摘要
目的:建立人血浆中头孢曲松的高效液相色谱测定法(HPLC)。方法:血浆样品经10%三氯醋酸沉淀蛋白后,于ZORBAX Eclipse XDB-C18色谱柱(4.6mm×250mm,5μm)上,以含10mmol·L^-1戊烷磺酸钠的10mmol·L^-1。磷酸氢二钾缓冲溶液(以磷酸调节pH值为6.0)-乙腈(94:6)为流动相进行色谱分离,柱温为25℃,紫外检测波长为254nm。结果:线性范围0.2~10mg·L^-1,沉淀蛋白回收率81.6%~84.4%,加样回收率98.0%~100.5%,日内RSD2.27%~3.65%,日间RSD4.42%~5.13%。结论:本法准确可靠,可用于人血浆中头孢曲松的测定。
OBJECTIVE To establish an HPLC method for the determination of ceftriaxone in human plasma. METHODS 10% Trichloraeetie acid was used as deproteinizing agent for the plasma samples. The chromatographic separation was conducted on ZORBAX Eclipse XDB-C18 (4.6 mm×250 mm,5μm) column. The mobile phase consisted of acetonitrile-10 mmol·L^-1 phosphate buffer(6:94) containing 10 mmol·L^-1 sodium pentanesulfonat, adjusted to pH 6.0 with orthophosphoric acid. The temperature of column was at 25°C, the wavelength of detection was 254 nm. RESULTS The calibration curve was linear within 0.2-10 mg·L^-1. The deprotein recovery of ceftriaxone was 81.6%-84.4^. The recovery of methodology was 98.0%-100.5% with the with-day RSD of 2.27%-3.65%,and the between-day RSD of 4.42%-5.13%. CONCLUSION This method is accurate and reliable. It has been applied successfully to the determination of ceftriaxone in human plasma.
出处
《中国医院药学杂志》
CAS
CSCD
北大核心
2006年第3期290-291,共2页
Chinese Journal of Hospital Pharmacy