0000000000189942

AUTHOR

Christine Seidl

0000-0003-0342-1559

showing 11 related works from this author

Trans -Cyclooctene-Functionalized PeptoBrushes with Improved Reaction Kinetics of the Tetrazine Ligation for Pretargeted Nuclear Imaging

2020

Tumor targeting using agents with slow pharmacokinetics represents a major challenge in nuclear imaging and targeted radionuclide therapy as they most often result in low imaging contrast and high radiation dose to healthy tissue. To address this challenge, we developed a polymer-based targeting agent that can be used for pretargeted imaging and thus separates tumor accumulation from the imaging step in time. The developed targeting agent is based on polypeptide-graft-polypeptoid polymers (PeptoBrushes) functionalized with trans-cyclooctene (TCO). The complementary In-111-labeled imaging agent is a 1,2,4,5-tetrazine derivative, which can react with aforementioned TCO-modified PeptoBrushes i…

pretargeted imagingGeneral Physics and Astronomy02 engineering and technology010402 general chemistry01 natural sciencesArticlechemistry.chemical_compoundTetrazinetetrazine ligationCycloocteneGeneral Materials Sciencepolypeptide-graft-polypeptoidsPretargetingchemistry.chemical_classificationGeneral EngineeringPolymerEPR effectPeptoBrush021001 nanoscience & nanotechnologynanomedicineSmall moleculeCombinatorial chemistryImaging agent0104 chemical scienceschemistrySPECTNanomedicineBioorthogonal chemistry0210 nano-technologyACS Nano
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Polymeric Nanoparticles: Polymeric Nanoparticles with Neglectable Protein Corona (Small 18/2020)

2020

BiomaterialsMaterials scienceChemical engineeringAsymmetrical Flow Field-Flow FractionationDrug deliveryGeneral Materials ScienceProtein CoronaGeneral ChemistryPolymeric nanoparticlesBiotechnologySmall
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Polymeric Nanoparticles with Neglectable Protein Corona

2020

Small : nano micro 16(18), 1907574 (2020). doi:10.1002/smll.201907574

540 Chemistry and allied sciencesDispersity610 Medizinmicellar structuresNanoparticleProtein Corona02 engineering and technology010402 general chemistry01 natural sciencesPolyethylene GlycolsBiomaterialschemistry.chemical_compoundAdsorption610 Medical sciencesHumansGeneral Materials ScienceParticle SizeGel electrophoresisChemistryasymmetrical flow field-flow fractionationSarcosineGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesChemical engineering540 Chemiedrug deliveryNanoparticlesParticleProtein CoronaParticle sizePeptides0210 nano-technologyHydrophobic and Hydrophilic InteractionsEthylene glycolBiotechnologySmall
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Tetrazine- and trans -cyclooctene-functionalised polypept(o)ides for fast bioorthogonal tetrazine ligation

2020

The inverse electron demand Diets-Alder (IEDDA) reaction-initiated ligation between 1,2,4,5-tetra-zines (Tz) and trans-cyclooctenes (TCO) is one of the fastest bioorthogonal reactions known today and is therefore increasingly used for in vivo click chemistry. Described herein is the synthesis of Tz- and TCO-functionalised polypeptides, polypeptoids and polypeptide-block-polypeptoids (polypept(o) ides) by ring-opening polymerisation of the corresponding N-carboxyanhydrides using Tz- or TCO-functional amine initiators. Despite the reactivity of tetrazines, polymers with low dispersity and high end group integrity can be obtained as observed by gel permeation chromatography (GPC), nuclear magn…

Polymers and PlasticsChemistryOrganic ChemistryBioengineering02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesBiochemistryCombinatorial chemistry0104 chemical sciencesGel permeation chromatographyMiniemulsionEnd-groupchemistry.chemical_compoundTetrazineCycloocteneClick chemistryReactivity (chemistry)Bioorthogonal chemistry0210 nano-technologyPolymer Chemistry
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Density of conjugated antibody determines the extent of Fc receptor dependent capture of nanoparticles by liver sinusoidal endothelial cells

2021

Despite considerable progress in the design of multifunctionalized nanoparticles (NPs) that selectively target specific cell types, their systemic application often results in unwanted liver accumulation. The exact mechanisms for this general observation are still unclear. Here we asked whether the number of cell-targeting antibodies per NP determines the extent of NP liver accumulation and also addressed the mechanisms by which antibody-coated NPs are retained in the liver. We used polysarcosine-based peptobrushes (PBs), which in an unmodified form remain in the circulation for >24 h due to the absence of a protein corona formation and low unspecific cell binding, and conjugated them with …

