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Folate-targeted nanostructured chitosan/chondroitin sulfate complex carriers for enhanced delivery of bortezomib to colorectal cancer cells

Folate-targeting self-assembled nanoparticles (NPs) using biocompatible and biodegradable natural polymers chitosan (Cs) and chondroitin sulfate (Chs) were developed to address the major challenge in cancer treatment, the selective delivery of nanoparticles to the target site. In this study, we succ...

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Detalles Bibliográficos
Autores principales: Soe, Zar Chi, Poudel, Bijay Kumar, Nguyen, Hanh Thuy, Thapa, Raj Kumar, Ou, Wenquan, Gautam, Milan, Poudel, Kishwor, Jin, Sung Giu, Jeong, Jee-Heon, Ku, Sae Kwang, Choi, Han-Gon, Yong, Chul Soon, Kim, Jong Oh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shenyang Pharmaceutical University 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7032194/
https://www.ncbi.nlm.nih.gov/pubmed/32104437
http://dx.doi.org/10.1016/j.ajps.2018.09.004
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author Soe, Zar Chi
Poudel, Bijay Kumar
Nguyen, Hanh Thuy
Thapa, Raj Kumar
Ou, Wenquan
Gautam, Milan
Poudel, Kishwor
Jin, Sung Giu
Jeong, Jee-Heon
Ku, Sae Kwang
Choi, Han-Gon
Yong, Chul Soon
Kim, Jong Oh
author_facet Soe, Zar Chi
Poudel, Bijay Kumar
Nguyen, Hanh Thuy
Thapa, Raj Kumar
Ou, Wenquan
Gautam, Milan
Poudel, Kishwor
Jin, Sung Giu
Jeong, Jee-Heon
Ku, Sae Kwang
Choi, Han-Gon
Yong, Chul Soon
Kim, Jong Oh
author_sort Soe, Zar Chi
collection PubMed
description Folate-targeting self-assembled nanoparticles (NPs) using biocompatible and biodegradable natural polymers chitosan (Cs) and chondroitin sulfate (Chs) were developed to address the major challenge in cancer treatment, the selective delivery of nanoparticles to the target site. In this study, we successfully incorporated a hydrophobic drug, bortezomib (Bor), into folic acid (FA)-conjugated Cs/Chs self-assembled NPs (Bor/Cs/Chs-FA) for colorectal cancer therapy. The particle size and polydispersity index of Bor/Cs/Chs-FA were ∼196.5 ± 1.2 nm and ∼0.21 ± 0.5, respectively. A pH-dependent release profile was observed, facilitating cancer cell-targeted drug release under an acidic tumor microenvironment. Moreover, in vitro data revealed enhanced cellular uptake and apoptosis in folate receptor-expressing colorectal cancer cells (HCT-116 and HT-29) as compared to that in lung cancer cells (A549), which do not express folate receptors. Furthermore, intravenous administration of Bor/Cs/Chs-FA in a HCT-116 bearing xenograft mouse model showed that the NPs were a safe and effective drug delivery system. The results suggest that folate-targeted nanoparticle can be effectively applied for efficient chemotherapy of colorectal cancer.
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spelling pubmed-70321942020-02-26 Folate-targeted nanostructured chitosan/chondroitin sulfate complex carriers for enhanced delivery of bortezomib to colorectal cancer cells Soe, Zar Chi Poudel, Bijay Kumar Nguyen, Hanh Thuy Thapa, Raj Kumar Ou, Wenquan Gautam, Milan Poudel, Kishwor Jin, Sung Giu Jeong, Jee-Heon Ku, Sae Kwang Choi, Han-Gon Yong, Chul Soon Kim, Jong Oh Asian J Pharm Sci Research Article Folate-targeting self-assembled nanoparticles (NPs) using biocompatible and biodegradable natural polymers chitosan (Cs) and chondroitin sulfate (Chs) were developed to address the major challenge in cancer treatment, the selective delivery of nanoparticles to the target site. In this study, we successfully incorporated a hydrophobic drug, bortezomib (Bor), into folic acid (FA)-conjugated Cs/Chs self-assembled NPs (Bor/Cs/Chs-FA) for colorectal cancer therapy. The particle size and polydispersity index of Bor/Cs/Chs-FA were ∼196.5 ± 1.2 nm and ∼0.21 ± 0.5, respectively. A pH-dependent release profile was observed, facilitating cancer cell-targeted drug release under an acidic tumor microenvironment. Moreover, in vitro data revealed enhanced cellular uptake and apoptosis in folate receptor-expressing colorectal cancer cells (HCT-116 and HT-29) as compared to that in lung cancer cells (A549), which do not express folate receptors. Furthermore, intravenous administration of Bor/Cs/Chs-FA in a HCT-116 bearing xenograft mouse model showed that the NPs were a safe and effective drug delivery system. The results suggest that folate-targeted nanoparticle can be effectively applied for efficient chemotherapy of colorectal cancer. Shenyang Pharmaceutical University 2019-01 2018-10-20 /pmc/articles/PMC7032194/ /pubmed/32104437 http://dx.doi.org/10.1016/j.ajps.2018.09.004 Text en © 2018 Shenyang Pharmaceutical University. Published by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Soe, Zar Chi
Poudel, Bijay Kumar
Nguyen, Hanh Thuy
Thapa, Raj Kumar
Ou, Wenquan
Gautam, Milan
Poudel, Kishwor
Jin, Sung Giu
Jeong, Jee-Heon
Ku, Sae Kwang
Choi, Han-Gon
Yong, Chul Soon
Kim, Jong Oh
Folate-targeted nanostructured chitosan/chondroitin sulfate complex carriers for enhanced delivery of bortezomib to colorectal cancer cells
title Folate-targeted nanostructured chitosan/chondroitin sulfate complex carriers for enhanced delivery of bortezomib to colorectal cancer cells
title_full Folate-targeted nanostructured chitosan/chondroitin sulfate complex carriers for enhanced delivery of bortezomib to colorectal cancer cells
title_fullStr Folate-targeted nanostructured chitosan/chondroitin sulfate complex carriers for enhanced delivery of bortezomib to colorectal cancer cells
title_full_unstemmed Folate-targeted nanostructured chitosan/chondroitin sulfate complex carriers for enhanced delivery of bortezomib to colorectal cancer cells
title_short Folate-targeted nanostructured chitosan/chondroitin sulfate complex carriers for enhanced delivery of bortezomib to colorectal cancer cells
title_sort folate-targeted nanostructured chitosan/chondroitin sulfate complex carriers for enhanced delivery of bortezomib to colorectal cancer cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7032194/
https://www.ncbi.nlm.nih.gov/pubmed/32104437
http://dx.doi.org/10.1016/j.ajps.2018.09.004
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