Электронный архив

Synthesis, biological evaluation and structure-activity relationships of self-assembled and solubilization properties of amphiphilic quaternary ammonium derivatives of quinuclidine

Показать сокращенную информацию

dc.contributor.author Burilova E.
dc.contributor.author Pashirova T.
dc.contributor.author Lukashenko S.
dc.contributor.author Sapunova A.
dc.contributor.author Voloshina A.
dc.contributor.author Zhiltsova E.
dc.contributor.author Campos J.
dc.contributor.author Souto E.
dc.contributor.author Zakharova L.
dc.date.accessioned 2019-01-22T20:35:43Z
dc.date.available 2019-01-22T20:35:43Z
dc.date.issued 2018
dc.identifier.issn 0167-7322
dc.identifier.uri https://dspace.kpfu.ru/xmlui/handle/net/147877
dc.description.abstract © 2018 Elsevier B.V. This work deals with development of polyfunctional biocompatible cationic surfactant systems based on bioactive saturated bicyclic alkaloid quinuclidine. It is focused on the effect of the chemical structure of surfactants on their aggregation behavior, their physicochemical estimation of solubility of model water insoluble dye Orange OT and drugs, quercetin and rutin, microbiology and cytotoxicity. Quaternary ammonium derivatives of quinuclidine (Q-Nuc-n) with different hydrophobicity (R = CnH2n+1, where n = 14, 16, 18) were synthesized. Self-assembly of Q-Nuc-n was investigated by tensiometry, conductometry, spectrophotometry, fluorimetry and dynamic light scattering. The critical micelle concentration, thermodynamic and adsorption parameters at water-air interface, size and aggregation numbers of Q-Nuc-n micelles were determined. The looser packing of surfactant molecules in Q-Nuc-n micelles compared to its analogues, quaternized derivatives of 1,4‑diazabicyclo[2.2.2]octane (DABCO-n), was established. The hydrophobic dye Orange OT and drugs quercetin and rutin were solubilized in micellar Q-Nuc-n solutions better than in solutions of classical surfactant CTAB and its analogue DABCO-n. Solubilization capacity of Q-Nuc-18 is 5 times higher than that of classical surfactant CTAB. Q-Nuc-18 1.95 μg·mL−1 has also bactericidal and fungicidal activity 2 times (against S. aureus 209P) and 8 times (against B. cereus 8035) higher than antibiotics Norfloxacin and antifungal Ketoconazole. Q-Nuc-16 has the highest bactericidal activity. It is 6 times (against S. aureus 209P) and 15 times (against B. cereus 8035) higher than the bactericidal activity value of Norfloxacin. Synthesized cationic surfactants based on quinuclidine are new multifunctional biocompatible compounds with high potential in nanomedicine and biotechnology.
dc.relation.ispartofseries Journal of Molecular Liquids
dc.subject Antimicrobial activity
dc.subject Cytotoxicity
dc.subject Quaternary ammonium derivatives of quinuclidine
dc.subject Quercetin
dc.subject Rutin
dc.subject Solubilization
dc.title Synthesis, biological evaluation and structure-activity relationships of self-assembled and solubilization properties of amphiphilic quaternary ammonium derivatives of quinuclidine
dc.type Article
dc.relation.ispartofseries-volume 272
dc.collection Публикации сотрудников КФУ
dc.relation.startpage 722
dc.source.id SCOPUS01677322-2018-272-SID85054307666


Файлы в этом документе

Данный элемент включен в следующие коллекции

  • Публикации сотрудников КФУ Scopus [24551]
    Коллекция содержит публикации сотрудников Казанского федерального (до 2010 года Казанского государственного) университета, проиндексированные в БД Scopus, начиная с 1970г.

Показать сокращенную информацию

Поиск в электронном архиве


Расширенный поиск

Просмотр

Моя учетная запись

Статистика