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Development of a novel polycationic adsorbent for cryogel removal
K Miyamoto1, R Uchiyama, M Tokita
1Faculty of Engineering, Department of Chemistry for Materials, Mie University, 1515, Tsu, Mie 514, Kamihama-Chou, Japan. miyamoto@chem.mie-u.ac.jp
International Journal of Biological Macromolecules
|June 29, 2001
Summary
Rheumatism patients
Area of Science:
- Biochemistry
- Materials Science
- Medical Research
Background:
- Cryogel, a complex of plasma fibronectin (pFN) with extra domain A (EDA(+)FN) and fibrinogen (Fbg), forms in rheumatic patients' plasma due to heparin (HP) at low temperatures.
- EDA(+)FN presence in normal plasma is unusual, but its prevalence in rheumatism contributes to cryogelation, suggesting cryogel removal as a potential treatment.
- The HP-EDA(+)FN aggregate, a key cryogel component, exhibits anionic properties.
Purpose of the Study:
- To develop novel cationic materials for selectively removing the anionic HP-EDA(+)FN complex from plasma.
- To investigate the optimal amino group density on adsorbents for efficient cryogel component adsorption.
- To assess the therapeutic potential of cryogel removal in treating rheumatism.
Main Methods:
- Synthesis of cationic adsorbents with varying amino group densities.
- Testing the selective adsorption of the EDA(+)FN-HP complex using model patient plasma.
- Quantifying the removal efficiency of EDA(+)FN, pFN, and Fbg.
Main Results:
- Adsorbents with an amino group density of 100-130 micromol/g (dry weight) demonstrated selective adsorption of the EDA(+)FN-HP complex.
- An 80% elimination of EDA(+)FN was achieved.
- Significant removal of total fibronectin (pFN) (10%) and fibrinogen (Fbg) (10%) was also observed in model plasma.
Conclusions:
- Cationic materials with specific amino group densities can effectively and selectively remove cryogel components from plasma.
- This approach shows promise for developing novel therapeutic strategies targeting cryogel-related conditions like rheumatism.
- Further research is warranted to validate these findings in clinical settings.