Pharmaceutics & Pharmacokinetics Division, CSIR-Central Drug Research Institute, Lucknow, Uttar Pradesh, India.
Academy of Scientific & Innovative Research (AcSIR), Ghaziabad, Uttar Pradesh, India.
J Mass Spectrom. 2024 Jun;59(6):e5031. doi: 10.1002/jms.5031.
Managing ocular microbial infections typically requires pharmacotherapy using antibiotic eye drops, such as moxifloxacin hydrochloride (MFX), combined with an antifungal agent like amphotericin B (AB). We carried out and validated an LC-MS/MS assay to quantify these compounds in rabbit tear fluid in order to look into the pharmacokinetics of these two drugs. We employed a protein precipitation technique for the extraction of drugs under examination. A Waters Symmetry C column was used to separate the analytes and internal standard. The composition of the mobile phase was like (A) 0.1% v/v formic acid in water and (B) methanol. The detection of MFX and AB was accomplished through the utilization of positive ion electrospray ionization under multiple reaction monitoring mode. The linearity curves for both analytes exhibited an acceptable trendline across a concentration range of 2.34-300 ng/mL for MFX and 7.81-1000 ng/mL for AB in surrogate rabbit tear fluid. The lower limit of quantitation for MFX was 2.34 ng/mL, while for AB, it was 7.81 ng/mL. The approach was strictly validated, encompassing tests of selectivity, linearity (with r > 0.99), precision, accuracy, matrix effects, and stability. Consequently, we employed this method to evaluate the pharmacokinetics profiles of MFX and AB in rabbit tear fluid following single topical doses.
治疗眼部微生物感染通常需要使用抗生素眼药水进行药物治疗,如盐酸莫西沙星(MFX),并结合使用抗真菌药物,如两性霉素 B(AB)。我们开发并验证了一种 LC-MS/MS 测定法,以定量测定兔泪液中的这些化合物,从而研究这两种药物的药代动力学。我们采用蛋白沉淀技术提取待检药物。使用 Waters Symmetry C 柱分离分析物和内标。流动相的组成为(A)0.1%v/v 甲酸水溶液和(B)甲醇。通过正离子电喷雾电离在多重反应监测模式下检测 MFX 和 AB。两种分析物的线性曲线在替代兔泪液中均表现出可接受的趋势,MFX 的浓度范围为 2.34-300ng/mL,AB 的浓度范围为 7.81-1000ng/mL。MFX 的定量下限为 2.34ng/mL,AB 的定量下限为 7.81ng/mL。该方法经过严格验证,包括选择性、线性(r>0.99)、精密度、准确度、基质效应和稳定性测试。因此,我们采用该方法评估单次局部给药后 MFX 和 AB 在兔泪液中的药代动力学特征。