Aptamer-modified polymer nanoparticles for targeted drug delivery

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dc.identifier.uri http://dx.doi.org/10.15488/3104
dc.identifier.uri http://www.repo.uni-hannover.de/handle/123456789/3134
dc.contributor.author Modrejewski, Julia
dc.contributor.author Walter, Johanna-Gabriela
dc.contributor.author Kretschmer, Imme
dc.contributor.author Kemal, Evren
dc.contributor.author Green, Mark
dc.contributor.author Belhadj, Hamza
dc.contributor.author Blume, Cornelia
dc.contributor.author Scheper, Thomas
dc.date.accessioned 2018-04-18T12:21:27Z
dc.date.available 2018-04-18T12:21:27Z
dc.date.issued 2016
dc.identifier.citation Modrejewski, J.; Walter, J.-G.; Kretschmer, I.; Kemal, E.; Green, M. et al.: Aptamer-modified polymer nanoparticles for targeted drug delivery. In: BioNanoMaterials 17 (2016), Nr. Februar, S. 43-51. DOI: https://doi.org/10.1515/bnm-2015-0027
dc.description.abstract The purpose of this study was to develop a model system for targeted drug delivery. This system should enable targeted drug release at a certain tissue in the body. In conventional drug delivery systems, drugs are often delivered unspecifically resulting in unwarranted adverse effects. To circumvent this problem, there is an increasing demand for the development of intelligent drug delivery systems allowing a tissue-specific mode of delivery. Within this study, nanoparticles consisting of two biocompatible polymers are used. Because of their small size, nanoparticles are well-suited for effective drug delivery. The small size affects their movement through cell and tissue barriers. Their cellular uptake is easier when compared to larger drug delivery systems. Paclitaxel was encapsulated into the nanoparticles as a model drug, and to achieve specific targeting an aptamer directed against lung cancer cells was coupled to the nanoparticles surface. Nanoparticles were characterized by dynamic light scattering (DLS), transmission electron microscopy (TEM), fourier transform infrared spectroscopy (FTIR), and nanotracking analysis (NTA). Also their surface charge was characterized from ζ-potential measurements. Their preparation was optimized and subsequently specificity of drug-loaded and aptamer-functionalized nanoparticles was investigated using lung cancer cells. © 2016 by De Gruyter. eng
dc.language.iso eng
dc.publisher Berlin : De Gruyter
dc.relation.ispartofseries BioNanoMaterials 17 (2016), Nr. Februar
dc.rights Es gilt deutsches Urheberrecht. Das Dokument darf zum eigenen Gebrauch kostenfrei genutzt, aber nicht im Internet bereitgestellt oder an Außenstehende weitergegeben werden. Dieser Beitrag ist aufgrund einer (DFG-geförderten) Allianz- bzw. Nationallizenz frei zugänglich.
dc.subject aptamer eng
dc.subject HOOC-PEG-PCL eng
dc.subject mPEG-PCL eng
dc.subject nanoparticles eng
dc.subject aptamer eng
dc.subject copolymer eng
dc.subject nanocarrier eng
dc.subject paclitaxel eng
dc.subject antineoplastic activity eng
dc.subject Article eng
dc.subject cancer cell eng
dc.subject controlled study eng
dc.subject drug delivery system eng
dc.subject drug dosage form comparison eng
dc.subject drug release eng
dc.subject drug solubility eng
dc.subject female eng
dc.subject high performance liquid chromatography eng
dc.subject human eng
dc.subject human cell eng
dc.subject hydrodynamics eng
dc.subject in vitro study eng
dc.subject infrared spectroscopy eng
dc.subject lung cancer eng
dc.subject nanoencapsulation eng
dc.subject particle size eng
dc.subject photon correlation spectroscopy eng
dc.subject polymerization eng
dc.subject priority journal eng
dc.subject process optimization eng
dc.subject surface charge eng
dc.subject transmission electron microscopy eng
dc.subject zeta potential eng
dc.subject.ddc 610 | Medizin, Gesundheit ger
dc.title Aptamer-modified polymer nanoparticles for targeted drug delivery eng
dc.type Article
dc.type Text
dc.relation.issn 2193-0651
dc.relation.doi https://doi.org/10.1515/bnm-2015-0027
dc.bibliographicCitation.volume 17
dc.bibliographicCitation.firstPage 43
dc.bibliographicCitation.lastPage 51
dc.description.version publishedVersion
tib.accessRights frei zug�nglich


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