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Encapsulation and release of non-fluorescent crystal violet confined in bile-salt aggregates

In this work, the entrapment of non-fluorescent dye Crystal Violet (CV) in presence of bio-mimetic confined bile-salt aggregates has been studied. The photophysical characteristic properties of CV have been carried out by changing different kinds of hydrophilic head groups and hydrophobic skeletons...

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Autores principales: Sharma, Prachi, Sohal, Neeraj, Maity, Banibrata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8695816/
https://www.ncbi.nlm.nih.gov/pubmed/35423564
http://dx.doi.org/10.1039/d0ra06599d
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author Sharma, Prachi
Sohal, Neeraj
Maity, Banibrata
author_facet Sharma, Prachi
Sohal, Neeraj
Maity, Banibrata
author_sort Sharma, Prachi
collection PubMed
description In this work, the entrapment of non-fluorescent dye Crystal Violet (CV) in presence of bio-mimetic confined bile-salt aggregates has been studied. The photophysical characteristic properties of CV have been carried out by changing different kinds of hydrophilic head groups and hydrophobic skeletons of bile-salt aggregates (NaC, NaDC, NaTC and NaTGC). The main aim of this work is to modulate the solubility behaviour, fluorescence properties and elucidation of different kinds of non-covalent interaction of CV confined in bile-salt aggregates. To interpret the result, steady state absorption and fluorescence emission techniques have been employed. In aqueous buffer, the CV molecule is non-fluorescent in nature. The value of fluorescence quantum yield (Φ) is ∼10(−4). It has been observed that CV confined in bile-salt aggregates becomes highly fluorescent in nature. The enhancement of ‘Φ’ value of CV in bile-salt aggregates is ∼1000 fold compared to that of aqueous buffer medium. It has also been observed that in the presence of different bile-salt aggregates, CV exhibits remarkable enhancement of absorption and fluorescence emission spectral behaviour. The ground state and the excited state binding constant values of CV in the presence of different bile-salt aggregates have been determined. Moreover, the release of the dye molecule from the confined bile-salt aggregates to the aqueous medium has been executed. It has been found that addition of a very minute concentration of KCl salt (100 nm) to the bile-salt aggregates leads to extreme modification of their photophysical properties of CV. The absorption, fluorescence intensity, fluorescence quantum yield, ground state and excited state binding constant values, partition coefficient and aggregation number of CV molecules entrapped in bile-salt aggregates significantly reduces by addition of KCl. This result clearly confirms that CV releases from the confined system to the aqueous medium.
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spelling pubmed-86958162022-04-13 Encapsulation and release of non-fluorescent crystal violet confined in bile-salt aggregates Sharma, Prachi Sohal, Neeraj Maity, Banibrata RSC Adv Chemistry In this work, the entrapment of non-fluorescent dye Crystal Violet (CV) in presence of bio-mimetic confined bile-salt aggregates has been studied. The photophysical characteristic properties of CV have been carried out by changing different kinds of hydrophilic head groups and hydrophobic skeletons of bile-salt aggregates (NaC, NaDC, NaTC and NaTGC). The main aim of this work is to modulate the solubility behaviour, fluorescence properties and elucidation of different kinds of non-covalent interaction of CV confined in bile-salt aggregates. To interpret the result, steady state absorption and fluorescence emission techniques have been employed. In aqueous buffer, the CV molecule is non-fluorescent in nature. The value of fluorescence quantum yield (Φ) is ∼10(−4). It has been observed that CV confined in bile-salt aggregates becomes highly fluorescent in nature. The enhancement of ‘Φ’ value of CV in bile-salt aggregates is ∼1000 fold compared to that of aqueous buffer medium. It has also been observed that in the presence of different bile-salt aggregates, CV exhibits remarkable enhancement of absorption and fluorescence emission spectral behaviour. The ground state and the excited state binding constant values of CV in the presence of different bile-salt aggregates have been determined. Moreover, the release of the dye molecule from the confined bile-salt aggregates to the aqueous medium has been executed. It has been found that addition of a very minute concentration of KCl salt (100 nm) to the bile-salt aggregates leads to extreme modification of their photophysical properties of CV. The absorption, fluorescence intensity, fluorescence quantum yield, ground state and excited state binding constant values, partition coefficient and aggregation number of CV molecules entrapped in bile-salt aggregates significantly reduces by addition of KCl. This result clearly confirms that CV releases from the confined system to the aqueous medium. The Royal Society of Chemistry 2021-03-15 /pmc/articles/PMC8695816/ /pubmed/35423564 http://dx.doi.org/10.1039/d0ra06599d Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Sharma, Prachi
Sohal, Neeraj
Maity, Banibrata
Encapsulation and release of non-fluorescent crystal violet confined in bile-salt aggregates
title Encapsulation and release of non-fluorescent crystal violet confined in bile-salt aggregates
title_full Encapsulation and release of non-fluorescent crystal violet confined in bile-salt aggregates
title_fullStr Encapsulation and release of non-fluorescent crystal violet confined in bile-salt aggregates
title_full_unstemmed Encapsulation and release of non-fluorescent crystal violet confined in bile-salt aggregates
title_short Encapsulation and release of non-fluorescent crystal violet confined in bile-salt aggregates
title_sort encapsulation and release of non-fluorescent crystal violet confined in bile-salt aggregates
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8695816/
https://www.ncbi.nlm.nih.gov/pubmed/35423564
http://dx.doi.org/10.1039/d0ra06599d
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