Advances and challenges in sample preparation and analytical methods for water-soluble vitamins: Application in food, clinical, pharmaceutical samples

IF 3.1 3区 医学 Q2 CHEMISTRY, ANALYTICAL
Tikeshwari , Kamlesh Shrivas , Khushali Tandey , Anuradha Sharma , Nagendra Kumar Chandrawanshi , Kallol K. Ghosh
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Abstract

This review provides a comprehensive analysis of advances and challenges in the sample preparation and analytical methods for determining water-soluble vitamins (WSVs) in foods, clinical, and pharmaceutical samples. WSVs, including vitamin C and B-complex vitamins, are essential for various physiological functions such as energy metabolism, immune response, and neurological health. The accurate analysis of these vitamins is crucial for ensuring nutritional adequacy and preventing deficiencies. The paper explores the different separation and extraction techniques, such as acid and enzymatic hydrolysis, solid-phase extraction (SPE), ultrasound-assisted extraction (UAE), and Soxhlet extraction, highlighting their strengths and limitations. Analytical techniques like spectrophotometry, fluorometry, high-performance liquid chromatography (HPLC), liquid chromatography-mass spectrometry (LC-MS), and electrochemical methods are reviewed for their applicability in quantifying the WSVs. The review also addresses the challenges in WSV analysis in complex sample matrices, including vitamin stability, matrix effects, and method standardization, which impact the reliability of results. Furthermore, the revolutionary role of nanomaterials, particularly nanoparticles and quantum dots, in enhancing sensitivity for vitamin detection through colorimetric and fluorometric methods is discussed. Finally, different sample preparation and analytical techniques are employed for quantitative measurement of WSVs in foods (vegetables, fruits, and grains) clinical (urine, plasma, tears), pharmaceuticals (syrups, drugs) and metabolic studies. The review concludes by emphasizing the significance of these methodologies in improving the accuracy of WSV analysis, contributing valuable knowledge to the fields of nutrition, clinical and analytical chemistry and supporting public health strategies for preventing vitamin deficiencies.
水溶性维生素样品制备和分析方法的进展和挑战:在食品、临床和药物样品中的应用
本文综述了食品、临床和药物样品中水溶性维生素(WSVs)的制备和分析方法的进展和挑战。WSVs,包括维生素C和b族复合维生素,对能量代谢、免疫反应和神经系统健康等各种生理功能至关重要。对这些维生素的准确分析对于确保营养充足和预防缺乏至关重要。本文对酸酶水解、固相萃取(SPE)、超声辅助萃取(UAE)和索氏萃取等不同的分离提取技术进行了探讨,并重点介绍了它们的优点和局限性。综述了分光光度法、荧光法、高效液相色谱法、液相色谱-质谱法和电化学方法等分析技术在WSVs定量分析中的应用。本文还讨论了复杂样品基质中WSV分析的挑战,包括维生素稳定性、基质效应和方法标准化,这些都会影响结果的可靠性。此外,纳米材料的革命性作用,特别是纳米粒子和量子点,在提高灵敏度的维生素检测通过比色法和荧光法进行了讨论。最后,采用不同的样品制备和分析技术对食品(蔬菜、水果和谷物)、临床(尿液、血浆、泪液)、药物(糖浆、药物)和代谢研究中的wsv进行定量测量。综述最后强调了这些方法在提高WSV分析准确性、为营养、临床和分析化学领域提供宝贵知识以及支持预防维生素缺乏症的公共卫生战略方面的重要性。
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来源期刊
CiteScore
6.70
自引率
5.90%
发文量
588
审稿时长
37 days
期刊介绍: This journal is an international medium directed towards the needs of academic, clinical, government and industrial analysis by publishing original research reports and critical reviews on pharmaceutical and biomedical analysis. It covers the interdisciplinary aspects of analysis in the pharmaceutical, biomedical and clinical sciences, including developments in analytical methodology, instrumentation, computation and interpretation. Submissions on novel applications focusing on drug purity and stability studies, pharmacokinetics, therapeutic monitoring, metabolic profiling; drug-related aspects of analytical biochemistry and forensic toxicology; quality assurance in the pharmaceutical industry are also welcome. Studies from areas of well established and poorly selective methods, such as UV-VIS spectrophotometry (including derivative and multi-wavelength measurements), basic electroanalytical (potentiometric, polarographic and voltammetric) methods, fluorimetry, flow-injection analysis, etc. are accepted for publication in exceptional cases only, if a unique and substantial advantage over presently known systems is demonstrated. The same applies to the assay of simple drug formulations by any kind of methods and the determination of drugs in biological samples based merely on spiked samples. Drug purity/stability studies should contain information on the structure elucidation of the impurities/degradants.
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