Vegetable oil-based hybrid microparticles as a green and biocompatible system for subcutaneous drug delivery

被引:5
|
作者
Doufene, Koceila [1 ]
Basile, Ilaria [2 ]
Lebrun, Aurelien [3 ]
Pirot, Nelly [4 ,5 ]
Escande, Aurelie [6 ]
Chopineau, Joel [1 ]
Devoisselle, Jean-Marie [1 ]
Bettache, Nadir [7 ]
Aubert-Pouessel, Anne [1 ]
机构
[1] Univ Montpellier, CNRS, Inst Charles Gerhardt Montpellier ICGM, ENSCM, Montpellier, France
[2] NanoMedSyn, Montpellier, France
[3] Univ Montpellier, CNRS, Lab Mesures Phys LMP, Montpellier, France
[4] Univ Montpellier, Inst Rech Cancerol Montpellier IRCM, ICM, INSERM, Montpellier, France
[5] Univ Montpellier, CNRS, BioCampus Montpellier BCM, INSERM, Montpellier, France
[6] Univ Montpellier, CNRS, Hydrosci Montpellier HSM, IRD, Montpellier, France
[7] Univ Montpellier, CNRS, Inst Biomol Max Mousseron IBMM, ENSCM, Montpellier, France
关键词
Vegetable oil; Green process; Sol-gel; Estradiol; Subcutaneous drug delivery; Biocompatible; DISSOLUTION; RELEASE;
D O I
10.1016/j.ijpharm.2020.120070
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The aim of this study was to evidence the ability of vegetable oil-based hybrid microparticles (HMP) to be an efficient and safe drug delivery system after subcutaneous administration. The HMP resulted from combination of a thermostabilized emulsification process and a sol-gel chemistry. First of all, castor oil was successfully silylated by means of (3-Isocyanatopropyl)trimethoxysilane in solvent-free and catalyst-free conditions. Estradiol, as a model drug, was dissolved in silylated castor oil (ICOm) prior to emulsification, and then an optimal sol-gel crosslinking was achieved inside the ICOm microdroplets. The resulting estradiol-loaded microparticles were around 80 um in size and allowed to entrap 4 wt% estradiol. Their release kinetics in a PBS/octanol biphasic system exhibited a one-week release profile, and the released estradiol was fully active on HeLa EREluciferase ERa cells. The hybrid microparticles were cytocompatible during preliminary tests on NIH 3T3 fibroblasts (ISO 10993-5 standard) and they were fully biocompatible after subcutaneous injection on mice (ISO 10993-6 standard) underlining their high potential as a safe and long-acting subcutaneous drug delivery system.
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页数:9
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