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采用反相高效液相色谱-紫外检测法测定犬血浆和尿液中一种新型聚合物结合紫杉醇衍生物(PNU 166945)、游离紫杉醇和7-表紫杉醇。

Determination of a new polymer-bound paclitaxel derivative (PNU 166945), free paclitaxel and 7-epipaclitaxel in dog plasma and urine by reversed-phase high-performance liquid chromatography with UV detection.

作者信息

Fraier D, Cenacchi V, Frigerio E

机构信息

Pharmacia & Upjohn, Pharmacokinetics & Metabolism Department, Milan, Italy.

出版信息

J Chromatogr A. 1998 Feb 27;797(1-2):295-303. doi: 10.1016/s0021-9673(97)01204-1.

Abstract

A sensitive and selective high-performance liquid chromatographic method for the determination of PNU 166945, a new polymer-bound paclitaxel derivative, free paclitaxel and 7-epipaclitaxel in dog plasma and urine has been developed. The method involves a solid-phase extraction of free paclitaxel and its possible degradation product 7-epipaclitaxel from plasma and urine, previously buffered with an equal volume of 0.05 M or 1 M KH2PO4 respectively, on 1-ml cyanopropyl columns. Cartridges elution was performed with the mobile phase, 0.05 M (pH 4.6) monobasic potassium phosphate-acetonitrile mixture (45:55, v/v). The samples were chromatographed on a reversed-phase octyl 4-microns column with UV detection at 229 nm. The retention times of paclitaxel and 7-epipaclitaxel were about 14 and 22 min, respectively. Determination of total paclitaxel (free + polymer-bound) was performed after release of paclitaxel from the polymeric carrier by chemical hydrolysis at room temperature (22 degrees C) for 20 h. After addition of 0.5 ml of methanol-0.1 M KH2PO4 mixture (50:50, v/v, pH = 7.5) to 0.5 ml of plasma or urine, paclitaxel was analysed as described above. PNU 166945 concentration was then determined by subtraction of free from total paclitaxel. The linearity, precision, accuracy and recovery of the method were evaluated. The limit of quantitation of the method was 5 ng/ml for biological fluid for paclitaxel and 7-epipaclitaxel and 20 ng/ml for PNU 166945 (as paclitaxel equivalent).

摘要

已开发出一种灵敏且具选择性的高效液相色谱法,用于测定犬血浆和尿液中的新型聚合物结合紫杉醇衍生物PNU 166945、游离紫杉醇和7-表紫杉醇。该方法包括分别用等体积的0.05 M或1 M KH2PO4缓冲后的血浆和尿液,在1 ml氰丙基柱上对游离紫杉醇及其可能的降解产物7-表紫杉醇进行固相萃取。用流动相0.05 M(pH 4.6)磷酸二氢钾 - 乙腈混合物(45:55,v/v)进行柱洗脱。样品在4微米反相辛基柱上进行色谱分析,在229 nm处进行紫外检测。紫杉醇和7-表紫杉醇的保留时间分别约为14分钟和22分钟。通过在室温(22℃)下化学水解20小时从聚合物载体中释放出紫杉醇后,测定总紫杉醇(游离 + 聚合物结合)。向0.5 ml血浆或尿液中加入0.5 ml甲醇 - 0.1 M KH2PO4混合物(50:50,v/v,pH = 7.5)后,按上述方法分析紫杉醇。然后通过从总紫杉醇中减去游离紫杉醇来测定PNU 166945的浓度。对该方法进行了线性、精密度、准确度和回收率评估。该方法对生物流体中紫杉醇和7-表紫杉醇的定量限为5 ng/ml,对PNU 166945(以紫杉醇当量计)为20 ng/ml。

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