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Liposome-encapsulated hemoglobin using film hydration processing to form artificial red blood cells
S V Deshpande1, R L Beissinger
1Department of Chemical Engineering, Illinois Institute of Technology, Chicago 60616.
Summary
Liposome-encapsulated hemoglobin (LEH) production was optimized for yield and stability. LEH effectively delivered oxygen and supported life in rats with critically low hematocrit levels.
Area of Science:
- Biomaterials Science
- Biomedical Engineering
- Hematology
Background:
- Liposome-encapsulated hemoglobin (LEH) is a potential blood substitute.
- Optimizing LEH production is crucial for its clinical application.
- Understanding LEH properties is key to its efficacy.
Purpose of the Study:
- To investigate the impact of process parameters on LEH characteristics.
- To determine optimal conditions for high hemoglobin encapsulation efficiency and stability.
- To evaluate the oxygen-carrying capacity and in vivo performance of LEH.
Main Methods:
- Microfluidizer M110 used for LEH production.
- Lipid loading ratios and concentrations optimized.
- Transmission electron microscopy for particle size analysis.
- Rheological measurements for viscosity assessment.
- In vivo studies involving exchange-transfused rats.
Main Results:
- Maximum hemoglobin encapsulation efficiency achieved at 300 mumol lipid/ml.
- High encapsulated hemoglobin concentrations (up to 15.5 g/100 ml) prepared.
- Average vesicle size of optimal LEH batches approximately 155 nm.
- LEH viscosity higher than whole blood across tested shear rates.
- LEH demonstrated minimal hemoglobin leakage and supported survival in anemic rats.
Conclusions:
- Optimized microfluidization parameters yield stable LEH with high encapsulation efficiency.
- LEH exhibits suitable rheological properties and minimal leakage for potential transfusion.
- LEH effectively supports life in critical anemia, indicating its oxygen-carrying capability.