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一种通过固相萃取同时分离测定人血浆中游离和脂质体两性霉素B的简便快速的液相色谱-串联质谱法。

A convenient and rapid LC-MS/MS method for determination of free and liposomal amphotericin B in human plasma by simultaneous separation using SPE.

作者信息

Jin Yi, Wu Bowen, Gong Yuting, Wei Huanyu, Ma Ruihan, Wang Yue, Yuan Min, Xu Haiyan

机构信息

Department of Pharmaceutical Analysis, Pharmacy School, Shenyang Pharmaceutical University, Shenyang 110016, China.

Department of Pharmaceutical Analysis, Pharmacy School, Shenyang Pharmaceutical University, Shenyang 110016, China.

出版信息

J Pharm Biomed Anal. 2025 Sep 1;262:116884. doi: 10.1016/j.jpba.2025.116884. Epub 2025 Apr 10.

Abstract

Effective separation and specific detection of free and encapsulated drugs in bio-samples are critical to the pharmacokinetic investigation of liposomal medicine. In this study, a simple, convenient, reliable, and selective SPE separation method coupled with sensitive LC-MS/MS technique was developed and fully validated for the detection of liposomal amphotericin B (L-AMB) and non-liposomal amphotericin B (F-AMB) in human plasma. The simultaneous separation between L-AMB and F-AMB in plasma were realized using Oasis HLB SPE cartridge. L-AMB was collected in the aqueous eluate and F-AMB was eluted from the cartridge by methanol containing 1 % formic acid. The analyte and internal standard (natamycin) were separated on a ZORBAX Eclise XDB C18 column (2.1 × 50 mm, 3.5 μm) with gradient elution at a flow rate of 0.5 mL/min, employing a mobile phase that consisted of methanol (0.1 % formic acid) and 5 mM ammonium acetate solution (0.1 % formic acid). Mass spectrometry detection was performed in positive ion mode with electrospray ionization (ESI) interface by multiple reaction monitoring (MRM) method. The linearity range was 200-50000 ng/mL for L-AMB and 10.0-1600 ng/mL for F-AMB. A series of cross quality control samples was adopted to verify the selectivity, stability, and reproducibly of the quantification. Using our methodology, we quantified F-AMB and L-AMB without mutual interferences and obtained excellent incurred sample reanalysis (ISR) results for both analytes. The method was also successfully applied to a clinical study in healthy volunteers.

摘要

生物样品中游离药物和包封药物的有效分离及特异性检测对于脂质体药物的药代动力学研究至关重要。本研究开发了一种简单、便捷、可靠且具有选择性的固相萃取(SPE)分离方法,并结合灵敏的液相色谱-串联质谱(LC-MS/MS)技术,用于检测人血浆中的脂质体两性霉素B(L-AMB)和非脂质体两性霉素B(F-AMB),并进行了全面验证。使用Oasis HLB SPE小柱实现了血浆中L-AMB和F-AMB的同时分离。L-AMB收集于水洗脱液中,F-AMB用含1%甲酸的甲醇从柱上洗脱。分析物和内标(纳他霉素)在ZORBAX Eclise XDB C18柱(2.1×50 mm,3.5μm)上分离,采用梯度洗脱,流速为0.5 mL/min,流动相由甲醇(0.1%甲酸)和5 mM醋酸铵溶液(0.1%甲酸)组成。质谱检测采用电喷雾电离(ESI)接口,在正离子模式下通过多反应监测(MRM)方法进行。L-AMB的线性范围为200 - 50000 ng/mL,F-AMB的线性范围为10.0 - 1600 ng/mL。采用一系列交叉质量控制样品来验证定量的选择性、稳定性和重现性。使用我们的方法,我们对F-AMB和L-AMB进行了定量,无相互干扰,并获得了两种分析物的出色的基质加标样品再分析(ISR)结果。该方法还成功应用于健康志愿者的临床研究。

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