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粒径和抗酸剂对质粒DNA从均匀聚乳酸-羟基乙酸共聚物微球中的释放及稳定性的影响

Influence of particle size and antacid on release and stability of plasmid DNA from uniform PLGA microspheres.

作者信息

Varde Neelesh K, Pack Daniel W

机构信息

Department of Chemical and Biomolecular Engineering, University of Illinois, 600 S. Mathews Ave, Urbana, IL 61801 USA.

出版信息

J Control Release. 2007 Dec 20;124(3):172-80. doi: 10.1016/j.jconrel.2007.09.005. Epub 2007 Sep 21.

Abstract

PLGA microspheres are attractive DNA delivery vehicles due to their controlled release capabilities. One major problem with PLGA microspheres is that they develop an acidic microclimate as the polymer degrades, lowering the intraparticle pH, and potentially damaging the DNA. Antacids have recently shown promise in buffering this acidic microclimate and enhancing protein stability. We manufactured uniform plasmid DNA-encapsulating PLGA microspheres of two sizes (47, 80 microm diameter) and antacid concentrations (0, 3% Mg(OH)2). Microspheres with antacid had a homogeneous surface coverage of small pores, which resulted in a significant reduction of the burst effect. The 47 microm microspheres exhibited complete release of plasmid DNA over the course of two months. Incomplete release was observed from 80 microm spheres, though microspheres with 3% Mg(OH)2 showed a higher cumulative release, suggesting that the antacid at least partially aids in increasing the stability of DNA. SEM was used to visualize the surface pore evolution and cross-sectional microsphere structure over time. Subsequent image analysis was used to quantify the increase of surface pore sizes. Cross-sectional images showed increasing internal degradation and erosion, which resulted in a hollowing-out of microspheres. Our studies show that the incorporation of antacid into the microsphere structure has potential in addressing some of the major problems associated with DNA encapsulation and release in PLGA microspheres.

摘要

聚乳酸-羟基乙酸共聚物(PLGA)微球因其控释能力而成为有吸引力的DNA递送载体。PLGA微球的一个主要问题是,随着聚合物降解,它们会形成酸性微环境,降低颗粒内pH值,并可能损坏DNA。抗酸剂最近在缓冲这种酸性微环境和提高蛋白质稳定性方面显示出前景。我们制备了两种尺寸(直径47、80微米)和抗酸剂浓度(0、3%氢氧化镁)的均匀包裹质粒DNA的PLGA微球。含有抗酸剂的微球表面有均匀覆盖的小孔,这导致突释效应显著降低。47微米的微球在两个月内实现了质粒DNA的完全释放。80微米的微球观察到不完全释放,不过含有3%氢氧化镁的微球显示出更高的累积释放率,这表明抗酸剂至少部分有助于提高DNA的稳定性。使用扫描电子显微镜(SEM)观察表面孔隙随时间的演变以及微球的横截面结构。随后的图像分析用于量化表面孔径的增加。横截面图像显示内部降解和侵蚀增加,导致微球中空。我们的研究表明,将抗酸剂纳入微球结构在解决与PLGA微球中DNA包封和释放相关的一些主要问题方面具有潜力。

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