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      KCI등재 SCOPUS SCIE

      Validated HPLC Method for the Pharmacokinetic Study of Atenolol andChlorthalidone Combination Therapy in Korean Subjects

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      https://www.riss.kr/link?id=A104996695

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      다국어 초록 (Multilingual Abstract)

      A rapid, selective and sensitive reverse-phase HPLC methods for the determination of atenolol and chlorthalidone in human serum and whole blood were validated, and applied to the pharmacokinetic study of atenolol and chlorthalidone combination therapy. Atenolol and an internal standard, pindolol, were extracted from human serum by liquid-liquid extraction, and analyzed on a -Bondapak C18 10-mm column in a mobile phase of methanol-0.01 M potassium dihydrogenphosphate (30:70, v/v, adjusted to pH 3.5) and fluorescence detection (emission: 300 nm, excitation: 224 nm). Chlorthalidone and an internal standard, probenecid, were extracted form human whole blood by liquid-liquid extraction, and analyzed on a Luna C18 5-m column in a mobile phase of acetonitrile containing 77% 0.01 M sodium acetate and UV detection at 214 nm. These analysis were performed at three different laboratories using the same quality control (QC) samples. The chromatograms showed good resolution, sensitivity, and no interference by human serum and whole blood, respectively. The methods showed linear responses over a concentration range of 10-1,000 ng/mL for atenolol and 0.05-20 g/mL for chlorthalidone, with correlation coefficients of greater than 0.999 at all the three laboratories. Intra- and inter-day assay precision and accuracy fulfilled international requirements. Stability studies (freeze-thaw, short-, long-term, extracted sample and stock solution) showed that atenolol and chlorthalidone were stable. The lower limit of quantitation of atenolol and chlorthalidone were 10 ng/mL and 0.05 g/mL, respectively, which was sensitive enough for pharmacokinetic studies. These methods were applied to the pharmacokinetic study of atenolol and chlorthalidone in human volunteers following a single oral administration of Hyundai Tenoretic?? tablet (atenolol 50 mg and chlorthalidone 12.5 mg) at three different laboratories.
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      A rapid, selective and sensitive reverse-phase HPLC methods for the determination of atenolol and chlorthalidone in human serum and whole blood were validated, and applied to the pharmacokinetic study of atenolol and chlorthalidone combination therapy...

      A rapid, selective and sensitive reverse-phase HPLC methods for the determination of atenolol and chlorthalidone in human serum and whole blood were validated, and applied to the pharmacokinetic study of atenolol and chlorthalidone combination therapy. Atenolol and an internal standard, pindolol, were extracted from human serum by liquid-liquid extraction, and analyzed on a -Bondapak C18 10-mm column in a mobile phase of methanol-0.01 M potassium dihydrogenphosphate (30:70, v/v, adjusted to pH 3.5) and fluorescence detection (emission: 300 nm, excitation: 224 nm). Chlorthalidone and an internal standard, probenecid, were extracted form human whole blood by liquid-liquid extraction, and analyzed on a Luna C18 5-m column in a mobile phase of acetonitrile containing 77% 0.01 M sodium acetate and UV detection at 214 nm. These analysis were performed at three different laboratories using the same quality control (QC) samples. The chromatograms showed good resolution, sensitivity, and no interference by human serum and whole blood, respectively. The methods showed linear responses over a concentration range of 10-1,000 ng/mL for atenolol and 0.05-20 g/mL for chlorthalidone, with correlation coefficients of greater than 0.999 at all the three laboratories. Intra- and inter-day assay precision and accuracy fulfilled international requirements. Stability studies (freeze-thaw, short-, long-term, extracted sample and stock solution) showed that atenolol and chlorthalidone were stable. The lower limit of quantitation of atenolol and chlorthalidone were 10 ng/mL and 0.05 g/mL, respectively, which was sensitive enough for pharmacokinetic studies. These methods were applied to the pharmacokinetic study of atenolol and chlorthalidone in human volunteers following a single oral administration of Hyundai Tenoretic?? tablet (atenolol 50 mg and chlorthalidone 12.5 mg) at three different laboratories.

