Bender A, Schfer V, Steffan A M, Royer C, Kreuter J, Rübsamen-Waigmann H, von Briesen H
Institut für Pharmazeutische Technologie d. J.W. Goethe-Universität, Frankfurt am Main, Germany.
Res Virol. 1994 May-Aug;145(3-4):215-20. doi: 10.1016/s0923-2516(07)80025-2.
Nanoparticles are known to accumulate in the phagocytic cells of the mononuclear phagocyte system. Therefore, the use of this carrier system for the targeting of antiviral drugs to monocytes/macrophages (MO/MAC) is an attractive concept in the treatment of diseases involving MO/MAC, e.g. infection with HIV. In this study, the ability of macrophages isolated from peripheral blood of healthy blood donors to phagocytose and metabolize human serum albumin microspheres was investigated by transmission electron microscopy. Furthermore, nanoparticles manufactured using human serum albumin or polyhexylcyanoacrylate were loaded with nucleoside analogues (AZT and ddC) and tested for their ability to prevent HIV infection in MO/MAC cultures. Our results demonstrate the effectiveness of this drug-targeting system to one of the major target cells for HIV.
众所周知,纳米颗粒会在单核吞噬细胞系统的吞噬细胞中蓄积。因此,将这种载体系统用于将抗病毒药物靶向单核细胞/巨噬细胞(MO/MAC),在治疗涉及MO/MAC的疾病(如感染HIV)方面是一个有吸引力的概念。在本研究中,通过透射电子显微镜研究了从健康献血者外周血中分离出的巨噬细胞吞噬和代谢人血清白蛋白微球的能力。此外,用人血清白蛋白或聚己基氰基丙烯酸酯制造的纳米颗粒负载核苷类似物(齐多夫定和双脱氧胞苷),并测试其在MO/MAC培养物中预防HIV感染的能力。我们的结果证明了这种药物靶向系统对HIV的主要靶细胞之一的有效性。