Thrombolytic Potential of “Hydrodynamic Cavitation on a Chip” Concept: Insights into Clot Degradation

Abstract

Thrombolysis is essential for treating vascular conditions such as pulmonary embolism and deep vein thrombosis, yet current thrombolytic drug-based approaches have notable limitations in efficacy and safety. Hydrodynamic cavitation (HC) offers drug-free clot degradation through mechanical disruption. In this study, the effects of HC exposure on thrombolysis were investigated using Clot-on-a-Chip (CoC) platform. In this regard, the thrombolytic potential of HC exposure was evaluated by analyses involving hemolysis and fibrinolysis. Furthermore, the results were compared with Acoustic Cavitation (AC), a widely studied alternative. According to the obtained results, HC exposure (482 kPa, 120 s) resulted in 12.1% released hemoglobin and a 53.4% reduction in clot mass. In contrast, AC exposure (24 kHz, 50% amplitude, 30 s) led to a 1.3-fold greater mass reduction with 26.8% released hemoglobin, likely due to additional thermal effects. Morphological analyses revealed that HC treatment significantly reduced red blood cell density in a pressure- and time-dependent manner. Notably, HC treatment effectively eroded blood clots by hemolysis with slight fibrinolysis, whereas clot erosion in AC was primarily due to hemolysis. HC achieved thrombolysis comparable to or better than AC, offering a safer, more targeted strategy. The findings will advance mechanistic understanding of cavitation-induced clot degradation and support HC’s clinical potential for thrombosis treatment.

Supplementary files

Article information

Article type
Paper
Submitted
16 May 2025
Accepted
29 Sep 2025
First published
02 Oct 2025

Lab Chip, 2025, Accepted Manuscript

Thrombolytic Potential of “Hydrodynamic Cavitation on a Chip” Concept: Insights into Clot Degradation

A. A. Yetisgin, B. Ozogul, U. Akar, R. MERCİMEK, S. Seyedmirzaei Sarraf, T. Elverdi, E. Amani, D. Grishenkov, A. Kosar and M. Ghorbani, Lab Chip, 2025, Accepted Manuscript , DOI: 10.1039/D5LC00482A

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