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Dextran hydrofobically modified by sterically hindered phenols. / Filippov, S.K.; Porsch, B.; Sergeeva, O.Yu.; Olifirenko, A.S.; Lesnichin, S.B.; Domnina, N.S.; Komarova, E.A.; Lezov, A.V.; Garamus, V.M.; Walterova, Z.; Stepanek, P.

в: European Physical Journal E, Том 34, № 11, 2011, стр. 123-132.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

Harvard

Filippov, SK, Porsch, B, Sergeeva, OY, Olifirenko, AS, Lesnichin, SB, Domnina, NS, Komarova, EA, Lezov, AV, Garamus, VM, Walterova, Z & Stepanek, P 2011, 'Dextran hydrofobically modified by sterically hindered phenols', European Physical Journal E, Том. 34, № 11, стр. 123-132. https://doi.org/10.1140/epje/i2011-11123-7

APA

Filippov, S. K., Porsch, B., Sergeeva, O. Y., Olifirenko, A. S., Lesnichin, S. B., Domnina, N. S., Komarova, E. A., Lezov, A. V., Garamus, V. M., Walterova, Z., & Stepanek, P. (2011). Dextran hydrofobically modified by sterically hindered phenols. European Physical Journal E, 34(11), 123-132. https://doi.org/10.1140/epje/i2011-11123-7

Vancouver

Filippov SK, Porsch B, Sergeeva OY, Olifirenko AS, Lesnichin SB, Domnina NS и пр. Dextran hydrofobically modified by sterically hindered phenols. European Physical Journal E. 2011;34(11):123-132. https://doi.org/10.1140/epje/i2011-11123-7

Author

Filippov, S.K. ; Porsch, B. ; Sergeeva, O.Yu. ; Olifirenko, A.S. ; Lesnichin, S.B. ; Domnina, N.S. ; Komarova, E.A. ; Lezov, A.V. ; Garamus, V.M. ; Walterova, Z. ; Stepanek, P. / Dextran hydrofobically modified by sterically hindered phenols. в: European Physical Journal E. 2011 ; Том 34, № 11. стр. 123-132.

BibTeX

@article{5867e466be74460797c7a6215ea7d9a2,
title = "Dextran hydrofobically modified by sterically hindered phenols",
abstract = "The conformation properties of clinically relevant hybrid macromolecular antioxidants (dextran hydrophobically modified by sterically hindered phenols) in aqueous solution were characterized by a combination of dynamic light scattering (DLS), size exclusion chromatography (SEC), and small-angle neutron scattering (SANS). We were able to split and analyze separately two different types of polydispersity —polydispersity over molecular weights and the one over substitution degree. The properties of the hybrid macromolecules are determined by the number of hydrophobic antioxidants in a single molecule. An insertion of hydrophobic groups into a hydrophilic chain changes the conformation of a single conjugate macromolecule. We have established that with the increasing of a number of hydrophobic antioxidant groups, a conformational transition occurs where a single conjugate undergoes a transition from a Gaussian coil conformation to a more compact structure.",
author = "S.K. Filippov and B. Porsch and O.Yu. Sergeeva and A.S. Olifirenko and S.B. Lesnichin and N.S. Domnina and E.A. Komarova and A.V. Lezov and V.M. Garamus and Z. Walterova and P. Stepanek",
year = "2011",
doi = "10.1140/epje/i2011-11123-7",
language = "English",
volume = "34",
pages = "123--132",
journal = "European Physical Journal E",
issn = "1292-8941",
publisher = "Springer Nature",
number = "11",

}

RIS

TY - JOUR

T1 - Dextran hydrofobically modified by sterically hindered phenols

AU - Filippov, S.K.

AU - Porsch, B.

AU - Sergeeva, O.Yu.

AU - Olifirenko, A.S.

AU - Lesnichin, S.B.

AU - Domnina, N.S.

AU - Komarova, E.A.

AU - Lezov, A.V.

AU - Garamus, V.M.

AU - Walterova, Z.

AU - Stepanek, P.

PY - 2011

Y1 - 2011

N2 - The conformation properties of clinically relevant hybrid macromolecular antioxidants (dextran hydrophobically modified by sterically hindered phenols) in aqueous solution were characterized by a combination of dynamic light scattering (DLS), size exclusion chromatography (SEC), and small-angle neutron scattering (SANS). We were able to split and analyze separately two different types of polydispersity —polydispersity over molecular weights and the one over substitution degree. The properties of the hybrid macromolecules are determined by the number of hydrophobic antioxidants in a single molecule. An insertion of hydrophobic groups into a hydrophilic chain changes the conformation of a single conjugate macromolecule. We have established that with the increasing of a number of hydrophobic antioxidant groups, a conformational transition occurs where a single conjugate undergoes a transition from a Gaussian coil conformation to a more compact structure.

AB - The conformation properties of clinically relevant hybrid macromolecular antioxidants (dextran hydrophobically modified by sterically hindered phenols) in aqueous solution were characterized by a combination of dynamic light scattering (DLS), size exclusion chromatography (SEC), and small-angle neutron scattering (SANS). We were able to split and analyze separately two different types of polydispersity —polydispersity over molecular weights and the one over substitution degree. The properties of the hybrid macromolecules are determined by the number of hydrophobic antioxidants in a single molecule. An insertion of hydrophobic groups into a hydrophilic chain changes the conformation of a single conjugate macromolecule. We have established that with the increasing of a number of hydrophobic antioxidant groups, a conformational transition occurs where a single conjugate undergoes a transition from a Gaussian coil conformation to a more compact structure.

U2 - 10.1140/epje/i2011-11123-7

DO - 10.1140/epje/i2011-11123-7

M3 - Article

VL - 34

SP - 123

EP - 132

JO - European Physical Journal E

JF - European Physical Journal E

SN - 1292-8941

IS - 11

ER -

ID: 5358983