Kimura H, Ogura Y, Moritera T, Honda Y, Tabata Y, Ikada Y
Department of Ophthalmology, Faculty of Medicine, Kyoto University, Japan.
Curr Eye Res. 1994 May;13(5):353-60. doi: 10.3109/02713689409167299.
We investigated phagocytosis of biodegradable microspheres containing a drug by retinal pigment epithelial (RPE) cells and drug release within the cells to evaluate the potential usefulness of microspheres for intracellular drug delivery. The biodegradable polymers used were L-lactic acid, and DL-lactic acid with different molecular weights or the copolymers of different monomer compositions. The microspheres containing a non-bioactive fluorescent dye (rhodamine 6GX) as a model drug, were prepared by a solvent evaporation method. The in vitro release of the dye from the microspheres was examined. Phagocytosis of the microspheres by RPE cells was conducted to evaluate the extent of phagocytosis by phase-contrast microscopy and transmission electron microscopy. The RPE cells ingesting the microspheres at different stages were examined by fluorescent microscopy to estimate the intracellular release of the dye. The dye was released with time from every microsphere and the release was controlled by changing the type of polymers constituting microspheres. The microspheres containing the dye were phagocytosed by RPE cells and the dye was released intracellularly with time. The present study indicates that the drug incorporated in the microspheres was delivered into RPE cells by way of phagocytosis and released within the cells. It is concluded that this microsphere system is a promising delivery form capable of drug targeting to RPE cells.
我们研究了视网膜色素上皮(RPE)细胞对含有药物的可生物降解微球的吞噬作用以及细胞内的药物释放情况,以评估微球用于细胞内药物递送的潜在实用性。所使用的可生物降解聚合物为L-乳酸、不同分子量的DL-乳酸或不同单体组成的共聚物。通过溶剂蒸发法制备了含有非生物活性荧光染料(罗丹明6GX)作为模型药物的微球。检测了染料从微球中的体外释放情况。通过相差显微镜和透射电子显微镜对RPE细胞对微球的吞噬作用进行评估,以确定吞噬程度。通过荧光显微镜检查在不同阶段摄取微球的RPE细胞,以估计染料在细胞内的释放情况。染料随时间从每个微球中释放出来,并且通过改变构成微球的聚合物类型来控制释放。含有染料的微球被RPE细胞吞噬,并且染料随时间在细胞内释放。本研究表明,微球中所含的药物通过吞噬作用被递送至RPE细胞并在细胞内释放。得出的结论是,这种微球系统是一种有前景的递送形式,能够将药物靶向递送至RPE细胞。