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@ARTICLE{Bogomolova:189592,
author = {Bogomolova, Anna and Keller, Sandro and Klingler, Johannes
and Sedlak, Marian and Rak, Dmytro and Sturcova, Adriana and
Hruby, Martin and Stepanek, Petr and Filippov, Sergey K.},
title = {{S}elf-{A}ssembly {T}hermodynamics of p{H}-{R}esponsive
{A}mino-{A}cid-{B}ased {P}olymers with a {N}onionic
{S}urfactant},
journal = {Langmuir},
volume = {30},
number = {38},
issn = {1520-5827},
address = {Washington, DC},
publisher = {ACS Publ.},
reportid = {FZJ-2015-02730},
pages = {11307 - 11318},
year = {2014},
abstract = {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.},
cin = {JCNS (München) ; Jülich Centre for Neutron Science JCNS
(München) ; JCNS-FRM-II / Neutronenstreuung ; JCNS-1},
ddc = {670},
cid = {I:(DE-Juel1)JCNS-FRM-II-20110218 /
I:(DE-Juel1)JCNS-1-20110106},
pnm = {54G - JCNS (POF2-54G24)},
pid = {G:(DE-HGF)POF2-54G24},
experiment = {EXP:(DE-MLZ)KWS2-20140101},
typ = {PUB:(DE-HGF)16},
UT = {WOS:000342607000008},
pubmed = {pmid:25192406},
doi = {10.1021/la5031262},
url = {https://juser.fz-juelich.de/record/189592},
}