Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
Guest Molecules Release from MOF-808 and MOF-Based Hydrogel: An EPR Study. / Yazikova, Anastasiya A.; Tomilov, Aleksandr S.; Livanovich, Kanstantsin S. и др.
в: Journal of Physical Chemistry C, Том 129, № 49, 27.11.2025, стр. 21878-21886.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - Guest Molecules Release from MOF-808 and MOF-Based Hydrogel: An EPR Study
AU - Yazikova, Anastasiya A.
AU - Tomilov, Aleksandr S.
AU - Livanovich, Kanstantsin S.
AU - Smirnova, Kristina A.
AU - Kirilyuk, Igor A.
AU - Polienko, Yuliya F.
AU - Poryvaev, Artem S.
AU - Fedin, Matvey V.
N1 - The research was funded by Russian Science Foundation (No. 24-43-10002) and Belarusian Republican Foundation for Fundamental Research (BRFFR, No. X23RNFM-048).
PY - 2025/11/27
Y1 - 2025/11/27
N2 - Precise, long-term control of drug concentration in organs and tissues of patients remains a significant challenge in modern pharmaceutics. In this work we investigate the metal–organic framework MOF-808, both in its pristine form and incorporated into a carboxymethylcellulose/chitosan (CMC-chitosan) hydrogel polyelectrolyte dressing, as a prospective platform for controlled drug release. Using electron paramagnetic resonance (EPR) spectroscopy and spin probes (radicals) that model drug molecules, we demonstrate that the controllable release kinetics from MOF-808 into water strongly depends on the functional groups of the released guests. The MOF-808 effectively functions as a reservoir, maintaining a stable target concentration of guest molecules in practical water volumes. Furthermore, embedding the MOF particles into CMC-chitosan hydrogel creates convenient platform for practical applications. Although conjugation of MOF-808 and hydrogel leads to an extra release of the cargo radicals, upon their elimination the release profile approaches that of the pristine MOF-808. This study underscores the potential of MOF-808 for sustained drug release applications and highlights critical considerations for its integration into composite hydrogel materials using EPR spectroscopy as the primary investigative tool.
AB - Precise, long-term control of drug concentration in organs and tissues of patients remains a significant challenge in modern pharmaceutics. In this work we investigate the metal–organic framework MOF-808, both in its pristine form and incorporated into a carboxymethylcellulose/chitosan (CMC-chitosan) hydrogel polyelectrolyte dressing, as a prospective platform for controlled drug release. Using electron paramagnetic resonance (EPR) spectroscopy and spin probes (radicals) that model drug molecules, we demonstrate that the controllable release kinetics from MOF-808 into water strongly depends on the functional groups of the released guests. The MOF-808 effectively functions as a reservoir, maintaining a stable target concentration of guest molecules in practical water volumes. Furthermore, embedding the MOF particles into CMC-chitosan hydrogel creates convenient platform for practical applications. Although conjugation of MOF-808 and hydrogel leads to an extra release of the cargo radicals, upon their elimination the release profile approaches that of the pristine MOF-808. This study underscores the potential of MOF-808 for sustained drug release applications and highlights critical considerations for its integration into composite hydrogel materials using EPR spectroscopy as the primary investigative tool.
UR - https://www.scopus.com/pages/publications/105024692948
UR - https://www.mendeley.com/catalogue/f36f368c-88e9-35a9-a9ce-fc48b92148ee/
U2 - 10.1021/acs.jpcc.5c06713
DO - 10.1021/acs.jpcc.5c06713
M3 - Article
VL - 129
SP - 21878
EP - 21886
JO - Journal of Physical Chemistry C
JF - Journal of Physical Chemistry C
SN - 1932-7447
IS - 49
ER -
ID: 72827209