Liu Yanan, Peng Jiangning, Liang Yan, Li Yilin, Zhen Xiaolan, Li Hui
College of Chemistry and Pharmaceutical Engineering, Hebei University of Science and Technology, Shijiazhuang 050000, China.
College of Pharmacy, Hebei Medical University, Shijiazhuang 050000, China.
Molecules. 2025 May 18;30(10):2204. doi: 10.3390/molecules30102204.
Nucleoside reverse transcriptase inhibitors (NRTIs) and platinum-based chemotherapeutics are widely utilized in cancer treatment. Evidence suggests that drug plasma concentrations are closely linked to both therapeutic efficacy and the risk of adverse effects. Consequently, developing therapeutic drug monitoring (TDM) methods is essential. Here, an effective procedure utilizing QuEChERS (Quick, Easy, Cheap, Effective, Rugged, and Safe) techniques for preparing samples and UPLC-MS/MS for simultaneously measuring eight NRTIs and platinum-based drugs in human plasma is described. Chromatographic separation was conducted with an Agilent Eclipse Plus C18 column (4.6 × 100 mm, 3.5 μm) with acetonitrile with 0.1% formic acid as Phase A and 0.1% formic acid in water as Phase B, achieving complete separation within 10 min. The target analytes-lamivudine, telbivudine, emtricitabine, entecavir, tenofovir, nedaplatin, oxaliplatin, and adefovir dipivoxil-exhibited strong linearity within the 10-1000 ng/mL and 1-100 ng/mL ranges, showing correlations (r) ≥ 0.9962. The method demonstrated excellent accuracy (-6.72% to 7.82%) and selectivity (84.53%-110.49%), as well as satisfactory recovery and stability. Overall, this analytical approach can be used to detect the combination of eight NRTIs and platinum-based drugs in human plasma. This method enables plasma drug-level monitoring in real time, with applications for individualized treatment approaches.
核苷类逆转录酶抑制剂(NRTIs)和铂类化疗药物在癌症治疗中被广泛应用。有证据表明,药物血浆浓度与治疗效果和不良反应风险密切相关。因此,开发治疗药物监测(TDM)方法至关重要。在此,描述了一种利用QuEChERS(快速、简便、廉价、有效、耐用和安全)技术制备样品以及超高效液相色谱-串联质谱法(UPLC-MS/MS)同时测定人血浆中八种NRTIs和铂类药物的有效程序。采用安捷伦Eclipse Plus C18柱(4.6×100 mm,3.5μm)进行色谱分离,以含0.1%甲酸的乙腈为A相,含0.1%甲酸的水溶液为B相,在10分钟内实现完全分离。目标分析物——拉米夫定、替比夫定、恩曲他滨、恩替卡韦、替诺福韦、奈达铂、奥沙利铂和阿德福韦酯——在10 - 1000 ng/mL和1 - 100 ng/mL范围内呈现出良好的线性,相关性(r)≥0.9962。该方法具有出色的准确度(-6.72%至7.82%)和选择性(84.53% - 110.49%),以及令人满意的回收率和稳定性。总体而言,这种分析方法可用于检测人血浆中八种NRTIs和铂类药物的组合。该方法能够实时监测血浆药物水平,适用于个体化治疗方案。