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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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (2/2 displayed)

  • 2020Extracellular matrix decorated polycaprolactone scaffolds for improved mesenchymal stem/stromal cell osteogenesis towards a patient‐tailored bone tissue engineering approach60citations
  • 2016Dissolution enhancement of active pharmaceutical ingredients by therapeutic deep eutectic systems214citations

Places of action

Chart of shared publication
Moura, Carla S.
1 / 1 shared
Ferreira, Frederico Castelo
1 / 4 shared
Udangawa, Ranodhi N.
1 / 1 shared
Linhardt, Robert J.
1 / 2 shared
Carvalho, Marta S.
1 / 5 shared
Vashishth, Deepak
1 / 1 shared
Silva, Cláudia L. Da
1 / 1 shared
Cabral, Joaquim M. S.
1 / 4 shared
Barreiros, Susana
1 / 15 shared
Barreiros, S.
1 / 9 shared
Andrade, Maria Madalena Dionísio
1 / 31 shared
Paiva, A.
1 / 17 shared
Silva, J. C.
1 / 3 shared
Reis, Rui L.
1 / 189 shared
De Sá-Nogueira, Isabel
1 / 4 shared
Duarte, A. R. C.
1 / 56 shared
Paiva, Alexandre
1 / 45 shared
Mano, Francisca
1 / 7 shared
Dionisio, M.
1 / 7 shared
Ferreira, Ana
1 / 3 shared
Duarte, Ana Rita C.
1 / 69 shared
Sa-Nogueira, I.
1 / 2 shared
Reis, Rui Luís
1 / 1359 shared
Aroso, I. M.
1 / 12 shared
Aroso, Ivo M.
1 / 7 shared
Mano, F.
1 / 4 shared
Ferreira, A. S. D.
1 / 2 shared
Chart of publication period
2020
2016

Co-Authors (by relevance)

  • Moura, Carla S.
  • Ferreira, Frederico Castelo
  • Udangawa, Ranodhi N.
  • Linhardt, Robert J.
  • Carvalho, Marta S.
  • Vashishth, Deepak
  • Silva, Cláudia L. Da
  • Cabral, Joaquim M. S.
  • Barreiros, Susana
  • Barreiros, S.
  • Andrade, Maria Madalena Dionísio
  • Paiva, A.
  • Silva, J. C.
  • Reis, Rui L.
  • De Sá-Nogueira, Isabel
  • Duarte, A. R. C.
  • Paiva, Alexandre
  • Mano, Francisca
  • Dionisio, M.
  • Ferreira, Ana
  • Duarte, Ana Rita C.
  • Sa-Nogueira, I.
  • Reis, Rui Luís
  • Aroso, I. M.
  • Aroso, Ivo M.
  • Mano, F.
  • Ferreira, A. S. D.
OrganizationsLocationPeople

article

Dissolution enhancement of active pharmaceutical ingredients by therapeutic deep eutectic systems

  • Barreiros, Susana
  • Barreiros, S.
  • Andrade, Maria Madalena Dionísio
  • Paiva, A.
  • Silva, J. C.
  • Reis, Rui L.
  • De Sá-Nogueira, Isabel
  • Duarte, A. R. C.
  • Paiva, Alexandre
  • Mano, Francisca
  • Dionisio, M.
  • Ferreira, Ana
  • Duarte, Ana Rita C.
  • Sa-Nogueira, I.
  • Reis, Rui Luís
  • Aroso, I. M.
  • Aroso, Ivo M.
  • Silva, João C.
  • Mano, F.
  • Ferreira, A. S. D.
Abstract

<p>A therapeutic deep eutectic system (THEDES) is here defined as a deep eutectic solvent (DES) having an active pharmaceutical ingredient (API) as one of the components. In this work, THEDESs are proposed as enhanced transporters and delivery vehicles for bioactive molecules. THEDESs based on choline chloride (ChCl) or menthol conjugated with three different APIs, namely acetylsalicylic acid (AA), benzoic acid (BA) and phenylacetic acid (PA), were synthesized and characterized for thermal behaviour, structural features, dissolution rate and antibacterial activity. Differential scanning calorimetry and polarized optical microscopy showed that ChCl:PA (1:1), ChCl:AA (1:1), menthol:AA (3:1), menthol:BA (3:1), menthol:PA (2:1) and menthol:PA (3:1) were liquid at room temperature. Dissolution studies in PBS led to increased dissolution rates for the APIs when in the form of THEDES, compared to the API alone. The increase in dissolution rate was particularly noticeable for menthol-based THEDES. Antibacterial activity was assessed using both Gram-positive and Gram-negative model organisms. The results show that all the THEDESs retain the antibacterial activity of the API. Overall, our results highlight the great potential of THEDES as dissolution enhancers in the development of novel and more effective drug delivery systems.</p>

Topics
  • impedance spectroscopy
  • differential scanning calorimetry
  • optical microscopy