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Enhanced local bioavailability of single or compound drugs delivery to the inner ear through application of PLGA nanoparticles via round window administration

In this paper, the potential of poly(d,l-lactide-co-glycolide acid) (PLGA) nanoparticles (NPs) for carrying single or compound drugs traversing the round window membrane (RWM) was examined after the round window (RW) administration of different NPs to guinea pigs. First, coumarin-6 was incorporated...

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Autores principales: Cai, Hui, Wen, Xingxing, Wen, Lu, Tirelli, Nicola, Zhang, Xiao, Zhang, Yue, Su, Huanpeng, Yang, Fan, Chen, Gang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4257110/
https://www.ncbi.nlm.nih.gov/pubmed/25489245
http://dx.doi.org/10.2147/IJN.S72555
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author Cai, Hui
Wen, Xingxing
Wen, Lu
Tirelli, Nicola
Zhang, Xiao
Zhang, Yue
Su, Huanpeng
Yang, Fan
Chen, Gang
author_facet Cai, Hui
Wen, Xingxing
Wen, Lu
Tirelli, Nicola
Zhang, Xiao
Zhang, Yue
Su, Huanpeng
Yang, Fan
Chen, Gang
author_sort Cai, Hui
collection PubMed
description In this paper, the potential of poly(d,l-lactide-co-glycolide acid) (PLGA) nanoparticles (NPs) for carrying single or compound drugs traversing the round window membrane (RWM) was examined after the round window (RW) administration of different NPs to guinea pigs. First, coumarin-6 was incorporated into PLGA NPs as a fluorescent probe to investigate its ability to cross the RWM. Then, PLGA NPs with salvianolic acid B (Sal B), tanshinone IIA (TS IIA), and total panax notoginsenoside (PNS) including notoginsenoside R(1) (R(1)), ginsenoside Rg(1) (Rg(1)), and ginsenoside Rb(1) (Rb(1)) were developed to evaluate whether NPs loaded with compound drugs would pass through the RWM and improve the local bioavailability of these agents. PLGA NPs loaded with single or compound drugs were prepared by the emulsification solvent evaporation method, and their particle size distribution, particle morphology, and encapsulation efficiency were characterized. In vitro release study showed sustained-release profiles of Sal B, TS IIA, and PNS from the NPs. The pharmacokinetic results showed that NPs applied to the RWM significantly improved drug distribution within the inner ear. The AUC(0–t) of coumarin-6 in the perilymph (PL) following RW administration of NPs was 4.7-fold higher than that of coumarin-6 solution, and the C(max) was 10.9-fold higher. Furthermore, the AUC(0–t) of R(1), Rg(1), and Rb(1) were 4.0-, 3.1-, and 7.1-fold greater, respectively, after the application of NPs compared to the compound solution, and the C(max) were, respectively, 14.4-, 10.0-, and 16.7-fold higher. These findings suggest that PLGA NPs with unique properties at the nanoscale dimensions have a powerful ability to transport single or compound drugs into the PL through the RWM and remarkably enhance the local bioavailability of the encapsulated drugs in the inner ear. The use of PLGA NPs as nanoscale delivery vehicles to carry drugs across the RWM may be a promising strategy for the treatment of inner ear diseases.
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spelling pubmed-42571102014-12-08 Enhanced local bioavailability of single or compound drugs delivery to the inner ear through application of PLGA nanoparticles via round window administration Cai, Hui Wen, Xingxing Wen, Lu Tirelli, Nicola Zhang, Xiao Zhang, Yue Su, Huanpeng Yang, Fan Chen, Gang Int J Nanomedicine Original Research In this paper, the potential of poly(d,l-lactide-co-glycolide acid) (PLGA) nanoparticles (NPs) for carrying single or compound drugs traversing the round window membrane (RWM) was examined after the round window (RW) administration of different NPs to guinea pigs. First, coumarin-6 was incorporated into PLGA NPs as a fluorescent probe to investigate its ability to cross the RWM. Then, PLGA NPs with salvianolic acid B (Sal B), tanshinone IIA (TS IIA), and total panax notoginsenoside (PNS) including notoginsenoside R(1) (R(1)), ginsenoside Rg(1) (Rg(1)), and ginsenoside Rb(1) (Rb(1)) were developed to evaluate whether NPs loaded with compound drugs would pass through the RWM and improve the local bioavailability of these agents. PLGA NPs loaded with single or compound drugs were prepared by the emulsification solvent evaporation method, and their particle size distribution, particle morphology, and encapsulation efficiency were characterized. In vitro release study showed sustained-release profiles of Sal B, TS IIA, and PNS from the NPs. The pharmacokinetic results showed that NPs applied to the RWM significantly improved drug distribution within the inner ear. The AUC(0–t) of coumarin-6 in the perilymph (PL) following RW administration of NPs was 4.7-fold higher than that of coumarin-6 solution, and the C(max) was 10.9-fold higher. Furthermore, the AUC(0–t) of R(1), Rg(1), and Rb(1) were 4.0-, 3.1-, and 7.1-fold greater, respectively, after the application of NPs compared to the compound solution, and the C(max) were, respectively, 14.4-, 10.0-, and 16.7-fold higher. These findings suggest that PLGA NPs with unique properties at the nanoscale dimensions have a powerful ability to transport single or compound drugs into the PL through the RWM and remarkably enhance the local bioavailability of the encapsulated drugs in the inner ear. The use of PLGA NPs as nanoscale delivery vehicles to carry drugs across the RWM may be a promising strategy for the treatment of inner ear diseases. Dove Medical Press 2014-12-01 /pmc/articles/PMC4257110/ /pubmed/25489245 http://dx.doi.org/10.2147/IJN.S72555 Text en © 2014 Cai 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
Cai, Hui
Wen, Xingxing
Wen, Lu
Tirelli, Nicola
Zhang, Xiao
Zhang, Yue
Su, Huanpeng
Yang, Fan
Chen, Gang
Enhanced local bioavailability of single or compound drugs delivery to the inner ear through application of PLGA nanoparticles via round window administration
title Enhanced local bioavailability of single or compound drugs delivery to the inner ear through application of PLGA nanoparticles via round window administration
title_full Enhanced local bioavailability of single or compound drugs delivery to the inner ear through application of PLGA nanoparticles via round window administration
title_fullStr Enhanced local bioavailability of single or compound drugs delivery to the inner ear through application of PLGA nanoparticles via round window administration
title_full_unstemmed Enhanced local bioavailability of single or compound drugs delivery to the inner ear through application of PLGA nanoparticles via round window administration
title_short Enhanced local bioavailability of single or compound drugs delivery to the inner ear through application of PLGA nanoparticles via round window administration
title_sort enhanced local bioavailability of single or compound drugs delivery to the inner ear through application of plga nanoparticles via round window administration
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4257110/
https://www.ncbi.nlm.nih.gov/pubmed/25489245
http://dx.doi.org/10.2147/IJN.S72555
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