Supramolecular host-guest interactions of pseudoginsenoside F11 (cas 19340-14-8) with β- and γ-cyclodextrin: Spectroscopic/spectrometric and computational studies

Add time:08/04/2019    Source:sciencedirect.com

Pseudoginsenoside F11 (cas 19340-14-8) (PF11) was described considering its complexation capabilities with β- and γ-cyclodextrin. A merged computational/experimental approach was used, and it was found that the PF11 molecule form a stable inclusion complex with the γ-cyclodextrin, with an association constant of 1.66 × 104 M−1, while it is not able to form an analogously one with the β-cyclodextrin. Nuclear magnetic resonance spectroscopy (1H NMR, 2D ROESY, and DOSY) and mass spectrometry experiments were used for the study and characterization of the supramolecular complex revealing the effective inclusion of the PF11 in the γ-cyclodextrin cavity. The thermodynamic parameters and the geometry of the PF11/cyclodextrin inclusion complex were studied by molecular dynamics simulations and semi-empirical calculations. The results of this study might lead the way for new PF11/γ-cyclodextrin formulations with advanced bioavailability and targeting.

We also recommend Trading Suppliers and Manufacturers of F11 (cas 19340-14-8). Pls Click Website Link as below: cas 19340-14-8 suppliers

Prev:Biodegradation of Diclofenac by the bacterial strain Labrys portucalensis F11 (cas 19340-14-8)
Next:Pseudoginsenoside-F11 (cas 19340-14-8) Protects against Transient Cerebral Ischemia Injury in Rats Involving Repressing Calcium Overload)