Szabolcs Béni

Dr. Szabolcs Béni

Semmelweis University, Budapest, Hungary
orcid

Research Focus & Metrics

Academic Career Length

23Years (2004-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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27 December 2012 in Journal of Proteome Research
Verified
Journal Article
Closed access
GBGregory A. Barding
Gregory A. Barding
Szabolcs BéniSzabolcs Béni
Szabolcs Béni
TFTakeshi Fukao
Takeshi Fukao
JBJulia Bailey-Serres
Julia Bailey-Serres
CLCynthia K. Larive
Cynthia K. Larive

1 October 2007 in International Journal of Pharmaceutics
Verified
Journal Article
Closed access
LBL Budai
L Budai
MHM Hajdu
M Hajdu
MBM Budai
M Budai
PGP Grof
P Grof
Szabolcs BéniSzabolcs Béni
Szabolcs Béni
IAI Antal
I Antal

13 December 2004 in Journal of Medicinal Chemistry
Verified
Journal Article
Closed access
ZSZoltán Szakács
Zoltán Szakács
Szabolcs BéniSzabolcs Béni
Szabolcs Béni
ZVZoltán Varga
Zoltán Varga
LŐLászló Ferenc Őrfi
László Ferenc Őrfi
GKGyörgy Kéri
György Kéri
BNBela Noszal
Bela Noszal

3 September 2010 in Analytical and Bioanalytical Chemistry
Verified
Journal Article
Open access
PDF file
Szabolcs BéniSzabolcs Béni
Szabolcs Béni
JLJohn F. K. Limtiaco
John F. K. Limtiaco
CLCynthia K. Larive
Cynthia K. Larive
This review discusses recent developments in analytical methods available for the sensitive separation, detection and structural characterization of heparin contaminants. The adulteration of raw heparin with oversulfated chondroitin sulfate (OSCS) in 2007–2008 spawned a global crisis resulting in extensive revisions to the pharmacopeia monographs on heparin and prompting the FDA to recommend the development of additional physicochemical methods for the analysis of heparin purity. The analytical chemistry community quickly responded to this challenge, developing a wide variety of innovative approaches, several of which are reported in this special issue. This review provides an overview of methods of heparin isolation and digestion, discusses known heparin contaminants, including OSCS, and summarizes recent publications on heparin impurity analysis using sensors, near-IR, Raman, and NMR spectroscopy, as well as electrophoretic and chromatographic separations. Schematic illustrating the process for heparin impurity characterization

19 July 2011 in Annual Review of Analytical Chemistry
Verified
Journal Article
Closed access
CJChristopher J. Jones
Christopher J. Jones
Szabolcs BéniSzabolcs Béni
Szabolcs Béni
JLJohn F.K. Limtiaco
John F.K. Limtiaco
DLDerek J. Langeslay
Derek J. Langeslay
CLCynthia K. Larive
Cynthia K. Larive
Although heparin is an important and widely prescribed pharmaceutical anticoagulant, its high degree of sequence microheterogeneity and size polydispersity make molecular-level characterization challenging. Unlike nucleic acids and proteins that are biosynthesized through template-driven assembly processes, heparin and the related glycosaminoglycan heparan sulfate are actively remodeled during biosynthesis through a series of enzymatic reactions that lead to variable levels of O- and N-sulfonation and uronic acid epimers. As summarized in this review, heparin sequence information is determined through a bottom-up approach that relies on depolymerization reactions, size- and charge-based separations, and sensitive mass spectrometric and nuclear magnetic resonance experiments to determine the structural identity of component oligosaccharides. The structure-elucidation process, along with its challenges and opportunities for future analytical improvements, is reviewed and illustrated for a heparin-derived hexasaccharide.

20 December 2011 in Chemistry – A European Journal
Verified
Journal Article
Closed access
PDF file
BVBalázs R. Varga
Balázs R. Varga
MKMihály Kállay
Mihály Kállay
KHKrisztina Hegyi
Krisztina Hegyi
Szabolcs BéniSzabolcs Béni
Szabolcs Béni
PKPéter Kele
Péter Kele