Related Experiment Videos
Summary
Coating colloidal particles with poloxamer 407 hinders liver and spleen uptake. This allows targeted delivery of microspheres to the bone marrow for diagnostic and therapeutic applications.
Area of Science:
- Biomedical Engineering
- Nanotechnology
- Drug Delivery Systems
Background:
- Intravenously administered colloidal particles are typically cleared by the liver and spleen.
- Limited particle delivery to the bone marrow restricts its use in diagnostics and therapeutics.
Purpose of the Study:
- To develop a method for enhancing microsphere deposition in the bone marrow.
- To investigate the potential of poloxamer 407 as a coating agent for colloidal particles.
Main Methods:
- Model microspheres were coated with the block co-polymer poloxamer 407.
- The biodistribution of coated microspheres was evaluated, focusing on liver, spleen, and bone marrow uptake.
Main Results:
- Coating with poloxamer 407 significantly reduced uptake by reticuloendothelial cells in the liver and spleen.
- A preferential accumulation of coated microspheres was observed in the bone marrow.
Conclusions:
- Poloxamer 407 coating effectively shields colloidal particles from rapid clearance.
- This approach enables targeted delivery of microspheres to the bone marrow, opening avenues for radiodiagnosis and bone marrow disease treatment.