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Fiber-optic triggered release of liposome in vivo: implication of personalized chemotherapy

The aim of this research is to provide proof of principle by applying the fiber-optic triggered release of photo-thermally responsive liposomes embedded with gold nanoparticles (AuNPs) using a 200 μm fiber with 65 mW and 532 nm excitation for topical release in vivo. The tunable delivery function ca...

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Autores principales: Huang, Huei-Ling, Lu, Pei-Hsuan, Yang, Hung-Chih, Lee, Gi-Da, Li, Han-Ru, Liao, Kuo-Chih
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4542555/
https://www.ncbi.nlm.nih.gov/pubmed/26316748
http://dx.doi.org/10.2147/IJN.S85915
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author Huang, Huei-Ling
Lu, Pei-Hsuan
Yang, Hung-Chih
Lee, Gi-Da
Li, Han-Ru
Liao, Kuo-Chih
author_facet Huang, Huei-Ling
Lu, Pei-Hsuan
Yang, Hung-Chih
Lee, Gi-Da
Li, Han-Ru
Liao, Kuo-Chih
author_sort Huang, Huei-Ling
collection PubMed
description The aim of this research is to provide proof of principle by applying the fiber-optic triggered release of photo-thermally responsive liposomes embedded with gold nanoparticles (AuNPs) using a 200 μm fiber with 65 mW and 532 nm excitation for topical release in vivo. The tunable delivery function can be paired with an apoptosis biosensor based on the same fiber-optic configuration for providing real-time evaluation of chemotherapy efficacy in vivo to perform as a personalized chemotherapy system. The pattern of topical release triggered by laser excitation conveyed through optical fibers was monitored by the increase in fluorescence resulting from the dilution of self-quenching (75 mM) fluorescein encapsulated in liposomes. In in vitro studies (in 37°C phosphate buffer saline), the AuNP-embedded liposomes showed a more efficient triggered release (74.53%±1.63% in 40 minutes) than traditional temperature-responsive liposomes without AuNPs (14.53%±3.17%) or AuNP-liposomes without excitation (21.92%±2.08%) by spectroscopic measurements. Using the mouse xenograft studies, we first demonstrated that the encapsulation of fluorescein in liposomes resulted in a more substantial content retention (81%) in the tumor than for free fluorophores (14%) at 120 minutes after administration from in vivo fluorescence imaging. Furthermore, the preliminary results also suggested the tunable release capability of the system by demonstrating consecutive triggered releases with fiber-optic guided laser excitation.
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spelling pubmed-45425552015-08-27 Fiber-optic triggered release of liposome in vivo: implication of personalized chemotherapy Huang, Huei-Ling Lu, Pei-Hsuan Yang, Hung-Chih Lee, Gi-Da Li, Han-Ru Liao, Kuo-Chih Int J Nanomedicine Original Research The aim of this research is to provide proof of principle by applying the fiber-optic triggered release of photo-thermally responsive liposomes embedded with gold nanoparticles (AuNPs) using a 200 μm fiber with 65 mW and 532 nm excitation for topical release in vivo. The tunable delivery function can be paired with an apoptosis biosensor based on the same fiber-optic configuration for providing real-time evaluation of chemotherapy efficacy in vivo to perform as a personalized chemotherapy system. The pattern of topical release triggered by laser excitation conveyed through optical fibers was monitored by the increase in fluorescence resulting from the dilution of self-quenching (75 mM) fluorescein encapsulated in liposomes. In in vitro studies (in 37°C phosphate buffer saline), the AuNP-embedded liposomes showed a more efficient triggered release (74.53%±1.63% in 40 minutes) than traditional temperature-responsive liposomes without AuNPs (14.53%±3.17%) or AuNP-liposomes without excitation (21.92%±2.08%) by spectroscopic measurements. Using the mouse xenograft studies, we first demonstrated that the encapsulation of fluorescein in liposomes resulted in a more substantial content retention (81%) in the tumor than for free fluorophores (14%) at 120 minutes after administration from in vivo fluorescence imaging. Furthermore, the preliminary results also suggested the tunable release capability of the system by demonstrating consecutive triggered releases with fiber-optic guided laser excitation. Dove Medical Press 2015-08-14 /pmc/articles/PMC4542555/ /pubmed/26316748 http://dx.doi.org/10.2147/IJN.S85915 Text en © 2015 Huang et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. 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
Huang, Huei-Ling
Lu, Pei-Hsuan
Yang, Hung-Chih
Lee, Gi-Da
Li, Han-Ru
Liao, Kuo-Chih
Fiber-optic triggered release of liposome in vivo: implication of personalized chemotherapy
title Fiber-optic triggered release of liposome in vivo: implication of personalized chemotherapy
title_full Fiber-optic triggered release of liposome in vivo: implication of personalized chemotherapy
title_fullStr Fiber-optic triggered release of liposome in vivo: implication of personalized chemotherapy
title_full_unstemmed Fiber-optic triggered release of liposome in vivo: implication of personalized chemotherapy
title_short Fiber-optic triggered release of liposome in vivo: implication of personalized chemotherapy
title_sort fiber-optic triggered release of liposome in vivo: implication of personalized chemotherapy
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4542555/
https://www.ncbi.nlm.nih.gov/pubmed/26316748
http://dx.doi.org/10.2147/IJN.S85915
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