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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...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Shenyang Pharmaceutical University
2019
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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. |
format | Online Article Text |
id | pubmed-7032194 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Shenyang Pharmaceutical University |
record_format | MEDLINE/PubMed |
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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