Podsiadlo Paul, Sinani Vladimir A, Bahng Joong Hwan, Kam Nadine Wong Shi, Lee Jungwoo, Kotov Nicholas A
Departments of Chemical Engineering, University of Michigan, Ann Arbor, Michigan 48109, USA.
Langmuir. 2008 Jan 15;24(2):568-74. doi: 10.1021/la702782k. Epub 2007 Dec 5.
6-mercaptopurine and its riboside derivatives are some of the most widely utilized anti-leukemic and anti-inflammatory drugs. Their short biological half-life and severe side effects limit their use. A new delivery method for these drugs based on 4-5 nm gold nanoparticles can potentially resolve these issues. We have found substantial enhancement of the antiproliferative effect against K-562 leukemia cells of Au nanoparticles bearing 6-mercaptopurine-9-beta-d-ribofuranoside compared to the same drug in typically administered free form. The improvement was attributed to enhanced intracellular transport followed by the subsequent release in lysosomes. Enhanced activity and nanoparticle carriers will make possible the reduction of the overall concentration of the drug, renal clearance, and, thus, side effects. The nanoparticles with mercaptopurine also showed excellent stability over 1 year without loss of inhibitory activity.
6-巯基嘌呤及其核糖苷衍生物是一些应用最为广泛的抗白血病和抗炎药物。它们较短的生物半衰期和严重的副作用限制了其使用。一种基于4-5纳米金纳米颗粒的这些药物新递送方法有可能解决这些问题。我们发现,与通常以游离形式给药的相同药物相比,负载6-巯基嘌呤-9-β-D-呋喃核糖苷的金纳米颗粒对K-562白血病细胞的抗增殖作用有显著增强。这种改善归因于细胞内转运增强,随后在溶酶体中释放。增强的活性和纳米颗粒载体将有可能降低药物的总体浓度、肾清除率,从而减少副作用。含有巯基嘌呤的纳米颗粒在1年多的时间里也表现出优异的稳定性,且没有丧失抑制活性。