利用液相色谱-质谱法检测吸毒者手指和脚趾甲中的 3-4 亚甲二氧基苯丙胺

Nandini Bansod, Mani P Goutam
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引用次数: 0

摘要

有关药物滥用和药物使用的信息。近年来,人体指甲中的药物分析已证明了其在法医毒理学应用、鉴定子宫内药物暴露、监测药物治疗计划和治疗药物监测方面的重要价值。与传统基质(血液和尿液)相比,指甲具有各种优势,包括更长的检测时间(数月至数年)、非侵入性样本采集以及易于储存和运输。这些优点使指甲成为法医毒理学和治疗药物监测的重要基质。由于指甲中的滥用药物和药物浓度较低,而且角质化基质非常复杂,因此分析技术需要更加灵敏,样品制备也至关重要。本研究旨在开发一种简单的高效液相色谱-质谱(LC-MS)方法,用于鉴定和定量指甲和脚趾甲剪片中的 3,4-亚甲二氧基苯丙胺(MDA)。手指和脚趾甲剪片采集自印度 M.P. 省 Ujjain 一家康复中心的六名接受治疗的吸毒者。首先对指甲片进行去污处理,然后在 370°C 下用 1 M NaOH 进行水解,用乙酸乙酯提取,再用甲醇稀释,最后进行 LC-MS 分析。使用 MDA 标准物质在 0.5 至 30 纳克/毫升的浓度范围内构建了校准曲线。在标准溶液中的检出限为 1.10 纳克/毫升,定量限为 3.67 纳克/毫升,而在加标指甲片中的检出限和定量限分别为 1.21 和 4.6 纳克/毫克。所开发的方法在原始指甲片中取得了显著的结果,在六个滥用者样本中,指甲中的平均浓度范围为 0.12 纳克/毫克,脚趾甲中的平均浓度范围为 0.08 纳克/毫克。结果表明,即使在吸食毒品 90 天之后,所开发的新方法仍能检测出指甲片中的 3,4-甲基内含安非他明 MDA 药物。
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Detection of 3-4 Methylenedioxyamphetamine from Drug Abuser’s Fingers and Toenails using Liquid Chromatography with Mass Spectroscopy
information regarding drug abuse and pharmaceutical use. In recent years, drug analysis in human nail clippings has proven its significant value in forensic toxicological applications, identification of in utero drug exposure, monitoring of drug treatment programmes, and therapeutic drug monitoring. Nails have various advantages over conventional matrices (blood and urine), which include a longer detection window (months to years), non-invasive sample collection, and easy storage and transportation. These aspects make nails a very significant matrix for forensic toxicology and therapeutic drug monitoring. Because of the low concentrations of drugs of abuse and pharmaceuticals present in nails and the complexity of the keratinized matrix, analytical techniques need to be more sensitive, and sample preparation is crucial. The aim of the present study is to develop a simple, high-performance liquid chromatography-mass spectroscopy (LC-MS) method for the identification and quantitation of 3,4-methylenedioxyamphetamine (MDA) in fingernail and toenail clippings. Finger and toenail clippings were collected from six users undergoing treatment at a rehab center in Ujjain, M.P., India. Nail clippings were initially decontaminated, then hydrolyzed in 1 M NaOH at 370°C, extracted with ethyl acetate, diluted with methanol, and then subjected to LC-MS analysis. The calibration curve was constructed over the 0.5 to 30 ng/mL concentration range using the MDA reference standard. The limit of detection was calculated at 1.10 ng/mL and the limit of quantification was recorded at 3.67 ng/mL in standard solutions, whereas the respective values in spiked nail clippings were 1.21 and 4.6 ng/mg. The developed method has obtained significant results in original nail clippings with mean concentration ranges of 0.12 ng/mg in fingernails and 0.08 ng/mg in toenails in six abuser samples. The new method developed has been found to be capable of detecting the 3,4-methylendioxyamphetamine MDA drug in nail clippings even after 90 days of drug intake.
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