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通过高效液相色谱法测定壳聚糖的分子量分布

Determination of molecular-weight distribution of chitosan by high-performance liquid chromatography.

作者信息

Wu A C, Bough W A, Conrad E C, Alden K E

出版信息

J Chromatogr. 1976 Nov 17;128(1):87-99. doi: 10.1016/s0021-9673(00)84034-0.

Abstract

Optimal conditions for using high-performance liquid chromatography (HPLC) in the size exclusion mode have been determined for measuring the molecular-weight (MW) distribution of chitosan samples. Physical separation according to molecular size was accomplished on the stationary phase of glass supports having controlled pore sizes ranging from 2500 to 40 A. Selection of column combinations was based on the requirements to resolve the higher MW fraction of chitosan and to give a linear calibration curve within the required MW range. The best combination of glass pore sizes and column lengths in two foot sections joined sequentially was: 2500 A (2 ft.), 1500 A (4 ft.), 550 A (6 ft.), 250 A (2 ft), 100 A (2 ft.), and 40 A (2 ft.). A loading study showed that an injection load of 500 mug, i.e. 100 mul at 5 g/l or 50 mul at 10 g/l (w/v), was the optimal load to give reproducible elution volumes, precision in quantitation, and minimum viscosity effects. The best calibration curve using defined dextran standards was obtained from the geometric mean of Mw (weight average MW) and Mn (number average MW) values and peak elution volumes. Precision in determining MW distribution of chitosan as well as dextran standards was better than 5% relative standard deviation, and the differences between these results and the manufacturer's data on the dextran standards were 6 to -17%. The MW distribution of a selected chitosan samples in 2% acetic acid thus determined was Mw = 2,055,000, Mn = 936,000, dispersity = 2.16, and the most abundant species was around 1,103,000. Analysis time for the HPLC separation was less than 20 min per sample. Chitosan is an effective coagulating agent for the treatment of food processing wastes and activated sludge from biological treatment systems. It is manufactured from chitin in shrimp and crab wastes. The rapid methods developed here for determining the MW distribution of chitosan preparations will be used to optimize the manufacturing process and guide the selection of more effective chitosan products.

摘要

已确定在尺寸排阻模式下使用高效液相色谱法(HPLC)测量壳聚糖样品分子量(MW)分布的最佳条件。根据分子大小进行的物理分离是在孔径控制在2500至40埃范围内的玻璃载体固定相上完成的。柱组合的选择基于分离壳聚糖较高分子量部分以及在所需MW范围内给出线性校准曲线的要求。依次连接的两个英尺长的柱段中玻璃孔径和柱长的最佳组合是:2500埃(2英尺)、1500埃(4英尺)、550埃(6英尺)、250埃(2英尺)、100埃(2英尺)和40埃(2英尺)。一项进样研究表明,500微克的进样量,即5克/升时100微升或10克/升(w/v)时50微升,是获得可重现洗脱体积、定量精度和最小粘度影响的最佳进样量。使用定义的葡聚糖标准品获得的最佳校准曲线是由Mw(重均分子量)和Mn(数均分子量)值以及峰洗脱体积的几何平均值得出的。测定壳聚糖以及葡聚糖标准品MW分布的精度优于5%相对标准偏差,这些结果与葡聚糖标准品制造商数据之间的差异为6%至 -17%。由此确定的选定壳聚糖样品在2%乙酸中的MW分布为Mw = 2,055,000,Mn = 936,000,分散度 = 2.16,最丰富的物种约为1,103,000。HPLC分离每个样品的分析时间少于20分钟。壳聚糖是处理食品加工废水和生物处理系统中活性污泥的有效凝聚剂。它由虾蟹废弃物中的几丁质制成。这里开发的用于测定壳聚糖制剂MW分布的快速方法将用于优化制造工艺并指导选择更有效的壳聚糖产品。

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