Bioreducible hyaluronic acid conjugates as siRNA carrier for tumor targeting

Title
Bioreducible hyaluronic acid conjugates as siRNA carrier for tumor targeting
Authors
윤홍열김현령Gurusamy Saravanakumar허로운채수영엄우람김광명권익찬이준영이두성박재찬박재형
Keywords
Hyaluronic acid; Bioreducible conjugate; Stability; Tumor targetability; siRNA
Issue Date
2013-12
Publisher
Journal of controlled release
Citation
VOL 172, NO 3, 653-661
Abstract
The successful clinical translation of siRNA-based therapeutics requires efficient carrier systems that can specifically deliver siRNA within the cytosol of the target cells. Although numerous polymeric nanocarriers forming ionic complexes with siRNA have been investigated for cancer therapy, their poor stability and lack of tumor targetability have impeded their in vivo applications. To surmount these limitations, we synthesized a novel type of biodegradable hyaluronic acid-graft-poly(dimethylaminoethyl methacrylate) (HPD) conjugate that can form complexes with siRNA and be chemically crosslinked via the formation of the disulfide bonds under facile conditions. The crosslinked siRNA-HPD (C-siRNA-HPD) complexes exhibited high stability in a 50% serum solution, as compared to the uncrosslinked siRNA-HPD (U-siRNA-HPD) complexes and free siRNA. Both the C-siRNA-HPD and U-siRNA-HPD complexes were efficiently taken up by the CD44-overexpressing melanoma cells (B16F10), but not by the normal fibroblast cells (NIH3T3). When the RFP-expressing B16F10 cells were treated with the complexes or free siRNA, the C-siRNA-HPD complexes showed the highest decrease in RFP expression. In vivo studies demonstrated the selective accumulation of C-siRNA-HPD complexes at the tumor site after their systemic administration into tumor-bearingmice, resulting in an efficient gene silencing effect.Overall, these results suggest that the HPD conjugate could be used as an efficient carrier for the tumor-targeted delivery of siRNA.
URI
http://pubs.kist.re.kr/handle/201004/47261
ISSN
01683659
Appears in Collections:
KIST Publication > Article
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