Department of Pharmacy, Faculty of Health and Medical Sciences, University of Copenhagen , Universitetsparken 2, DK-2100, Copenhagen, Denmark.
Biomacromolecules. 2012 Mar 12;13(3):905-17. doi: 10.1021/bm201821x. Epub 2012 Feb 28.
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.
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。