Davda Jasmine, Labhasetwar Vinod
Department of Pharmaceutical Sciences, College of Pharmacy, 986025 Nebraska Medical Center, Omaha, NE 68198-6025, USA.
Int J Pharm. 2002 Feb 21;233(1-2):51-9. doi: 10.1016/s0378-5173(01)00923-1.
Endothelium is an important target for drug or gene therapy because of its important role in the biological system. In this paper, we have characterized nanoparticle uptake by endothelial cells in cell culture. Nanoparticles were formulated using poly DL-lactide-co-glycolide polymer containing bovine serum albumin as a model protein and 6-coumarin as a fluorescent marker. It was observed that the cellular uptake of nanoparticles depends on the time of incubation and the concentration of nanoparticles in the medium. The uptake of nanoparticles was rapid with confocal microscopy demonstrating their localization mostly in the cytoplasm. The mitogenic study demonstrated biocompatability of nanoparticles with the cells. The study thus demonstrates that nanoparticles could be used for localizing therapeutic agents or gene into endothelial cells. Nanoparticles localized in the endothelium could provide prolonged drug effects because of their sustained release characterics, and also could protect the encapsulated agent from enzymatic degradation.
内皮细胞是药物或基因治疗的重要靶点,因为它在生物系统中发挥着重要作用。在本文中,我们对细胞培养中内皮细胞摄取纳米颗粒的情况进行了表征。纳米颗粒是用含有牛血清白蛋白作为模型蛋白和6-香豆素作为荧光标记的聚DL-丙交酯-乙交酯聚合物制备的。观察到纳米颗粒的细胞摄取取决于孵育时间和培养基中纳米颗粒的浓度。纳米颗粒的摄取很快,共聚焦显微镜显示它们大多定位在细胞质中。促有丝分裂研究证明了纳米颗粒与细胞的生物相容性。因此,该研究表明纳米颗粒可用于将治疗剂或基因定位到内皮细胞中。由于其缓释特性,定位在内皮细胞中的纳米颗粒可以提供延长的药物作用,并且还可以保护包封的药物免受酶降解。