A rapid, sensitive method for clinical monitoring of ketamine and norketamine by ultra-high-performance reverse-phase liquid chromatography tandem mass spectrometry.

IF 2.1 4区 医学 Q3 MEDICAL LABORATORY TECHNOLOGY Annals of Clinical Biochemistry Pub Date : 2024-07-01 Epub Date: 2023-12-30 DOI:10.1177/00045632231224215
Nicholas Armfield, Bernhard Frank, Carrie Chadwick
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引用次数: 0

Abstract

Background: Ketamine is an NMDAR antagonist with aggregating use across many areas of medicine. P450 enzymes heavily metabolise ketamine, where norketamine is a first pass formed metabolite following initial N-demethylation. Serum ketamine monitoring is becoming increasingly important, requiring a sensitive method with a robust lower limit of quantitation.

Methods: Samples were prepared using protein precipitation or solid phase extraction. Ion suppression was investigated to optimise sample preparation technique, followed by reverse-phase chromatography coupled with tandem mass spectrometry to analyse extractions using a Waters Xevo TQ-S Micro and associated Acquity chromatography systems. Performance characteristics were analysed to validate the assay.

Results: Ketamine and norketamine retention times were 1.28 and 1.23 min, respectively. Ketamine and norketamine precursor ions fragmented into 2 distinguishable product ions (238.14 > 207.18/125.06 and 224.1 > 178.96/124.86). Performance characteristics include an assay recovery of 103.7% (ketamine) and 96.3% (norketamine), lower limit of quantitation 36.2 µg/L (ketamine) and 38.9 µg/L (norketamine), and intra-assay imprecision ≤ 7.04% on average.

Conclusions: A robust and reproducible assay with limited sample preparation has been designed and validated. The linearity of the assay covers all ranges of interest reported in the literature. Ion suppression was clearly reduced via use of solid phase extraction. The method will form the basis of ketamine monitoring and providing valuable patient information on tolerance and metabolism.

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利用超高效液相色谱-质谱联用技术(UPLC-MSMS)快速、灵敏地进行氯胺酮和诺卡因临床监测的方法。
背景:氯胺酮是一种 NMDAR 拮抗剂,在许多医学领域都有广泛应用。P450 酶会对氯胺酮进行大量代谢,其中氯胺酮是在最初的 N-去甲基化后形成的首过代谢物[1]。血清氯胺酮监测变得越来越重要,需要一种灵敏度高、定量下限稳健的方法:方法:采用蛋白沉淀或固相萃取法制备样品。对离子抑制进行了研究,以评估样品制备技术,然后使用反相色谱法和串联质谱法对使用沃特世 Xevo TQ-s 和相关 Acquity 色谱系统进行的提取物进行分析。对性能特征进行了分析,以验证该检测方法:氯胺酮和诺卡因的保留时间分别为 1.28 分钟和 1.23 分钟。氯胺酮和去甲氯胺酮前体离子碎裂成2个可区分的产物离子(238.14 > 207.18/125.06 和 224.1 > 178.96/124.86)。分析回收率为103.7%(氯胺酮)和96.3%(诺卡他明),定量下限为36.2µg/L(氯胺酮)和38.9µg/L(诺卡他明),测定内不精密度平均≤7.04%:我们设计并验证了一种只需少量样品制备的稳健且可重复的检测方法。该检测方法的线性范围涵盖了文献报道的所有相关范围。通过使用固相萃取,离子抑制明显减少。该方法将成为氯胺酮监测的基础,并为患者提供有关耐受性和代谢的宝贵信息。
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来源期刊
Annals of Clinical Biochemistry
Annals of Clinical Biochemistry Biochemistry, Genetics and Molecular Biology-Clinical Biochemistry
CiteScore
5.20
自引率
4.50%
发文量
61
期刊介绍: Annals of Clinical Biochemistry is the fully peer reviewed international journal of the Association for Clinical Biochemistry and Laboratory Medicine. Annals of Clinical Biochemistry accepts papers that contribute to knowledge in all fields of laboratory medicine, especially those pertaining to the understanding, diagnosis and treatment of human disease. It publishes papers on clinical biochemistry, clinical audit, metabolic medicine, immunology, genetics, biotechnology, haematology, microbiology, computing and management where they have both biochemical and clinical relevance. Papers describing evaluation or implementation of commercial reagent kits or the performance of new analysers require substantial original information. Unless of exceptional interest and novelty, studies dealing with the redox status in various diseases are not generally considered within the journal''s scope. Studies documenting the association of single nucleotide polymorphisms (SNPs) with particular phenotypes will not normally be considered, given the greater strength of genome wide association studies (GWAS). Research undertaken in non-human animals will not be considered for publication in the Annals. Annals of Clinical Biochemistry is also the official journal of NVKC (de Nederlandse Vereniging voor Klinische Chemie) and JSCC (Japan Society of Clinical Chemistry).
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