TY  - JOUR
A1  - Fasciotti, Maira
A1  - Sanvido, Gustavo B.
A1  - Santos, Vanessa G.
A1  - Lalli, Priscila M.
A1  - McCullagh, Michael
A1  - de Sa, Gilberto F.
A1  - Daroda, Romeu J.
A1  - Peter, Martin G.
A1  - Eberlin, Marcos N.
T1  - Separation of isomeric disaccharides by traveling wave ion mobility mass spectrometry using CO2 as drift gas
JF  - Journal of mass spectrometr
N2  - The use of CO2 as a massive and polarizable drift gas is shown to greatly improve peak-to-peak resolution (Rp-p), as compared with N2, for the separation of disaccharides in a Synapt G2 traveling wave ion mobility cell. Near or baseline Rp-p was achieved for three pairs of sodiated molecules of disaccharide isomers, that is, cellobiose and sucrose (Rp-p?=?0.76), maltose and sucrose (Rp-p?=?1.04), and maltose and lactose (Rp-p?=?0.74). Ion mobility mass spectrometry using CO2 as the drift gas offers therefore an attractive alternative for fast and efficient separation of isomeric disaccharides.
KW  - isomer resolution
KW  - oligosaccharides
KW  - traveling wave ion mobility mass spectrometry
KW  - polarizable drift gases
Y1  - 2012
U6  - https://doi.org/10.1002/jms.3089
SN  - 1076-5174
VL  - 47
IS  - 12
SP  - 1643
EP  - 1647
PB  - Wiley-Blackwell
CY  - Hoboken
ER  - 
TY  - JOUR
A1  - Issaree, Arisara
A1  - Vijayakrishnan, Balakumar
A1  - Abdelnur, Patricia V.
A1  - Corilo, Yuri E.
A1  - Riccio, Maria F.
A1  - Sanvido, Gustavo B.
A1  - Eberlin, Marcos N.
A1  - Peter, Martin G.
T1  - Mass spectrometry of aminoglucan oligosaccharides using electrospray ionization MS/MS and MS/MS/MS
Y1  - 2009
ER  - 
TY  - JOUR
A1  - Pereira, Fernanda S.
A1  - Nascimento, Heliara D. L.
A1  - Magalhaes, Alvicler
A1  - Peter, Martin G.
A1  - Bataglion, Giovana Anceski
A1  - Eberlin, Marcos N.
A1  - Gonzalez, Eduardo R. P.
T1  - ESI(+)-MS and GC-MS study of the hydrolysis of N-azobenzyl derivatives of chitosan
JF  - Molecules
N2  - New N-p-chloro-, N-p-bromo-, and N-p-nitrophenylazobenzylchitosan derivatives, as well as the corresponding azophenyl and azophenyl-p-sulfonic acids, were synthesized by coupling N-benzylvchitosan with aryl diazonium salts. The synthesized molecules were analyzed by UV-Vis, FT-IR, H-1-NMR and N-15-NMR spectroscopy. The capacity of copper chelation by these materials was studied by AAS. Chitosan and the derivatives were subjected to hydrolysis and the products were analyzed by ESI(+)-MS and GC-MS, confirming the formation of N-benzyl chitosan. Furthermore, the MS results indicate that a nucleophilic aromatic substitution (SnAr) reaction occurs under hydrolysis conditions, yielding chloroaniline from N-p-bromo-, and N-p-nitrophenylazo-benzylchitosan as well as bromoaniline from N-p-chloro-, and N-p-nitrophenylazobenzyl-chitosan.
KW  - chitosan
KW  - N-azobenzylchitosan
KW  - ESI-MS
KW  - GC-MS
KW  - SnAr reaction
Y1  - 2014
U6  - https://doi.org/10.3390/molecules191117604
SN  - 1420-3049
VL  - 19
IS  - 11
SP  - 17604
EP  - 17618
PB  - MDPI
CY  - Basel
ER  - 
TY  - JOUR
A1  - Vijayakrishnan, Balakumar
A1  - Issaree, Arisara
A1  - Corilo, Yuri E.
A1  - Ferreira, Christina Ramires
A1  - Eberlin, Marcos N.
A1  - Peter, Martin G.
T1  - MSn of the six isomers of (GlcN)(2)(GlcNAc)(2) aminoglucan tetrasaccharides (diacetylchitotetraoses) rules of fragmentation for the sodiated molecules and application to sequence analysis of hetero-chitooligosaccharides
JF  - Carbohydrate polymers : an international journal devoted to scientific and technological aspects of industrially important polysaccharides
N2  - The six possible isomers of di-N-acetylchitotetraoses [AADD, ADDA, ADAD, DADA, DAAD, and DDAA, where D stands for 2-amino-2-deoxy-3-D-glucose (GlcN) and A for 2-acetamido-2-deoxy-beta-D-glucose (GlcNAc)] were analyzed by ESI(+)-MSn. Collision induced dissociation via MSn experiments were performed for the sodiated molecules of m/z 769 [M+Na](+) for each isomer, and fragments were generated mainly by glycosidic bond and cross-ring cleavages. Rules of fragmentation were then established. A reducing end D residue yields the (O.2)A(4) cross-ring [M-59+Na](+) fragment of m/z 710 as the most abundant, whereas isomers containing a reducing end A prefer to lose water to form the [M-18+Na](+) ion of m/z 751, as well as abundant (O.2)A(4) cross-ring [M-101+Na](+) fragments of m/z 668 and B-3 [M-221+Na](+) ions of m/z 548. MS3 of C- and Y-type ions shows analogous fragmentation behaviour that allows identification of the reducing end next-neighbour residue. Due to gas-phase anchimeric assistance, B-type cleavage between the glycosidic oxygen and the anomeric carbon atom is favoured when the glycon is an A residue. Relative ion abundances are generally in the order B >> C > Y, but may vary depending on the next neighbour towards the non-reducing end. These fragmentation rules were used for partial sequence analysis of hetero-chitooligosaccharides of the composition D(2)A(3), D(3)A(3), D(2)A(4), D(4)A(3), and D(3)A(4).
KW  - Chitosan
KW  - Fragmentation
KW  - Oligosaccharides
KW  - Sequence analysis
KW  - Tandem mass spectrometry
Y1  - 2011
U6  - https://doi.org/10.1016/j.carbpol.2010.04.041
SN  - 0144-8617
VL  - 84
IS  - 2
SP  - 713
EP  - 726
PB  - Elsevier
CY  - Oxford
ER  -