Department of Pharmacy and Pharmaceutical Technology, Faculty of Pharmacy, University of Granada, Spain.
Curr Drug Targets. 2011 Jul 1;12(8):1151-65. doi: 10.2174/138945011795906570.
It is a fact that chemotherapy agents have little specificity for cancer cells, this leading to low concentrations into the tumor interstititum and severe side effects on healthy tissues. The formulation of lipid-based nanomedicines against cancer has been hypothesized to improve drug localization into the tumor tissue and to increase the anticancer efficacy of concentional drugs, while minimizing their systemic adverse effects. In this review, special attention is devoted to the analysis of the state-of-the-art in the development of lipid-based drug carriers against cancer. Specifically, the most significant in vitro and in vivo results on the use of niosomes, liposomes, and solid lipid nanoparticles are revised. It is concluded that biodistribution profiles of chemotherapy agents can be controlled by their loading to such nanoplatforms. Lipid-based nanomedicines offer an interesting approach to the delivery of anticancer drugs to brain tumors, and to reverse multi-drug resistance of cancer cells. Finally, a deep evaluation of the applicability of drug delivery strategies in the formulation of lipid-based nanoplatforms is carried out. They involve active drug targeting (including ligand-mediated delivery, and stimuli-sensitive carriers), and passive drug targeting (through the enhanced permeability and retention effect) to tumors.
事实上,化疗药物对癌细胞的特异性很小,这导致药物在肿瘤间质中的浓度较低,并对健康组织产生严重的副作用。针对癌症的基于脂质的纳米药物的制剂被假设可以改善药物在肿瘤组织中的定位,并提高常规药物的抗癌疗效,同时最小化其全身不良反应。在这篇综述中,特别关注分析针对癌症的基于脂质的药物载体的最新进展。具体来说,对使用囊泡、脂质体和固体脂质纳米粒的最显著的体外和体内结果进行了修订。结论是,通过将化疗药物负载到这些纳米平台上,可以控制其生物分布特征。基于脂质的纳米药物为将抗癌药物递送到脑肿瘤以及逆转癌细胞的多药耐药性提供了一种有趣的方法。最后,对基于脂质的纳米平台制剂中药物传递策略的适用性进行了深入评估。它们涉及主动药物靶向(包括配体介导的递药和刺激敏感载体)和被动药物靶向(通过增强的通透性和保留效应)到肿瘤。