Posch W, Lindner W
Institute of Pharmaceutical Chemistry, University of Graz, Austria.
Biomed Chromatogr. 1989 Jul;3(4):153-6. doi: 10.1002/bmc.1130030403.
An automated column-switching HPLC system is described for the simultaneous determination of midodrine, an alpha-adrenergic stimulating drug, and its active metabolite, ST-1059. Serum or plasma (850 microliters) is directly injected onto a RP18 (30 micrograms particle size) pre-column (9 x 4 mm ID) which acts as an on-line liquid-solid extractor and analyte enrichment system. The injection is followed by washing steps. The fraction containing the analytes is transferred onto an analytical RP18 column via step gradient elution where the final analysis is performed. Fluorescence detection is used (lambda ex 290 nm and lambda em 322 nm), and method detection limits of 0.8 ng/mL plasma were reached. These were sufficiently low to determine the plasma concentration-time profiles for both compounds following oral administration of 2.5 mg and 5 mg midodrine hydrochloride. The assay in serum or plasma was linear in the range of 1 to 15 ng analyte/mL, the recovery was greater than 95%, and the reproducibility was sufficient. The assay was rugged and was maintained by routinely changing the home-made, dry packed pre-column every 20th serum injection.
描述了一种自动柱切换高效液相色谱系统,用于同时测定α-肾上腺素能刺激药物米多君及其活性代谢物ST-1059。将血清或血浆(850微升)直接注入到RP18(粒径30微克)预柱(9×4毫米内径)上,该预柱用作在线液固萃取器和分析物富集系统。进样后进行洗涤步骤。含有分析物的馏分通过梯度洗脱转移到分析型RP18柱上进行最终分析。采用荧光检测(激发波长290纳米,发射波长322纳米),血浆中的方法检测限达到0.8纳克/毫升。这些检测限足够低,能够测定口服2.5毫克和5毫克盐酸米多君后两种化合物的血浆浓度-时间曲线。血清或血浆中的测定在1至15纳克分析物/毫升范围内呈线性,回收率大于95%,重现性良好。该测定方法耐用,通过每20次血清进样常规更换自制的干填充预柱来维持。