在血中测定可纳的UPLC-MS/MS方法及其在墨西哥候选血病患者中的应用
Karla Paulina Valero Rivera1, Martin Magaña Aquino2, Julia Sagahón Azúa1
1Departamento de Farmacia, Facultad de Ciencias Químicas, Universidad Autónoma de San Luis Potosí, #6 Ave. Manuel Nava, San Luis Potosí, C.P.78210, México.
Bioanalysis
|September 5, 2024
概括
一种新的超高性能液态色谱法准确地量化了人体血中的可纳. 这种快速和选择性测定适用于监测候选血病患者,可能改善治疗结果.
科学领域:
- 分析化学 分析化学
- 药理动力学 药理动力学
背景情况:
- 精确量化抗真菌药物,如可纳对于治疗系统性真菌感染,如候选性血症至关重要.
- 现有的分析方法可能缺乏常规临床监测所需的速度或灵敏度.
研究的目的:
- 开发和验证一种快速而准确的分析方法,用于在人体血中量化可纳.
- 确保该方法符合美国食品和药物管理局 (FDA) 的指导方针.
主要方法:
- 超高性能液态染色学与双重质谱学 (UHPLC-MS/MS) 相结合.
- 简单的蛋白质沉,使用乙尼来制备样本.
- 在Acquity UHPLC HSS T3 列上进行异离子化.
主要成果:
- 该方法表现出极好的线性 (r2 > 0.999) 和在1-50μg/mL范围内稳定性.
- 日内和日间精度显示变化系数从1.4%到6.6%.
- 成功分析了来自候选血病患者的27个血样本.
结论:
- 开发的UHPLC-MS/MS方法是准确,精确和快速的,用于在人体血中量化可纳.
- 简单的样本准备和缩短的分析时间使其非常适合在成人候选血病患者的临床应用.
- 这种方法可以帮助优化可纳治疗,改善患者的治疗结果.
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