首页> 外文期刊>Scientia pharmaceutica >Validated HPLC Method for Concurrent Determination of Antipyrine, Carbamazepine, Furosemide and Phenytoin and its Application in Assessment of Drug Permeability through Caco-2 Cell Monolayers
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Validated HPLC Method for Concurrent Determination of Antipyrine, Carbamazepine, Furosemide and Phenytoin and its Application in Assessment of Drug Permeability through Caco-2 Cell Monolayers

机译:高效液相色谱法同时测定安替比林,卡马西平,呋塞米和苯妥英钠的验证方法及其在通过Caco-2细胞单层膜评估药物透过性中的应用

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摘要

The present work explains the development and validation of a simple, rapid and sensitive liquid chromatographic method for the simultaneous determination of antipyrine (ANT), carbamazepine (CBZ), furosemide (FSD) and phenytoin (PHTN). Chromatographic analysis was carried out by a reversed phase technique on a C18 column, using water pH 3.0 and 50:50 mixtures of methanol and acetonitrile (58:42 v/v) as the mobile phase, at a flow-rate of 1.0 ml/min and a column temperature of 40℃. Detection was carried out at 205 nm for CBZ and PHTN and at 230 nm for ANT and FSD. The proposed method was evaluated for validation parameters including linearity, range, accuracy, precision, limit of detection (LOD), limit of quantification (LOQ) and specificity. Elution of drugs ANT, FSD, PHTN, and CBZ was observed at 4.1, 5.1, 12.3 and 13.5 min, respectively. The method was found to be linear (R~2≥ 0.999) in the concentration range of 5-100 uM, with an acceptable accuracy and relative standard deviation. Results of intra- and inter-day validation (n=3) showed the method to be efficient for routine determination of these permeability markers in Caco-2 cell monolayer permeability studies. The method was successfully utilized for determination of standard compounds in Caco-2 permeability experiments.
机译:本工作解释了同时测定安替比林(ANT),卡马西平(CBZ),速尿(FSD)和苯妥英钠(PHTN)的简单,快速和灵敏的液相色谱方法的开发和验证。通过反相技术在C18色谱柱上进行色谱分析,使用pH 3.0的水和甲醇与乙腈的50:50混合物(58:42 v / v)作为流动相,流速为1.0 ml /分钟,柱温为40℃。对于CBZ和PHTN在205 nm处进行检测,对于ANT和FSD在230 nm处进行检测。对提出的方法的验证参数进行了评估,包括线性,范围,准确性,精密度,检测限(LOD),定量限(LOQ)和特异性。分别在4.1、5.1、12.3和13.5分钟观察到药物ANT,FSD,PHTN和CBZ的洗脱。发现该方法在5-100 uM的浓度范围内是线性的(R〜2≥0.999),具有可接受的准确性和相对标准偏差。日内和日间验证的结果(n = 3)表明该方法可有效地常规测定Caco-2细胞单层通透性研究中的这些通透性标志物。该方法已成功用于Caco-2渗透性实验中标准化合物的测定。

著录项

  • 来源
    《Scientia pharmaceutica》 |2012年第1期|p.89-100|共12页
  • 作者单位

    Department of Pharmaceutical Technology (Formulations), National Institute of Pharmaceutical Education and Research (NIPER), S.A.S. Nagar, Mohali, Punjab-160 062, India;

    Department of Pharmaceutics, National Institute of Pharmaceutical Education and Research (NIPER),S.A.S. Nagar, Mohali, Punjab-160 062, India;

    Department of Pharmaceutics, National Institute of Pharmaceutical Education and Research (NIPER),S.A.S. Nagar, Mohali, Punjab-160 062, India;

    Department of Pharmaceutics, National Institute of Pharmaceutical Education and Research (NIPER),S.A.S. Nagar, Mohali, Punjab-160 062, India;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    validation; HPLC; caco-2 cell monolayer; phenazone; carbamazepine; furosemide; phenytoin;

    机译:验证;HPLC;caco-2细胞单层;吩a卡马西平速尿苯妥英;
  • 入库时间 2022-08-18 01:33:33

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