CAJ | 학술논문

建立了利用蛋白沉淀提取血浆中61种常见的中枢神经系统药物并用高效液相色谱-二极管阵列检测器(HPLC-DAD)分析的方法.1 mL血浆样品中加入1.5 mL乙腈,旋涡混合后,离心,上清液过滤后直接采用HPLC测定.选用Agilent TC-C18色谱柱(250 mm×4.6 mm,5 μm),以磷酸盐缓冲液和乙腈为流动相进行梯度洗脱,流速1.5 mL/min,柱温35 ℃,检测波长210 nm.61种药物的回收率均大于80%,相对标准偏差为0.94% ～11.23% .采用乙腈沉淀蛋白,方法简便、快速、回收率高且稳定,能够作为系统毒物分析的通用前处理方法.该蛋白沉淀方法与HPLC-DAD技术结合,可应用于61种药物的分析.
건립료이용단백침정제취혈장중61충상견적중추신경계통약물병용고효액상색보-이겁관진렬검측기(HPLC-DAD)분석적방법.1 mL혈장양품중가입1.5 mL을정,선와혼합후,리심,상청액과려후직접채용HPLC측정.선용Agilent TC-C18색보주(250 mm×4.6 mm,5 μm),이린산염완충액화을정위류동상진행제도세탈,류속1.5 mL/min,주온35 ℃,검측파장210 nm.61충약물적회수솔균대우80%,상대표준편차위0.94% ～11.23% .채용을정침정단백,방법간편、쾌속、회수솔고차은정,능구작위계통독물분석적통용전처리방법.해단백침정방법여HPLC-DAD기술결합,가응용우61충약물적분석.
A method was established for the determination of 61 central nervous system drugs in plasma by using protein precipitation combined with high performance liquid chromatogra-phy-diode array detection (HPLC-DAD). A volume of 1. 5 mL acetonitrile was added into 1 mL plasma, after vortex, centrifugation and filtration, the supernatant was directly injected into HPLC. The separation was performed on an Agilent TC-C18 column (250 mm ×4. 6 mm, 5 μm) with acetonitrile and phosphate buffer solution as mobile phase by gradient elution at a flow rate of 1. 5 mL/min. The detection wavelength was 210 nm; full spectra were recorded from 200-364 nm. The recoveries of 61 drugs were larger than 80% with the relative standard devia-tions (RSDs) ranged from 0.94% to 11.23%. The protein precipitation method is simple, rap-id , low-cost with good recoveries, reproducibility and suitable for the general pretreatment of the systematic toxicological analysis (STA) of the 61 drugs.