Zendelovska Dragica, Pavlovska Kristina, Atanasovska Emilija, Gjorgjievska Kalina, Petrusevska Marija
Institute of Preclinical and Clinical Pharmacology and Toxicology, Ss. Cyril and Methodius University, Medical Faculty, 50 Divizija bb,1000 Skopje, Republic of Macedonia.
Pril (Makedon Akad Nauk Umet Odd Med Nauki). 2017 Dec 1;38(3):89-96. doi: 10.2478/prilozi-2018-0009.
Herein, we present a simple and rapid high performance liquid chromatographic (HPLC) method with UV-detection for the direct determination of diazepam in whole blood and serum that can be used for monitoring diazepam levels in clinical samples analysis. The isolation of diazepam and the internal standard bromazepam from serum and whole blood samples was performed using solid phase extraction method with RP select B cartridges. The analytes were separated employing a reversed phase C8 column with a mobile phase composed of 0.1 % (V/V) triethylamine in water (pH 3.5) and acetonitrile (63:37, V/V). UV detection was carried out at 240 nm. Linearity was achieved in the range from 10.0-1000.0 ng/ml for serum and whole blood. The method was applied to spiked and real biological samples after an oral administration of 10 mg diazepam. In conclusion, the proposed method is simple, rapid and provides efficient clean-up of the complex biological matrix and high recovery of diazepam.
在此,我们提出一种简单快速的高效液相色谱(HPLC)方法,采用紫外检测直接测定全血和血清中的地西泮,可用于临床样本分析中地西泮水平的监测。使用RP select B柱固相萃取法从血清和全血样本中分离地西泮和内标物溴西泮。采用反相C8柱,流动相由0.1%(V/V)三乙胺的水溶液(pH 3.5)和乙腈(63:37,V/V)组成,对分析物进行分离。在240 nm处进行紫外检测。血清和全血中地西泮的线性范围为10.0 - 1000.0 ng/ml。该方法应用于口服10 mg地西泮后的加标和实际生物样本。总之,所提出的方法简单、快速,能有效净化复杂的生物基质,且地西泮回收率高。