TANDEM MASS SPECTROMETRY CHARACTERIZATION OF ESTERIFIED CYCLODEXTRINS

Peptu, C; Harabagiu, V

HERO ID

3575130

Reference Type

Journal Article

Year

2013

HERO ID 3575130
In Press No
Year 2013
Title TANDEM MASS SPECTROMETRY CHARACTERIZATION OF ESTERIFIED CYCLODEXTRINS
Authors Peptu, C; Harabagiu, V
Journal Digest Journal of Nanomaterials and Biostructures
Volume 8
Issue 4
Page Numbers 1551-1561
Abstract The tandem mass spectrometry (MS/MS) characterization of cyclodextrin derivatives, namely randomly esterified 6-O-(3-hydroxybutyril)-beta-cyclodextrin (HBCD) and triacetyl-beta-cyclodextrin (TABCD) is described. The chosen compounds share certain structural similarities which are exploited in order to establish a general approach in their tandem MS characterization. The TABCD commercial product is fully esterified and presents in single stage MS a single peak while HBCD presents a molecular weight distribution due to the variation of the substitution degree. HBCD product was obtained via ring opening of beta-butyrolactone in the presence of beta-cyclodextrin (CD). First, the specific fragmentation pathways are established for protonated and sodiated TABCD parent ions and, based on the established fragmentation behaviour, HBCD compounds are analyzed. Our findings indicate that in MS/MS analysis of esterified cyclodextrins the cleavage of the substituents can be selectively induced thus offering information on the substitution patterns. Moreover, we demonstrate, using tandem MS technique, that beta-butyrolactone monomer units are attached to the CD molecule not as oligomer chains but as singly esterified molecules.
Wosid WOS:000327818000020
Is Certified Translation No
Dupe Override No
Is Public Yes
Keyword beta-cyclodextrin; beta-butyrolactone; tryacetil-beta-cyclodextrin; ESI MS; Tandem MS; Collision induced dissociations