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西谷椰种子缓释改性淀粉的合成、表征及评价。

Synthesis, characterization and evaluation of release retardant modified starches of Lagenaria siceraria seeds.

机构信息

Department of Pharmaceutical Sciences, Birla Institute of technology, Mesra, Ranchi, 835215, India.

出版信息

Int J Biol Macromol. 2013 Oct;61:396-403. doi: 10.1016/j.ijbiomac.2013.07.027. Epub 2013 Aug 3.

Abstract

Starch isolated from under-utilized seeds of five different cultivars of Lagenaria siceraria (Mol.) standley (Cucurbitaceae) was carboxymethylated. The influence of the degree of substitution (DS) on physicochemical properties and drug release properties of starches was studied. The physicochemical profiles of the derivatives were assessed by means of FT-IR, XRD, SEM, elemental analysis, reaction efficiency, water binding capacity, swelling power, powder characteristics and visual estimation. The highest values of the DS obtained when the carboxymethylation was performed at 45 °C for 4h. Scanning electron microscopy (SEM) showed that after carboxymethylation, the granular appearance of the native starch was distorted. The new bands at 1576.87 cm(-1) and 1423.81 cm(-1) in Fourier transform infrared (FT-IR) indicated that the starch granules were substituted. Wide-angle X-ray diffractometry revealed that crystallinity was reduced significantly after carboxymethylation. Powder studies revealed that these starches possess potential for pharmaceutical applications. The matrix tablets were found to release the drug by Korsmeyer and Peppas kinetics. The carboxymethylated starches with high DS can be used as a drug release retardant in sustained release formulations, as the drug dissolution rate of native starches was significantly lower than the modified starches.

摘要

从五种不同品种的 Lagenaria siceraria(葫芦科)未充分利用的种子中分离出的淀粉进行了羧甲基化。研究了取代度(DS)对淀粉理化性质和药物释放性质的影响。通过傅里叶变换红外光谱(FT-IR)、X 射线衍射(XRD)、扫描电子显微镜(SEM)、元素分析、反应效率、结合水能力、溶胀能力、粉末特性和直观评估来评估衍生物的物理化学特征。当羧甲基化在 45°C 下进行 4 小时时,获得了最高的 DS 值。扫描电子显微镜(SEM)表明,羧甲基化后,天然淀粉的颗粒外观发生了变形。傅里叶变换红外光谱(FT-IR)中 1576.87 cm(-1) 和 1423.81 cm(-1)处的新带表明淀粉颗粒被取代。广角 X 射线衍射表明,羧甲基化后结晶度显著降低。粉末研究表明,这些淀粉具有药物应用的潜力。发现这些基质片剂通过 Korsmeyer 和 Peppas 动力学释放药物。具有高 DS 的羧甲基化淀粉可用作缓释制剂中的药物释放阻滞剂,因为天然淀粉的药物溶解速率明显低于改性淀粉。

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