Establishment and Validation of High-Performance Liquid Chromatography—Tandem Mass Spectrometry for Simultaneous Assessment of Amlodipine and Indapamide in Human Plasma

IF 1.7 3区 化学 Q4 BIOCHEMICAL RESEARCH METHODS
Duc Tuan Nguyen, Thu Le Anh Do, Sil Thanh Nguyen, Thi Anh Huynh Huynh, Vo Thi Kim Khuyen, Tho Vinh Minh Chau Do
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Abstract

Background

Hypertension is a major cause of premature death worldwide despite the availability of a number of antihypertensive medication monotherapies. Therefore, several polytherapies have been prescribed, among which the combination of amlodipine with indapamide is often the preferred choice to control blood pressure, especially in the elderly, because of its efficacy and safety. To ensure the quality of this combination drug, a versatile procedure for the simultaneous quantification of components is required. Thus, this study aims to develop a liquid chromatography - tandem mass spectrometric procedure and validate according to FDA and EMA guidelines to determine amlodipine and indapamide in human plasma.

Methods

A liquid–liquid extraction with tert-butyl methyl ether and ethyl acetate (1:1) was applied to extract the compounds. Amlodipine was ionized with positive electrospray ionization and detected by multiple reaction monitoring mode, while indapamide was ionized with negative electrospray ionization and detected by selected ion monitoring mode. Samples were chromatographically analyzed on a C18 column (150 × 4.6 mm; 3.5 μm), eluted by the mobile phase of methanol and 0.025% formic acid (90:10, v/v).

Results

Linearity ranged from 0.29- to 17.14-ng/mL amlodipine, from 1.14- to 68.57-ng/mL indapamide. The lower limit of quantitation of amlodipine and indapamide is 0.29- and 1.14-ng/mL, respectively. The validation using furosemide as an internal standard showed that the specificity, intra- and interday precision and accuracy, matrix effect, sample carryover, dilution, and stability were in the acceptable range.

Conclusions

The method met validation criteria of US-FDA and EMA guidelines, thereby recommended for application in in vivo bioavailability and bioequivalence assessment of fixed-dose combinations of amlodipine with indapamide.

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高效液相色谱-串联质谱法同时测定人血浆中氨氯地平和吲达帕胺含量的建立与验证
背景:尽管有许多抗高血压药物单一疗法,高血压仍是世界范围内过早死亡的主要原因。因此,有几种综合疗法被开处方,其中氨氯地平与吲达帕胺联用往往是控制血压的首选,特别是在老年人中,因为它的有效性和安全性。为了保证这种联合药物的质量,需要一种通用的同时定量成分的方法。因此,本研究旨在建立一种液相色谱-串联质谱方法,并根据FDA和EMA的指南进行验证,以测定人血浆中的氨氯地平和吲达帕胺。方法采用叔丁基甲基醚和乙酸乙酯(1:1)液液萃取法提取。氨氯地平采用正电喷雾电离,采用多反应监测模式检测;吲达帕胺采用负电喷雾电离,采用选择离子监测模式检测。样品在C18色谱柱(150 × 4.6 mm; 3.5 μm)上进行色谱分析,流动相为甲醇和0.025%甲酸(90:10,v/v)。结果氨氯地平线性范围为0.29 ~ 17.14 ng/mL,吲达帕胺线性范围为1.14 ~ 68.57 ng/mL。氨氯地平和吲达帕胺的定量下限分别为0.29 ng/mL和1.14 ng/mL。以速尿为内标进行验证,特异性、内、日间精密度和准确度、基质效应、样品携带、稀释度、稳定性均在可接受范围内。结论该方法符合US-FDA和EMA指南的验证标准,可用于氨氯地平与吲达帕胺固定剂量联合使用的体内生物利用度和生物等效性评价。
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来源期刊
CiteScore
4.10
自引率
5.00%
发文量
219
审稿时长
2.6 months
期刊介绍: Rapid Communications in Mass Spectrometry is a journal whose aim is the rapid publication of original research results and ideas on all aspects of the science of gas-phase ions; it covers all the associated scientific disciplines. There is no formal limit on paper length ("rapid" is not synonymous with "brief"), but papers should be of a length that is commensurate with the importance and complexity of the results being reported. Contributions may be theoretical or practical in nature; they may deal with methods, techniques and applications, or with the interpretation of results; they may cover any area in science that depends directly on measurements made upon gaseous ions or that is associated with such measurements.
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