Please use this identifier to cite or link to this item: https://doi.org/10.4155/bio-2017-0006
Title: Development of bioanalytical assays for variegin, a peptide-based bivalent direct thrombin inhibitor
Authors: Shih, Norrapat
de Carvalho, Leonardo Pinto
Lee, Yie Hou
Rocha, Mauricio Macario
Pereira Barbosa, Adriano Henrique
de Sousa, Jose Marconi A
Carvalho, Antonio Carlos de C
Kini, R Manjunatha 
Chan, Mark Y 
Keywords: Science & Technology
Life Sciences & Biomedicine
Physical Sciences
Biochemical Research Methods
Chemistry, Analytical
Biochemistry & Molecular Biology
Chemistry
anticoagulant
bioanalytical assays
LC-MS/MS
thrombin amidolytic assay
thrombin time
PERCUTANEOUS CORONARY INTERVENTION
TANDEM MASS-SPECTROMETRY
PLASMA
BIVALIRUDIN
THERAPY
HEPARIN
DABIGATRAN
TRIAL
Issue Date: 1-May-2017
Publisher: FUTURE SCI LTD
Citation: Shih, Norrapat, de Carvalho, Leonardo Pinto, Lee, Yie Hou, Rocha, Mauricio Macario, Pereira Barbosa, Adriano Henrique, de Sousa, Jose Marconi A, Carvalho, Antonio Carlos de C, Kini, R Manjunatha, Chan, Mark Y (2017-05-01). Development of bioanalytical assays for variegin, a peptide-based bivalent direct thrombin inhibitor. BIOANALYSIS 9 (9) : 693-705. ScholarBank@NUS Repository. https://doi.org/10.4155/bio-2017-0006
Abstract: Aim: Variegin is an anticoagulant peptide that will be tested in porcine models of percutaneous coronary intervention. We developed three bioanalytical assays for variegin quantitation and utilized these methods to evaluate pharmacokinetics of variegin in pigs. Results & methodology: The LC-MS/MS, thrombin amidolytic and modified thrombin time assays had a quantitation range of 21.6-5541.7, 10.8-5541.7 and 5.4-5541.7 nM in human plasma, respectively. The elimination half-lives obtained using the LC-MS/MS, modified thrombin time and thrombin amidolytic assays were 52.3 ± 4.4, 50.4 ± 5.9 and 67.7 ± 6.3 min, respectively. Conclusion: We developed three bioanalytical assays for a novel direct thrombin inhibitor, variegin. The thrombin time assay is optimized for variegin quantitation during future porcine studies and clinical trials.
Source Title: BIOANALYSIS
URI: https://scholarbank.nus.edu.sg/handle/10635/206031
ISSN: 17576180
17576199
DOI: 10.4155/bio-2017-0006
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