可溶性马铃薯淀粉对非常规象脚山药淀粉预糊化性能的影响。

Riya Banerjee, K. Jayaram Kumar
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摘要

近年来,研究人员一直在探索替代淀粉给药的来源。传统的选择,如玉米、土豆和大米淀粉已被广泛使用,但对可持续性的担忧促使了对非常规淀粉的研究。象脚山药淀粉来源于一种农业聚合物,由于其广泛的可用性而受到欢迎。淀粉从根本上不适合大多数应用;它们必须经过物理和/或化学改变,以最大限度地发挥其优势和/或减少其缺点。由于化学毒性,淀粉改性通常采用廉价的物理技术。本研究旨在评价象脚山药淀粉对马铃薯淀粉理化性质和给药性能的影响。预糊化是一个关键的过程,通过傅里叶变换红外光谱分析证实,预糊化可以增加直链淀粉的含量,改善淀粉的流动特性。场发射扫描电镜图像显示改性后淀粉颗粒结构完全破坏。用预糊化淀粉混合制成的片剂与单独用预糊化淀粉制成的片剂相比,药物释放速度较慢。值得注意的是,在混合物中加入马铃薯淀粉会导致更持久的药物释放。因此,变性淀粉在提高难溶性药物的溶解度方面有多种应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Effect of Soluble Potato Starch on the Pregelatinization Properties of Non‐Conventional Elephant Foot Yam Starch.
Abstract In recent years, researchers have been exploring alternative sources of starch for drug delivery. Traditional options like corn, potato, and rice starches have been widely used, but sustainability concerns have prompted the investigation of nonconventional starches. Elephant foot yam starch, derived from an agricultural polymer, has gained popularity due to its wide availability. Starches are fundamentally unsuited for the majority of applications; they must be physically and/or chemically altered to maximize their advantages and/or minimize their drawbacks. Due to the chemical toxicity, starch modification is often done using physical techniques that are inexpensive. This study aims to evaluate the impact of elephant foot yam starch on the physicochemical properties and drug delivery of potato starch. Pregelatinization, a crucial process, is found to increase amylose content and improves starch flow properties, as confirmed by Fourier‐transform infrared spectroscopy analysis showing gelatinization in the mixture. Field emission scanning electron microscopy images reveal complete disruption of the starch granular structure after modification. Tablets made with a mixture of pregelatinized starches exhibit a slower drug release compared to those with pregelatinized starch alone. Notably, inclusion of potato starch in the mixture results in a more sustained drug release. Hence, modified starches have diverse applications for enhancing solubility of poorly soluble drugs.
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