淀粉与纤维素协同加工制备新型药用赋形剂的物理性质及应用研究。

IF 4.8 3区 医学 Q2 CHEMISTRY, MEDICINAL
Pharmaceuticals Pub Date : 2025-09-17 DOI:10.3390/ph18091389
Yong Bi, Hanfang Lei, Ying Fang, Simeng Wang, Jihui Tang
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引用次数: 0

摘要

目的:研究预糊化淀粉(PS)与微晶纤维素(MCC)在不同配比下的结构特征、粉体特性及其性能变化。方法:采用扫描电镜(SEM)观察MCC在PS基质内的包埋。傅里叶变换红外光谱(FTIR)和x射线衍射(XRD)分析表明,淀粉与MCC在加工过程中没有化学相互作用。通过多种指标(如卡尔指数)评估共加工材料的物理性能,并通过多种指标(如抗拉强度和稀释能力)评估其在制药应用中的性能。结果:FTIR/XRD分析证实,在共加工过程中没有出现新的化学物质,再加上SEM证据表明MCC-PS结构具有物理互锁,最终表明结构重组是通过物理机制发生的。MCC比例的增加提高了共加工材料的抗拉强度,同时降低了卡尔指数、粒径、抽头密度、堆积密度、溶胀和水溶性含量。选择共处理样品(PS:MCC = 7:3)用于配方中。与物理混合物相比,共处理材料具有更好的压实性,并且在压实性较差的模型药物(包括利萘欣和灵栀孢子粉)中具有良好的稀释能力,并且具有更高的生物惰性。结论:PS和MCC共处理具有良好的压实性和稀释能力。该共加工赋形剂证明了在口服固体剂型(例如片剂)的直接压缩生产中的适用性,为高载药量制剂提供了明显的优势。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Study on the Physical Properties and Application of a Novel Pharmaceutical Excipient Made from Starch and Cellulose Co-Processing.

Objective: This article investigated the structural characteristics, powder properties, and performance variations of co-processed pregelatinized starch (PS) and microcrystalline cellulose (MCC) at varying ratios. Methods: Scanning Electron Microscopy (SEM) revealed the embedding of MCC within the PS matrix. Fourier-transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD) analysis indicated no chemical interaction between the starch and MCC during processing. The physical properties of the co-processed materials were evaluated using multiple indicators, such as the Carr index, and their properties in pharmaceutical applications were evaluated using multiple indicators, such as tensile strength and dilution capacity. Results:The absence of new chemical substances during co-processing, as confirmed by FTIR/XRD analyses, coupled with SEM evidence of a physically interlocked MCC-PS architecture, conclusively demonstrates that structural reorganization occurred via physical mechanisms.An increase in the MCC proportion enhanced the tensile strength of the co-processed material while decreasing the Carr's index, particle size, tapped density, bulk density, swelling, and water-soluble content. A co-processed sample (PS:MCC = 7:3) was selected for application in formulations. The co-processed material exhibited superior compactibility compared to a physical mixture and demonstrated favorable dilution capacity in poorly compactible model drugs, including Linaoxin and Lingzhi spore powder, as well as higher biological inertness. Conclusions: These findings suggest that the co-processed PS and MCC possess excellent compactibility and dilution capacity. The co-processed excipient demonstrates applicability in direct compression manufacturing of oral solid dosage forms (e.g., tablets), offering distinct advantages for high drug-loading formulations.

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来源期刊
Pharmaceuticals
Pharmaceuticals Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
6.10
自引率
4.30%
发文量
1332
审稿时长
6 weeks
期刊介绍: Pharmaceuticals (ISSN 1424-8247) is an international scientific journal of medicinal chemistry and related drug sciences.Our aim is to publish updated reviews as well as research articles with comprehensive theoretical and experimental details. Short communications are also accepted; therefore, there is no restriction on the maximum length of the papers.
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