scholarly journals How validated receptor occupancy flow cytometry assays can impact decisions and support drug development

2015 ◽  
Vol 90 (2) ◽  
pp. 150-158 ◽  
Author(s):  
Maxime Moulard ◽  
Marie-Laure Ozoux
2015 ◽  
Vol 90 (2) ◽  
pp. 177-190 ◽  
Author(s):  
Karen J. Quadrini ◽  
Anne Charlotte Hegelund ◽  
Kasia E. Cortes ◽  
Chengsen Xue ◽  
Susan M. Kennelly ◽  
...  

2016 ◽  
Vol 90 (2) ◽  
pp. 110-116 ◽  
Author(s):  
Jennifer J. Stewart ◽  
Cherie L. Green ◽  
Nicholas Jones ◽  
Meina Liang ◽  
Yuanxin Xu ◽  
...  

1999 ◽  
Vol 19 (03) ◽  
pp. 134-138
Author(s):  
Gitta Kühnel ◽  
A. C. Matzdorff

SummaryWe studied the effect of GPIIb/IIIa-inhibitors on platelet activation with flow cytometry in vitro. Citrated whole blood was incubated with increasing concentrations of three different GPIIb/IIIa-inhibitors (c7E3, DMP728, XJ757), then thrombin or ADP were added and after 1 min the sample was fixed. Samples without c7E3 but with 0.1 U/ml thrombin had a decrease in platelet count. Samples with increasing concentrations of c7E3 had a lesser or no decrease in platelet count. The two other inhibitors (DMP 725, XJ757) gave similar results. GPIIb/IIIa-inhibitors prevent aggregate formation and more single platelets remain in the blood sample. The agonist-induced decrease in platelet count correlates closely with the concentration of the GPIIb/IIIa inhibitor and receptor occupancy. This correlation may be used as a simple measure for inhibitor activity in whole blood.


Author(s):  
Alessandra Audia ◽  
Gregory Bannish ◽  
Rachel Bunting ◽  
Chelsea Riveley

Author(s):  
Padma Narayanan ◽  
Renold J. Capocasale ◽  
Nianyu Li ◽  
Peter J. Bugelski

Author(s):  
Leanne Flye-Blakemore ◽  
Christèle Gonneau ◽  
Nithianandan Selliah ◽  
Ajay Grover ◽  
Sriram Ramanan ◽  
...  

Bioanalysis ◽  
2021 ◽  
Author(s):  
Vellalore N Kakkanaiah ◽  
Katie Matys ◽  
Patrick Bennett

Flow cytometer is a powerful cellular analysis tool consists of three main components; fluidics, optics and electronics. Flow cytometry methods have been used in all stages of drug development as like ligand binding assays (LBA). Both LBA and flow cytometry methods require specific interaction between the critical reagents and the analytes. Antibodies and their conjugates, viable dyes and permeabilizing buffer are the main critical reagents in flow cytometry methods. Similarly, antibodies, engineered proteins and their conjugates are the main critical reagents in LBA. The main difference between the two methods is the lack of true reference standards for flow cytometry cellular analysis.


2015 ◽  
Vol 90 (2) ◽  
pp. 117-127 ◽  
Author(s):  
Meina Liang ◽  
Martin Schwickart ◽  
Amy K. Schneider ◽  
Inna Vainshtein ◽  
Christopher Del Nagro ◽  
...  

2016 ◽  
Vol 90 (2) ◽  
pp. 141-149 ◽  
Author(s):  
Cherie L. Green ◽  
Jennifer J. Stewart ◽  
Carl-Magnus Högerkorp ◽  
Alan Lackey ◽  
Nicholas Jones ◽  
...  

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