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Antitumor activity of sorafenib-incorporated nanoparticles of dextran/poly(dl-lactide-co-glycolide) block copolymer

Sorafenib-incoporated nanoparticles were prepared using a block copolymer that is composed of dextran and poly(DL-lactide-co-glycolide) [DexbLG] for antitumor drug delivery. Sorafenib-incorporated nanoparticles were prepared by a nanoprecipitation-dialysis method. Sorafenib-incorporated DexbLG nanop...

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Autores principales: Kim, Do Hyung, Kim, Min-Dae, Choi, Cheol-Woong, Chung, Chung-Wook, Ha, Seung Hee, Kim, Cy Hyun, Shim, Yong-Ho, Jeong, Young-Il, Kang, Dae Hwan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3292832/
https://www.ncbi.nlm.nih.gov/pubmed/22283905
http://dx.doi.org/10.1186/1556-276X-7-91
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author Kim, Do Hyung
Kim, Min-Dae
Choi, Cheol-Woong
Chung, Chung-Wook
Ha, Seung Hee
Kim, Cy Hyun
Shim, Yong-Ho
Jeong, Young-Il
Kang, Dae Hwan
author_facet Kim, Do Hyung
Kim, Min-Dae
Choi, Cheol-Woong
Chung, Chung-Wook
Ha, Seung Hee
Kim, Cy Hyun
Shim, Yong-Ho
Jeong, Young-Il
Kang, Dae Hwan
author_sort Kim, Do Hyung
collection PubMed
description Sorafenib-incoporated nanoparticles were prepared using a block copolymer that is composed of dextran and poly(DL-lactide-co-glycolide) [DexbLG] for antitumor drug delivery. Sorafenib-incorporated nanoparticles were prepared by a nanoprecipitation-dialysis method. Sorafenib-incorporated DexbLG nanoparticles were uniformly distributed in an aqueous solution regardless of the content of sorafenib. Transmission electron microscopy of the sorafenib-incorporated DexbLG nanoparticles revealed a spherical shape with a diameter < 300 nm. Sorafenib-incorporated DexbLG nanoparticles at a polymer/drug weight ratio of 40:5 showed a relatively uniform size and morphology. Higher initial drug feeding was associated with increased drug content in nanoparticles and in nanoparticle size. A drug release study revealed a decreased drug release rate with increasing drug content. In an in vitro anti-proliferation assay using human cholangiocarcinoma cells, sorafenib-incorporated DexbLG nanoparticles showed a similar antitumor activity as sorafenib. Sorafenib-incorporated DexbLG nanoparticles are promising candidates as vehicles for antitumor drug targeting.
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spelling pubmed-32928322012-03-06 Antitumor activity of sorafenib-incorporated nanoparticles of dextran/poly(dl-lactide-co-glycolide) block copolymer Kim, Do Hyung Kim, Min-Dae Choi, Cheol-Woong Chung, Chung-Wook Ha, Seung Hee Kim, Cy Hyun Shim, Yong-Ho Jeong, Young-Il Kang, Dae Hwan Nanoscale Res Lett Nano Express Sorafenib-incoporated nanoparticles were prepared using a block copolymer that is composed of dextran and poly(DL-lactide-co-glycolide) [DexbLG] for antitumor drug delivery. Sorafenib-incorporated nanoparticles were prepared by a nanoprecipitation-dialysis method. Sorafenib-incorporated DexbLG nanoparticles were uniformly distributed in an aqueous solution regardless of the content of sorafenib. Transmission electron microscopy of the sorafenib-incorporated DexbLG nanoparticles revealed a spherical shape with a diameter < 300 nm. Sorafenib-incorporated DexbLG nanoparticles at a polymer/drug weight ratio of 40:5 showed a relatively uniform size and morphology. Higher initial drug feeding was associated with increased drug content in nanoparticles and in nanoparticle size. A drug release study revealed a decreased drug release rate with increasing drug content. In an in vitro anti-proliferation assay using human cholangiocarcinoma cells, sorafenib-incorporated DexbLG nanoparticles showed a similar antitumor activity as sorafenib. Sorafenib-incorporated DexbLG nanoparticles are promising candidates as vehicles for antitumor drug targeting. Springer 2012-01-27 /pmc/articles/PMC3292832/ /pubmed/22283905 http://dx.doi.org/10.1186/1556-276X-7-91 Text en Copyright ©2012 Kim et al; licensee Springer. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Nano Express
Kim, Do Hyung
Kim, Min-Dae
Choi, Cheol-Woong
Chung, Chung-Wook
Ha, Seung Hee
Kim, Cy Hyun
Shim, Yong-Ho
Jeong, Young-Il
Kang, Dae Hwan
Antitumor activity of sorafenib-incorporated nanoparticles of dextran/poly(dl-lactide-co-glycolide) block copolymer
title Antitumor activity of sorafenib-incorporated nanoparticles of dextran/poly(dl-lactide-co-glycolide) block copolymer
title_full Antitumor activity of sorafenib-incorporated nanoparticles of dextran/poly(dl-lactide-co-glycolide) block copolymer
title_fullStr Antitumor activity of sorafenib-incorporated nanoparticles of dextran/poly(dl-lactide-co-glycolide) block copolymer
title_full_unstemmed Antitumor activity of sorafenib-incorporated nanoparticles of dextran/poly(dl-lactide-co-glycolide) block copolymer
title_short Antitumor activity of sorafenib-incorporated nanoparticles of dextran/poly(dl-lactide-co-glycolide) block copolymer
title_sort antitumor activity of sorafenib-incorporated nanoparticles of dextran/poly(dl-lactide-co-glycolide) block copolymer
topic Nano Express
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3292832/
https://www.ncbi.nlm.nih.gov/pubmed/22283905
http://dx.doi.org/10.1186/1556-276X-7-91
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