dc.contributor.author
Paulus, Florian
dc.contributor.author
Steinhilber, Dirk
dc.contributor.author
Welker, Pia
dc.contributor.author
Mangoldt, Dorothea
dc.contributor.author
Licha, Kai
dc.contributor.author
Depner, Harald
dc.contributor.author
Sigrist, Stephan
dc.contributor.author
Haag, Rainer
dc.date.accessioned
2018-06-08T04:04:26Z
dc.date.available
2014-10-21T12:00:07.767Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/16525
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-20706
dc.description.abstract
A set of six hydrophobically derivatized polymers based on polyglycerol
sulfates have been investigated to determine the influence of scaffold
architecture on the encapsulation properties of hydrophobic guests. Each of
three block and statistical copolymers has been synthesized with phenyl,
naphthyl, and biphenyl substituents in a one-pot procedure. The copolymers
have been functionalized with sulfate groups in order to introduce an
electrostatically repulsive surface that can stabilize the aggregated
carriers. In addition, sulfates provide a highly active targeting moiety for
inflammation and cellular uptake. UV measurements show a supramolecular
encapsulation of the investigated guest molecules in the low μM range. The
transport studies with pyrene and an indocarbocyanine dye further indicated a
core–shell-type architecture which provides a distinct amphiphilicity as
required for supramolecular guest complexation. The combination of a host
functionality with an active sulfate targeting moiety has been used to
investigate the structure related cellular transport properties.
en
dc.rights.uri
http://creativecommons.org/licenses/by-nc/3.0/
dc.subject.ddc
500 Naturwissenschaften und Mathematik::540 Chemie
dc.title
Structure related transport properties and cellular uptake of hyperbranched
polyglycerol sulfates with hydrophobic cores
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation
Polymer Chemistry. - 5 (2014), 17, S. 5020-5028
dc.identifier.sepid
39619
dcterms.bibliographicCitation.doi
10.1039/C4PY00430B
dcterms.bibliographicCitation.url
http://xlink.rsc.org/?DOI=C4PY00430B
refubium.affiliation
Biologie, Chemie, Pharmazie
de
refubium.funding
OpenAccess Publikation in Allianzlizenz
refubium.funding.id
Au-006333
refubium.mycore.fudocsId
FUDOCS_document_000000021182
refubium.resourceType.isindependentpub
no
refubium.mycore.derivateId
FUDOCS_derivate_000000004623
dcterms.accessRights.openaire
open access
dcterms.isPartOf.issn
1759-9954