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绿胶束高效液相色谱法分析三种血管紧张素转换酶抑制剂与其与氢氯噻嗪混合物,并通过拟合 Foley 模型来模拟它们的保留行为。

Green micellar HPLC analysis of three angiotensin-converting enzyme inhibitors in their mixtures with hydrochlorothiazide and modeling of their retention behavior by fitting to Foley's model.

机构信息

Department of Pharmaceutical Analytical Chemistry, Faculty of Pharmacy, Mansoura University, Mansoura, Egypt.

出版信息

J Sep Sci. 2017 Sep;40(18):3646-3654. doi: 10.1002/jssc.201700622. Epub 2017 Aug 28.

DOI:10.1002/jssc.201700622
PMID:28722342
Abstract

We present an environmentally friendly method for the analysis of three angiotensin-converting enzyme inhibitors and hydrochlorothiazide simultaneously using a green micellar eluent for the first time. The chromatographic separation of enalapril maleate, lisinopril dihydrate, benazepril hydrochloride, and hydrochlorothiazide was implemented on an octadecyl silica column with a solution containing sodium dodecyl sulfate (0.12 M), 1-propyl alcohol (10% v/v), triethylamine (0.3% v/v), and H PO (0.02 M) at pH 3.6 as the mobile phase and UV detection at 210 nm. Validity of the method was confirmed and it exhibited good linearity within the ranges of 5.0-50.0 μg/mL for hydrochlorothiazide and 10.0-60.0 μg/mL for the three angiotensin-converting enzyme inhibitors with a limit of detection of 0.39 to 1.15 μg/mL for all the studied drugs. The developed micellar high-performance liquid chromatography method enables the quantification of the targeted angiotensin-converting enzyme inhibitors in combined tablets with hydrochlorothiazide by isocratic elution. There is no need for special precautions to prevent broadening and splitting of their chromatographic peaks. The method fulfills the society rights for safe and green analytical methods. The retention behavior of the four studied drugs was fitted to Foley's model and their association equilibria to the micelles (K ) and to the surface-modified stationary phase (K ) were calculated.

摘要

我们首次提出了一种使用绿色胶束洗脱液同时分析三种血管紧张素转换酶抑制剂和氢氯噻嗪的环境友好方法。马来酸依那普利、赖诺普利二水合物、盐酸贝那普利和氢氯噻嗪的色谱分离是在十八烷基硅烷柱上进行的,流动相为含有十二烷基硫酸钠(0.12 M)、1-丙醇(10%v/v)、三乙胺(0.3%v/v)和 H PO (0.02 M)的溶液,在 pH 3.6 下进行,并在 210nm 处进行 UV 检测。该方法的有效性得到了验证,并且对于氢氯噻嗪的 5.0-50.0μg/mL 和三种血管紧张素转换酶抑制剂的 10.0-60.0μg/mL 的范围内,均表现出良好的线性关系,所有研究药物的检测限为 0.39 至 1.15μg/mL。所开发的胶束高效液相色谱法可通过等度洗脱定量测定含氢氯噻嗪的复方片剂中的目标血管紧张素转换酶抑制剂。无需特别注意防止其色谱峰变宽和分裂。该方法符合社会对安全和绿色分析方法的权利要求。四种研究药物的保留行为符合 Foley 模型,并且它们与胶束(K)和表面修饰固定相(K)的缔合平衡也被计算出来。

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