Polydiacetylene Liposome Microarray toward Facile Measurement of Platelet Activation in Whole Blood.
Deokwon SeoTerry C MajorDo Hyun KangSungbaek SeoKangwon LeeRobert H BartlettJinsang KimPublished in: ACS sensors (2021)
The necessity of a simple measurement of platelet activation has been increasing in clinical medicine to regulate the proper dose of the antiplatelet drugs for patients having clinical outcomes in acute situations such as angina pectoris, stroke, or peripheral vascular disease or procedures involving angioplasty or coronary thrombolysis. We developed a self-signaling polydiacetylene (PDA) liposome microarray to detect activated platelets from whole blood samples in a single step. A specific antibody, 9F9 antibody, to platelet-bound fibrinogen was selected and conjugated to the PDA liposome microarray to quantify the fibrinogen-bound platelets. The developed PDA liposome-9F9 microarray generated an intense fluorescence signal when activated platelets in whole blood were introduced and also successfully distinguished the reduced platelet activation in the presence of Tirofiban, a model antiplatelet drug. The results of this single-step benchtop assay incorporates simple, sensitive, and rapid attributes that can detect the extent of platelet activation prior to needed clinical procedures.
Keyphrases
- coronary artery disease
- coronary artery
- ejection fraction
- newly diagnosed
- intensive care unit
- atrial fibrillation
- heart failure
- photodynamic therapy
- prognostic factors
- liver failure
- emergency department
- drug induced
- percutaneous coronary intervention
- red blood cell
- respiratory failure
- gold nanoparticles
- blood brain barrier
- highly efficient