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      KCI등재 SCIE SCOPUS

      Determination of the L-Enantiomer of Nateglinide in Pharmaceutical Formulations by Micellar Electrokinetic Chromatography

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      https://www.riss.kr/link?id=A104665351

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      다국어 초록 (Multilingual Abstract)

      An analytical micellar electrokinetic chromatographic method was developed and validated for the determination of the L-enantiomer of nateglinide. Separations were carried out in a 50 μm, 64.5/56 fused-silica capillary. The optimized conditions inclu...

      An analytical micellar electrokinetic chromatographic method was developed and validated for the determination of the L-enantiomer of nateglinide. Separations were carried out in a 50 μm, 64.5/56 fused-silica capillary. The optimized conditions included 75 mM borate buffer, pH 9.2, containing 50 mM of sodium dodecyl sulfate and 25 mg/mL of methyl-β-cyclodextrin as background electrolyte, an applied voltage of 20 kV and a temperature of 15, UV detector at 210 nm. The assay was validated for the L-enantiomer of nateglinide. The limit of detection and quantification were 0.07 and 0.2% respectively. Intraday precision was ranged between 0.12 and 1.7%. Interday precision ranged between 0.73 and 1.73%. The assay was applied to the determination of the L-enantiomer of nateglinide in pharmaceutical formulations.

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      참고문헌 (Reference)

      1 Hu, S, "The mechanisms underlying the unique pharmacodynamics of nateglide" 46 (46): M37-M43, 2003

      2 Keilson, L, "Synergistic Effects of Nateglinide and Meal Administration on Insulin Secretion in Patients with Type 2 Diabetes Mellitus" 85 : 1081-1086, 2000

      3 Yanyan, Z, "Study of protein binding of acidic drug, nateglinide in human plasma albumin solution by high performance capillary electrophoresis/frontal analysis" 7 : 860-864, 2003

      4 Li, B, "Simultaneous chiral separation of geometry isomers and enantiomers of nateglinide by capillary electrophoresis with mixture of CD derivations as chiral selector" 41 : 3177-3186, 2008

      5 Bauer, S, "Rapid and simple method for the analysis of nateglinide in human plasma using HPLC analysis with UV detection" 31 : 551-555, 2003

      6 Yin, J, "Rapid and efficient chiral separation of nateglinide and its L-enantiomer on monolithic molecularly imprinted polymers" 1090 : 68-75, 2005

      7 Tamura, M, "Pharmacokinetics of nateglinide enantiomers and their metabolites in Goto-Kakizaki rats, a model for type 2 diabetes mellitus" 22 : 92-98, 2010

      8 Walle, T, "Pharmacokinetic parameters obtained with racemates" 7 : 155-158, 1986

      9 Shinkai, H, "N-(Cyclohexylcarbonyl)-D-phenylalanines and related compounds.A new oral hypoglycemic agents. 2" 32 : 1436-1441, 1989

      10 Hu, S, "Interaction of nateglinide with KATP channel in β-cells underlies its unique insulinotropic action" 442 : 163-171, 2002

      1 Hu, S, "The mechanisms underlying the unique pharmacodynamics of nateglide" 46 (46): M37-M43, 2003

      2 Keilson, L, "Synergistic Effects of Nateglinide and Meal Administration on Insulin Secretion in Patients with Type 2 Diabetes Mellitus" 85 : 1081-1086, 2000

      3 Yanyan, Z, "Study of protein binding of acidic drug, nateglinide in human plasma albumin solution by high performance capillary electrophoresis/frontal analysis" 7 : 860-864, 2003

      4 Li, B, "Simultaneous chiral separation of geometry isomers and enantiomers of nateglinide by capillary electrophoresis with mixture of CD derivations as chiral selector" 41 : 3177-3186, 2008

      5 Bauer, S, "Rapid and simple method for the analysis of nateglinide in human plasma using HPLC analysis with UV detection" 31 : 551-555, 2003

      6 Yin, J, "Rapid and efficient chiral separation of nateglinide and its L-enantiomer on monolithic molecularly imprinted polymers" 1090 : 68-75, 2005

      7 Tamura, M, "Pharmacokinetics of nateglinide enantiomers and their metabolites in Goto-Kakizaki rats, a model for type 2 diabetes mellitus" 22 : 92-98, 2010

      8 Walle, T, "Pharmacokinetic parameters obtained with racemates" 7 : 155-158, 1986

      9 Shinkai, H, "N-(Cyclohexylcarbonyl)-D-phenylalanines and related compounds.A new oral hypoglycemic agents. 2" 32 : 1436-1441, 1989

      10 Hu, S, "Interaction of nateglinide with KATP channel in β-cells underlies its unique insulinotropic action" 442 : 163-171, 2002

      11 "Guideline Q2 (R1)" 2005

      12 Whitelaw, D. C, "Effects of the new oral hypoglycaemic agent nateglinide on insulin secretion in type 2 diabetes mellitus" 17 : 225-229, 2000

      13 Maddi, S, "Development and validation of a stereoselective HPLC method for the determination of the in vitro transport of nateglinide enantiomers in rat intestine" 30 : 1875-1880, 2007

      14 Qi, M, "Determination of the LEnantiomer of Nateglinide in a Bulk Drug Substance by Chiral Reversed-Phase Liquid Chromatography" 26 : 1839-1845, 2003

      15 Blanco, M, "Choice of chiral selector for enantioseparation by capillary electrophoresis" 22 : 428-439, 2003

      16 Yang, G, "Chiral Separation of Nateglinide and its L Enantiomer on a Molecularly Imprinted Polymer-Based Stationary Phase" 59 : 705-708, 2004

      17 Yang, G, "Chiral Separation of N-(trans-4-isopropylcyclohexylcarbonyl)-D, L-phenylalanine isomers by High Performance Liquid Chromatography" 56 : 515-518, 2002

      18 Sato, H, "Analysis of enantiomers of a new antidiabetic agent in plasma by highperformance liquid chromatography" 12 : 445-455, 1989

      19 Sangaraju, S, "A validated chiral LC method for the enantiomeric separation of nateglinide and the quantitative dertermination of its Lenantiomer" 69 : 1123-1127, 2009

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2010-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2008-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2006-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2004-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2001-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      1998-07-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 1.96 0.2 1.44
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      1.07 0.87 0.439 0.05
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