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用于递送BMP-2质粒DNA的PLGA/HAp复合支架的制备与表征

Fabrication and characterization of PLGA/HAp composite scaffolds for delivery of BMP-2 plasmid DNA.

作者信息

Nie Hemin, Wang Chi-Hwa

机构信息

Department of Chemical and Biomolecular Engineering, National University of Singapore, Singapore, Singapore.

出版信息

J Control Release. 2007 Jul 16;120(1-2):111-21. doi: 10.1016/j.jconrel.2007.03.018. Epub 2007 Apr 1.

Abstract

The objective of this study is to construct complex of DNA and PLGA/HAp composite scaffold for bone tissue engineering. Naked DNA has low transfection efficiency so DNA loaded chitosan particles are used nowadays in gene delivery due to their high transfection efficiency, but unfortunately this is accompanied by strong immunological reaction of cells. In order to preserve the advantage of polymeric particles and reduce immunological effect at the same time, a new DNA release system is developed which makes possible sustained DNA release with negligible immunological effects. Poly (lactide-co-glycolide) (PLGA)/Hydroxylapatite (HAp) composite scaffolds with different HAp contents (0%, 5% and 10%) are fabricated by an electrospinning method and DNA is incorporated into the scaffolds in 3 ways (i.e. naked DNA, encapsulation of DNA/chitosan nanoparticles into scaffolds after fiber fabrication by dripping, and encapsulation of DNA/chitosan nanoparticles into scaffold by mixing with PLGA/HAp solution before fiber fabrication). All the scaffolds are characterized by SEM, XRD, DSC and GC-MS and the results show that the scaffolds are non-woven, nano- to micro-fibered membrane structures composed predominantly of PLGA with amorphous dispersion of HAp nanoparticles inside polymeric matrix. In vitro release tests were carried out on 9 different scaffolds to check the effects of HAp contents and the encapsulation ways of DNA on the release properties. These effects are also tested by human marrow stem cells (hMSCs) by comparing their cell attachment ability, cell viability and DNA transfection efficiency. It is demonstrated that the addition of HAp nanoparticles increased the release rate of DNA for both naked and encapsulated DNA. Cell culture experiments show that the scaffolds with encapsulated DNA/chitosan nanoparticles have higher cell attachment, higher cell viablility and desirable transfection efficiency of DNA. The observations show that DNA/chitosan nanoparticles encapsulated PLGA/HAp composite scaffold is promising for use in bone regeneration.

摘要

本研究的目的是构建用于骨组织工程的DNA与聚乳酸-羟基乙酸共聚物/羟基磷灰石(PLGA/HAp)复合支架。裸DNA的转染效率较低,因此由于壳聚糖颗粒具有较高的转染效率,目前在基因递送中使用负载DNA的壳聚糖颗粒,但不幸的是,这伴随着细胞强烈的免疫反应。为了保留聚合物颗粒的优势并同时降低免疫效应,开发了一种新的DNA释放系统,该系统能够实现DNA的持续释放,且免疫效应可忽略不计。通过静电纺丝法制备了具有不同HAp含量(0%、5%和10%)的聚(乳酸-乙醇酸)(PLGA)/羟基磷灰石(HAp)复合支架,并通过3种方式将DNA掺入支架中(即裸DNA、在纤维制备后通过滴注将DNA/壳聚糖纳米颗粒包封到支架中、以及在纤维制备前通过与PLGA/HAp溶液混合将DNA/壳聚糖纳米颗粒包封到支架中)。所有支架均通过扫描电子显微镜(SEM)、X射线衍射(XRD)、差示扫描量热法(DSC)和气相色谱-质谱联用仪(GC-MS)进行表征,结果表明,支架为非织造的纳米至微米纤维膜结构,主要由PLGA组成,HAp纳米颗粒以无定形形式分散在聚合物基质中。对9种不同的支架进行了体外释放试验,以检查HAp含量和DNA包封方式对释放性能的影响。还通过人骨髓干细胞(hMSCs)比较其细胞附着能力、细胞活力和DNA转染效率来测试这些影响。结果表明,添加HAp纳米颗粒可提高裸DNA和包封DNA的释放速率。细胞培养实验表明,包封有DNA/壳聚糖纳米颗粒的支架具有更高的细胞附着率、更高的细胞活力和理想的DNA转染效率。观察结果表明,包封有DNA/壳聚糖纳米颗粒的PLGA/HAp复合支架在骨再生方面具有应用前景。

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