Li Jingjing, Zhang Xuemei, Wang Meng, Li Xuejuan, Mu Hongjie, Wang Aiping, Liu Wanhui, Li Youxin, Wu Zimei, Sun Kaoxiang
School of Pharmacy, Collaborative Innovation Center of Advanced Drug Delivery System and Biotech Drugs in Universities of Shandong, Key Laboratory of Molecular Pharmacology and Drug Evaluation (Yantai University), Ministry of Education, Yantai University, Yantai 264005, PR China.
School of Pharmacy, Collaborative Innovation Center of Advanced Drug Delivery System and Biotech Drugs in Universities of Shandong, Key Laboratory of Molecular Pharmacology and Drug Evaluation (Yantai University), Ministry of Education, Yantai University, Yantai 264005, PR China; Luye Pharmaceutical Co., Ltd., Shandong Province, PR China.
Int J Pharm. 2016 Mar 30;501(1-2):112-23. doi: 10.1016/j.ijpharm.2016.01.068. Epub 2016 Jan 29.
The dual-ligand dendritic polyamidoamine-(polyethylene glycol)n-cyclic RGDyC peptide-(TAT peptide) (PPnR(T)) with various supplied molar ratios of polyethylene glycol (PEG) to polyamidoamine (PAMAM) (n=5, 15, 30) were designed as drug-carriers for the treatment of neovascular diseases; their targeting and penetrating effects were subsequently evaluated. (1)H NMR demonstrated PPnR(T) was successfully synthesized. Compared with the unmodified PAMAM, in vitro cytotoxicity of PPnR(T) to αvβ3 negative cells (αvβ3-) was significantly reduced, whereas the lethality to pathologic neovascular endothelial cells (αvβ3+) was efficiently increased compared to PPn. Compared to PP5R(T) and PP15R(T), PP30R(T) exhibited the most selective and efficient cellular uptake by human umbilical vein endothelial cells (HUVECs, αvβ3+). Membrane interaction study indicated the cellular uptake process of PP30R(T) of HUVECs mainly involved specific RGD-αvβ3 recognition as well as electrostatic interactions. Intracellular localization results confirmed PP30R(T) was distributed in the cytoplasm in HUVECs. 3D tumor spheroids penetration studies demonstrated that PP30R(T) penetrated the A549 cells to reach the depths of the avascular tumor spheroids. In vivo imaging further demonstrated that PP30R(T) achieved profoundly improved distribution in tumor tissues where angiogenesis existed. Therefore, the bi-functional dendrimer PP30R(T) displayed great potential as a nano-carrier for targeted drug delivery both in vitro and in vivo, and had broad prospects as nanocarriers for the targeted treatment of neovascular diseases.
设计了具有不同聚乙二醇(PEG)与聚酰胺-胺(PAMAM)摩尔比(n = 5、15、30)的双配体树枝状聚酰胺-胺-(聚乙二醇)n-环RGDyC肽-(TAT肽)(PPnR(T))作为治疗新生血管疾病的药物载体;随后评估了它们的靶向和穿透效果。核磁共振氢谱(1H NMR)表明PPnR(T)已成功合成。与未修饰的PAMAM相比,PPnR(T)对αvβ3阴性细胞(αvβ3-)的体外细胞毒性显著降低,而与PPn相比,对病理性新生血管内皮细胞(αvβ3+)的杀伤力有效增加。与PP5R(T)和PP15R(T)相比,PP30R(T)在人脐静脉内皮细胞(HUVECs,αvβ3+)中表现出最具选择性和高效的细胞摄取。膜相互作用研究表明,HUVECs对PP30R(T)的细胞摄取过程主要涉及特异性RGD-αvβ3识别以及静电相互作用。细胞内定位结果证实PP30R(T)分布于人脐静脉内皮细胞的细胞质中。三维肿瘤球体穿透研究表明,PP30R(T)穿透A549细胞,到达无血管肿瘤球体的深度。体内成像进一步表明,PP30R(T)在存在血管生成的肿瘤组织中的分布有显著改善。因此,双功能树枝状大分子PP30R(T)在体外和体内作为靶向药物递送的纳米载体都显示出巨大潜力,作为新生血管疾病靶向治疗的纳米载体具有广阔前景。