TY - JOUR
T1 - Functional platelet aggregation analysis using digital optofluidic scattering quantitation
AU - Qin, Shan
AU - Fu, Rongxin
AU - Yang, Fan
AU - Gao, Weibo
AU - Hou, Jialu
AU - Li, Hang
AU - Zhang, Shuailong
N1 - Publisher Copyright:
© 2023 SPIE.
PY - 2023
Y1 - 2023
N2 - Platelet aggregation rate is a crucial indicator for platelet function testing in clinical practice. Currently, the most common method for detecting platelet aggregation rate is by using a platelet aggregation analyzer to detect platelet-rich plasma or washed platelets. This method works based on the principle of light transmittance ratio, which measures the difference of the light transmittance before and after the reaction between the sample and the inducer to represent the aggregation rate of the sample. Although this method only requires a few minutes to complete after the sample is collected and processed, it requires a large sample volume. Moreover, it cannot accurately detect samples with low aggregation rate and chyle blood due to the slight difference in light transmittance before and after the reaction, which poses significant challenges for doctors in the clinical diagnosis and treatment determination for platelet aggregation dysfunction. To overcome this limitation, we propose a novel method for assessing platelet aggregation rate by leveraging the capabilities of digital microfluidics for automated precision manipulation of minute liquid droplets.
AB - Platelet aggregation rate is a crucial indicator for platelet function testing in clinical practice. Currently, the most common method for detecting platelet aggregation rate is by using a platelet aggregation analyzer to detect platelet-rich plasma or washed platelets. This method works based on the principle of light transmittance ratio, which measures the difference of the light transmittance before and after the reaction between the sample and the inducer to represent the aggregation rate of the sample. Although this method only requires a few minutes to complete after the sample is collected and processed, it requires a large sample volume. Moreover, it cannot accurately detect samples with low aggregation rate and chyle blood due to the slight difference in light transmittance before and after the reaction, which poses significant challenges for doctors in the clinical diagnosis and treatment determination for platelet aggregation dysfunction. To overcome this limitation, we propose a novel method for assessing platelet aggregation rate by leveraging the capabilities of digital microfluidics for automated precision manipulation of minute liquid droplets.
KW - digital microfluidics
KW - label-free biosensor
KW - optofluidics
KW - platelet aggregation
KW - scattering quantitation
UR - http://www.scopus.com/inward/record.url?scp=85181986030&partnerID=8YFLogxK
U2 - 10.1117/12.2685606
DO - 10.1117/12.2685606
M3 - Conference article
AN - SCOPUS:85181986030
SN - 0277-786X
VL - 12770
JO - Proceedings of SPIE - The International Society for Optical Engineering
JF - Proceedings of SPIE - The International Society for Optical Engineering
IS - 1
M1 - 127701K
T2 - Optics in Health Care and Biomedical Optics XIII 2023
Y2 - 14 October 2023 through 16 October 2023
ER -