Highly Sensitive, Selective and Validated Spectrofluorimetric Assay for Novel Oxazolidinone Antibiotic: Tedizolid Phosphate in Pharmaceutical Dosage Form and Human Plasma

Basma M. Tawfik, M. Rizk, M. Sultan, R. El-Eryan
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Abstract

Objectives: In this work we presented a highly sensitive, selective and validated method for determination of tedizolid phosphate (TEDP) antibiotic, based on its native fluorescence in aqueous solution. Methods: The maximum fluorescence intensity was measured at 408 nm after excitation at 298 nm after optimization of all experimental conditions. Results: The measured fluorescence was directly proportional to the concentration of the drug over the range of 2-30 ng/mL with a limit of detection of 0.13 and limit of quantification of 0.44 ng/mL The method succeeded to determine TEDP in its pharmaceutical dosage form and in human plasma with mean % recovery of 100.49 ±1.32 and 99.40 ± 2.18 respectively. Conclusion: The developed data was found to be with a good agreement with a valid method. The method was validated according to ICH guidelines for determination of the drug in its pure form and dosage form and according to FDA Guidance for Industry, Bioanalytical Method Validation for determination of TEDP in human plasma.
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药物剂型和人血浆中新型恶唑烷酮类抗生素磷酸二唑脂的高灵敏度、选择性和有效的荧光光谱分析
目的:建立了一种高灵敏度、高选择性、高可靠性的方法,利用磷酸盐二唑脂(tedizolid phosphate, TEDP)在水溶液中的天然荧光测定其含量。方法:优化所有实验条件后,在298 nm处激发后,在408 nm处测量最大荧光强度。结果:在2 ~ 30 ng/mL范围内,荧光值与药物浓度成正比,检测限为0.13,定量限为0.44 ng/mL,成功测定了TEDP在药物剂型和人血浆中的含量,平均%回收率分别为100.49±1.32和99.40±2.18。结论:所建立的数据与有效的方法吻合较好。该方法根据ICH指南进行了纯度和剂型测定,并根据FDA工业指南,生物分析方法验证用于测定人血浆中TEDP。
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