Literature DB >> 24844700

Poly(N-isopropylacrylamide-co-methacrylic acid) pH/thermo-responsive porous hydrogels as self-regulated drug delivery system.

Marieta Constantin1, Sanda Bucatariu1, Valeria Harabagiu1, Irina Popescu1, Paolo Ascenzi2, Gheorghe Fundueanu3.   

Abstract

A dual drug delivery system based on a "biosensor" (pH-sensitive unit) and a delivery component (thermosensitive hydrogel) was developed. The pH/thermosensitive hydrogel is able to restore the thermosensitive characteristics after electrostatic interaction of the pH-sensitive units with selected biologically active compounds that act as triggering agents. The poly(N-isopropylacrylamide-co-methacrylic acid) (poly(NIPAAm-co-MA)) was synthesized as an interesting pH/thermo-responsive copolymer by free radical polymerization method. Due to the presence of carboxylic groups in MA units, the copolymer loses its thermosensitivity at physiological pH and temperature. However, when the negatively-charged carboxylic groups of the pH-sensitive units interact electrostatically with the positively-charged drugs with hydrophobic character propranolol, lidocaine or metoclopramide, taken as model biologically active compounds, the copolymer restores the thermosensitive properties around the physiological pH and temperature. The poly(NIPAAm-co-MA) linear copolymer was converted into pH/thermo-responsive porous microgels using oligomers of NIPAAm above their LCST, as porogens. Accordingly, the swelling/collapsing processes of the microgels occur only after the interaction with the positively-charged hydrophobic drugs. The hydrophobic drug acts as a triggering agent and the pH/temperature sensitive hydrogel turns as a biosensor (pH-sensitive units) and a delivery component (thermosensitive hydrogel).
Copyright © 2014 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Lower critical solution temperature; Self-regulated drug delivery system; Stimuli-sensitive polymer; Volume phase transition temperature; pH/thermoresponsive copolymer

Mesh:

Substances:

Year:  2014        PMID: 24844700     DOI: 10.1016/j.ejps.2014.05.005

Source DB:  PubMed          Journal:  Eur J Pharm Sci        ISSN: 0928-0987            Impact factor:   4.384


  5 in total

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