Darren Creek

Dr. Darren Creek

Monash Institute of Pharmaceutical Sciences, Faculty of Pharmacy and Pharmaceutical Sciences, Monash University (Parkville campus), 381 Royal Parade, Parkville, Victoria 3052, Australia
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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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26 May 2012 in Metabolomics
Verified
Journal Article
Closed access
PDF file
WDWarwick Dunn
Warwick Dunn
AEAlexander Erban
Alexander Erban
RWRalf J. M. Weber
Ralf J. M. Weber
DCDarren Creek
Darren Creek
MBMarie Brown
Marie Brown
MVMark Viant
Mark Viant

4 February 2012 in Bioinformatics
Verified
Journal Article
Open access
PDF file
DCDarren Creek
Darren Creek
AJAndris Jankevics
Andris Jankevics
KBKarl E. V. Burgess
Karl E. V. Burgess
Rainer BreitlingRainer Breitling
Rainer Breitling
MBMichael P. Barrett
Michael P. Barrett
Summary: The application of emerging metabolomics technologies to the comprehensive investigation of cellular biochemistry has been limited by bottlenecks in data processing, particularly noise filtering and metabolite identification. IDEOM provides a user-friendly data processing application that automates filtering and identification of metabolite peaks, paying particular attention to common sources of noise and false identifications generated by liquid chromatography–mass spectrometry (LC–MS) platforms. Building on advanced processing tools such as mzMatch and XCMS, it allows users to run a comprehensive pipeline for data analysis and visualization from a graphical user interface within Microsoft Excel, a familiar program for most biological scientists. Availability and implementation: IDEOM is provided free of charge at http://mzmatch.sourceforge.net/ideom.html, as a macro-enabled spreadsheet (.xlsb). Implementation requires Microsoft Excel (2007 or later). R is also required for full functionality. Contact:michael.barrett@glasgow.ac.uk Supplementary Information: Supplementary data are available at Bioinformatics online.

21 October 2011 in Analytical Chemistry
Verified
Journal Article
Closed access
DCDarren Creek
Darren Creek
AJAndris Jankevics
Andris Jankevics
Rainer BreitlingRainer Breitling
Rainer Breitling
DWDavid G. Watson
David G. Watson
MBMichael P. Barrett
Michael P. Barrett
KBKarl E. V. Burgess
Karl E. V. Burgess

7 February 2011 in Proceedings of the National Academy of Sciences
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Journal Article
Closed access
PDF file
SCSusan A. Charman
Susan A. Charman
SASarah Arbe-Barnes
Sarah Arbe-Barnes
IBIan C. Bathurst
Ian C. Bathurst
RBReto Brun
Reto Brun
MCMichael Campbell
Michael Campbell
JVJonathan Vennerstrom
Jonathan Vennerstrom
Ozonide OZ439 is a synthetic peroxide antimalarial drug candidate designed to provide a single-dose oral cure in humans. OZ439 has successfully completed Phase I clinical trials, where it was shown to be safe at doses up to 1,600 mg and is currently undergoing Phase IIa trials in malaria patients. Herein, we describe the discovery of OZ439 and the exceptional antimalarial and pharmacokinetic properties that led to its selection as a clinical drug development candidate. In vitro, OZ439 is fast-acting against all asexual erythrocytic Plasmodium falciparum stages with IC 50 values comparable to those for the clinically used artemisinin derivatives. Unlike all other synthetic peroxides and semisynthetic artemisinin derivatives, OZ439 completely cures Plasmodium berghei -infected mice with a single oral dose of 20 mg/kg and exhibits prophylactic activity superior to that of the benchmark chemoprophylactic agent, mefloquine. Compared with other peroxide-containing antimalarial agents, such as the artemisinin derivatives and the first-generation ozonide OZ277, OZ439 exhibits a substantial increase in the pharmacokinetic half-life and blood concentration versus time profile in three preclinical species. The outstanding efficacy and prolonged blood concentrations of OZ439 are the result of a design strategy that stabilizes the intrinsically unstable pharmacophoric peroxide bond, thereby reducing clearance yet maintaining the necessary Fe(II)-reactivity to elicit parasite death.

8 April 2014 in Metabolomics
Verified
Journal Article
Closed access
PDF file
DCDarren Creek
Darren Creek
WDWarwick Dunn
Warwick Dunn
OFOliver Fiehn
Oliver Fiehn
JGJulian L. Griffin
Julian L. Griffin
RHRobert Hall
Robert Hall
JWJean-Luc Wolfender
Jean-Luc Wolfender

25 February 2014 in Bioanalysis
Verified
Journal Article
Closed access
ACAchuthanunni Chokkathukalam
Achuthanunni Chokkathukalam
DKDong-Hyun Kim
Dong-Hyun Kim
MBMichael P. Barrett
Michael P. Barrett
Rainer BreitlingRainer Breitling
Rainer Breitling
DCDarren Creek
Darren Creek
The rapid emergence of metabolomics has enabled system-wide measurements of metabolites in various organisms. However, advances in the mechanistic understanding of metabolic networks remain limited...