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Facilitated permeation of insulin across TR146 cells by cholic acid derivatives-modified elastic bilosomes

BACKGROUND: Buccal delivery of insulin is still a challenging issue for the researchers due to the presence of permeability barrier (buccal mucosa) in the buccal cavity. The main objective of this study was to investigate the safety, effectiveness, and potential of various liposomes containing diffe...

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Autores principales: Bashyal, Santosh, Seo, Jo-Eun, Keum, Taekwang, Noh, Gyubin, Choi, Young Wook, Lee, Sangkil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6135218/
https://www.ncbi.nlm.nih.gov/pubmed/30233179
http://dx.doi.org/10.2147/IJN.S168310
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author Bashyal, Santosh
Seo, Jo-Eun
Keum, Taekwang
Noh, Gyubin
Choi, Young Wook
Lee, Sangkil
author_facet Bashyal, Santosh
Seo, Jo-Eun
Keum, Taekwang
Noh, Gyubin
Choi, Young Wook
Lee, Sangkil
author_sort Bashyal, Santosh
collection PubMed
description BACKGROUND: Buccal delivery of insulin is still a challenging issue for the researchers due to the presence of permeability barrier (buccal mucosa) in the buccal cavity. The main objective of this study was to investigate the safety, effectiveness, and potential of various liposomes containing different bile salts to improve the permeation of insulin across in vitro TR146 buccal cell layers. METHODS: Elastic bilosomes containing soy lecithin and bile salt edge activators (sodium cholate [SC], sodium taurocholate [STC], sodium glycocholate [SGC], sodium deoxyglycocholate [SDGC], or sodium deoxytaurocholate [SDTC]) were fabricated by thin-film hydration method. The prepared liposomes were characterized, and in vitro permeation studies were performed. The fluorescein isothiocyanate-insulin-loaded elastic bilosomes were used to evaluate the quantitative and qualitative cellular uptake studies. RESULTS: The prepared elastic bilosomes had a particle size and an entrapment efficiency of ~140–150 nm and 66%–78%, respectively. SDGC-lipo (SDGC-incorporated liposome) was observed to be the most superior with an enhancement ratio (ER) of 5.24 (P<0.001). The SC-incorporated liposome (SC-lipo) and SDTC-incorporated liposome (SDTC-lipo) also led to a significant enhancement with ERs of 3.20 and 3.10 (P<0.05), respectively, compared with insulin solution. These results were further supported by quantitative and qualitative cellular uptake studies performed employing fluorescence-activated cell sorting analysis and confocal microscopy, respectively. The relative median fluorescence intensity values of elastic bilosomes were counted in the order of SDGC-lipo > SC-lipo > SDTC-lipo > SGC-incorporated liposome > STC-incorporated liposome, and similarity in the permeability profile of the employed elastic bilosomes was noted. CONCLUSION: This study presents the employment of various derivatives of cholic acid-loaded elastic bilosomes as a promising strategy to enhance the permeation of insulin through buccal route.
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spelling pubmed-61352182018-09-19 Facilitated permeation of insulin across TR146 cells by cholic acid derivatives-modified elastic bilosomes Bashyal, Santosh Seo, Jo-Eun Keum, Taekwang Noh, Gyubin Choi, Young Wook Lee, Sangkil Int J Nanomedicine Original Research BACKGROUND: Buccal delivery of insulin is still a challenging issue for the researchers due to the presence of permeability barrier (buccal mucosa) in the buccal cavity. The main objective of this study was to investigate the safety, effectiveness, and potential of various liposomes containing different bile salts to improve the permeation of insulin across in vitro TR146 buccal cell layers. METHODS: Elastic bilosomes containing soy lecithin and bile salt edge activators (sodium cholate [SC], sodium taurocholate [STC], sodium glycocholate [SGC], sodium deoxyglycocholate [SDGC], or sodium deoxytaurocholate [SDTC]) were fabricated by thin-film hydration method. The prepared liposomes were characterized, and in vitro permeation studies were performed. The fluorescein isothiocyanate-insulin-loaded elastic bilosomes were used to evaluate the quantitative and qualitative cellular uptake studies. RESULTS: The prepared elastic bilosomes had a particle size and an entrapment efficiency of ~140–150 nm and 66%–78%, respectively. SDGC-lipo (SDGC-incorporated liposome) was observed to be the most superior with an enhancement ratio (ER) of 5.24 (P<0.001). The SC-incorporated liposome (SC-lipo) and SDTC-incorporated liposome (SDTC-lipo) also led to a significant enhancement with ERs of 3.20 and 3.10 (P<0.05), respectively, compared with insulin solution. These results were further supported by quantitative and qualitative cellular uptake studies performed employing fluorescence-activated cell sorting analysis and confocal microscopy, respectively. The relative median fluorescence intensity values of elastic bilosomes were counted in the order of SDGC-lipo > SC-lipo > SDTC-lipo > SGC-incorporated liposome > STC-incorporated liposome, and similarity in the permeability profile of the employed elastic bilosomes was noted. CONCLUSION: This study presents the employment of various derivatives of cholic acid-loaded elastic bilosomes as a promising strategy to enhance the permeation of insulin through buccal route. Dove Medical Press 2018-09-06 /pmc/articles/PMC6135218/ /pubmed/30233179 http://dx.doi.org/10.2147/IJN.S168310 Text en © 2018 Bashyal 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
Bashyal, Santosh
Seo, Jo-Eun
Keum, Taekwang
Noh, Gyubin
Choi, Young Wook
Lee, Sangkil
Facilitated permeation of insulin across TR146 cells by cholic acid derivatives-modified elastic bilosomes
title Facilitated permeation of insulin across TR146 cells by cholic acid derivatives-modified elastic bilosomes
title_full Facilitated permeation of insulin across TR146 cells by cholic acid derivatives-modified elastic bilosomes
title_fullStr Facilitated permeation of insulin across TR146 cells by cholic acid derivatives-modified elastic bilosomes
title_full_unstemmed Facilitated permeation of insulin across TR146 cells by cholic acid derivatives-modified elastic bilosomes
title_short Facilitated permeation of insulin across TR146 cells by cholic acid derivatives-modified elastic bilosomes
title_sort facilitated permeation of insulin across tr146 cells by cholic acid derivatives-modified elastic bilosomes
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6135218/
https://www.ncbi.nlm.nih.gov/pubmed/30233179
http://dx.doi.org/10.2147/IJN.S168310
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