Different Microfluidic Environments for In Vitro Testing of Lipid Nanoparticles against Osteosarcoma

Mitxelena-Iribarren, Oihane and Lizarbe-Sancha, Sara and Campisi, Jay and Arana, Sergio and Mujika, Maite (2021) Different Microfluidic Environments for In Vitro Testing of Lipid Nanoparticles against Osteosarcoma. Bioengineering, 8 (6). p. 77. ISSN 2306-5354

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Abstract

The use of lipid nanoparticles as biodegradable shells for controlled drug delivery shows promise as a more effective and targeted tumor treatment than traditional treatment methods. Although the combination of target therapy with nanotechnology created new hope for cancer treatment, methodological issues during in vitro validation of nanovehicles slowed their application. In the current work, the effect of methotrexate (MTX) encapsulated in different matrices was evaluated in a dynamic microfluidic platform. Effects on the viability of osteosarcoma cells in the presence of recirculation of cell media, free MTX and two types of blank and drug-containing nanoparticles were successfully assessed in different tumor-mimicking microenvironments. Encapsulated MTX was more effective than the equal dose free drug treatment, as cell death significantly increased under the recirculation of both types of drug-loaded nanoparticles in all concentrations. In fact, MTX-nanoparticles reduced cell population 50 times more than the free drug when 150-µM drug dose was recirculated. Moreover, when compared to the equivalent free drug dose recirculation, cell number was reduced 60 and 100 points more under recirculation of each nanoparticle with a 15-µM drug concentration. Thus, the results obtained with the microfluidic model present MTX-lipid nanoparticles as a promising and more effective therapy for pediatric osteosarcoma treatment than current treatment options.

Item Type: Article
Subjects: Journal Eprints > Engineering
Depositing User: Managing Editor
Date Deposited: 14 Feb 2023 07:32
Last Modified: 01 Jul 2024 06:21
URI: http://repository.journal4submission.com/id/eprint/614

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