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Self-assembling surfactant-like peptide A(6)K as potential delivery system for hydrophobic drugs
BACKGROUND: Finding a suitable delivery system to improve the water solubility of hydrophobic drugs is a critical challenge in the development of effective formulations. In this study, we used A(6)K, a self-assembling surfactant-like peptide, as a carrier to encapsulate and deliver hydrophobic pyren...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4315539/ https://www.ncbi.nlm.nih.gov/pubmed/25670898 http://dx.doi.org/10.2147/IJN.S71696 |
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author | Chen, Yongzhu Tang, Chengkang Zhang, Jie Gong, Meng Su, Bo Qiu, Feng |
author_facet | Chen, Yongzhu Tang, Chengkang Zhang, Jie Gong, Meng Su, Bo Qiu, Feng |
author_sort | Chen, Yongzhu |
collection | PubMed |
description | BACKGROUND: Finding a suitable delivery system to improve the water solubility of hydrophobic drugs is a critical challenge in the development of effective formulations. In this study, we used A(6)K, a self-assembling surfactant-like peptide, as a carrier to encapsulate and deliver hydrophobic pyrene. METHODS: Pyrene was mixed with A(6)K by magnetic stirring to form a suspension. Confocal laser scanning microscopy, transmission electron microscopy, dynamic light scattering, atomic force microscopy, fluorescence, and cell uptake measurements were carried out to study the features and stability of the nanostructures, the state and content of pyrene, as well as the pyrene release profile. RESULTS: The suspension formed contained pyrene monomers trapped in the hydrophobic cores of the micellar nanofibers formed by A(6)K, as well as nanosized pyrene crystals wrapped up and stabilized by the nanofibers. The two different encapsulation methods greatly increased the concentration of pyrene in the suspension, and formation of pyrene crystals wrapped up by A(6)K nanofibers might be the major contributor to this effect. Furthermore, the suspension system could readily release and transfer pyrene into living cells. CONCLUSION: A(6)K could be further exploited as a promising delivery system for hydrophobic drugs. |
format | Online Article Text |
id | pubmed-4315539 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-43155392015-02-10 Self-assembling surfactant-like peptide A(6)K as potential delivery system for hydrophobic drugs Chen, Yongzhu Tang, Chengkang Zhang, Jie Gong, Meng Su, Bo Qiu, Feng Int J Nanomedicine Original Research BACKGROUND: Finding a suitable delivery system to improve the water solubility of hydrophobic drugs is a critical challenge in the development of effective formulations. In this study, we used A(6)K, a self-assembling surfactant-like peptide, as a carrier to encapsulate and deliver hydrophobic pyrene. METHODS: Pyrene was mixed with A(6)K by magnetic stirring to form a suspension. Confocal laser scanning microscopy, transmission electron microscopy, dynamic light scattering, atomic force microscopy, fluorescence, and cell uptake measurements were carried out to study the features and stability of the nanostructures, the state and content of pyrene, as well as the pyrene release profile. RESULTS: The suspension formed contained pyrene monomers trapped in the hydrophobic cores of the micellar nanofibers formed by A(6)K, as well as nanosized pyrene crystals wrapped up and stabilized by the nanofibers. The two different encapsulation methods greatly increased the concentration of pyrene in the suspension, and formation of pyrene crystals wrapped up by A(6)K nanofibers might be the major contributor to this effect. Furthermore, the suspension system could readily release and transfer pyrene into living cells. CONCLUSION: A(6)K could be further exploited as a promising delivery system for hydrophobic drugs. Dove Medical Press 2015-01-23 /pmc/articles/PMC4315539/ /pubmed/25670898 http://dx.doi.org/10.2147/IJN.S71696 Text en © 2015 Chen 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 Chen, Yongzhu Tang, Chengkang Zhang, Jie Gong, Meng Su, Bo Qiu, Feng Self-assembling surfactant-like peptide A(6)K as potential delivery system for hydrophobic drugs |
title | Self-assembling surfactant-like peptide A(6)K as potential delivery system for hydrophobic drugs |
title_full | Self-assembling surfactant-like peptide A(6)K as potential delivery system for hydrophobic drugs |
title_fullStr | Self-assembling surfactant-like peptide A(6)K as potential delivery system for hydrophobic drugs |
title_full_unstemmed | Self-assembling surfactant-like peptide A(6)K as potential delivery system for hydrophobic drugs |
title_short | Self-assembling surfactant-like peptide A(6)K as potential delivery system for hydrophobic drugs |
title_sort | self-assembling surfactant-like peptide a(6)k as potential delivery system for hydrophobic drugs |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4315539/ https://www.ncbi.nlm.nih.gov/pubmed/25670898 http://dx.doi.org/10.2147/IJN.S71696 |
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