Estimation of Eravacycline Dihydrochloride in Biological Matrices by LC-MS/MS

B. S. Prasad, Sekharan Jaya Kumari
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引用次数: 1

Abstract

Objective: The validated protein precipitation method was applied for estimation of Eravacycline dihydrochloride in human plasma with Rolitetracycline hydrochloride as an internal standard (ISTD) by using HPLC-ESI-MS/ MS. Methods: The chromatographic separation was achieved with 20mM Ammonium acetate (pH-3.0):Methanol:Acetontrile (20:20:60,%v/v) using the TELOS LU C18 (2) 5μm, 100 x 4.6 mm. The total analysis time was 3 min and flow rate was set to 0.5 mL/min. Results: The mass transitions of Eravacycline dihydrochloride and Rolitetracycline hydrochloride obtained were m/z 632.5®84.3 and 436.2®84.3. The standard curve shows correlation coefficient (s) greater than 0.999 with a range of 15.00-120.00 pg/ml using the linear regression model. Conclusion: The method was suitable and conveniently applicable to pharmacokinetic and bioavailability studies for estimation of Eravacycline in biological matrices by HPLC-ESI-MS/MS.
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LC-MS/MS法测定生物基质中盐酸依拉瓦环素的含量
目的:以盐酸罗利特环素为内标(ISTD),采用高效液相色谱- esi -质谱联用技术(HPLC-ESI-MS/ ms)测定人血浆中盐酸依拉瓦环素的含量。方法:采用20mM乙酸铵(pH-3.0):甲醇:乙腈(20:20:60,%v/v),色谱柱为TELOS LU C18 (2) 5μm, 100 × 4.6 mm。总分析时间为3 min,流速为0.5 mL/min。结果:得到的盐酸依拉瓦环素和盐酸罗利特环素的质量转移率分别为m/z 632.5®84.3和436.2®84.3。在15.00 ~ 120.00 pg/ml的线性回归范围内,标准曲线的相关系数大于0.999。结论:该方法适用于高效液相色谱- esi -MS/MS法测定伊拉瓦环素在生物基质中的药动学和生物利用度研究。
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