Hurst R, Hennessey P
Prep Biochem. 1982;12(3):275-88. doi: 10.1080/00327488208065568.
A preparative method is described for continuous flow fractionation of heparin according to charge density in two-phase systems of butanol-hexadecylpyridinium chloride/aquaous NaCl. The separation is carried out on a "Slowly-Rotating Coil" device for countercurrent chromatography with 6 coil units and a sample capacity of 80 mg heparin. A turbidometric method is described which can be used to rapidly quantify the distribution of heparin. Characterization of fractions showed that linear charge density, binding constant for acridine orange, and specific activities in a "global" plasma anticoagulant assay and in a specific activities in a specific biochemical thrombin-inhibition assay varied with the NaCl concentration in the eluting phase. Some partial resolution of the two functional activities was observed. The fractions are much more homogeneous in composition than are the usual heparin preparations and may be useful as standards or in structure-function studies.
描述了一种制备方法,用于在丁醇-十六烷基氯化吡啶/氯化钠水溶液的两相系统中根据电荷密度对肝素进行连续流分级分离。分离在具有6个盘管单元且样品容量为80mg肝素的用于逆流色谱的“慢转盘管”装置上进行。描述了一种比浊法,可用于快速定量肝素的分布。级分的表征表明,线性电荷密度、吖啶橙结合常数以及在“整体”血浆抗凝测定中的比活性和在特定生化凝血酶抑制测定中的比活性随洗脱相中氯化钠浓度而变化。观察到两种功能活性有一定程度的分离。这些级分在组成上比通常的肝素制剂更均匀,可用作标准品或用于结构-功能研究。