Improving antiangiogenesis and anti-tumor activity of curcumin by biodegradable polymeric micelles
- Authors
- Gong, C., Deng, S., Wu, Q., Xiang, M., Wei, X., Li, L., Gao, X., Wang, B., Sun, L., Chen, Y., Li, Y., Liu, L., Qian, Z., and Wei, Y.
- ID
- ZDB-PUB-121205-28
- Date
- 2013
- Source
- Biomaterials 34(4): 1413-1432 (Journal)
- Registered Authors
- Keywords
- curcumin, micelles, biodegradable, polymer, tumor, antiangiogenesis
- MeSH Terms
-
- Absorbable Implants*
- Angiogenesis Inhibitors/administration & dosage
- Animals
- Antineoplastic Agents/administration & dosage
- Antineoplastic Agents/chemistry
- Cell Line, Tumor
- Curcumin/administration & dosage*
- Curcumin/chemistry*
- Metabolic Clearance Rate
- Mice
- Mice, Inbred C57BL
- Micelles
- Nanocapsules/administration & dosage*
- Nanocapsules/chemistry
- Neoplasms, Experimental/drug therapy*
- Neoplasms, Experimental/pathology
- Neovascularization, Pathologic/drug therapy*
- Neovascularization, Pathologic/pathology
- Tissue Distribution
- Treatment Outcome
- PubMed
- 23164423 Full text @ Biomaterials
For developing aqueous formulation and improving anti-tumor activity of curcumin (Cur), we prepared Cur encapsulated MPEG-PCL micelles by solid dispersion method without using any surfactants or toxic organic solvent. Cur micelles could be lyophilized into powder form without any cryoprotector or excipient, and the re-dissolved Cur micelles are homogenous and stable. Molecular modeling study suggested that Cur tended to interact with PCL serving as a core embraced by PEG as a shell. After Cur was encapsulated into polymeric micelles, cytotoxicity and cellular uptake were both increased. Cur micelles had a stronger inhibitory effect on proliferation, migration, invasion, and tube formation of HUVECs than free Cur. Besides, Cur micelles showed a sustained in vitro release behavior and slow extravasation from blood vessels in transgenic zebrafish model. Embryonic angiogenesis and tumor-induced angiogenesis were both dramatically inhibited by Cur micelles in transgenic zebrafish model. Furthermore, Cur micelles were more effective in inhibiting tumor growth and prolonged survival in both subcutaneous and pulmonary metastatic LL/2 tumor models. In pharmacokinetic and tissue distribution studies, Cur micelles showed higher concentration and longer retention time in plasma and tumors. Our findings suggested that Cur micelles may have promising applications in pulmonary carcinoma therapy.