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Gold nanorod-encapsulated biodegradable polymeric matrix for combined photothermal and chemo-cancer therapy

PURPOSE: A biocompatible nanocomplex system co-encapsulated with gold nanorods (AuNRs) and doxorubicin (DOX) was investigated for its potentials on the combined photothermal- and chemotherapy. MATERIALS AND METHODS: Hydrophobic AuNRs were synthesized by the hexadecyltrimethyl-ammonium bromide (CTAB)...

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Autores principales: Chuang, Chun-Chiao, Cheng, Chih-Chi, Chen, Pei-Ying, Lo, Chieh, Chen, Yi-Ning, Shih, Min-Hsiung, Chang, Chien-Wen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6306055/
https://www.ncbi.nlm.nih.gov/pubmed/30613145
http://dx.doi.org/10.2147/IJN.S177851
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author Chuang, Chun-Chiao
Cheng, Chih-Chi
Chen, Pei-Ying
Lo, Chieh
Chen, Yi-Ning
Shih, Min-Hsiung
Chang, Chien-Wen
author_facet Chuang, Chun-Chiao
Cheng, Chih-Chi
Chen, Pei-Ying
Lo, Chieh
Chen, Yi-Ning
Shih, Min-Hsiung
Chang, Chien-Wen
author_sort Chuang, Chun-Chiao
collection PubMed
description PURPOSE: A biocompatible nanocomplex system co-encapsulated with gold nanorods (AuNRs) and doxorubicin (DOX) was investigated for its potentials on the combined photothermal- and chemotherapy. MATERIALS AND METHODS: Hydrophobic AuNRs were synthesized by the hexadecyltrimethyl-ammonium bromide (CTAB)-mediated seed growth method, and then, they received two-step surface modifications of polyethylene glycol (PEG) and dodecane. The AuNR/DOX/poly(lactic-co-glycolic acid) (PLGA) nanocomplexes were prepared by emulsifying DOX, AuNR, and PLGA into aqueous polyvinyl alcohol solution by sonication. Human serum albumin (HSA) was used to coat the nanocomplexes to afford HSA/AuNR/DOX–PLGA (HADP). Size and surface potential of the HADP nanocomplexes were determined by using a Zetasizer. Cytotoxicity and cellular uptake of the HADP were analyzed by using MTT assay and flow cytometry, respectively. In vitro anticancer effects of the HADP were studied on various cancer cell lines. To assess the therapeutic efficacy, CT26 tumor-bearing mice were intravenously administered with HADP nanocomplexes and laser treatments, followed by monitoring of the tumor growth and body weight. RESULTS: Size and surface potential of the HADP nanocomplexes were 245.8 nm and -8.6 mV, respectively. Strong photothermal effects were verified on the AuNR-loaded PLGA nanoparticles (NPs) in vitro. Rapid and repeated drug release from the HADP nanocomplexes was successfully achieved by near-infrared (NIR) irradiations. HSA significantly promoted cellular uptake of the HADP nanocomplexes to murine colon cancer cells as demonstrated by cell imaging and flow cytometric studies. By combining photothermal and chemotherapy, the HADP nanocomplexes exhibited strong synergistic anticancer effects in vitro and in vivo. CONCLUSION: An NIR-triggered drug release system by encapsulating hydrophobic AuNR and DOX inside the PLGA NPs has been successfully prepared in this study. The HADP NPs show promising combined photothermal- and chemotherapeutic effects without inducing undesired side effects on a murine colon cancer animal model.
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spelling pubmed-63060552019-01-04 Gold nanorod-encapsulated biodegradable polymeric matrix for combined photothermal and chemo-cancer therapy Chuang, Chun-Chiao Cheng, Chih-Chi Chen, Pei-Ying Lo, Chieh Chen, Yi-Ning Shih, Min-Hsiung Chang, Chien-Wen Int J Nanomedicine Original Research PURPOSE: A biocompatible nanocomplex system co-encapsulated with gold nanorods (AuNRs) and doxorubicin (DOX) was investigated for its potentials on the combined photothermal- and chemotherapy. MATERIALS AND METHODS: Hydrophobic AuNRs were synthesized by the hexadecyltrimethyl-ammonium bromide (CTAB)-mediated seed growth method, and then, they received two-step surface modifications of polyethylene glycol (PEG) and dodecane. The AuNR/DOX/poly(lactic-co-glycolic acid) (PLGA) nanocomplexes were prepared by emulsifying DOX, AuNR, and PLGA into aqueous polyvinyl alcohol solution by sonication. Human serum albumin (HSA) was used to coat the nanocomplexes to afford HSA/AuNR/DOX–PLGA (HADP). Size and surface potential of the HADP nanocomplexes were determined by using a Zetasizer. Cytotoxicity and cellular uptake of the HADP were analyzed by using MTT assay and flow cytometry, respectively. In vitro anticancer effects of the HADP were studied on various cancer cell lines. To assess the therapeutic efficacy, CT26 tumor-bearing mice were intravenously administered with HADP nanocomplexes and laser treatments, followed by monitoring of the tumor growth and body weight. RESULTS: Size and surface potential of the HADP nanocomplexes were 245.8 nm and -8.6 mV, respectively. Strong photothermal effects were verified on the AuNR-loaded PLGA nanoparticles (NPs) in vitro. Rapid and repeated drug release from the HADP nanocomplexes was successfully achieved by near-infrared (NIR) irradiations. HSA significantly promoted cellular uptake of the HADP nanocomplexes to murine colon cancer cells as demonstrated by cell imaging and flow cytometric studies. By combining photothermal and chemotherapy, the HADP nanocomplexes exhibited strong synergistic anticancer effects in vitro and in vivo. CONCLUSION: An NIR-triggered drug release system by encapsulating hydrophobic AuNR and DOX inside the PLGA NPs has been successfully prepared in this study. The HADP NPs show promising combined photothermal- and chemotherapeutic effects without inducing undesired side effects on a murine colon cancer animal model. Dove Medical Press 2018-12-21 /pmc/articles/PMC6306055/ /pubmed/30613145 http://dx.doi.org/10.2147/IJN.S177851 Text en © 2019 Chuang et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Chuang, Chun-Chiao
Cheng, Chih-Chi
Chen, Pei-Ying
Lo, Chieh
Chen, Yi-Ning
Shih, Min-Hsiung
Chang, Chien-Wen
Gold nanorod-encapsulated biodegradable polymeric matrix for combined photothermal and chemo-cancer therapy
title Gold nanorod-encapsulated biodegradable polymeric matrix for combined photothermal and chemo-cancer therapy
title_full Gold nanorod-encapsulated biodegradable polymeric matrix for combined photothermal and chemo-cancer therapy
title_fullStr Gold nanorod-encapsulated biodegradable polymeric matrix for combined photothermal and chemo-cancer therapy
title_full_unstemmed Gold nanorod-encapsulated biodegradable polymeric matrix for combined photothermal and chemo-cancer therapy
title_short Gold nanorod-encapsulated biodegradable polymeric matrix for combined photothermal and chemo-cancer therapy
title_sort gold nanorod-encapsulated biodegradable polymeric matrix for combined photothermal and chemo-cancer therapy
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6306055/
https://www.ncbi.nlm.nih.gov/pubmed/30613145
http://dx.doi.org/10.2147/IJN.S177851
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