Payan E, Jouzeau J Y, Lapicque F, Muller N, Payan J P, Gegout P, Bertin P, Netter P
Laboratoire de Pharmacologie Clinique et URA CNRS 1288, Faculté de Médecine, Vandoeuvre les Nancy, France.
J Chromatogr. 1991 May 3;566(1):9-18. doi: 10.1016/0378-4347(91)80106-m.
A high-performance liquid chromatographic method for the determination of hyaluronic acid levels in synovial fluids has been developed. The hyaluronidase sample digests, containing an internal standard (benzoic acid), were separated on a reversed-phase octadecylsilyl column eluted with 0.01 M tetrabutylammonium phosphate-acetonitrile (83:17, v/v) at pH 7.35. The determination was made on 1:10 diluted samples, by using a calibration curve from 50 to 500 micrograms/ml of human umbilical cord hyaluronic acid. For validation, the synovial fluids were simultaneously analysed by this method and a radiometric method: a high correlation was found between the two (correlation coefficient 0.94). The proposed method can be used to determine specifically the high hyaluronic acid levels of synovial fluids without interferences from other glycosaminoglycans or non-steroidal anti-inflammatory drug treatment.
已开发出一种用于测定滑液中透明质酸水平的高效液相色谱法。含有内标(苯甲酸)的透明质酸酶样品消化液在反相十八烷基硅柱上分离,该柱用pH 7.35的0.01 M磷酸四丁铵 - 乙腈(83:17,v/v)洗脱。通过使用50至500微克/毫升人脐带透明质酸的校准曲线,对1:10稀释的样品进行测定。为进行验证,同时用该方法和放射性方法分析滑液:两者之间发现高度相关(相关系数0.94)。所提出的方法可用于特异性测定滑液中的高透明质酸水平,而不受其他糖胺聚糖或非甾体抗炎药治疗的干扰。