Biodistributionbiologymedicine.diagnostic_testChemistryCellGeneral EngineeringFc receptorGeneral Physics and AstronomyEndothelial CellsDendritic cellReceptors FcFlow cytometryCell biologymedicine.anatomical_structureLiverbiology.proteinmedicineSystemic administrationNanoparticlesGeneral Materials ScienceTissue DistributionAntibodyReceptor
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Investigation of α-amino acid N-carboxyanhydrides by X-ray diffraction for controlled ring-opening polymerization

2019

Abstract The need for a scalable synthesis of not sequence defined polypeptides as biomaterials is met by the ring-opening polymerization of α-amino acid N-carboxyanhydrides (NCAs). Even though this polymerization technique appears straight forward, it holds pitfalls in terms of reproducibility and overall control over the polymerization conditions, which depends, beside choice of solvent or initiator, significantly on reagent purity. In addition, the synthesis of monomers can lead to the formation of racemic amino acids. Thus, in this work, we describe the benefits of highly pure monomers in order to control nucleophilic ring-opening polymerization NCAs. Hereby, monomer purity is investiga…

chemistry.chemical_classificationOrganic ChemistrySequence (biology)BiochemistryRing-opening polymerizationAmino acidchemistry.chemical_compoundMonomerchemistryNucleophilePolymerizationReagentDrug DiscoveryX-ray crystallographyPolymer chemistryTetrahedron Letters
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Polysarcosine-Based Lipids: From Lipopolypeptoid Micelles to Stealth-Like Lipids in Langmuir Blodgett Monolayers.

2016

Amphiphiles and, in particular, PEGylated lipids or alkyl ethers represent an important class of non-ionic surfactants and have become key ingredients for long-circulating (“stealth”) liposomes. While poly-(ethylene glycol) (PEG) can be considered the gold standard for stealth-like materials, it is known to be neither a bio-based nor biodegradable material. In contrast to PEG, polysarcosine (PSar) is based on the endogenous amino acid sarcosine (N-methylated glycine), but has also demonstrated stealth-like properties in vitro, as well as in vivo. In this respect, we report on the synthesis and characterization of polysarcosine based lipids with C14 and C18 hydrocarbon chains and their end g…

polysarcosine; polypeptoids; surfactants; lipids; NCA polymerization; PSarcosinylated lipidsPolymers and PlasticsDispersity02 engineering and technologypolysarcosineDegree of polymerization010402 general chemistry01 natural sciencesMicelleRing-opening polymerizationLangmuir–Blodgett filmArticlesurfactantslipidslcsh:QD241-441PSarcosinylated lipidslcsh:Organic chemistryMonolayerPolymer chemistryOrganic chemistrypolypeptoidsNCA polymerizationChemistryGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesEnd-groupCritical micelle concentrationlipids (amino acids peptides and proteins)0210 nano-technologyPolymers
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CCDC 1874607: Experimental Crystal Structure Determination

2019

Related Article: Olga Schäfer, Dieter Schollmeyer, Alexander Birke, Regina Holm, Kerstin Johann, Christian Muhl, Christine Seidl, Benjamin Weber, Matthias Barz|2019|Tetrahedron Lett.|60|272|doi:10.1016/j.tetlet.2018.12.028

Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates3-methyl-13-oxazolidine-25-dione
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CCDC 1874606: Experimental Crystal Structure Determination

2019

Related Article: Olga Schäfer, Dieter Schollmeyer, Alexander Birke, Regina Holm, Kerstin Johann, Christian Muhl, Christine Seidl, Benjamin Weber, Matthias Barz|2019|Tetrahedron Lett.|60|272|doi:10.1016/j.tetlet.2018.12.028

N-epsilon-t-butyloxycarbonyl-L-lysine N-carboxyanhydrideSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1874603: Experimental Crystal Structure Determination

2019

Related Article: Olga Schäfer, Dieter Schollmeyer, Alexander Birke, Regina Holm, Kerstin Johann, Christian Muhl, Christine Seidl, Benjamin Weber, Matthias Barz|2019|Tetrahedron Lett.|60|272|doi:10.1016/j.tetlet.2018.12.028

Space GroupCrystallographyS-[(25-dioxo-13-oxazolidin-4-yl)methyl] ethanesulfonothioateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1874604: Experimental Crystal Structure Determination

2019

Related Article: Olga Schäfer, Dieter Schollmeyer, Alexander Birke, Regina Holm, Kerstin Johann, Christian Muhl, Christine Seidl, Benjamin Weber, Matthias Barz|2019|Tetrahedron Lett.|60|272|doi:10.1016/j.tetlet.2018.12.028

Space GroupCrystallographyCrystal SystemS-[(25-dioxo-13-oxazolidin-4-yl)methyl] propane-2-sulfonothioateCrystal StructureCell ParametersExperimental 3D Coordinates
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