TY - GEN
T1 - Dynamic Topology-Aware Flow Path Construction and Scheduling Optimization for Multilayered Continuous-Flow Microfluidic Biochips
AU - Lian, Meng
AU - Yang, Shucheng
AU - Li, Mengchu
AU - Tseng, Tsun Ming
AU - Schlichtmann, Ulf
N1 - Publisher Copyright:
© 2025 Institute of Electrical and Electronics Engineers Inc.. All rights reserved.
PY - 2025/3/4
Y1 - 2025/3/4
N2 - Multilayered continuous-flow microfluidic biochips are highly valued for their miniaturization and high bio-application throughput. However, challenges arise as the dynamic connections of channels, adjusted to satisfy varying demands of fluid transportation at different moments, complicate the execution of bioassays. The existing methods often focus on device binding and operation scheduling during high-level synthesis but overlook the topological connections within the microfluidic network. This oversight leads to mismanagement of conflicts between fluid transportations and erroneous assumptions about constant flow velocities, resulting in decreased accuracy and efficiency or even infeasibility of bioassay execution. To address this problem, we mathematically model the flow velocity that varies according to the dynamic changes of the topological connections between the on-chip components during the execution of the bioassay. Further integrating the flow velocity model into the high-level synthesis, we propose a quadratic programming (QP) method that constructs flow paths and optimizes scheduling schemes to minimize the bioassay completion time. Experimental results confirm that, compared with the state-of-the-art approach, our method shortened the bioassay completion time by an average of 40.9%.
AB - Multilayered continuous-flow microfluidic biochips are highly valued for their miniaturization and high bio-application throughput. However, challenges arise as the dynamic connections of channels, adjusted to satisfy varying demands of fluid transportation at different moments, complicate the execution of bioassays. The existing methods often focus on device binding and operation scheduling during high-level synthesis but overlook the topological connections within the microfluidic network. This oversight leads to mismanagement of conflicts between fluid transportations and erroneous assumptions about constant flow velocities, resulting in decreased accuracy and efficiency or even infeasibility of bioassay execution. To address this problem, we mathematically model the flow velocity that varies according to the dynamic changes of the topological connections between the on-chip components during the execution of the bioassay. Further integrating the flow velocity model into the high-level synthesis, we propose a quadratic programming (QP) method that constructs flow paths and optimizes scheduling schemes to minimize the bioassay completion time. Experimental results confirm that, compared with the state-of-the-art approach, our method shortened the bioassay completion time by an average of 40.9%.
KW - high-level synthesis
KW - multilayered continuous-flow microfluidic biochip
KW - quadratic programming
UR - http://www.scopus.com/inward/record.url?scp=105000247034&partnerID=8YFLogxK
U2 - 10.1145/3658617.3697779
DO - 10.1145/3658617.3697779
M3 - Conference contribution
AN - SCOPUS:105000247034
T3 - Proceedings of the Asia and South Pacific Design Automation Conference, ASP-DAC
SP - 1364
EP - 1371
BT - ASP-DAC 2025 - 30th Asia and South Pacific Design Automation Conference, Proceedings
PB - Institute of Electrical and Electronics Engineers Inc.
T2 - 30th Asia and South Pacific Design Automation Conference, ASP-DAC 2025
Y2 - 20 January 2025 through 23 January 2025
ER -