(1): 9-19.

      3. T. Satyanarayana Raju*, O. Vishweshwari Kutty,V. Ganesh, P. Yadagiri Swamy. A validated stabilityindica

      ting LC method for the separation of enantiomer and potential impurities of Linezolid using polar organic mode. Journal of Pharmaceutical Analysis, 2012, 2(4): 272-278.

      JPA Prize Medal

      Fig. 2 Separation of anticoagulants with fused-core columns of different selectivities. Columns: 50 mm × 4.6 mm Halo C18, 50 mm × 4.6 mm Halo RP-amide, 50 mm × 4.6 mm Halo phenyl-hexyl; mobile phase: A/B = 40/60; A = 0.1% formic acid, pH 2.6; B = methanol/acetonitrile,50/50; flowrate: 2.0 mL/min; temperature: 45 oC; pressure: 210 bar;detector, UV: 254 nm; 1 μL injection; andsolutes: (1) uracil, (2)4-hydroxycoumarin, (3) coumarin, (4) 6-chloro-4-hydroxycoumarin, (5)warfarin, (6) coumatetralyl, and (7) coumachlor, i = impurity.

      Fig. 3 Complete degradation profile of Linezolid along with the % impurity formation and corresponding mass nos. of impurities.

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