Journal
PURE AND APPLIED CHEMISTRY
Volume 81, Issue 8, Pages 1345-1355Publisher
WALTER DE GRUYTER GMBH
DOI: 10.1351/PAC-CON-08-11-10
Keywords
solid-state NMR; porous silica; encapsulation; confinement; drug delivery
Categories
Funding
- FAME European Network of Excellence (FP6)
Ask authors/readers for more resources
In this contribution, we present a solid-state NMR approach to characterize drug-model molecules as ibuprofen, benzoic acid, and lauric acid, encapsulated in MCM-41 silica and submitted to strong confinement effects. In particular, we show that by a careful choice of the solid-state NMR sequences, it is possible to efficiently characterize these highly mobile molecules and their interactions with the pore surface. Thus, we demonstrate that C-13 NMR spectroscopy is a powerful tool to characterize and even quantify entrapped and non-entrapped species by using either single-pulse excitation (SPE) or cross-polarization (CP). Whereas the standard (H-1)-C-13 CP experiment is of poor efficiency for mobile species, we show that 13C signal-to-noise (SIN) ratio can be significantly improved through H-1-C-13 cross-relaxation (namely, nuclear Overhauser effect, nOe) by using a H-1 power-gated technique. The long transversal relaxation times [T-2(H-1) up to 22 ms] observed allow the setup of J-coupling-based experiments such as 2D {H-1}-C-13 heteronuclear multiple-quantum coherence (HMQC) in order to fully characterize the encapsulated molecules. Thus, we demonstrate that the use of sequences derived from solution-state NMR such as these two latter experiments is highly efficient to characterize highly mobile organic molecules trapped in mesopores. Finally, we show that I H spin diffusion-based experiments can give useful information on the proximities between trapped molecules and the silica surface.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available