Synthesis, characterisation and in vitro release of paclitaxel‐loaded polymeric micelles
Source abstract
Abstract
A novel folic acid (FA) poly (ethylene oxide) (PEO)/poly (lactic acid) (PLA) block copolymer conjugate (FA‐PEO‐PLA) was successfully synthesised by a two‐step reaction. FA‐PEO‐PLA can form mixed micelles with low critical micelle concentration (3.2 × 10 −3 wt%). The physical properties and the structure of micelles were characterised by size distribution and transmission electron microscopy. The micelles exhibited uniform spherical structure and the average diameter was 107.9 nm with narrow size distribution (polydispersity index 0.214). Paclitaxel was loaded in micelles and the encapsulation efficiency of paclitaxel was 43%. The in vitro release of paclitaxel from micelles was initially fast in the first 8 h followed by sustained release. The Weibull model was the most appropriate mechanism for describing the release procedure. These results indicated that the FA‐PEO‐PLA can be used as a carrier for hydrophobic anticancer drugs.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Nanoparticle-Based Drug Delivery · biodegradable polymer synthesis and properties · Advanced Polymer Synthesis and Characterization
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Life Science Jiangxi Science and Technology Normal University Nanchang 330013 People's Republic of China
State Key Laboratory of Food Science and Technology Nanchang University Nanchang 330047 People's Republic of China
Jiangxi Institute of Analysis and Test Nanchang 330029 People's Republic of China
Funding
National Natural Science Foundation of China · Natural Science Foundation of Jiangxi Province
References (22)
Show source-provided references
1. 10.1049/mnl.2013.046110.1049/mnl.2013.0461 ↗
2. 10.1039/c0jm04410e10.1039/c0jm04410e ↗
3. 10.1016/j.jconrel.2014.03.02610.1016/j.jconrel.2014.03.026 ↗
4. 10.1016/j.jconrel.2009.11.01210.1016/j.jconrel.2009.11.012 ↗
5. 10.1016/j.biortech.2010.05.09210.1016/j.biortech.2010.05.092 ↗
6. 10.1016/j.ijpharm.2006.10.02010.1016/j.ijpharm.2006.10.020 ↗
7. 10.1016/j.progpolymsci.2010.06.00310.1016/j.progpolymsci.2010.06.003 ↗
8. 10.1016/j.phrs.2010.03.00510.1016/j.phrs.2010.03.005 ↗
9. 10.1039/C2CS35265F10.1039/C2CS35265F ↗
10. 10.1016/j.biomaterials.2011.04.00610.1016/j.biomaterials.2011.04.006 ↗
11. 10.1016/j.biomaterials.2009.02.01110.1016/j.biomaterials.2009.02.011 ↗
12. 10.1021/ar700081510.1021/ar7000815 ↗
13. 10.1016/j.colsurfb.2015.11.01810.1016/j.colsurfb.2015.11.018 ↗
14. 10.1016/j.eurpolymj.2015.05.00310.1016/j.eurpolymj.2015.05.003 ↗
15. 10.1002/app.3112510.1002/app.31125 ↗
16. 10.1016/j.colsurfb.2013.06.01910.1016/j.colsurfb.2013.06.019 ↗
17. 10.1016/j.ejps.2012.04.01110.1016/j.ejps.2012.04.011 ↗
18. 10.1016/j.apsusc.2012.10.13110.1016/j.apsusc.2012.10.131 ↗
19. 10.1016/j.colsurfb.2012.07.03010.1016/j.colsurfb.2012.07.030 ↗
20. 10.2217/nnm.12.3110.2217/nnm.12.31 ↗
21. 10.1016/j.nano.2011.05.01610.1016/j.nano.2011.05.016 ↗
22. 10.1016/j.jconrel.2007.10.00210.1016/j.jconrel.2007.10.002 ↗