KFU. Card publication. Supramolecular assemblies involving calix[4]resorcinol and surfactant with pH-induced morphology transition for drug encapsulation

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SUPRAMOLECULAR ASSEMBLIES INVOLVING CALIX[4]RESORCINOL AND SURFACTANT WITH PH-INDUCED MORPHOLOGY TRANSITION FOR DRUG ENCAPSULATION

Form of presentation

Articles in international journals and collections

Year of publication

2018

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Authors, employees of KFU

Ziganshina Albina Yulduzovna, author

Bibliographic description in the original language

R. R. Kashapov, S. V. Kharlamov, Y. S. Razuvayeva, A. Yu. Ziganshina, I. R. Nizameev, M. K. Kadirov, Sh. K. Latypov, L. Ya. Zakharova, Supramolecular assemblies involving calix[4]resorcinol and surfactant with pH-induced morphology transition for drug encapsulation // J. Mol. Liq. – 2018. – 261. – 218–224.

Annotation

The present investigations concern the mixed aggregation of anionic surfactant sodium dodecyl sulfate (SDS) and aminomethylated calix[4]resorcinol (ACR) with ethylsulfonate groups on the lower rim. The interaction between these compounds was investigated by DOSY NMR, tensiometry, conductometry, dynamic and electrophoretic light scattering, atomic force microscopy and drug solubilization. The mixed supramolecular systems based on ACR and SDS can be derived due to pH-switchable properties. Supramolecular assembly took place in acidic medium which caused protonation of the amine groups of ACR and thereby the interaction of charged species in solution. Remarkably, the globular SDS micelles were observed to transform into rod-like micelles in the presence of ACR at lower pH, which can be used to encapsulate the hydrophobic guest molecules.

Keywords

calix[4]resorcinol

The name of the journal

Journal of Molecular Liquids

URL

https://www.sciencedirect.com/science/article/abs/pii/S0167732218308602?via%3Dihub

Please use this ID to quote from or refer to the card

https://repository.kpfu.ru/eng/?p_id=262905&p_lang=2

Full metadata record

Field DC	Value	Language
dc.contributor.author	Ziganshina Albina Yulduzovna	ru_RU
dc.date.accessioned	2018-01-01T00:00:00Z	ru_RU
dc.date.available	2018-01-01T00:00:00Z	ru_RU
dc.date.issued	2018	ru_RU
dc.identifier.citation	R. R. Kashapov, S. V. Kharlamov, Y. S. Razuvayeva, A. Yu. Ziganshina, I. R. Nizameev, M. K. Kadirov, Sh. K. Latypov, L. Ya. Zakharova, Supramolecular assemblies involving calix[4]resorcinol and surfactant with pH-induced morphology transition for drug encapsulation // J. Mol. Liq. – 2018. – 261. – 218–224.	ru_RU
dc.identifier.uri	https://repository.kpfu.ru/eng/?p_id=262905&p_lang=2	ru_RU
dc.description.abstract	Journal of Molecular Liquids	ru_RU
dc.description.abstract	The present investigations concern the mixed aggregation of anionic surfactant sodium dodecyl sulfate (SDS) and aminomethylated calix[4]resorcinol (ACR) with ethylsulfonate groups on the lower rim. The interaction between these compounds was investigated by DOSY NMR, tensiometry, conductometry, dynamic and electrophoretic light scattering, atomic force microscopy and drug solubilization. The mixed supramolecular systems based on ACR and SDS can be derived due to pH-switchable properties. Supramolecular assembly took place in acidic medium which caused protonation of the amine groups of ACR and thereby the interaction of charged species in solution. Remarkably, the globular SDS micelles were observed to transform into rod-like micelles in the presence of ACR at lower pH, which can be used to encapsulate the hydrophobic guest molecules.	ru_RU
dc.language.iso	ru	ru_RU
dc.subject		ru_RU
dc.title	Supramolecular assemblies involving calix[4]resorcinol and surfactant with pH-induced morphology transition for drug encapsulation	ru_RU
dc.type	Articles in international journals and collections	ru_RU