Back to Search Start Over

A Biocompatible Multilayer Film from an Asymmetric Picolinium-Containing Polycation with Fast Visible-Light/NIR-Degradability.

Authors :
Zhang H
Zhou T
Shen J
Zhang P
Chen X
Chen Y
Yu Y
Source :
Macromolecular rapid communications [Macromol Rapid Commun] 2019 Nov; Vol. 40 (22), pp. e1900441. Date of Electronic Publication: 2019 Sep 25.
Publication Year :
2019

Abstract

Finely tuning the photodegradation behavior of the layer-by-layer (LbL) film from the view of controlling the chemical structure of the film-building polymer is still a challenge in related fields. To meet this requirement, a photodegradable polymer (P1) is rationally designed for assembling a visible-light-degradable multilayer film with polystyrene sulfonate (PSS). Compared with similar photopolymers (P2 and P3), this asymmetric picolinium-containing polymer can significantly enhance the degradation rate of as-prepared LbL films; under the same degradation condition, the degradation rate of (P1/PSS)10 is 3 and 6.6 times that of (P2/PSS)10 and (P3/PSS)10, respectively. Moreover, near-infrared light (NIR) is available for triggering the degradation of this film with the assistance of upconversion nanoparticles of YbTm@Lu. The cell cytotoxicity and cell proliferation experiments reveal that P1 is nontoxic and favorable for cell proliferation at concentrations of up to 500 μg mL <superscript>-1</superscript> . As for (PSS/P1)10 films, the ratio of cell number of these two samples ((PSS/P1)10 modified: photodegraded) increases dramatically and reaches about 1.67:1 after 72 h incubation. On the basis of these results, it is anticipated that P1 and this LbL film is an exceptional candidate for visible-light/NIR degradable materials in materials and biological science, medicine, and optics.<br /> (© 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Details

Language :
English
ISSN :
1521-3927
Volume :
40
Issue :
22
Database :
MEDLINE
Journal :
Macromolecular rapid communications
Publication Type :
Academic Journal
Accession number :
31553508
Full Text :
https://doi.org/10.1002/marc.201900441