A Novel Folic Acid Receptor-Targeted Drug Delivery System Based on Curcumin-Loaded β-Cyclodextrin Nanoparticles for Cancer Treatment
Weiyong Hong,1,2,* Fangyuan Guo,2,* Nan Yu,2 Sanjun Ying,2 Bang Lou,2 Jiangqing Wu,2 Ying Gao,2 Xugang Ji,2 Haiying Wang,1 Aiqin Li,3 Guoping Wang,4 Gensheng Yang2 1Department of Pharmacy, Taizhou Municipal Hospital, Taizhou, 318000, People’s Republic of China; 2College of Pharmaceut...
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doaj-6bd0ad5072a54513b21b5dc7c512dc7a2021-07-04T20:03:22ZengDove Medical PressDrug Design, Development and Therapy1177-88812021-06-01Volume 152843285566463A Novel Folic Acid Receptor-Targeted Drug Delivery System Based on Curcumin-Loaded β-Cyclodextrin Nanoparticles for Cancer TreatmentHong WGuo FYu NYing SLou BWu JGao YJi XWang HLi AWang GYang GWeiyong Hong,1,2,* Fangyuan Guo,2,* Nan Yu,2 Sanjun Ying,2 Bang Lou,2 Jiangqing Wu,2 Ying Gao,2 Xugang Ji,2 Haiying Wang,1 Aiqin Li,3 Guoping Wang,4 Gensheng Yang2 1Department of Pharmacy, Taizhou Municipal Hospital, Taizhou, 318000, People’s Republic of China; 2College of Pharmaceutical Science, Zhejiang University of Technology, Hangzhou, 310014, People’s Republic of China; 3Zhejiang Share Bio-Pharm Co., Ltd, Hangzhou, 310019, People’s Republic of China; 4Zhejiang Dayang Biotech Group Co., Ltd, Hangzhou, 311616, People’s Republic of China*These authors contributed equally to this workCorrespondence: Gensheng YangCollege of Pharmaceutical Science, Zhejiang University of Technology, Hangzhou, 310014, People’s Republic of ChinaTel +86571-88871077Fax +86571-88320913Email yanggs@zjut.edu.cnPurpose: A novel folate receptor-targeted β-cyclodextrin (β-CD) drug delivery vehicle was constructed to improve the bioavailability, biosafety, and drug loading capacity of curcumin. Controlled release and targeted delivery was achieved by modifying the nanoparticles with folic acid (FA).Methods: Folate-conjugated β-CD-polycaprolactone block copolymers were synthesized and characterized. Curcumin-loaded nanoparticles (FA-Cur-NPs) were structured by self-assembly. The physicochemical properties, stability, release behavior and tumor-targeting ability of the fabricated nanoparticles were studied.Results: The average particle size and drug loading of FA-Cur-NPs was 151.8 nm and 20.27%, respectively. Moreover, the FA-Cur-NPs exhibited good stability in vitro for 72 h. The drug release profiles showed that curcumin from FA-Cur-NPs was released significantly faster in a pH 6.4 phosphate buffered solution (PBS) than in pH 7.4, indicating that curcumin can be enriched around the tumor site compared with normal cells. Additionally, the internalization of FA-Cur-NPs was aided by FA receptor-mediated endocytosis, and its cytotoxicity was proportional to the cellular uptake efficiency. Furthermore, in vivo studies confirmed that FA-Cur-NPs exhibited marked accumulation in the tumor site and excellent antitumor activity.Conclusion: These findings suggest that FA-Cur-NPs are a promising approach for improving cancer therapy through active targeting and controllable release.Keywords: curcumin, β-CD-polycaprolactone copolymers, folate receptor, targeted drug delivery, HeLa cellshttps://www.dovepress.com/a-novel-folic-acid-receptor-targeted-drug-delivery-system-based-on-cur-peer-reviewed-fulltext-article-DDDTcurcuminβ-cd-polycaprolactone copolymersfolate receptortargeted drug deliveryhela cells |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Hong W Guo F Yu N Ying S Lou B Wu J Gao Y Ji X Wang H Li A Wang G Yang G |
spellingShingle |
Hong W Guo F Yu N Ying S Lou B Wu J Gao Y Ji X Wang H Li A Wang G Yang G A Novel Folic Acid Receptor-Targeted Drug Delivery System Based on Curcumin-Loaded β-Cyclodextrin Nanoparticles for Cancer Treatment Drug Design, Development and Therapy curcumin β-cd-polycaprolactone copolymers folate receptor targeted drug delivery hela cells |
