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交联冷冻干燥明胶基质的特性和扫描电子显微镜研究及其药物扩散和释放动力学研究。

Characterization and scanning electron microscopic investigation of crosslinked freeze dried gelatin matrices for study of drug diffusivity and release kinetics.

机构信息

School of Medical Science and Technology, Indian Institute of Technology Kharagpur, Kharagpur 721302, India.

出版信息

Micron. 2012 Feb;43(2-3):311-20. doi: 10.1016/j.micron.2011.09.007. Epub 2011 Oct 13.

Abstract

Drug delivery is a promising technique to enhance the therapeutic efficacy of the drug. However, properties of carrier materials require intense improvement for effective transport of drug molecules. In the current study, attempts have been made to develop freeze dried gelatin matrices cross linked with genipin at various temperatures (5°C, 15°C and 25°C) prior to freeze-drying (-80°C). The freeze dried matrices thus obtained at the said temperatures are characterized for crosslinking density, compression strength, swelling behaviors. The matrix crosslinked at 25°C showed highest Flory-Rehner crosslinking density (467 ± 46) (p<0.05), highest compressive strength (12.36 ± 0.12) (p<0.05) and lowest equilibrium water content. In this context, scanning electron microscopy (SEM) was performed to study the surface morphology (size and shape of pores) of the crosslinked matrices. These images were further processed for quantitative analysis of morphological features, viz., areas, radius, ferret diameter, length of major and minor axis and eccentricity using MATLAB toolboxes. These quantitative analyses correlate transport and the release kinetics of model anti-inflammatory drug (indomethacin) from crosslinked matrices in vitro to tune as a controllable delivery system. The diffusional exponent (n) for all constructs ranging from 0.61 to 0.69 (p<0.05) (0.45<n<0.89) indicated non-Fickian release kinetics.

摘要

药物传递是一种有前途的技术,可以提高药物的治疗效果。然而,载体材料的性质需要得到极大的改善,才能有效输送药物分子。在目前的研究中,尝试在冷冻干燥(-80°C)之前,用京尼平在不同温度(5°C、15°C 和 25°C)交联各种冷冻干燥明胶基质。在所述温度下获得的冻干基质的交联密度、压缩强度和溶胀行为。在 25°C 交联的基质表现出最高的 Flory-Rehner 交联密度(467±46)(p<0.05)、最高的压缩强度(12.36±0.12)(p<0.05)和最低的平衡含水量。在这种情况下,进行扫描电子显微镜(SEM)以研究交联基质的表面形态(孔的大小和形状)。使用 MATLAB 工具箱对这些图像进行进一步处理,以定量分析形态特征,即面积、半径、福雷特直径、长轴和短轴的长度以及偏心度。这些定量分析将交联基质中模型抗炎药物(吲哚美辛)的体外传输和释放动力学相关联,以将其调谐为可控的递药系统。所有构建体的扩散指数(n)在 0.61 到 0.69 之间(p<0.05)(0.45<n<0.89),表明非菲克扩散释放动力学。

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