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Hydrogels in endovascular embolization. V. Antitumour agent methotrexate-containing p(HEMA)
1Institute of Macromolecular Chemistry, Czechoslovak Academy of Sciences, Prague.
Biomaterials
|January 1, 1992
Summary
This study evaluated a polymeric carrier, p(HEMA)-Hex-MTX, for methotrexate delivery. The carrier showed minimal impact on blood and surrounding tissues, with sustained drug diffusion.
Area of Science:
- Biomaterials Science
- Polymer Chemistry
- Drug Delivery Systems
Background:
- Methotrexate (MTX) is a chemotherapy drug with potential for localized delivery.
- Polymeric carriers offer controlled release of therapeutic agents.
- The aminohexyl derivative of 2-hydroxyethyl methacrylate and ethylene dimethacrylate (p(HEMA)-Hex) was investigated as a potential carrier.
Purpose of the Study:
- To assess the biocompatibility of a p(HEMA)-Hex-MTX polymeric carrier.
- To evaluate the effects of the carrier on blood morphology and coagulation.
- To examine the host tissue response to the implanted carrier over time.
Main Methods:
- Spherical p(HEMA)-Hex particles were loaded with methotrexate (MTX).
- The carrier's impact on donor blood morphology and coagulation was analyzed.
- Tissue response was evaluated in rabbit blood vessels after implantation for various durations.
Main Results:
- The p(HEMA)-Hex-MTX carrier demonstrated minimal alterations to blood morphology.
- Key blood coagulation indicators remained largely unaffected by the carrier.
- Surrounding living tissues showed acceptable responses to the material over time.
- Methotrexate diffused from the embolic material for several days.
Conclusions:
- The p(HEMA)-Hex-MTX polymeric carrier is biocompatible.
- The carrier exhibits a favorable safety profile for localized drug delivery.
- Sustained release of methotrexate is achievable with this system.