Journal
JOURNAL OF EXPERIMENTAL NANOSCIENCE
Volume 4, Issue 3, Pages 269-275Publisher
TAYLOR & FRANCIS LTD
DOI: 10.1080/17458080802516909
Keywords
nano-aggregate; protein delivery; chitosan; pluronic
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Funding
- Korea government (MOST) [R01-2004-000-10164-0]
- Gyeonggi Provincial Government
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Polymeric micelle or self-aggregate formations have received much attention as carriers for drug delivery systems because of their high efficiency for drug delivery. Our recent results in the formation of nano-aggregates using chemically modified chitosan encouraged us to investigate the possibility of applying them as drug carriers. Therefore, we investigated a novel chitosan-based nano-aggregate as a drug carrier for sustained protein release. Thermosensitive chitosan-Pluronic (CP) was prepared by grafting monocarboxy Pluronic F127 onto the chitosan using 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide and N-hydroxysuccinimide. Bovine serum albumin (BSA)-loaded CP nano-aggregate was prepared by the direct dissolution method based on thermosensitive property of the CP copolymer. The physico-chemical properties of CP nano-aggregates were characterised by critical aggregate concentration, dynamic light scattering, and -potential. In vitro release studies were investigated with BSA as a model protein at 37 degrees C. BSA released from the CP nano-aggregates for about 6 h. The results suggest that CP nano-aggregates can potentially be efficient nanocarriers for protein delivery.
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