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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Characterization of PMMA-b-PDMAEMA aggregates in aqueous solutions

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Author(s):
Saraiva, G. K. V. [1] ; de Souza, V. V. [1] ; Coutinho de Oliveira, L. [1, 2] ; Noronha, M. L. C. [3, 4] ; Masini, J. C. [5] ; Chaimovich, H. [1] ; Salinas, R. K. [1] ; Florenzano, F. H. [6] ; Cuccovia, I. M. [1]
Total Authors: 9
Affiliation:
[1] Univ Sao Paulo, Dept Bioquim, Inst Quim, Sao Paulo - Brazil
[2] INRS Inst Armand Frappier, 531 Blvd Prairies, Laval, PQ H7V 1B7 - Canada
[3] Univ Fed Alfenas, Inst Ciencias Exatas, Alfenas - Brazil
[4] Ctr Univ Itajuba, Itajuba - Brazil
[5] Univ Sao Paulo, Dept Quim Fundamental, Inst Quim, Sao Paulo - Brazil
[6] Univ Sao Paulo, Dept Engn Mat, Escola Engn Lorena, Lorena, SP - Brazil
Total Affiliations: 6
Document type: Journal article
Source: COLLOID AND POLYMER SCIENCE; v. 297, n. 4, p. 557-569, APR 2019.
Web of Science Citations: 0
Abstract

Diblock amphiphilic copolymers form aggregates in some solvents. Such aggregates exhibit different morphologies, depending mainly on the polar/apolar block ratios. Aggregation of copolymers with polar block excess leads to micelle-like aggregates, known as polymeric micelles, which can be used as vehicles for drug and gene delivery, water decontamination, and catalysis. Here, we synthesized by RAFT polymerization three different polymers namely {[}dimethyl 2-(aminoethyl) methacrylate] (PDMAEMA), poly (methyl methacrylate) (PMMA) copolymers, and PDMAEMA-block-PMMA and characterized their aggregates by NMR spectroscopy and pH titrations. We investigated correlations between their chemical structure, aggregation behavior, protonation degree, and chain conformation in the corona. Decreased amine protonation in the copolymers reduced the electrostatic repulsion, and the apparent pK(a) of the amino groups approached that of isolated amine. These effects increased compactness and sizes of the polymers and their aggregates at higher pH as reflected by the increased NMR line widths. (AU)

FAPESP's process: 13/08166-5 - Interfacial chemistry: drugs, peptides and ezymes interactions with membrane models
Grantee:Iolanda Midea Cuccovia
Support Opportunities: Research Projects - Thematic Grants
FAPESP's process: 16/07490-1 - Structural studies of the Na+/Ca2+ exchanger and of proteins from the Zika virus by Nuclear Magnetic Resonance spectroscopy in solution
Grantee:Roberto Kopke Salinas
Support Opportunities: Regular Research Grants