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Thermodynamically stable vesicle formation of biodegradable double mPEG-tailed amphiphiles with sulfonate head group

The development of efficient, biodegradable and biocompatible surfactants has become a pressing need because of adverse effects of surface-active compounds on the aquatic environment and human health. Cleavable surfactants containing a labile functional group have the ability to eliminate some of th...

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Autores principales: Ghosh, Rita, Dey, Joykrishna, Kumar, B. V. N. Phani
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9056604/
https://www.ncbi.nlm.nih.gov/pubmed/35516463
http://dx.doi.org/10.1039/d0ra05613h
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author Ghosh, Rita
Dey, Joykrishna
Kumar, B. V. N. Phani
author_facet Ghosh, Rita
Dey, Joykrishna
Kumar, B. V. N. Phani
author_sort Ghosh, Rita
collection PubMed
description The development of efficient, biodegradable and biocompatible surfactants has become a pressing need because of adverse effects of surface-active compounds on the aquatic environment and human health. Cleavable surfactants containing a labile functional group have the ability to eliminate some of these problems. Consequently, PEGylated amphiphiles have found widespread applications in pharmaceutics, household purposes, and drug delivery. Herein we report synthesis and characterization of two novel amphiphiles which to our knowledge are the first examples of double PEG-tailed amphiphiles with an anionic head group. Considering their chemical structure, they are expected to be biodegradable, biocompatible, milder and less irritant than conventional surfactants. The solution behavior of these newly developed amphiphiles was thoroughly investigated in aqueous buffer (pH 7.0) at 25 °C. The surface activity of the compounds in aqueous buffer was studied by surface tension measurements. The self-assembly properties were investigated by various techniques such as fluorescence and NMR spectroscopy, dynamic light scattering, transmission electron microscopy, atomic force microscopy, and isothermal titration calorimetry. Both molecules were found to be surface active in water and exhibit spontaneous vesicle formation in the absence of any additives at room temperature. As in the cases of conventional surfactants, the self-assembly is driven by the hydrophobic effect. The vesicles produced in aqueous media were shown to encapsulate hydrophobic dyes and exhibit structural transitions upon addition of salts. The sensitivity of the vesicles to change in environments qualifies them for potential use in drug delivery.
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spelling pubmed-90566042022-05-04 Thermodynamically stable vesicle formation of biodegradable double mPEG-tailed amphiphiles with sulfonate head group Ghosh, Rita Dey, Joykrishna Kumar, B. V. N. Phani RSC Adv Chemistry The development of efficient, biodegradable and biocompatible surfactants has become a pressing need because of adverse effects of surface-active compounds on the aquatic environment and human health. Cleavable surfactants containing a labile functional group have the ability to eliminate some of these problems. Consequently, PEGylated amphiphiles have found widespread applications in pharmaceutics, household purposes, and drug delivery. Herein we report synthesis and characterization of two novel amphiphiles which to our knowledge are the first examples of double PEG-tailed amphiphiles with an anionic head group. Considering their chemical structure, they are expected to be biodegradable, biocompatible, milder and less irritant than conventional surfactants. The solution behavior of these newly developed amphiphiles was thoroughly investigated in aqueous buffer (pH 7.0) at 25 °C. The surface activity of the compounds in aqueous buffer was studied by surface tension measurements. The self-assembly properties were investigated by various techniques such as fluorescence and NMR spectroscopy, dynamic light scattering, transmission electron microscopy, atomic force microscopy, and isothermal titration calorimetry. Both molecules were found to be surface active in water and exhibit spontaneous vesicle formation in the absence of any additives at room temperature. As in the cases of conventional surfactants, the self-assembly is driven by the hydrophobic effect. The vesicles produced in aqueous media were shown to encapsulate hydrophobic dyes and exhibit structural transitions upon addition of salts. The sensitivity of the vesicles to change in environments qualifies them for potential use in drug delivery. The Royal Society of Chemistry 2020-09-02 /pmc/articles/PMC9056604/ /pubmed/35516463 http://dx.doi.org/10.1039/d0ra05613h Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Ghosh, Rita
Dey, Joykrishna
Kumar, B. V. N. Phani
Thermodynamically stable vesicle formation of biodegradable double mPEG-tailed amphiphiles with sulfonate head group
title Thermodynamically stable vesicle formation of biodegradable double mPEG-tailed amphiphiles with sulfonate head group
title_full Thermodynamically stable vesicle formation of biodegradable double mPEG-tailed amphiphiles with sulfonate head group
title_fullStr Thermodynamically stable vesicle formation of biodegradable double mPEG-tailed amphiphiles with sulfonate head group
title_full_unstemmed Thermodynamically stable vesicle formation of biodegradable double mPEG-tailed amphiphiles with sulfonate head group
title_short Thermodynamically stable vesicle formation of biodegradable double mPEG-tailed amphiphiles with sulfonate head group
title_sort thermodynamically stable vesicle formation of biodegradable double mpeg-tailed amphiphiles with sulfonate head group
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9056604/
https://www.ncbi.nlm.nih.gov/pubmed/35516463
http://dx.doi.org/10.1039/d0ra05613h
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