DNase I-Responsive Calixpyridinium-Mediated DNA Aggregation

In this work, cationic macrocyclic calixpyridinium was employed as a new strategy to condense DNA. Moreover, the degradation of DNA by DNase I could lead to the calixpyridinium-DNA supramolecular aggregates being dissipated. Therefore, the present system is potentially applicable as the targeted dru...

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Détails bibliographiques
Publié dans:Langmuir : the ACS journal of surfaces and colloids. - 1985. - 35(2019), 32 vom: 13. Aug., Seite 10505-10511
Auteur principal: Wang, Kui (Auteur)
Autres auteurs: Ren, Xiao-Wei, Wang, Xiao-Yan, Xing, Si-Yang, Zhu, Bo-Lin, Liu, Chang
Format: Article en ligne
Langue:English
Publié: 2019
Accès à la collection:Langmuir : the ACS journal of surfaces and colloids
Sujets:Journal Article Research Support, Non-U.S. Gov't Calixarenes 130036-26-9 DNA 9007-49-2 Deoxyribonuclease I EC 3.1.21.1
Description
Résumé:In this work, cationic macrocyclic calixpyridinium was employed as a new strategy to condense DNA. Moreover, the degradation of DNA by DNase I could lead to the calixpyridinium-DNA supramolecular aggregates being dissipated. Therefore, the present system is potentially applicable as the targeted drug delivery model at DNase I-overexpressed sites
Description:Date Completed 13.08.2020
Date Revised 13.08.2020
published: Print-Electronic
Citation Status MEDLINE
ISSN:1520-5827
DOI:10.1021/acs.langmuir.9b01116