4.8 Article

19F NMR Spectroscopy as a Highly Sensitive Method for the Direct Monitoring of Confined Crystallization within Nanoporous Materials

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 55, 期 31, 页码 8904-8908

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201602936

关键词

drug delivery; flufenamic acid; mesoporous silica; nanocrystals; solid-state NMR spectroscopy

资金

  1. University of East Anglia
  2. EPSRC Directed Assembly Network
  3. EPSRC CASE studentship - EPSRC
  4. Bristol-Myers Squibb [EP/I501517/1]
  5. EPSRC [EP/J007803/1]
  6. EPSRC [EP/J007803/1] Funding Source: UKRI
  7. Engineering and Physical Sciences Research Council [1039855, EP/J007803/1] Funding Source: researchfish

向作者/读者索取更多资源

The introduction of fluorine into the structure of pharmaceuticals has been an effective strategy for tuning their pharmacodynamic properties, with more than 40 new drugs entering the market in the last 15 years. In this context, F-19 NMR spectroscopy can be viewed as a useful method for investigating the host-guest chemistry of pharmaceuticals in nanosized drug-delivery systems. Although the interest in confined crystallization, nanosized devices, and porous catalysts is gradually increasing, understanding of the complex phase behavior of organic molecules confined within nanochambers or nanoreactors is still lacking. Using F-19 magicangle-spinning NMR spectroscopy, we obtained detailed mechanistic insight into the crystallization of flufenamic acid (FFA) in a confined environment of mesoporous silica materials with different pore diameters (3.2-29 nm), providing direct experimental evidence for the formation of a molecular-liquid-like layer besides crystalline confined FFA form I.

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