Modified QuEChERS-LC-MS/MS Method for Forensic Quantification and Validation of Acyclovir and Amantadine from Biological Matrices

Q4 Chemistry Asian Journal of Chemistry Pub Date : 2024-07-25 DOI:10.14233/ajchem.2024.31691
Priyanka Gopi, Chintan Singh, Majji Sai Sudha Rani, R. K. Sarin, Prateek Pandya
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Abstract

Antiviral drugs exhibit various toxic effects such as teratogenicity, carcinogenicity and surprisingly neurotoxic effects that mimics that of drugs of abuse as indicated by the in silico toxicological studies performed and corroborated with published literature. Despite extensive studies on antiviral drugs, their forensic implications regarding individual toxicity, drug interactions, overdose and abuse have been overlooked. Consequently, there is a critical need to develop an analytical strategy for forensic detection of these antivirals. In this study, a simple and selective LC-MS/MS method is developed to determine toxic antivirals acyclovir and amantadine in urine, saliva and gastric fluid. The modified QuEChERS extraction was followed by chromatography on a C18 column with a gradient mobile phase of 5 mM ammonium formate and 0.1% formic acid in methanol. Detection was performed using a triple quadrupole tandem mass spectrometer. The validation of method, adhering to SWGTOX guidelines, demonstrated excellent linearity, precision and accuracy, covering a linear range of 5-200 ng/mL for both drugs. The limit of detection ranged from 14 to 20 ng/mL and the limit of quantification ranged from 40 to 63 ng/mL for acyclovir and amantadine. Finally, the validated method was successfully applied to the forensic detection of antiviral drugs in gastric lavage, exhibiting robustness and reproducibility.
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用于生物基质中阿昔洛韦和金刚烷胺的法医定量和验证的改良 QuEChERS-LC-MS/MS 方法
抗病毒药物表现出各种毒性作用,如致畸、致癌和令人惊讶的神经毒性作用,这些作用与已发表的文献中提到的滥用药物的作用相似。尽管对抗病毒药物进行了广泛的研究,但它们在个体毒性、药物相互作用、过量和滥用方面的法医影响却被忽视了。因此,亟需开发一种法医检测这些抗病毒药物的分析策略。本研究开发了一种简单且具有选择性的 LC-MS/MS 方法,用于检测尿液、唾液和胃液中的毒性抗病毒药物阿昔洛韦和金刚烷胺。采用改良的 QuEChERS 萃取技术,以 5 mM 甲酸铵和 0.1% 甲酸甲醇为流动相,在 C18 色谱柱上进行梯度洗脱。使用三重四极杆串联质谱仪进行检测。该方法的线性、精密度和准确度均符合SWGTOX指南的要求,两种药物的线性范围为5-200 ng/mL。阿昔洛韦和金刚烷胺的检出限为14-20纳克/毫升,定量限为40-63纳克/毫升。最后,该验证方法成功地应用于洗胃液中抗病毒药物的法医检测,表现出稳健性和重现性。
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来源期刊
Asian Journal of Chemistry
Asian Journal of Chemistry 化学-化学综合
CiteScore
0.80
自引率
0.00%
发文量
229
审稿时长
4 months
期刊介绍: Information not localized
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