Self-assembly thermodynamics of pH-responsive amino-acid-based polymers with a nonionic surfactant

The behavior of pH-responsive polymers poly(N-methacryloyl-l-valine) (P1), poly(N-methacryloyl-l-phenylalanine) (P2), and poly(N-methacryloylglycyne-l-leucine) (P3) has been studied in the presence of the nonionic surfactant Brij98. The pure polymers phase-separate in an acidic medium with critical...

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Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1985. - 30(2014), 38 vom: 30. Sept., Seite 11307-18
1. Verfasser: Bogomolova, Anna (VerfasserIn)
Weitere Verfasser: Keller, Sandro, Klingler, Johannes, Sedlak, Marian, Rak, Dmytro, Sturcova, Adriana, Hruby, Martin, Stepanek, Petr, Filippov, Sergey K
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2014
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Amino Acids Plant Oils Polymers Surface-Active Agents Polyethylene Glycols 3WJQ0SDW1A polyethylene glycol oleyl ether 9004-98-2
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520 |a The behavior of pH-responsive polymers poly(N-methacryloyl-l-valine) (P1), poly(N-methacryloyl-l-phenylalanine) (P2), and poly(N-methacryloylglycyne-l-leucine) (P3) has been studied in the presence of the nonionic surfactant Brij98. The pure polymers phase-separate in an acidic medium with critical pHtr values of 3.7, 5.5, and 3.4, respectively. The addition of the surfactant prevents phase separation and promotes reorganization of polymer molecules. The nature of the interaction between polymer and surfactant depends on the amino acid structure in the side chain of the polymer. This effect was investigated by dynamic light scattering, isothermal titration calorimetry, electrophoretic measurements, small-angle neutron scattering, and infrared spectroscopy. Thermodynamic analysis revealed an endothermic association reaction in P1/Brij98 mixture, whereas a strong exothermic effect was observed for P2/Brij98 and P3/Brij98. Application of regular solution theory for the analysis of experimental enthalpograms indicated dominant hydrophobic interactions between P1 and Brij98 and specific interactions for the P2/Brij98 system. Electrophoretic and dynamic light scattering measurements support the applicability of the theory to these cases. The specific interactions can be ascribed to hydrogen bonds formed between the carboxylic groups of the polymer and the oligo(ethylene oxide) head groups of the surfactant. Thus, differences in polymer-surfactant interactions between P1 and P2 polymers result in different structures of polymer-surfactant complexes. Specifically, small-angle neutron scattering revealed pearl-necklace complexes and "core-shell" structures for P1/Brij98 and P2/Brij98 systems, respectively. These results may help in the design of new pH-responsive site-specific micellar drug delivery systems or pH-responsive membrane-disrupting agents 
650 4 |a Journal Article 
650 4 |a Research Support, Non-U.S. Gov't 
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650 7 |a Plant Oils  |2 NLM 
650 7 |a Polymers  |2 NLM 
650 7 |a Surface-Active Agents  |2 NLM 
650 7 |a Polyethylene Glycols  |2 NLM 
650 7 |a 3WJQ0SDW1A  |2 NLM 
650 7 |a polyethylene glycol oleyl ether  |2 NLM 
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700 1 |a Keller, Sandro  |e verfasserin  |4 aut 
700 1 |a Klingler, Johannes  |e verfasserin  |4 aut 
700 1 |a Sedlak, Marian  |e verfasserin  |4 aut 
700 1 |a Rak, Dmytro  |e verfasserin  |4 aut 
700 1 |a Sturcova, Adriana  |e verfasserin  |4 aut 
700 1 |a Hruby, Martin  |e verfasserin  |4 aut 
700 1 |a Stepanek, Petr  |e verfasserin  |4 aut 
700 1 |a Filippov, Sergey K  |e verfasserin  |4 aut 
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