依托泊苷负载纳米颗粒的高效液相色谱荧光检测及药代动力学研究。

Arzneimittel-Forschung-Drug Research Pub Date : 2012-12-01 Epub Date: 2012-11-28 DOI:10.1055/s-0032-1330019
H-Z Yang, L Liu, X Xu
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引用次数: 1

摘要

建立了高效液相色谱-荧光检测法测定犬血浆中依托泊苷的含量及药动学研究。血浆样品预处理包括500µL血浆的液-液萃取。色谱分离采用Gemini C18色谱柱,流动相为甲醇(a)和水(B)的混合物(0~5 min, a体积为45-50%,5~10 min, a体积为50-90%),流速为0.4 ml/min。这些结果表明,当前测定法的准确度和精密度在《工业指南:生物分析方法验证》中规定的测定验证建议范围内。依托泊苷纳米颗粒及注射药动学参数分别为T1/2、2.26(0.71)、1.74 (0.43)h, Cmax、13.24(5.32)、8.12(3.61)µg/ml;AUC0-t, 41.32(7.33)和16.53(4.12)µg·ml - 1·h;AUC0 -∞,49.54(9.62)和19.64(8.22)µg·ml - 1·h;MRT分别为3.13(0.54)和2.06 (0.33)h, CL分别为7.35(1.53)和12.61 (2.22)h。该方法得到了充分验证,并成功应用于静脉注射后依托泊苷在犬体内的临床前药代动力学研究。滴。
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Fluorescence detection of etoposide-loaded nanoparticles by HPLC and pharmacokinetics study.

A simple HPLC with fluorescence detection method was developed for determination and pharmacokinetic study of Etoposide in dog plasma.Plasma sample pretreatment involved liquid-liquid extraction of 500 µL plasma. The chromatographic separation was carried out on a Gemini C18 column with a mixture of methanol (A) and water (B) (0~5 min, volume of A was 45-50%, 5~10 min, volume of A was 50-90%) used as mobile phase at a flow rate of 0.4 ml/min.These results indicated that the accuracy and precision of the current assay were within the recommendations for assay validation as stipulated in "Guidance for Industry: Bioanalytical Method Validation". Etoposide nanoparticles and injection pharmacokinetic parameters were as follows: T1/2, 2.26 (0.71) and 1.74 (0.43) h;Cmax, 13.24 (5.32) and 8.12 (3.61) µg/ml; AUC0-t, 41.32 (7.33) and 16.53 (4.12) µg · ml - 1 · h; AUC0-∞, 49.54 (9.62) and 19.64 (8.22) µg · ml - 1 · h; MRT, 3.13 (0.54) and 2.06 (0.33) h and CL 7.35 (1.53) and 12.61 (2.22), respectively.This method was fully validated and successfully applied to a preclinical pharmacokinetic study of Etoposide in dogs after i. v. drip administration.

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