author_facet |
Hong W Guo F Yu N Ying S Lou B Wu J Gao Y Ji X Wang H Li A Wang G Yang G |
author_sort |
Hong W |
title |
A Novel Folic Acid Receptor-Targeted Drug Delivery System Based on Curcumin-Loaded β-Cyclodextrin Nanoparticles for Cancer Treatment |
title_short |
A Novel Folic Acid Receptor-Targeted Drug Delivery System Based on Curcumin-Loaded β-Cyclodextrin Nanoparticles for Cancer Treatment |
title_full |
A Novel Folic Acid Receptor-Targeted Drug Delivery System Based on Curcumin-Loaded β-Cyclodextrin Nanoparticles for Cancer Treatment |
title_fullStr |
A Novel Folic Acid Receptor-Targeted Drug Delivery System Based on Curcumin-Loaded β-Cyclodextrin Nanoparticles for Cancer Treatment |
title_full_unstemmed |
A Novel Folic Acid Receptor-Targeted Drug Delivery System Based on Curcumin-Loaded β-Cyclodextrin Nanoparticles for Cancer Treatment |
title_sort |
novel folic acid receptor-targeted drug delivery system based on curcumin-loaded β-cyclodextrin nanoparticles for cancer treatment |
publisher |
Dove Medical Press |
series |
Drug Design, Development and Therapy |
issn |
1177-8881 |
publishDate |
2021-06-01 |
description |
Weiyong Hong,1,2,* Fangyuan Guo,2,* Nan Yu,2 Sanjun Ying,2 Bang Lou,2 Jiangqing Wu,2 Ying Gao,2 Xugang Ji,2 Haiying Wang,1 Aiqin Li,3 Guoping Wang,4 Gensheng Yang2 1Department of Pharmacy, Taizhou Municipal Hospital, Taizhou, 318000, People’s Republic of China; 2College of Pharmaceutical Science, Zhejiang University of Technology, Hangzhou, 310014, People’s Republic of China; 3Zhejiang Share Bio-Pharm Co., Ltd, Hangzhou, 310019, People’s Republic of China; 4Zhejiang Dayang Biotech Group Co., Ltd, Hangzhou, 311616, People’s Republic of China*These authors contributed equally to this workCorrespondence: Gensheng YangCollege of Pharmaceutical Science, Zhejiang University of Technology, Hangzhou, 310014, People’s Republic of ChinaTel +86571-88871077Fax +86571-88320913Email yanggs@zjut.edu.cnPurpose: A novel folate receptor-targeted β-cyclodextrin (β-CD) drug delivery vehicle was constructed to improve the bioavailability, biosafety, and drug loading capacity of curcumin. Controlled release and targeted delivery was achieved by modifying the nanoparticles with folic acid (FA).Methods: Folate-conjugated β-CD-polycaprolactone block copolymers were synthesized and characterized. Curcumin-loaded nanoparticles (FA-Cur-NPs) were structured by self-assembly. The physicochemical properties, stability, release behavior and tumor-targeting ability of the fabricated nanoparticles were studied.Results: The average particle size and drug loading of FA-Cur-NPs was 151.8 nm and 20.27%, respectively. Moreover, the FA-Cur-NPs exhibited good stability in vitro for 72 h. The drug release profiles showed that curcumin from FA-Cur-NPs was released significantly faster in a pH 6.4 phosphate buffered solution (PBS) than in pH 7.4, indicating that curcumin can be enriched around the tumor site compared with normal cells. Additionally, the internalization of FA-Cur-NPs was aided by FA receptor-mediated endocytosis, and its cytotoxicity was proportional to the cellular uptake efficiency. Furthermore, in vivo studies confirmed that FA-Cur-NPs exhibited marked accumulation in the tumor site and excellent antitumor activity.Conclusion: These findings suggest that FA-Cur-NPs are a promising approach for improving cancer therapy through active targeting and controllable release.Keywords: curcumin, β-CD-polycaprolactone copolymers, folate receptor, targeted drug delivery, HeLa cells |
topic |
curcumin β-cd-polycaprolactone copolymers folate receptor targeted drug delivery hela cells |
url |
https://www.dovepress.com/a-novel-folic-acid-receptor-targeted-drug-delivery-system-based-on-cur-peer-reviewed-fulltext-article-DDDT |
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