Tianjin Neurological Institute, Tianjin Medical University General Hospital, China.
Int J Pharm. 2012 Sep 15;434(1-2):209-14. doi: 10.1016/j.ijpharm.2012.06.003. Epub 2012 Jun 9.
CADY-1 is an amphipathic peptide that possesses cell-penetrating activity. As an amphipathic peptide, CADY-1 is capable of forming complexes by self-assembly, and they are these complexes that possess cell-penetrating activity. This distinct characteristic of CADY-1 makes it a potent cell-penetrating drug delivery system. Doxorubicin is a widely used cytotoxic anti-cancer drug but is limited by its toxicity. Although the liposomal formulation of doxorubicin ameliorates its toxicity, its complicated synthesis remains an obstacle to its wide clinical use. In this study, our findings revealed that CADY-1 and doxorubicin form a stable complex at optimised molar ratios in a self-assembling manner. Formation of the complex extended the blood residence time of doxorubicin in a similar fashion to that of liposomal doxorubicin. In addition, the complex was capable of carrying doxorubicin across the cell membrane, which increased the therapeutic index of doxorubicin. Experimental animals treated with a CADY-1/doxorubicin complex exhibited better tolerance and anti-tumour activity than animals treated with either liposomal doxorubicin or the free form of doxorubicin. Collectively, the findings in this study support the advantages of using complexes formed by the self-assembled peptide CADY-1 and suggest that CADY-1 is a potent drug delivery system.
CADY-1 是一种具有穿膜活性的两亲肽。作为一种两亲肽,CADY-1 能够通过自组装形成复合物,正是这些复合物具有穿膜活性。CADY-1 的这一独特特性使其成为一种有效的穿膜药物递送系统。多柔比星是一种广泛应用的细胞毒性抗癌药物,但由于其毒性而受到限制。尽管多柔比星的脂质体制剂改善了其毒性,但复杂的合成仍然是其广泛临床应用的障碍。在本研究中,我们的发现表明 CADY-1 和多柔比星以自组装的方式在优化的摩尔比下形成稳定的复合物。该复合物的形成以类似于脂质体多柔比星的方式延长了多柔比星在血液中的停留时间。此外,该复合物能够携带多柔比星穿过细胞膜,从而提高多柔比星的治疗指数。用 CADY-1/多柔比星复合物治疗的实验动物比用脂质体多柔比星或游离多柔比星治疗的动物表现出更好的耐受性和抗肿瘤活性。总之,本研究的结果支持使用自组装肽 CADY-1 形成的复合物的优势,并表明 CADY-1 是一种有效的药物递送系统。