Intramuscular delivery of DNA releasing microspheres: Microsphere properties and transgene expression

被引:38
作者
Jang, JH
Shea, LD
机构
[1] Univ Calif Berkeley, Dept Chem Engn, Berkeley, CA 94720 USA
[2] Northwestern Univ, Dept Biol & Chem Engn, Evanston, IL 60208 USA
[3] Northwestern Univ, Dept Biomed Engn, Evanston, IL 60208 USA
关键词
poly (lactide-co-glycolide); gene therapy; drug delivery; microspheres;
D O I
10.1016/j.jconrel.2006.01.013
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Plasmid-loaded microspheres can provide localized and sustained release into the target tissue, and thus have the potential to enhance the efficiency of naked DNA at promoting transgene expression. In this report, microsphere design parameters are investigated by correlating the extent and duration of transgene expression intramuscularly to the polymer molecular weight and the mass of DNA delivered. Plasmid DNA was incorporated into poly (lactide-co-glycolide) microspheres using a cryogenic double emulsion process, and microspheres were injected intramuscularly. Bolus injection of naked plasmid was used for control, which exhibited transfection of muscle cells with transgene expression that g radually decreased over time. Microspheres fabricated from low molecular weight polymer had expression levels that increased from day I to day 92, which subsequently decreased through day 174. Decreasing the microsphere mass delivered resulted in steady expression during the same time. However, microspheres fabricated with high molecular weight polymer had expression for only 14 days. Intramuscular injection resulted in a foreign body response to the microspheres, and these infiltrating cells adjacent were primarily transfected. This understanding of microsphere properties that determine transgene expression and the distribution of transfected cells may facilitate their application to fields such as tissue engineering or DNA vaccines. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:120 / 128
页数:9
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