Department of Materials Science and Engineering, National Chiao Tung University, 1001 Ta-Hseuh Road, Hsinchu City, 300 Taiwan, ROC.
J Control Release. 2012 Aug 10;161(3):942-8. doi: 10.1016/j.jconrel.2012.05.038. Epub 2012 May 28.
Thermo-gelling injectable nanogels, with no burst release of loaded drug, were prepared by a simple route by combining self assembled nanocapsules of amphiphilically modified chitosan with glycerophosphate di-sodium salt and glycerol. The potential as a depot drug delivery system was demonstrated in vivo through the therapeutic effect of ethosuximide (ESM) loaded nanogels, suppressing spike wave discharges (SWDs) in Long Evan rat model. Simultaneously clearance of gels from the site of administration was monitored non-invasively using MRI. The gel structure was characterized using TEM and SEM, confirming the gels to be an assembly of nanocapsules and using two-photon microscopy to visualize the network structure. In vitro drug release studies using ESM revealed that the nanogels exhibited extended, mostly Fickian release. Finally, all investigated formulations displayed excellent cytotoxicity data determined by MTT assay using human retinal pigmented epithelium cells. All presented properties are highly desirable for injectable depot gels for drug delivery.
温敏型注射纳米凝胶,所载药物无突释现象,通过将两亲性改性壳聚糖纳米胶囊与甘油磷酸二钠和甘油结合,采用简单的方法制备。通过负载乙琥胺(ESM)纳米凝胶在长牡蛎大鼠模型中的治疗效果,证明了其作为储库药物递送系统的潜力,抑制棘波放电(SWD)。同时,使用 MRI 非侵入性地监测从给药部位清除凝胶。使用 TEM 和 SEM 对凝胶结构进行了表征,证实了凝胶是纳米胶囊的组装体,并使用双光子显微镜可视化网络结构。使用 ESM 进行的体外药物释放研究表明,纳米凝胶表现出延长的、主要是菲克扩散释放。最后,所有研究的制剂在使用人视网膜色素上皮细胞的 MTT 测定法确定细胞毒性数据时都表现出优异的结果。所有呈现的性质对于用于药物递送的可注射储库凝胶都是非常理想的。