## Various noncovalent complexes between native and derivatized cyclodextrins (CDs ) and barbiturates were studied using capillary electrophoresis (CE) and electrospray ionization mass spectrometry (ESI-MS). This paper involves the study of four aspects of CD-barbiturate noncovalent inclusion compl
Study of the lorazepam: cyclodextrin inclusion complexes using electrospray ionization mass spectrometry
✍ Scribed by Renata Kobetić; Branko S Jursic; Sidney Bonnette; Jane S.-C Tsai; Salamone J Salvatore
- Book ID
- 104231238
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- French
- Weight
- 134 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
As an example of drug-cyclodextrin interactions in aqueous media, the cyclodextrin complexation of lorazepam was studied by electrospray ionization mass spectroscopy (ES-MS). It was concluded that highly concentrated aqueous hydroxypropylcyclodextrins are more suited for the drug complexation and that the inclusion complex includes one molecule of the drug with two and three cyclodextrin molecules as well as two molecules of the drug with three molecules of hydroxypropylcyclodextrins. It was postulated that in the hydroxycyclodextrin cavity the drug molecule decomposes via the elimination of one molecule of formaldehyde.
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## Abstract Non‐covalent inclusion complexes formed between an anti‐inflammatory drug, oleanolic acid (OA), and α‐, β‐ and γ‐cyclodextrins (CDs) were investigated by means of solubility studies and electrospray ionization tandem mass spectrometry (ESI‐MS^__n__^). The order of calculated association
A series of supramolecular complexes of various cycludextrins (CDs) was studied. Among the 13 CD complexes synthesized, 11 could be characterizied by electrospray ionization mass spectrometry. Different supramolecular entities, with host: guest ratios of 1 : 1 and 2: 1, were observed.