Knobloch J E, Shaklee P N
Scientific Protein Laboratories, Waunakee, Wisconsin 53597, USA.
Anal Biochem. 1997 Feb 15;245(2):231-41. doi: 10.1006/abio.1996.9984.
The absolute molecular weight (M(r)) distribution of seven low-molecular-weight (LMW) heparin products was determined by size-exclusion chromatography (SEC) coupled with multiangle laser light scattering (MALLS) detection. The SEC/MALLS technique does not rely on relative M(r) standards for column calibration and yields absolute M(r) estimates directly from the angular dependence of scattered light intensity as a function of concentration, as formulated by light scattering theory. The SEC/MALLS method we describe is rapid, precise, and accurate. In 1 h it yields results from triplicate injections that agree well with the manufacturers' own independent analyses and that exhibit coefficients of variation of approximately 1%. By eliminating the requirement for finite quantities of highly purified, well-characterized M(r) standards derived from heparin, the present procedure represents a clear improvement over relative methods of M(r) determination. Thus, it is concluded that the SEC/MALLS method is ideally suited to routine quality control of commercial LMW-heparin products.
采用尺寸排阻色谱法(SEC)结合多角度激光光散射(MALLS)检测,测定了七种低分子量(LMW)肝素产品的绝对分子量(M(r))分布。SEC/MALLS技术不依赖相对M(r)标准品进行柱校准,而是根据光散射理论,直接从散射光强度随浓度的角度依赖性得出绝对M(r)估计值。我们所描述的SEC/MALLS方法快速、精确且准确。在1小时内,三次进样的结果与制造商自己的独立分析结果高度一致,变异系数约为1%。通过消除对有限量源自肝素的高度纯化、特征明确的M(r)标准品的需求,本方法相较于相对分子量测定方法有明显改进。因此,得出结论:SEC/MALLS方法非常适合商业LMW肝素产品的常规质量控制。