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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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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Vuoriluoto, Maija

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VTT Technical Research Centre of Finland

in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (7/7 displayed)

  • 2022Optical properties of an organic-inorganic hybrid film made of regenerated cellulose doped with light-scattering TiO2 particles21citations
  • 2021Manufacture of all-wood sawdust-based particle board using ionic liquid-facilitated fusion process18citations
  • 2017Engineering Nanocellulose Biointerfaces Toward Bioactivity and Strengthcitations
  • 2017Engineering Nanocellulose Biointerfaces Toward Bioactivity and Strength ; Nanoselluloosabiorajapintojen ominaisuuksien muokkaus33citations
  • 2016Control of Protein Affinity of Bioactive Nanocellulose and Passivation Using Engineered Block and Random Copolymers22citations
  • 2016Cellulose nanofibril film as a piezoelectric sensor material278citations
  • 2015Effect of molecular architecture of PDMAEMA-POEGMA random and block copolymers on their adsorption on regenerated and anionic nanocelluloses and evidence of interfacial water expulsion33citations

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Chart of shared publication
Orelma, Hannes
4 / 15 shared
Hokkanen, Ari
1 / 13 shared
Harlin, Ali
1 / 47 shared
Mäkelä, Tapio
1 / 21 shared
Tanaka, Atsushi
1 / 12 shared
Korpela, Antti
1 / 5 shared
Khakalo, Alexey
1 / 14 shared
Zhu, Baolei
2 / 7 shared
Johansson, Leena Sisko
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Rojas, Orlando J.
3 / 51 shared
Tuukkanen, Sampo
1 / 22 shared
Mettänen, Marja
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Pammo, Arno
1 / 2 shared
Sarlin, Essi Linnea
1 / 51 shared
Siponkoski, Tuomo
1 / 1 shared
Rajala, Satu
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Juuti, Jari
1 / 9 shared
Franssila, Sami
1 / 16 shared
Laine, Janne
1 / 11 shared
Poutanen, Mikko
1 / 3 shared
Walther, Andreas
1 / 24 shared
Johansson, Leena-Sisko
1 / 7 shared
Chart of publication period
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Co-Authors (by relevance)

  • Orelma, Hannes
  • Hokkanen, Ari
  • Harlin, Ali
  • Mäkelä, Tapio
  • Tanaka, Atsushi
  • Korpela, Antti
  • Khakalo, Alexey
  • Zhu, Baolei
  • Johansson, Leena Sisko
  • Rojas, Orlando J.
  • Tuukkanen, Sampo
  • Mettänen, Marja
  • Pammo, Arno
  • Sarlin, Essi Linnea
  • Siponkoski, Tuomo
  • Rajala, Satu
  • Juuti, Jari
  • Franssila, Sami
  • Laine, Janne
  • Poutanen, Mikko
  • Walther, Andreas
  • Johansson, Leena-Sisko
OrganizationsLocationPeople

article

Control of Protein Affinity of Bioactive Nanocellulose and Passivation Using Engineered Block and Random Copolymers

  • Orelma, Hannes
  • Vuoriluoto, Maija
  • Zhu, Baolei
  • Johansson, Leena Sisko
  • Rojas, Orlando J.
Abstract

We passivated TEMPO-oxidized cellulose nanofibrils(TOCNF) toward human immunoglobulin G (hIgG) bymodification with block and random copolymers ofpoly(2-(dimethylamino)ethyl methacrylate) (PDMAEMA) andpoly(oligo(ethylene glycol) methyl ether methacrylate)(POEGMA). The block copolymers reversibly adsorbed onTOCNF and were highly effective in preventing nonspecificinteractions with hIgG, especially if short PDMAEMAblocks were used. In such cases, total protein rejectionwas achieved. This is in contrast to typical blockingagents, which performed poorly. When an anti-human IgGbiointerface was installed onto the passivated TOCNF,remarkably high affinity antibody-antigen interactionswere observed (0.90 ± 0.09 mg/m2). This is in contrast tothe nonpassivated biointerface, which resulted in asignificant false response. In addition, regeneration ofthe biointerface was possible by low pH aqueous wash.Protein A from Staphylococcus aureus was also utilized tosuccessfully increase the sensitivity for human IgGrecognition (1.28 ± 0.11 mg/m2). Overall, the developedsystem based on TOCNF modified with multifunctionalpolymers can be easily deployed as bioactive materialwith minimum fouling and excellent selectivity.

Topics
  • impedance spectroscopy
  • random
  • cellulose
  • copolymer
  • block copolymer
  • random copolymer