Microfluidics-based encapsulation of isoniazid in egg white/carrageenan microparticles for sustained release

The prevalence of tuberculosis continuously grows and there is an imperious need to improve the therapeutic efficacy of approved drugs for clinical use. Here we report the encapsulation of isoniazid (INH) in egg white/κ-carrageenan microparticles, which are intended for drug vehiculation through the...

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Autores principales: Robinson C. Marengo, Luciano N. Mengatto, María L. Olivares, Claudio L.A. Berli
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Lenguaje:EN
Publicado: Elsevier 2021
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spelling oai:doaj.org-article:7d26e44d0f4b410bbf1c59a546017d1f2021-11-28T04:39:44ZMicrofluidics-based encapsulation of isoniazid in egg white/carrageenan microparticles for sustained release2667-025910.1016/j.fhfh.2021.100041https://doaj.org/article/7d26e44d0f4b410bbf1c59a546017d1f2021-01-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S2667025921000339https://doaj.org/toc/2667-0259The prevalence of tuberculosis continuously grows and there is an imperious need to improve the therapeutic efficacy of approved drugs for clinical use. Here we report the encapsulation of isoniazid (INH) in egg white/κ-carrageenan microparticles, which are intended for drug vehiculation through the gastrointestinal tract and controlled release in the ileum. Spherical and highly monodisperse microparticles (255 mm average diameter) were obtained by droplet-based microfluidics and subsequent microwave irradiation. The entire amount of INH added to the particles was encapsulated. Infrared spectra revealed the formation of esters, hydrogen bonding, and Maillard reaction in the biopolymer matrix. In vitro release experiments were carried out in media that systematically emulate the stomach and intestinal tract conditions: 37 °C, NaCl 0.05 mol/L, pH 1.6, for the first 2 h, and Tris–HCl 0.1 mol/L, pH 7, for the next 24 h. A small fraction of the loaded INH was released in the first medium and most of the drug was progressively delivered in the second medium. The release profiles of microparticles were analyzed by using classical kinetic models, which enabled to hypothesize the release mechanism of INH from the biopolymer matrix. This knowledge, together with the ability to control the governing parameters of microfluidic elaboration, opens further possibilities for designing optimal prototypes for sustained release.Robinson C. MarengoLuciano N. MengattoMaría L. OlivaresClaudio L.A. BerliElsevierarticleIsoniazidEncapsulationMicrofluidicsEgg white/carrageenanDrug releaseNutrition. Foods and food supplyTX341-641Nutritional diseases. Deficiency diseasesRC620-627ENFood Hydrocolloids for Health, Vol 1, Iss , Pp 100041- (2021)
institution DOAJ
collection DOAJ
language EN
topic Isoniazid
Encapsulation
Microfluidics
Egg white/carrageenan
Drug release
Nutrition. Foods and food supply
TX341-641
Nutritional diseases. Deficiency diseases
RC620-627
spellingShingle Isoniazid
Encapsulation
Microfluidics
Egg white/carrageenan
Drug release
Nutrition. Foods and food supply
TX341-641
Nutritional diseases. Deficiency diseases
RC620-627
Robinson C. Marengo
Luciano N. Mengatto
María L. Olivares
Claudio L.A. Berli
Microfluidics-based encapsulation of isoniazid in egg white/carrageenan microparticles for sustained release
description The prevalence of tuberculosis continuously grows and there is an imperious need to improve the therapeutic efficacy of approved drugs for clinical use. Here we report the encapsulation of isoniazid (INH) in egg white/κ-carrageenan microparticles, which are intended for drug vehiculation through the gastrointestinal tract and controlled release in the ileum. Spherical and highly monodisperse microparticles (255 mm average diameter) were obtained by droplet-based microfluidics and subsequent microwave irradiation. The entire amount of INH added to the particles was encapsulated. Infrared spectra revealed the formation of esters, hydrogen bonding, and Maillard reaction in the biopolymer matrix. In vitro release experiments were carried out in media that systematically emulate the stomach and intestinal tract conditions: 37 °C, NaCl 0.05 mol/L, pH 1.6, for the first 2 h, and Tris–HCl 0.1 mol/L, pH 7, for the next 24 h. A small fraction of the loaded INH was released in the first medium and most of the drug was progressively delivered in the second medium. The release profiles of microparticles were analyzed by using classical kinetic models, which enabled to hypothesize the release mechanism of INH from the biopolymer matrix. This knowledge, together with the ability to control the governing parameters of microfluidic elaboration, opens further possibilities for designing optimal prototypes for sustained release.
format article
author Robinson C. Marengo
Luciano N. Mengatto
María L. Olivares
Claudio L.A. Berli
author_facet Robinson C. Marengo
Luciano N. Mengatto
María L. Olivares
Claudio L.A. Berli
author_sort Robinson C. Marengo
title Microfluidics-based encapsulation of isoniazid in egg white/carrageenan microparticles for sustained release
title_short Microfluidics-based encapsulation of isoniazid in egg white/carrageenan microparticles for sustained release
title_full Microfluidics-based encapsulation of isoniazid in egg white/carrageenan microparticles for sustained release
title_fullStr Microfluidics-based encapsulation of isoniazid in egg white/carrageenan microparticles for sustained release
title_full_unstemmed Microfluidics-based encapsulation of isoniazid in egg white/carrageenan microparticles for sustained release
title_sort microfluidics-based encapsulation of isoniazid in egg white/carrageenan microparticles for sustained release
publisher Elsevier
publishDate 2021
url https://doaj.org/article/7d26e44d0f4b410bbf1c59a546017d1f
work_keys_str_mv AT robinsoncmarengo microfluidicsbasedencapsulationofisoniazidineggwhitecarrageenanmicroparticlesforsustainedrelease
AT lucianonmengatto microfluidicsbasedencapsulationofisoniazidineggwhitecarrageenanmicroparticlesforsustainedrelease
AT marialolivares microfluidicsbasedencapsulationofisoniazidineggwhitecarrageenanmicroparticlesforsustainedrelease
AT claudiolaberli microfluidicsbasedencapsulationofisoniazidineggwhitecarrageenanmicroparticlesforsustainedrelease
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