Materials Map

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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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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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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (2/2 displayed)

  • 2021Carbon fiber reinforced polymers for implantable medical devices74citations
  • 2012Glucose-functionalized, serum-stable polymeric micelles from the combination of anionic and RAFT polymerizations62citations

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Trani, Nicola Di
1 / 1 shared
Liu, Hsuan Chen
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Grattoni, Alessandro
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Cicalo, Roberto
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Chua, Corrine Ying Xuan
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Nucci, Maria Concetta
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Ferrari, Mauro
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Lolli, Graziano
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Hernandez, Nathanael
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Ho, Jeremy
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Susnjar, Antonia
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Rhudy, Jessica
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Scorrano, Giovanni
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Yin, Ligeng
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Dalsin, Molly C.
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Reineke, Theresa M.
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2021
2012

Co-Authors (by relevance)

  • Trani, Nicola Di
  • Liu, Hsuan Chen
  • Grattoni, Alessandro
  • Cicalo, Roberto
  • Chua, Corrine Ying Xuan
  • Nucci, Maria Concetta
  • Ferrari, Mauro
  • Lolli, Graziano
  • Hernandez, Nathanael
  • Ho, Jeremy
  • Susnjar, Antonia
  • Rhudy, Jessica
  • Scorrano, Giovanni
  • Yin, Ligeng
  • Dalsin, Molly C.
  • Reineke, Theresa M.
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article

Glucose-functionalized, serum-stable polymeric micelles from the combination of anionic and RAFT polymerizations

  • Yin, Ligeng
  • Sizovs, Antons
  • Dalsin, Molly C.
  • Reineke, Theresa M.
Abstract

<p>Poly(ethylene-alt-propylene)-poly[(N,N-dimethylacrylamide) -grad-(2-methacrylamido glucopyranose)] (PEP-poly(DMA-grad-MAG), or PG) diblock terpolymers were synthesized by combining anionic and reversible addition-fragmentation chain transfer (RAFT) polymerizations. An ω-trithiocarbonate-functionalized PEP homopolymer served as the macromolecular chain transfer agent (macroCTA), and RAFT copolymerizations of DMA and a trimethylsilyl-protected MAG (TMS-MAG) monomer gave a family of PG diblock terpolymers after hydrolysis. The terpolymers had similar degrees of polymerization, and the MAG content ranged from 3.5 to 39 mol % in the hydrophilic block. At 70°C, the reactivity ratios of DMA (1) and TMS-MAG (2) were determined to be r <sub>1</sub> = 1.86 ± 0.07 and r <sub>2</sub> = 0.16 ± 0.01, and thus the poly(meth)acrylamide blocks in the PG diblock terpolymers were likely to be gradient copolymers. Micellar dispersions from PG diblock polymers in water were examined by cryogenic transmission electron microscopy (cryo-TEM) and dynamic light scattering (DLS). Spherical micelles with core radii of ca. 7 nm and overall hydrodynamic radii of ca. 15 nm were the predominant morphologies observed in all samples prepared by sequential nanoprecipitation and dialysis. The electron-dense MAG moieties greatly increased the native contrast of the micellar coronae, which were clearly viewed as gray halos around the micellar cores in samples with relatively large MAG content. The stability of the glucose-installed micelles was tested in four biologically relevant media, from simple phosphate-buffered saline (PBS) to fetal bovine serum (FBS), using a combination of DLS and cryo-TEM measurements. Micellar dispersions from a PG diblock terpolymer with 16 mol % of MAG of the hydrophilic block were stable in 100% FBS over at least 14 h, suggesting their minimal interactions with serum proteins. Control experiments suggested that micelles composed of PDMA alone in the corona had similar serum stabilities. These sugar-functionalized micelles hold promise as in vivo drug delivery vehicles to possibly prolong circulation time after intravenous administration.</p>

Topics
  • dispersion
  • experiment
  • transmission electron microscopy
  • copolymer
  • homopolymer
  • dynamic light scattering
  • gradient copolymer
  • dialysis