Yoshimura Y, Ohnishi K, Hamamura M, Oda T, Sohda T
Drug Safety Research Laboratories, Takeda Chemical Industries, Ltd., Osaka, Japan.
J Chromatogr. 1993 Mar 5;613(1):43-9. doi: 10.1016/0378-4347(93)80195-a.
An on-line urine clean-up system was developed for the simultaneous determination of free and total pyridinoline, hydroxylysyl-pyridinoline (HP) and lysylpyridinoline (LP) by high-performance liquid chromatography (HPLC) using a column-switching technique. The method is based on a combination of gel permeation chromatography (GPC) and ion-pair reversed-phase HPLC. In the GPC column, pyridinoline is preseparated from endogenous urinary substances with 0.03 M heptafluorobutyric acid (HFBA) as the mobile phase. After column switching, the eluate fraction containing pyridinoline is further separated by ion-pair chromatography using an octadecylsilica (ODS) column with 0.03 M HFBA-acetonitrile (81:19) as the mobile phase. The detection limits were 36 and 44 pmol/ml for free and total HP, respectively, and 44 pmol/ml for both free and total LP at a signal-to-noise ratio of 3. The coefficients of variation for free and total pyridinoline were 1.5 and 3.5%, respectively. The determination of one sample including the clean-up is completed within 25 min. This system is precise and is useful for the determination of pyridinoline in large amounts of urine. The usefulness of pyridinoline as a biomedical marker for bone resorption was also examined.
开发了一种在线尿液净化系统,用于通过高效液相色谱(HPLC)结合柱切换技术同时测定游离和总吡啶啉、羟赖氨酰吡啶啉(HP)和赖氨酰吡啶啉(LP)。该方法基于凝胶渗透色谱(GPC)和离子对反相HPLC的结合。在GPC柱中,以0.03 M七氟丁酸(HFBA)为流动相,将吡啶啉与内源性尿液物质进行预分离。柱切换后,含有吡啶啉的洗脱液部分通过离子对色谱法进一步分离,使用十八烷基硅胶(ODS)柱,以0.03 M HFBA - 乙腈(81:19)为流动相。在信噪比为3时,游离和总HP的检测限分别为36和44 pmol/ml,游离和总LP的检测限均为44 pmol/ml。游离和总吡啶啉的变异系数分别为1.5%和3.5%。包括净化在内的一个样品的测定在25分钟内完成。该系统精确,可用于大量尿液中吡啶啉的测定。还研究了吡啶啉作为骨吸收生物医学标志物的实用性。