Hemn A H Barzani, Seerwan Hamadameen Sulaiman, Rebaz Anwar Omer, Ali Hussein Mer, Hoshyar Saadi Ali
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Chromatographic methods, especially high-performance liquid chromatography (HPLC) and liquid chromatography-mass spectrometry (LC-MS/MS), remain the most robust techniques, offering excellent sensitivity (LOD: 10-50 ng/mL for HPLC; as low as 0.7-15 ng/mL for LC-MS/MS) with rapid analysis times. While LC-MS/MS provides superior detection, it is limited by high costs and technical expertise requirements. Electrochemical methods, particularly voltammetry, stand out for their affordability, rapid analysis, and feasibility in decentralized laboratories, achieving LOD values as low as 0.01-0.05 µM. Spectrophotometric approaches, primarily UV-Vis, remain the simplest and most cost-effective options, making them useful for routine quality control, though with reduced selectivity and higher detection limits. Key analytical challenges include Methyldopa's low concentration in biological fluids, chemical instability, and matrix interferences. This review provides a comparative evaluation of chromatographic, spectrophotometric, and electrochemical techniques, emphasizing the need for portable, low-cost platforms to expand accessibility in therapeutic monitoring. 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引用次数: 0
摘要
甲基多巴是一种中枢作用的α2-肾上腺素能激动剂,仍然是一种重要的降压药物,特别是用于孕妇和肾功能受损患者。它的临床意义导致了广泛的研究,旨在开发可靠的分析方法,以准确、敏感和选择性地测定药物配方和生物基质。相关文献检索自Scopus、Web of Science、ScienceDirect、PubMed和谷歌Scholar,仅限于英文出版物。这篇综述批判性地考察了用于甲基多巴定量的各种分析方法,概述了它们的原理、优势、局限性以及在先进和资源有限环境中的适用性。色谱方法,特别是高效液相色谱(HPLC)和液相色谱-质谱(LC-MS/MS),仍然是最可靠的技术,具有优异的灵敏度(HPLC的LOD: 10-50 ng/mL, LC-MS/MS低至0.7-15 ng/mL)和快速的分析时间。虽然LC-MS/MS提供了卓越的检测,但它受到高成本和技术专长要求的限制。电化学方法,特别是伏安法,以其可负担性,快速分析和分散实验室的可行性而脱颖而出,LOD值低至0.01-0.05µM。分光光度法,主要是紫外-可见,仍然是最简单和最具成本效益的选择,使其可用于常规质量控制,尽管选择性较低,检测限较高。主要的分析挑战包括甲基多巴在生物流体中的低浓度、化学不稳定性和基质干扰。这篇综述提供了色谱、分光光度和电化学技术的比较评价,强调需要便携式、低成本的平台来扩大治疗监测的可及性。总的来说,它为推进甲基多巴分析和改善不同医疗保健环境中的临床管理提供了关键的见解。
Analytical techniques for methyldopa and metabolites: a comprehensive review.
Methyldopa, a centrally acting α2-adrenergic agonist, remains a key antihypertensive drug, particularly prescribed for pregnant and renal-impaired patients. Its clinical significance has led to extensive research aimed at developing reliable analytical methods for its accurate, sensitive, and selective determination in pharmaceutical formulations and biological matrices. Relevant literature was retrieved from Scopus, Web of Science, ScienceDirect, PubMed, and Google Scholar, restricted to English-language publications. This review critically examines the diverse analytical approaches used for Methyldopa quantification, outlining their principles, advantages, limitations, and applicability in both advanced and resource-limited settings. Chromatographic methods, especially high-performance liquid chromatography (HPLC) and liquid chromatography-mass spectrometry (LC-MS/MS), remain the most robust techniques, offering excellent sensitivity (LOD: 10-50 ng/mL for HPLC; as low as 0.7-15 ng/mL for LC-MS/MS) with rapid analysis times. While LC-MS/MS provides superior detection, it is limited by high costs and technical expertise requirements. Electrochemical methods, particularly voltammetry, stand out for their affordability, rapid analysis, and feasibility in decentralized laboratories, achieving LOD values as low as 0.01-0.05 µM. Spectrophotometric approaches, primarily UV-Vis, remain the simplest and most cost-effective options, making them useful for routine quality control, though with reduced selectivity and higher detection limits. Key analytical challenges include Methyldopa's low concentration in biological fluids, chemical instability, and matrix interferences. This review provides a comparative evaluation of chromatographic, spectrophotometric, and electrochemical techniques, emphasizing the need for portable, low-cost platforms to expand accessibility in therapeutic monitoring. Overall, it offers critical insights for advancing Methyldopa analysis and improving clinical management in diverse healthcare settings.
期刊介绍:
Drug Metabolism Reviews consistently provides critically needed reviews of an impressive array of drug metabolism research-covering established, new, and potential drugs; environmentally toxic chemicals; absorption; metabolism and excretion; and enzymology of all living species. Additionally, the journal offers new hypotheses of interest to diverse groups of medical professionals including pharmacologists, toxicologists, chemists, microbiologists, pharmacokineticists, immunologists, mass spectroscopists, as well as enzymologists working in xenobiotic biotransformation.