Towards an Improved anti‐HIV Activity of NRTI via Metal–Organic Frameworks Nanoparticles

Valentina Agostoni(Université Paris-Sud), Tamim Chalati(Université Paris-Sud), Patricia Horcajada(Université Paris-Sud), H. Willaime(Université Paris-Sud), Resmi Anand(Institute of Organic Synthesis and Photoreactivity), Nicolas Sémiramoth(Université Paris-Sud), Tarek Baâti(Centre National de la Recherche Scientifique), Shaun Hall(École Nationale Supérieure de Chimie de Montpellier), Guillaume Maurin(École Nationale Supérieure de Chimie de Montpellier), Hélène Chacun(Université Paris-Sud), Kawthar Bouchemal(Université Paris-Sud), Charlotte Martineau(Centre National de la Recherche Scientifique), Françis Taulelle(Centre National de la Recherche Scientifique), Patrick Couvreur(Université Paris-Sud), Christine Rogez‐Kreuz(Commissariat à l'Énergie Atomique et aux Énergies Alternatives), Pascal Clayette(Commissariat à l'Énergie Atomique et aux Énergies Alternatives), Sandra Monti(Institute of Organic Synthesis and Photoreactivity), Christian Serre(Centre National de la Recherche Scientifique), Ruxandra Gref(Université Paris-Sud)
Advanced Healthcare Materials
June 17, 2013
Cited by 152Open Access
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Abstract

Nanoscale mesoporous iron carboxylates metal-organic frameworks (nanoMOFs) have recently emerged as promising platforms for drug delivery, showing biodegradability, biocompatibility and important loading capability of challenging highly water-soluble drugs such as azidothymidine tryphosphate (AZT-TP). In this study, nanoMOFs made of iron trimesate (MIL-100) were able to act as efficient molecular sponges, quickly adsorbing up to 24 wt% AZT-TP with entrapment efficiencies close to 100%, without perturbation of the supramolecular crystalline organization. These data are in agreement with molecular modelling predictions, indicating maximal loadings of 33 wt% and preferential location of the drug in the large cages. Spectrophotometry, isothermal titration calorimetry, and solid state NMR investigations enable to gain insight on the mechanism of interaction of AZT and AZT-TP with the nanoMOFs, pointing out the crucial role of phosphates strongly coordinating with the unsaturated iron(III) sites. Finally, contrarily to the free AZT-TP, the loaded nanoparticles efficiently penetrate and release their cargo of active triphosphorylated AZT inside major HIV target cells, efficiently protecting against HIV infection.


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