FRANÇAIS
A showcase of ÉTS researchers’ publications and other contributions
SEARCH

The influence of adsorption incorporation mechanism on the release of isoniazid by montmorillonite

de Carvalho Arjona, Jessica, Ulsen, Carina, Tada, Dayane, Valenzuela Diaz, Francisco Rolando and Demarquette, Nicole Raymonde. 2025. « The influence of adsorption incorporation mechanism on the release of isoniazid by montmorillonite ». Journal of Drug Delivery Science and Technology, vol. 108.
Compte des citations dans Scopus : 1.

[thumbnail of Demarquette-N-2025-30932.pdf]
Preview
PDF
Demarquette-N-2025-30932.pdf - Published Version
Use licence: Creative Commons CC BY-NC-ND.

Download (4MB) | Preview

Abstract

Studies on the use of clay as a drug delivery vehicle have increased in recent years. Its applicability in the pharmaceutical field offers a low-cost solution to addressing drug side effects. Among the drugs that may benefit from a controlled release system is isoniazid (INH), a medication used in tuberculosis treatment. However, to enhance the clay-drug loading capacity and improve sustained drug release, the interaction between clay and drug must be thoroughly understood. This study used montmorillonite (Mtt) to develop Mtt-INH hybrids. Adsorption mechanisms were investigated under two pH conditions. At pH 7, where the drug is in its neutral state, two adsorption phases: the formation of a monolayer (20 mg/g) hybrid (a), followed by multilayer adsorption which can exceed 50 mg/g, hybrid (b) were achieved. At pH 2, where the drug protonates and carries a positive charge, the highest loading capacity of 100 mg/g, (hybrid (c) was achieved at the lowest drug concentration. Different from previous studies, the INH release profile was influenced by the amount adsorbed and the clay-drug interactions. For the hybrids (a) and (c), which correspond to monolayer adsorption, the release profile in intestine pH conditions closely followed the Zero Order Model, (R2 > 0.93). These hybrids exhibited slower release rates than hybrid (b) consistent with their stronger clay-drug interactions observed during adsorption. In vitro cytocompatibility assays demonstrated that neither pristine clay nor hybrid (c) was cytotoxic to fibroblast cells, supporting the potential of Mtt-based systems for pharmaceutical applications. The results may guide future studies to optimize controlled drug release by considering the expected application and the interactions between the clay-drug system and the pH during the adsorption process.

Item Type: Peer reviewed article published in a journal
Professor:
Professor
Demarquette, Nicole R.
Affiliation: Génie mécanique
Date Deposited: 12 May 2025 20:40
Last Modified: 14 May 2025 14:50
URI: https://espace2.etsmtl.ca/id/eprint/30932

Actions (login required)

View Item View Item