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Characterization of the Block Structure and Molecular Weight of Sodium Alginates

糖醛酸 化学 表征(材料科学) 色谱法 海藻酸钠 摩尔质量分布 圆二色性 分析化学(期刊) 聚合物 材料科学 有机化学 立体化学 多糖 纳米技术
作者
Fiona A. Johnson,Duncan Q.M. Craig,Amanda D. Mercer
出处
期刊:Journal of Pharmacy and Pharmacology [Oxford University Press]
卷期号:49 (7): 639-643 被引量:144
标识
DOI:10.1111/j.2042-7158.1997.tb06085.x
摘要

Sodium alginates are widely used within the pharmaceutical sciences, yet the molecular characteristics of these materials are frequently not stated. In this study, a range of characterization techniques is applied to five sodium alginate samples and the data compared, both between techniques and with the information obtained from the manufacturer. The mannuronic acid to guluronic acid (MG) ratio and the distribution of uronic acid residues of five sodium alginate samples have been measured using circular dichroism and NMR, with circular dichroism yielding MG ratios between 42.1 and 63.6%, depending on the grade of alginate used. The MG ratios obtained from NMR studies were in broad agreement with these values, and the technique also yielded information on the distribution of uronic acid residues within each batch; this was again found to vary considerably (NG > 1 values ranging from 6.9 to 17.5). It was noted that samples with similar MG ratios could have markedly different chain-distribution characteristics. The uronic acid ratio ranges obtained from the manufacturers were found to be in good agreement with those found experimentally. Intrinsic viscosity measurements were used to compare the molecular weights of the samples; values between approximately 12,000 and 180,000 were obtained for the different batches. The study has enabled comparison of different methods for characterization of sodium alginate samples, highlighting their relative merits and the possible protocols that might be adopted. A critical discussion is given of the individual and combined use of these techniques and the relevance of such studies to the rational design and quality control of alginate-based pharmaceutical systems.
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