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聚电解质复合物载硫酸皮肤素海藻酸钠复合微球用于组织再生的递送。

Delivery of dermatan sulfate from polyelectrolyte complex-containing alginate composite microspheres for tissue regeneration.

机构信息

Department of Pharmacy, Faculty of Health and Medical Sciences, University of Copenhagen , Universitetsparken 2, DK-2100, Copenhagen, Denmark.

出版信息

Biomacromolecules. 2012 Mar 12;13(3):905-17. doi: 10.1021/bm201821x. Epub 2012 Feb 28.

DOI:10.1021/bm201821x
PMID:22296594
Abstract

Dermatan sulfate (DS) is a glycosaminoglycan (GAG) with a great potential as a new therapeutic agent in tissue engineering. The aim of the present study was to investigate the formation of polyelectrolyte complexes (PECs) between chitosan and dermatan sulfate (CS/DS) and delivery of DS from PEC-containing alginate/chitosan/dermatan sulfate (Alg/CS/DS) microspheres for application in tissue regeneration. The CS/DS complexes were initially formed at different conditions including varying CS/DS ratio (positive/negative charge ratio), buffer, and pH. The obtained CS/DS complexes exhibited stronger electrostatic interaction, smaller complex size, and more stable colloidal structure when chitosan was in large excess (CS/DS 3:1) and prepared at pH 3.5 as compared to pH 5 using acetate buffer. The CS/DS complexes were subsequently incorporated into an alginate matrix by spray drying to form Alg/CS/DS composite microspheres with a DS encapsulation efficiency of 90-95%. The excessive CS induced a higher level of sustained DS release into Tris buffer (pH 7.4) from the microspheres formulated at pH 3.5; however, the amount of CS did not have a significant effect on the release from the microspheres formulated at pH 5. Significant cell proliferation was stimulated by the DS released from the microspheres in vitro. The present results provide a promising drug delivery strategy using PECs for sustained release of DS from microspheres intended for site-specific drug delivery and ultimately for use in tissue engineering.

摘要

硫酸皮肤素(DS)是一种具有巨大潜力的糖胺聚糖(GAG),可作为组织工程中的新型治疗剂。本研究旨在研究壳聚糖和硫酸皮肤素(CS/DS)之间形成聚电解质复合物(PEC),以及将 DS 从 PEC 含海藻酸盐/壳聚糖/硫酸皮肤素(Alg/CS/DS)微球中递送到体内,用于组织再生。CS/DS 复合物最初是在不同条件下形成的,包括不同的 CS/DS 比(正/负电荷比)、缓冲液和 pH 值。与使用醋酸盐缓冲液在 pH5 相比,当壳聚糖过量(CS/DS 3:1)并在 pH3.5 下制备时,所得 CS/DS 复合物表现出更强的静电相互作用、更小的复合物尺寸和更稳定的胶体结构。CS/DS 复合物随后通过喷雾干燥掺入海藻酸盐基质中,形成具有 90-95%DS 包封效率的 Alg/CS/DS 复合微球。过量的 CS 从在 pH3.5 下配制的微球中诱导 DS 以更高水平持续释放到 Tris 缓冲液(pH7.4)中;然而,CS 的量对在 pH5 下配制的微球的释放没有显著影响。DS 从微球中体外释放可显著刺激细胞增殖。本研究结果为使用 PEC 从微球中持续释放 DS 提供了一种有前途的药物输送策略,用于实现特定部位药物输送,并最终用于组织工程。

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