Thermoresponsive curcumin/DsiRNA nanoparticle gels for the treatment of diabetic wounds: Synthesis and drug release
Aim: Chitosan (CS) has been extensively studied as drug delivery systems for wound healing. Results/methodology: CS nanoparticles were loaded with curcumin (Cur) and DsiRNA against prostaglandin transporter gene and they were incorporated into 20 and 25% w/v Pluronic F-127. The gels were later analy...
Published in: | Therapeutic Delivery |
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Newlands Press Ltd
2017
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Online Access: | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85011340333&doi=10.4155%2ftde-2016-0075&partnerID=40&md5=3515835b396825211d5fb1238d0ca5db |
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2-s2.0-85011340333 Katas H.; Wen C.Y.; Siddique M.I.; Hussain Z.; Mohd Fadhil F.H. Thermoresponsive curcumin/DsiRNA nanoparticle gels for the treatment of diabetic wounds: Synthesis and drug release 2017 Therapeutic Delivery 8 3 10.4155/tde-2016-0075 https://www.scopus.com/inward/record.uri?eid=2-s2.0-85011340333&doi=10.4155%2ftde-2016-0075&partnerID=40&md5=3515835b396825211d5fb1238d0ca5db Aim: Chitosan (CS) has been extensively studied as drug delivery systems for wound healing. Results/methodology: CS nanoparticles were loaded with curcumin (Cur) and DsiRNA against prostaglandin transporter gene and they were incorporated into 20 and 25% w/v Pluronic F-127. The gels were later analyzed for their rheology, gelation temperature (Tgel), morphology, drug incorporation and in vitro drug release. The particle size was in the range of 231 ± 17-320 ± 20 nm, depending on CS concentration. The gels had Tgel of 23-28°C and exhibited sustained drug release with high accumulated amount of drugs over 48 h. Conclusion: A thermo-sensitive gel containing Cur/DsiRNA CS nanoparticles was successfully developed and has a great potential to be further developed. © 2017 Future Science Ltd. Newlands Press Ltd 20415990 English Article |
author |
Katas H.; Wen C.Y.; Siddique M.I.; Hussain Z.; Mohd Fadhil F.H. |
spellingShingle |
Katas H.; Wen C.Y.; Siddique M.I.; Hussain Z.; Mohd Fadhil F.H. Thermoresponsive curcumin/DsiRNA nanoparticle gels for the treatment of diabetic wounds: Synthesis and drug release |
author_facet |
Katas H.; Wen C.Y.; Siddique M.I.; Hussain Z.; Mohd Fadhil F.H. |
author_sort |
Katas H.; Wen C.Y.; Siddique M.I.; Hussain Z.; Mohd Fadhil F.H. |
title |
Thermoresponsive curcumin/DsiRNA nanoparticle gels for the treatment of diabetic wounds: Synthesis and drug release |
title_short |
Thermoresponsive curcumin/DsiRNA nanoparticle gels for the treatment of diabetic wounds: Synthesis and drug release |
title_full |
Thermoresponsive curcumin/DsiRNA nanoparticle gels for the treatment of diabetic wounds: Synthesis and drug release |
title_fullStr |
Thermoresponsive curcumin/DsiRNA nanoparticle gels for the treatment of diabetic wounds: Synthesis and drug release |
title_full_unstemmed |
Thermoresponsive curcumin/DsiRNA nanoparticle gels for the treatment of diabetic wounds: Synthesis and drug release |
title_sort |
Thermoresponsive curcumin/DsiRNA nanoparticle gels for the treatment of diabetic wounds: Synthesis and drug release |
publishDate |
2017 |
container_title |
Therapeutic Delivery |
container_volume |
8 |
container_issue |
3 |
doi_str_mv |
10.4155/tde-2016-0075 |
url |
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85011340333&doi=10.4155%2ftde-2016-0075&partnerID=40&md5=3515835b396825211d5fb1238d0ca5db |
description |
Aim: Chitosan (CS) has been extensively studied as drug delivery systems for wound healing. Results/methodology: CS nanoparticles were loaded with curcumin (Cur) and DsiRNA against prostaglandin transporter gene and they were incorporated into 20 and 25% w/v Pluronic F-127. The gels were later analyzed for their rheology, gelation temperature (Tgel), morphology, drug incorporation and in vitro drug release. The particle size was in the range of 231 ± 17-320 ± 20 nm, depending on CS concentration. The gels had Tgel of 23-28°C and exhibited sustained drug release with high accumulated amount of drugs over 48 h. Conclusion: A thermo-sensitive gel containing Cur/DsiRNA CS nanoparticles was successfully developed and has a great potential to be further developed. © 2017 Future Science Ltd. |
publisher |
Newlands Press Ltd |
issn |
20415990 |
language |
English |
format |
Article |
accesstype |
|
record_format |
scopus |
collection |
Scopus |
_version_ |
1809678161004199936 |