Issue 16, 2024

A novel microfluidic tool for the evaluation of local drug delivery systems in simulated in vivo conditions

Abstract

A 3D-printed microfluidic tool for assessing local drug delivery systems (LDD) in simulated in vivo conditions was developed and evaluated. The device was designed considering the oral environment and dental applications, and it was fabricated with a high-precision resin 3D printer. Chitosan scaffolds loaded with different concentrations of doxycycline were used for evaluating our device. The concentration of the released drug was measured through in-line UV-VIS spectroscopy, and to verify the repeatability and accuracy of our measurements, comparisons with standard HPLC results were made (5% deviation). Cumulative drug release profiles in steady-state conditions were obtained and compared to the Weibull model. The behaviour of the LDD system in a dynamic environment was also evaluated during experiments where step changes in pH were introduced. It was demonstrated that under infection-like conditions, there is an immediate response from the polymer and a clear increase in the concentration of the released drug. Continuous flow and recirculation experiments were also conducted, revealing significant differences in the drug release profiles. Specifically, in the case of continuous flow, the quantity of the released drug is much higher due to the higher driving force for diffusion (concentration gradient). Overall, the proposed microfluidic tool proved to be ideal for evaluating LDD systems, as the in vivo microenvironment can be replicated in a better way than with currently used standard systems.

Graphical abstract: A novel microfluidic tool for the evaluation of local drug delivery systems in simulated in vivo conditions

Article information

Article type
Paper
Submitted
26 ferr 2024
Accepted
16 lugl 2024
First published
24 lugl 2024
This article is Open Access
Creative Commons BY-NC license

Lab Chip, 2024,24, 3840-3849

A novel microfluidic tool for the evaluation of local drug delivery systems in simulated in vivo conditions

W. A. Oates and A. D. Anastasiou, Lab Chip, 2024, 24, 3840 DOI: 10.1039/D4LC00181H

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