دورية
In VitroRelease from Polymeric Core/Shell Nanoparticles through the Lens of Multiscale Modeling
| العنوان: | In VitroRelease from Polymeric Core/Shell Nanoparticles through the Lens of Multiscale Modeling |
|---|---|
| المؤلفون: | Casalini, Tommaso, Treacher, Kevin, Grant, Iain, Marucci, Mariagrazia |
| المصدر: | Molecular Pharmaceutics; June 2024, Vol. 21 Issue: 6 p2684-2698, 15p |
| مستخلص: | The large number of studies involving nanoparticles for cancer therapy is due to their peculiar features: they protect loaded active molecules while extending circulation time and can extravasate from the blood flow to the tumor to deliver drugs directly in the target area. Mathematical modeling can provide a preliminary in silicoexploration of design space to optimize an experimental activity that often relies on a trial-and-error approach. However, because of the characteristic size of these vectors (10–1000 nm), numerous phenomena of interest occur at different time and length scales, making a single modeling technique insufficient to fully characterize the system of interest. In this work we employed a multiscale modeling approach, which bridges the phenomena of interest across different scales, to study the in vitrorelease from polymeric core/shell nanoparticles for cancer therapy loaded with an active compound assembled as a hydrophobic ion pair. The “computational microscope” provided by molecular dynamics simulations was used to track drug molecules through the release process at an atomic scale. The outcomes suggested that the drug is mainly partitioned in the polymer and released as hydrophobic ion pair rather than a free molecule, and that the hydrophobic ion pair is preferentially partitioned in Tween 20 micelles in the release media. A model at macroscale, aimed at describing the release rate and elucidating the release mechanism, was developed according to the results from molecular simulations and validated against experimental data. The outcomes provided insights that are challenging to be obtained experimentally and which supported the development and validation of a release model at macroscale. Overall, the adopted multiscale approach corroborated the experimental findings and provided significant insights into the mechanisms of release. |
| قاعدة البيانات: | Supplemental Index |
Find this issue from the American Chemical Society | تدمد: | 15438384 15438392 |
|---|---|
| DOI: | 10.1021/acs.molpharmaceut.3c00806 |