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Physicochemical Characterization of FRET-Labelled Chitosan Nanocapsules and Model Degradation Studies
Sub-micron o/w emulsions coated with chitosan have been used for drug delivery, quorum sensing inhibition, and vaccine development. To study interactions with biological systems, nanocapsules have been fluorescently labelled in previous works, but it is often difficult to distinguish the released la...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6215305/ https://www.ncbi.nlm.nih.gov/pubmed/30336593 http://dx.doi.org/10.3390/nano8100846 |
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author | Hoffmann, Stefan Gorzelanny, Christian Moerschbacher, Bruno Goycoolea, Francisco M. |
author_facet | Hoffmann, Stefan Gorzelanny, Christian Moerschbacher, Bruno Goycoolea, Francisco M. |
author_sort | Hoffmann, Stefan |
collection | PubMed |
description | Sub-micron o/w emulsions coated with chitosan have been used for drug delivery, quorum sensing inhibition, and vaccine development. To study interactions with biological systems, nanocapsules have been fluorescently labelled in previous works, but it is often difficult to distinguish the released label from intact nanocapsules. In this study, we present advanced-labelling strategies based on Förster Resonance Energy Transfer (FRET) measurements for chitosan-coated nanocapsules and investigate their dissolution and degradation. We used FRET measurements of nanocapsules loaded with equimolar concentrations of two fluorescent dyes in their oily core and correlated them with dynamic light scattering (DLS) count rate measurement and absorbance measurements during their disintegration by dissolution. Using count rate measurements, we also investigated the enzymatic degradation of nanocapsules using pancreatin and how protein corona formation influences their degradation. Of note, nanocapsules dissolved in ethanol, while FRET decreased simultaneously with count rate, and absorbance was caused by nanocapsule turbidity, indicating increased distance between dye molecules after their release. Nanocapsules were degradable by pancreatin in a dose-dependent manner, and showed a delayed enzymatic degradation after protein corona formation. We present here novel labelling strategies for nanocapsules that allow us to judge their status and an in vitro method to study nanocapsule degradation and the influence of surface characteristics. |
format | Online Article Text |
id | pubmed-6215305 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62153052018-11-14 Physicochemical Characterization of FRET-Labelled Chitosan Nanocapsules and Model Degradation Studies Hoffmann, Stefan Gorzelanny, Christian Moerschbacher, Bruno Goycoolea, Francisco M. Nanomaterials (Basel) Article Sub-micron o/w emulsions coated with chitosan have been used for drug delivery, quorum sensing inhibition, and vaccine development. To study interactions with biological systems, nanocapsules have been fluorescently labelled in previous works, but it is often difficult to distinguish the released label from intact nanocapsules. In this study, we present advanced-labelling strategies based on Förster Resonance Energy Transfer (FRET) measurements for chitosan-coated nanocapsules and investigate their dissolution and degradation. We used FRET measurements of nanocapsules loaded with equimolar concentrations of two fluorescent dyes in their oily core and correlated them with dynamic light scattering (DLS) count rate measurement and absorbance measurements during their disintegration by dissolution. Using count rate measurements, we also investigated the enzymatic degradation of nanocapsules using pancreatin and how protein corona formation influences their degradation. Of note, nanocapsules dissolved in ethanol, while FRET decreased simultaneously with count rate, and absorbance was caused by nanocapsule turbidity, indicating increased distance between dye molecules after their release. Nanocapsules were degradable by pancreatin in a dose-dependent manner, and showed a delayed enzymatic degradation after protein corona formation. We present here novel labelling strategies for nanocapsules that allow us to judge their status and an in vitro method to study nanocapsule degradation and the influence of surface characteristics. MDPI 2018-10-17 /pmc/articles/PMC6215305/ /pubmed/30336593 http://dx.doi.org/10.3390/nano8100846 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Hoffmann, Stefan Gorzelanny, Christian Moerschbacher, Bruno Goycoolea, Francisco M. Physicochemical Characterization of FRET-Labelled Chitosan Nanocapsules and Model Degradation Studies |
title | Physicochemical Characterization of FRET-Labelled Chitosan Nanocapsules and Model Degradation Studies |
title_full | Physicochemical Characterization of FRET-Labelled Chitosan Nanocapsules and Model Degradation Studies |
title_fullStr | Physicochemical Characterization of FRET-Labelled Chitosan Nanocapsules and Model Degradation Studies |
title_full_unstemmed | Physicochemical Characterization of FRET-Labelled Chitosan Nanocapsules and Model Degradation Studies |
title_short | Physicochemical Characterization of FRET-Labelled Chitosan Nanocapsules and Model Degradation Studies |
title_sort | physicochemical characterization of fret-labelled chitosan nanocapsules and model degradation studies |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6215305/ https://www.ncbi.nlm.nih.gov/pubmed/30336593 http://dx.doi.org/10.3390/nano8100846 |
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