- Author:
Li-Peng QIU
1
Author Information
- Publication Type:Journal Article
- Keywords: Copolymer micelle; Doxorubicin; Hyaluronic acid; Terminal modification
- From: Chinese Pharmaceutical Journal 2015;50(22):1973-1978
- CountryChina
- Language:Chinese
- Abstract: OBJECTIVE: To synthesize hyaluronic acid-octadecene (HOY) copolymers by terminal thiolation modification of hyaluronic acid (HA), prepare doxorubicin-loaded micelles and investigate its pharmaceutical characteristics. METHODS: HOY copolymers were synthesized through Michael addition reaction. The doxorubicin-loaded copolymer micelles were prepared with ultrasonic method, then the particle size, Zeta potential, encapsulation efficiency, drug loading efficiency and in vitro release behavior were studied. RESULTS: HOY copolymers were synthesized successfully. The particle size and Zeta potential of the drug-loaded micelles were (237.2±2.7) nm and (-22.37±0.38) mV, and the encapsulation efficiency and drug loading rate were (89.8±0.011)% and (5.4±0.007)%, respectively. Moreover, the accumulative release of doxorubicin in vitro was about 70% in 48 h, indicating that the drug was released slowly from the micelles. CONCLUSION: This study develops a new micellar system based on terminal modified HA, and provides a reference for the study of HA nanocarrier.