A drug delivery system obtained by hot-melt processing of zein plasticized by a pharmaceutically active ionic liquid
Author(s) -
Laurent Chaunier,
Lydie Viau,
Xavier Falourd,
Denis Lourdin,
Eric Leroy
Publication year - 2020
Publication title -
journal of materials chemistry b
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.316
H-Index - 101
eISSN - 2050-7518
pISSN - 2050-750X
DOI - 10.1039/d0tb00326c
Subject(s) - drug delivery , ionic liquid , amorphous solid , materials science , drug , chemical engineering , ionic bonding , delivery system , nanotechnology , biomedical engineering , organic chemistry , chemistry , pharmacology , ion , medicine , engineering , catalysis
Zein-based filaments containing 20 weight% [Lidocainium][Ibuprofenate] used as a doubly Active Pharmaceutical Ingredient-Ionic Liquid (API-IL) were obtained by extrusion at 130 °C. The plasticizing effect of the active ingredient on the zein amorphous matrix was assessed by differential scanning calorimetry, with a decrease in the glass transition temperature (T g ) from 77 °C, for the raw zein, to 53 °C. After storage under standard conditions (relative humidity 59%, 20 °C) the extrudates were rigid, with a high storage modulus (E') of about 3 GPa at ambient temperature. They had a main mechanical relaxation (T α ) beginning at 55 °C, leading to their flowing at temperatures above 130 °C, as determined by dynamic mechanical analysis, with E' below 1 MPa and tan δ above 1. Their structure was evaluated by wide angle X-ray scattering and NMR analysis was used to evaluate the API-IL stability after thermomechanical processing. Release experiments performed under simulated physiological conditions on filaments evidenced a release of 85% after 7 days immersion. These results demonstrate the advantage of using an API-IL as plasticizer of a resorbable biopolymer. The resulting material can be shaped by a continuous thermomechanical process and used as a drug delivery system.
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