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Bioartificial liver with whole blood perfusion
Yuichiro Ueda1, Hiroo Iwata, Hyun Joon Paek
1Institute for Frontier Medical Sciences, Kyoto University, Kyoto, Japan.
Summary
This study developed a bioartificial liver (BAL) device using porcine hepatocytes. The BAL system demonstrated effective detoxification and biocompatibility in vitro and in vivo canine models, showing promise as a liver assist device.
Area of Science:
- Biomedical Engineering
- Hepatology
- Regenerative Medicine
Background:
- Liver failure necessitates innovative treatment options.
- Bioartificial Liver (BAL) systems offer a potential solution by mimicking liver function.
- Developing a BAL that can perfuse whole blood is crucial for clinical application.
Purpose of the Study:
- To develop and evaluate a novel bioartificial liver (BAL) system for whole blood perfusion.
- To assess the detoxification capacity and biocompatibility of the BAL system.
- To investigate the protective mechanisms of the hollow fiber membrane against humoral immunity.
Main Methods:
- Preparation of BAL cartridges with porcine hepatocytes within hollow fibers.
- In vitro perfusion of human whole blood through the BAL system.
- Lidocaine loading tests to evaluate detoxification.
- Histological and immunohistochemical analysis (hematoxylin-eosin, MAC staining) of hepatocytes.
- In vivo assessment in a 24-hour canine model.
Main Results:
- The BAL system demonstrated sustained detoxification of lidocaine over 48 hours.
- Porcine hepatocytes maintained viability and integrity within the hollow fibers, with no observed Membrane Attack Complex (MAC) deposition.
- The hollow fiber membrane effectively protected hepatocytes from humoral immunity.
- In vivo studies showed no significant hemolysis or thrombus formation, indicating good biocompatibility.
Conclusions:
- The developed BAL system is a promising liver assist device capable of perfusing whole blood.
- The system exhibits effective detoxification and biocompatibility, crucial for potential clinical use.
- The hollow fiber design provides immune protection for the encapsulated hepatocytes.