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Interaction between covalent DNA gels and a cationic surfactant.
Diana Costa1, Per Hansson, Stefanie Schneider
1Physical Chemistry 1, Centre for Chemistry and Chemical Engineering, Lund University, Box 124, S-22100 Lund, Sweden. diana.costa@fkem1.lu.se
Biomacromolecules
|April 11, 2006
Summary
Double-stranded DNA gels interact with cetyltrimethylammonium bromide (CTAB), causing a significant 90% volume reduction. This occurs as CTAB forms complexes with DNA, even below its critical micelle concentration.
Area of Science:
- Materials Science
- Polymer Chemistry
- Physical Chemistry
Background:
- Covalently cross-linked double-stranded (ds) DNA gels are complex polyelectrolyte networks.
- Cetyltrimethylammonium bromide (CTAB) is a cationic surfactant known to interact with negatively charged polymers.
Purpose of the Study:
- To investigate the interaction between dsDNA gels and CTAB.
- To study the volume transition of dsDNA gels upon CTAB absorption.
- To characterize the size and formation of CTAB aggregates within the DNA gel.
Main Methods:
- Preparation of covalently cross-linked dsDNA gels.
- Absorption of CTAB from aqueous solutions.
- Time-resolved fluorescence quenching (TRFQ) to determine surfactant aggregate size.
- Measurement of gel volume changes at varying CTAB concentrations.
Main Results:
- DNA gels form complexes with CTAB micelles at concentrations below the critical micelle concentration (cmc).
- Small CTAB micelles (160 < N < 210) form at low concentrations, while larger micelles (N > 500) form at 1 mM CTAB.
- Surfactant binding is nearly quantitative when DNA is in excess.
- Gel volume decreases by 90% as the surfactant to DNA charge ratio (beta) increases from 0 to 1.
Conclusions:
- The interaction between dsDNA gels and CTAB leads to significant gel volume collapse.
- The formation of CTAB-DNA complexes and the size of CTAB aggregates are dependent on surfactant concentration.
- This study provides insights into polyelectrolyte-surfactant interactions and their effect on network volume.