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开发一种使用液相色谱-串联质谱法(LC-MS/MS)在亚纳克/毫升浓度下定量15聚体寡核苷酸的生物分析方法。

Development of a bioanalytical method for quantification of a 15-mer oligonucleotide at sub-ng/ml concentrations using LC-MS/MS.

作者信息

Hemsley Martyn, Ewles Matthew, Goodwin Lee

机构信息

Bioanalytical Services, Covance Laboratories, Harrogate HG3 1PY, UK.

出版信息

Bioanalysis. 2012 Jun;4(12):1457-69. doi: 10.4155/bio.12.117.

Abstract

LC-MS/MS provides a powerful technique for the selective quantification of therapeutic oligonucleotides; however, the LOQ (typically >1 ng/ml) may be higher than desirable for clinical bioanalysis. A method has been developed to allow quantification of a 15-mer unmodified DNA oligonucleotide in human plasma using SPE and UHPLC with MS/MS detection. The LOQ of this assay was 0.05 nM (∼250 pg/ml). This method was then further developed by the inclusion of online SPE to increase loading and apply additional sample cleanup. This allowed for improved assay precision at lower concentrations and increased signal, thus allowing the method to be validated over the range of 10-4000 pM (approximately 50-20,000 pg/ml). The method is accurate, precise and selective and it provides proof-of-concept for sub-ng/ml, high-throughput quantification of oligonucleotides using online SPE coupled to ion-pair, reversed-phase LC-MS/MS.

摘要

液相色谱-串联质谱(LC-MS/MS)为治疗性寡核苷酸的选择性定量提供了一种强大的技术;然而,定量下限(通常>1 ng/ml)可能高于临床生物分析的理想值。已开发出一种方法,可使用固相萃取(SPE)和超高效液相色谱(UHPLC)结合质谱/质谱检测,对人血浆中的15聚体未修饰DNA寡核苷酸进行定量。该测定法的定量下限为0.05 nM(约250 pg/ml)。然后通过加入在线SPE进一步改进该方法,以增加上样量并进行额外的样品净化。这使得在较低浓度下测定精密度得到提高,信号增强,从而使该方法在10 - 4000 pM(约50 - 20,000 pg/ml)范围内得到验证。该方法准确、精密且具有选择性,为使用在线SPE与离子对反相LC-MS/MS联用进行亚ng/ml级高通量寡核苷酸定量提供了概念验证。

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