Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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Materials Map under construction

The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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Stenzel, Martina

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (11/11 displayed)

  • 2016Polymer functional nanodiamonds by light-induced ligation20citations
  • 2009Formation efficiency of ABA blockcopolymers via enhanced spin capturing polymerization (ESCP): Locating the alkoxyamine function37citations
  • 2008Grafting thermoresponsive polymers onto honeycomb structured porous films using the RAFT process62citations
  • 2008Graft block copolymers of propargyl methacrylate and vinyl acetate via a combination of RAFT/MADIX and click chemistry: Reaction analysis110citations
  • 2007The Use of Novel F-RAFT Agents in High Temperature and High Pressure Ethene Polymerization: Can Control be Achieved?26citations
  • 2007Verification of Controlled Grafting of Styrene from Cellulose via Radiation-Induced RAFT Polymerization178citations
  • 2007Honeycomb structured porous films from amphiphilic block copolymers prepared via RAFT polymerization119citations
  • 2007Shell-cross-linked micelles containing cationic polymers synthesized via the RAFT process: toward a more biocompatible gene delivery system107citations
  • 2006Gold-loaded organic/inorganic nanocomposite honeycomb membranes26citations
  • 2006Effect of an added base on (4-cyanopentanoic acid)-4-dithiobenzoate mediated RAFT polymerization in water73citations
  • 2006Water-assisted formation of honeycomb structured porous films58citations

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Chart of shared publication
Trouillet, Vanessa
1 / 29 shared
Wuest, Kilian
1 / 2 shared
Junkers, Thomas
1 / 10 shared
Wong, Edgar
1 / 1 shared
Min, Eunhee
1 / 1 shared
Muller, Axel
1 / 2 shared
Hernandez-Guerrero, Maribel
2 / 2 shared
Bissett, Carla
1 / 1 shared
Hellaye, Maude Le
1 / 1 shared
Quemener, Damien
1 / 11 shared
Davis, Thomas
8 / 9 shared
Busch, Markus
1 / 2 shared
Roth, Marion
1 / 5 shared
Olgun, Olgun
1 / 1 shared
Barsbay, Murat
1 / 1 shared
Wong, Kok Hou
3 / 3 shared
Bernard, Julien
1 / 14 shared
Nguyen, T.
1 / 10 shared
Zhang, Ling
1 / 3 shared
Albertin, Luca
1 / 1 shared
Granville, Anthony
1 / 1 shared
Chart of publication period
2016
2009
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2007
2006

Co-Authors (by relevance)

  • Trouillet, Vanessa
  • Wuest, Kilian
  • Junkers, Thomas
  • Wong, Edgar
  • Min, Eunhee
  • Muller, Axel
  • Hernandez-Guerrero, Maribel
  • Bissett, Carla
  • Hellaye, Maude Le
  • Quemener, Damien
  • Davis, Thomas
  • Busch, Markus
  • Roth, Marion
  • Olgun, Olgun
  • Barsbay, Murat
  • Wong, Kok Hou
  • Bernard, Julien
  • Nguyen, T.
  • Zhang, Ling
  • Albertin, Luca
  • Granville, Anthony
OrganizationsLocationPeople

article

Shell-cross-linked micelles containing cationic polymers synthesized via the RAFT process: toward a more biocompatible gene delivery system

  • Bernard, Julien
  • Stenzel, Martina
  • Nguyen, T.
  • Zhang, Ling
  • Davis, Thomas
Abstract

Block copolymers poly(2-(dimethylamino) ethyl methacrylate)-b-poly(polyethylene glycol methacrylate) (PD-MAEMA-b-P(PEGMA)) were prepared via reversible addition fragmentation chain transfer polymerization (RAFT). The polymerization was found to proceed with the expected living behavior resulting in block copolymers with varying block sizes of low polydispersity (PDI < 1.3). The resulting block copolymer was self-assembled in an aqueous environment, leading to the formation of pH-responsive micelles. Further stabilization of the micellar system was performed in water using ethylene glycol dimethacrylate and the RAFT process to cross-link the shell. The cross-linked micelle was found to have properties significantly different from those of the uncross-linked block copolymer micelle. While a distinct critical micelle concentration (CMC) was observed using block copolymers, the CMC was absent in the cross-linked system. In addition, a better stability against disintegration was observed when altering the ionic strength such as the absence of changes of the hydrodynamic diameter with increasing NaCI concentration. Both cross-linked and uncross-linked micelles displayed good binding ability for genes. However, the cross-linked system exhibited a slightly superior tendency to bind oligonucleotides. Cytotoxicity tests confirmed a significant improvement of the biocompatibility of the synthesized cross-linked micelle compared to that of the highly toxic PDMAEMA. The cross-linked micelles were taken up by cells without causing any signs of cell damage, while the PDMAEMA homopolymer clearly led to cell death. © 2007 American Chemical Society.

Topics
  • strength
  • copolymer
  • homopolymer
  • block copolymer
  • polydispersity
  • biocompatibility