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 (4/4 displayed)

  • 2024Covalent Grafting of Functionalized MEW Fibers to Silk Fibroin Hydrogels to Obtain Reinforced Tissue Engineered Constructs8citations
  • 2021Lyophilization stabilizes clinical-stage core-crosslinked polymeric micelles to overcome cold chain supply challenges23citations
  • 2016A Kinetic Degradation Study of Curcumin in Its Free Form and Loaded in Polymeric Micelles83citations
  • 2014Covalent attachment of a three-dimensionally printed thermoplast to a gelatin hydrogel for mechanically enhanced cartilage constructs130citations

Places of action

Chart of shared publication
Ainsworth, Madison J.
1 / 2 shared
Rijen, Mattie Van
1 / 2 shared
Mihajlovic, Marko
1 / 2 shared
Ruijter, Mylène De
1 / 4 shared
Malda, Jos
2 / 39 shared
Viola, Martina
1 / 2 shared
Cedillo-Servin, Gerardo
1 / 5 shared
Castilho, Miguel
1 / 19 shared
Vermonden, Tina
2 / 14 shared
Shi, Yang
1 / 4 shared
Buhl, Eva Miriam
1 / 2 shared
Ojha, Tarun
1 / 2 shared
Hu, Qizhi
1 / 3 shared
Storm, Gert
1 / 5 shared
Rijcken, Cristianne J. F.
1 / 2 shared
Königs-Werner, Hiltrud
1 / 2 shared
Geijn, Michiel Van
1 / 1 shared
Hennink, Wim E.
3 / 18 shared
Bansal, Ruchi
1 / 3 shared
Bagheri, Mahsa
1 / 7 shared
Colombo, Claudio
1 / 2 shared
Wit, Jan
1 / 2 shared
Naksuriya, Ornchuma
1 / 2 shared
Okonogi, Siriporn
1 / 2 shared
Sastre Toraño, Javier
1 / 2 shared
Visser, Jetze
1 / 5 shared
Rahimian, Sima
1 / 2 shared
Dhert, Wouter J. A.
1 / 6 shared
Seyednejad, Hajar
1 / 2 shared
Gawlitta, Debby
1 / 3 shared
Boere, Kristel W. M.
1 / 2 shared
Chart of publication period
2024
2021
2016
2014

Co-Authors (by relevance)

  • Ainsworth, Madison J.
  • Rijen, Mattie Van
  • Mihajlovic, Marko
  • Ruijter, Mylène De
  • Malda, Jos
  • Viola, Martina
  • Cedillo-Servin, Gerardo
  • Castilho, Miguel
  • Vermonden, Tina
  • Shi, Yang
  • Buhl, Eva Miriam
  • Ojha, Tarun
  • Hu, Qizhi
  • Storm, Gert
  • Rijcken, Cristianne J. F.
  • Königs-Werner, Hiltrud
  • Geijn, Michiel Van
  • Hennink, Wim E.
  • Bansal, Ruchi
  • Bagheri, Mahsa
  • Colombo, Claudio
  • Wit, Jan
  • Naksuriya, Ornchuma
  • Okonogi, Siriporn
  • Sastre Toraño, Javier
  • Visser, Jetze
  • Rahimian, Sima
  • Dhert, Wouter J. A.
  • Seyednejad, Hajar
  • Gawlitta, Debby
  • Boere, Kristel W. M.
OrganizationsLocationPeople

article

Lyophilization stabilizes clinical-stage core-crosslinked polymeric micelles to overcome cold chain supply challenges

  • Shi, Yang
  • Buhl, Eva Miriam
  • Ojha, Tarun
  • Hu, Qizhi
  • Storm, Gert
  • Rijcken, Cristianne J. F.
  • Königs-Werner, Hiltrud
  • Steenbergen, Mies J. Van
  • Geijn, Michiel Van
  • Hennink, Wim E.
  • Bansal, Ruchi
  • Bagheri, Mahsa
  • Colombo, Claudio
  • Wit, Jan
Abstract

<p>Background: CriPec technology enables the generation of drug-entrapped biodegradable core-crosslinked polymeric micelles (CCPM) with high drug loading capacity, tailorable size, and drug release kinetics. Docetaxel (DTX)-entrapped CCPM, also referred to as CPC634, have demonstrated favorable pharmacokinetics, tolerability, and enhanced tumor uptake in patients. Clinical efficacy evaluation is ongoing. CPC634 is currently stored (shelf life &gt; 5 years) and shipped as a frozen aqueous dispersion at temperatures below −60°C, in order to prevent premature release of DTX and hydrolysis of the core-crosslinks. Consequently, like other aqueous nanomedicine formulations, CPC634 relies on cold chain supply, which is unfavorable for commercialization. Lyophilization can help to bypass this issue. Methods and results: Freeze-drying methodology for CCPM was developed by employing CPC634 as a model formulation, and sucrose and trehalose as cryoprotectants. We studied the residual moisture content and reconstitution behavior of the CPC634 freeze-dried cake, as well as the size, polydispersity index, morphology, drug retention, and release kinetics of reconstituted CPC634. Subsequently, the freeze-drying methodology was validated in an industrial setting, yielding a CPC634 freeze-dried cake with a moisture content of less than 0.1 wt%. It was found that trehalose-cryoprotected CPC634 could be rapidly reconstituted in less than 5 min at room temperature. Critical quality attributes such as size, morphology, drug retention, and release kinetics of trehalose-cryoprotected freeze-dried CPC634 upon reconstitution were identical to those of non-freeze-dried CPC634. Conclusion: Our findings provide proof-of-concept for the lyophilization of drug-containing CCPM and our methodology is readily translatable to large-scale manufacturing for future commercialization.</p>

Topics
  • impedance spectroscopy
  • morphology
  • dispersion
  • laser emission spectroscopy
  • drying
  • polydispersity