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      참고문헌 (Reference)

      1 "sensitive and selective high-performance liquid chromatographic method for analysis of chlorthalidone in whole blood" 416 : 420-425, 1987

      2 "Simultaneous determination of atenolol and amlodipine in tablets by high-performance thin-layer chromatography" 21 : 1137-1142, 2000

      3 "Simul- taneous determination of atenolol and chlorthalidone in plasma by high-performance liquid chromatography Application to pharmacokinetic studies in man" 698 : 187-194, 1997

      4 "Quantitation of atenolol, metoprolol, and propranolol in postmortem human fluid and tissue specimens via LC/APCI-MS" 156 (156): 106-117, 2006

      5 "Martindale-The complete drug reference 32nd ed." Pharmaceutical Press 825-, 1999

      6 "Korea Food & Drug Administration Notification No. 200260, Standard Protocol of Bioequivalence Test" 2002.11.

      7 "Error structure for the HPLC analysis for atenolol, metoprolol and propranolol: a useful weighting method in parameter estimation" 17 (17): 507-513, 1998

      8 "Determination of biological equivalence of two atenolol preparation" 25 (25): 567-571, 1987

      9 "Comparative bioavilability of two formulations containing atenolol and chlortalidone associated in a 4:1 fixed combination" 50 (50): 802-808, 2000

      10 "Comparative Bioavailability of Two Brands of Atenolol 100 mg Tablets (Tensotin and Tenormin) in Healthy Human Volunteers" 26 : 1-5, 2005

      1 "sensitive and selective high-performance liquid chromatographic method for analysis of chlorthalidone in whole blood" 416 : 420-425, 1987

      2 "Simultaneous determination of atenolol and amlodipine in tablets by high-performance thin-layer chromatography" 21 : 1137-1142, 2000

      3 "Simul- taneous determination of atenolol and chlorthalidone in plasma by high-performance liquid chromatography Application to pharmacokinetic studies in man" 698 : 187-194, 1997

      4 "Quantitation of atenolol, metoprolol, and propranolol in postmortem human fluid and tissue specimens via LC/APCI-MS" 156 (156): 106-117, 2006

      5 "Martindale-The complete drug reference 32nd ed." Pharmaceutical Press 825-, 1999

      6 "Korea Food & Drug Administration Notification No. 200260, Standard Protocol of Bioequivalence Test" 2002.11.

      7 "Error structure for the HPLC analysis for atenolol, metoprolol and propranolol: a useful weighting method in parameter estimation" 17 (17): 507-513, 1998

      8 "Determination of biological equivalence of two atenolol preparation" 25 (25): 567-571, 1987

      9 "Comparative bioavilability of two formulations containing atenolol and chlortalidone associated in a 4:1 fixed combination" 50 (50): 802-808, 2000

      10 "Comparative Bioavailability of Two Brands of Atenolol 100 mg Tablets (Tensotin and Tenormin) in Healthy Human Volunteers" 26 : 1-5, 2005

      11 "Bioavailability in man of atenolol and chlorthalidone from a combination formulation" 7 (7): 223-231, 1986

      12 "Bioavail- ability in man of atenolol and chlorthalidone from a combination formulation" 147-156, 1981

      13 "Bio- equivalence of Samchundang Atenolol Tablet to Tenolmin Tablet" 47 (47): 339-344, 2003

      14 "Analysis of chlorthalidone in whole blood by high-performance liquid chromatography" 375 : 438-443, 1986

      15 "A micromethod for the quantification of atenolol in plasma using high-performance liquid chroma- tography with fluorescence detection: Therapeutic drug monitoring of two patients with severe coronary insufficiency before cardiac surgery" 28 (28): 237-244, 2006

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
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      2010-06-09 학술지명변경 한글명 : 약제학회지 -> Journal of Pharmaceutical Investigation
      외국어명 : Jorunal of Korean Pharmaceutical Sciences -> Journal of Pharmaceutical Investigation
      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
      2005-06-16 학회명변경 영문명 : The Korean Society Of Pharmaceutics -> The Korean Society of Pharmaceutical Sciences and Technology KCI등재
      2004-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2001-07-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      1999-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.18 0.18 0.14
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.13 0.11 0.374 0.02
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