Gullotti Emily, Yeo Yoon
Weldon School of Biomedical Engineering, Purdue University, 206 South Martin Jischke Drive, West Lafayette, Indiana 47907, USA.
Mol Pharm. 2009 Jul-Aug;6(4):1041-51. doi: 10.1021/mp900090z.
One of the main goals of nanomedicine is to develop a nanocarrier that can selectively deliver anticancer drugs to the targeted tumors. Extensive efforts have resulted in several tumor-targeted nanocarriers, some of which are approved for clinical use. Most nanocarriers achieve tumor-selective accumulation through the enhanced permeability and retention effect. Targeting molecules such as antibodies, peptides, ligands, or nucleic acids attached to the nanocarriers further enhance their recognition and internalization by the target tissues. While both the stealth and targeting features are important for effective and selective drug delivery to the tumors, achieving both features simultaneously is often found to be difficult. Some of the recent targeting strategies have the potential to overcome this challenge. These strategies utilize the unique extracellular environment of tumors to change the long-circulating nanocarriers to release the drug or interact with cells in a tumor-specific manner. This review discusses the new targeting strategies with recent examples, which utilize the environmental stimuli to activate the nanocarriers. Traditional strategies for tumor-targeted nanocarriers are briefly discussed with an emphasis on their achievements and challenges.
纳米医学的主要目标之一是开发一种能够将抗癌药物选择性地递送至靶向肿瘤的纳米载体。经过大量努力,已经产生了几种肿瘤靶向纳米载体,其中一些已被批准用于临床。大多数纳米载体通过增强的渗透和滞留效应实现肿瘤选择性积累。附着在纳米载体上的靶向分子,如抗体、肽、配体或核酸,进一步增强了它们被靶组织识别和内化的能力。虽然隐身和靶向特性对于有效且选择性地将药物递送至肿瘤都很重要,但通常发现同时实现这两个特性很困难。一些最近的靶向策略有潜力克服这一挑战。这些策略利用肿瘤独特的细胞外环境,使长效循环纳米载体以肿瘤特异性方式释放药物或与细胞相互作用。本综述通过近期实例讨论了利用环境刺激激活纳米载体的新靶向策略。还简要讨论了肿瘤靶向纳米载体的传统策略,重点介绍了它们的成就和挑战。