2016
Orlistat interaction with sibutramine and carnitine. A physicochemical and theoretical study. Inés Nicolás-Vázquez, Jaime Hinojosa Torres, Julián Cruz Borbolla, René Miranda Ruvalcaba, Juan Manuel Aceves-Hernández. Journal of Molecular StructureVolume 1062, 24 March 2014, Pages 1?12.http://dx.doi.org/10.1016/j.molstruc.2013.12.072
Abstract
Chemical degradation of orlistat, (ORT) after melting and reaction of decomposition byproducts with sibutramine, SIB was studied. Interactions between the active pharmaceutical ingredients by using thermal analysis, TA, methods and other experimental techniques such as PXRD, IR and UV?vis spectroscopies were carried out to investigate chemical reactions between components. It was found that orlistat melts with decomposition and byproducts quickly affect sibutramine molecule and then reacting also with carnitine, CRN when the three active pharmaceutical ingredients (API?s) are mixed. However ORT byproducts do not react when ORT is mixed only with carnitine. It was found that compounds containing chlorine atoms react easily with orlistat when the temperature increases up to its melting point. Some reaction mechanisms of orlistat decomposition are proposed, the fragments in the mechanisms were found in the corresponding mass spectra. Results obtained indicate that special studies should be carried out in the formulation stage before the final composition of a poly-pill could be established. Similar results are commonly found for compounds very prone to react in presence of water, light and/or temperature. In order to explain the reactivity of orlistat with sibutramine and carnitine, theoretical calculations were carried out and the results are in agreement with the experimental results.
Study on the intramolecular transannular chalcogentin interactions in dithiastannecine compounds.
Synthesis and crystal structure of the N-8-(diphenyl-hydroxy-2-aminomethylpyridine)borane
Synthesis, characterization, and crystal structures of n-alkyldiorganodithiophosphates RS2P(OC6H4)2