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液相色谱法测定人血清中五种口服活性头孢菌素——头孢克肟、头孢克洛、头孢羟氨苄、头孢氨苄和头孢拉定。

Liquid-chromatographic determination of five orally active cephalosporins--cefixime, cefaclor, cefadroxil, cephalexin, and cephradine--in human serum.

作者信息

McAteer J A, Hiltke M F, Silber B M, Faulkner R D

机构信息

Pharmacodynamics Department, American Cyanamid Co., Pearl River, NY 10965.

出版信息

Clin Chem. 1987 Oct;33(10):1788-90.

PMID:3665031
Abstract

We report an isocratic "high-performance" liquid-chromatographic (HPLC) procedure for measurement of five orally administered cephalosporins (cefixime, cefaclor, cefadroxil, cephalexin, and cephradine) in 0.1 mL of human serum. Serum protein is precipitated with acetonitrile, the sample is centrifuged, and the supernate is evaporated under nitrogen. The residue is reconstituted in 0.1 mL of mobile phase, and 50 to 80 microL of this is injected onto a reversed-phase Altex Ultrasphere Octyl (C8) column. The five cephalosporins are resolved by elution with a pH 2.6 mobile phase of methanol/monobasic phosphate buffer (20/80) by vol), flow rate 2 mL/min. The column effluent is monitored at 240 nm. Cefixime serves as the internal standard for the analysis of the four other compounds, cephalexin as the internal standard for cefixime. We used two standard curves for all compounds: a low-range curve for concentrations commonly observed clinically and a higher-range curve for higher concentrations. The former were linear from 1.0 to 10 mg/L for cefaclor, cefadroxil, cephalexin, and cephradine and from 0.1 to 1 mg/L for cefixime. The high-concentration curves were linear from 1 to 10 mg/L for cefixime and from 10 to 100 mg/L for the other compounds. The detection limits were 0.1 mg/L for cefixime, 1 mg/L for the other cephalosporins. Mean within-run and day-to-day CVs were always less than 15% for all compounds studied.

摘要

我们报告了一种等度“高效”液相色谱(HPLC)方法,用于测定0.1 mL人血清中口服的5种头孢菌素(头孢克肟、头孢克洛、头孢羟氨苄、头孢氨苄和头孢拉定)。用乙腈沉淀血清蛋白,离心样品,上清液在氮气下蒸发。残渣用0.1 mL流动相复溶,取50至80 μL注入反相Altex Ultrasphere Octyl(C8)柱。用体积比为甲醇/磷酸二氢钠缓冲液(20/80)、pH 2.6的流动相以2 mL/min的流速洗脱,分离这5种头孢菌素。在240 nm处监测柱流出物。头孢克肟用作分析其他4种化合物的内标,头孢氨苄用作头孢克肟的内标。所有化合物我们都使用两条标准曲线:一条低浓度范围曲线用于临床常见浓度,一条高浓度范围曲线用于更高浓度。对于头孢克洛、头孢羟氨苄、头孢氨苄和头孢拉定,低浓度范围曲线在1.0至10 mg/L呈线性,对于头孢克肟在0.1至1 mg/L呈线性。高浓度曲线对于头孢克肟在1至10 mg/L呈线性,对于其他化合物在10至100 mg/L呈线性。检测限对于头孢克肟为0.1 mg/L,对于其他头孢菌素为1 mg/L。所有研究化合物的批内和日间平均变异系数均始终小于15%。

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