| Autor: |
Sherard MM; Department of Chemistry, Gottwald Center for the Sciences, University of Richmond, Richmond, VA 23173, USA., Kaplan JS; Department of Chemistry, Gottwald Center for the Sciences, University of Richmond, Richmond, VA 23173, USA., Simpson JH; Department of Chemistry, Gottwald Center for the Sciences, University of Richmond, Richmond, VA 23173, USA., Kittredge KW; Department of Chemistry, Joan P. Brock School of Math and Natural Sciences, Virginia Wesleyan College, Virginia Beach, VA 23455, USA., Leopold MC; Department of Chemistry, Gottwald Center for the Sciences, University of Richmond, Richmond, VA 23173, USA. |
| Abstrakt: |
Fentanyl (FTN) and synthetic analogs of FTN continue to ravage populations across the globe, including in the United States where opioids are increasingly being used and abused and are causing a staggering and growing number of overdose deaths each year. This growing pandemic is worsened by the ease with which FTN can be derivatized into numerous derivatives. Understanding the chemical properties/behaviors of the FTN class of compounds is critical for developing effective chemical detection schemes using nanoparticles (NPs) to optimize important chemical interactions. Halogen bonding (XB) is an intermolecular interaction between a polarized halogen atom on a molecule and e - -rich sites on another molecule, the latter of which is present at two or more sites on most fentanyl-type structures. Density functional theory (DFT) is used to identify these XB acceptor sites on different FTN derivatives. The high toxicity of these compounds necessitated a "fragmentation" strategy where smaller, non-toxic molecules resembling parts of the opioids acted as mimics of XB acceptor sites present on intact FTN and its derivatives. DFT of the fragments' interactions informed solution measurements of XB using 19 F NMR titrations as well as electrochemical measurements of XB at self-assembled monolayer (SAM)-modified electrodes featuring XB donor ligands. Gold NPs, known as monolayer-protected clusters (MPCs), were also functionalized with strong XB donor ligands and assembled into films, and their interactions with FTN "fragments" were studied using voltammetry. Ultimately, spectroscopy and TEM analysis were combined to study whole-molecule FTN interactions with the functionalized MPCs in solution. The results suggested that the strongest XB interaction site on FTN, while common to most of the drug's derivatives, is not strong enough to induce NP-aggregation detection but may be better exploited in sensing schemes involving films. |
