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)

  • 2023Preparation and investigation of a novel combination of Solanum nigrum-loaded, arabinoxylan-cross-linked β-cyclodextrin nanosponges for the treatment of cancer: in vitro, in vivo, and in silico evaluation4citations
  • 2023Laser Enhanced Combinatorial Chemo-photothermal Therapy of Green Synthesis Gold Nanoparticles Loaded with 6Mercaptopurine on Breast Cancer Model18citations

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Awan, Sajjad
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Al-Ghorbani, Mohammed
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Jawad, Zobia
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Alharbi, Osama
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Zaib, Sumera
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Khan, Imtiaz
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Shah, Hamid Saeed
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Thabet, Nadia A.
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Badr, Yehia A.
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2023

Co-Authors (by relevance)

  • Awan, Sajjad
  • Al-Ghorbani, Mohammed
  • Jawad, Zobia
  • Alharbi, Osama
  • Zaib, Sumera
  • Khan, Imtiaz
  • Shah, Hamid Saeed
  • Thabet, Nadia A.
  • Badr, Yehia A.
  • Faid, Amna H.
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article

Preparation and investigation of a novel combination of Solanum nigrum-loaded, arabinoxylan-cross-linked β-cyclodextrin nanosponges for the treatment of cancer: in vitro, in vivo, and in silico evaluation

  • Awan, Sajjad
  • Al-Ghorbani, Mohammed
  • Jawad, Zobia
  • Sliem, Mahmoud A.
  • Alharbi, Osama
  • Zaib, Sumera
  • Khan, Imtiaz
  • Shah, Hamid Saeed
Abstract

<jats:p><jats:bold>Introduction:</jats:bold> Cancer contributes to a high mortality rate worldwide spanning its diversity from genetics to resistant therapeutic response. To date emerging strategies to combat and manage cancer are particularly focused on the development of targeted therapies as conventional treatments account for the destruction of normal cells as well. In this regard, medicinal plant-based therapies are quite promising in imposing minimal side effects; however, limitations like poor bioavailability and stability of bioactive phytochemicals are associated with them. In parallel, nanotechnology provides nominal solution to deliver particular therapeutic agent without compromising its stability.</jats:p><jats:p><jats:bold>Methods:</jats:bold> In this study, <jats:italic>Solanum nigrum</jats:italic>, an effective medicinal plant, loaded arabinoxylan cross-linked β-cyclodextrin nanosponges (SN-AXCDNS) were designed to evaluate antitumor activity against breast cancer. Therefore, SN-AXCDNS were prepared by using cross-linker melt method and characterized by physicochemical and pharmacological parameters.</jats:p><jats:p><jats:bold>Results:</jats:bold> Hydrodynamic size, zeta potential and entrapment efficiency (EE%) were estimated as 226 ± 4 nm, −29.15 ± 5.71 mV and 93%, respectively. Surface morphology of nanocomposites showed spherical, smooth, and porous form. Antitumor pharmacological characterization showed that SN loaded nanosponge demonstrated higher cytotoxicity (22.67 ± 6.11 μg/mL), by inducing DNA damage as compared to void SN extract. Flow cytometry analysis reported that encapsulated extract promoted cell cycle arrest at sub-G1 (9.51%). Moreover, <jats:italic>in vivo</jats:italic> analysis demonstrates the reduction in tumor weight and 85% survival chances in nanosponge treated mice featuring its effectiveness. In addition, <jats:italic>in silico</jats:italic> analysis revealed that β-cyclodextrin potentially inhibits MELK in breast cancer cell lines (B.E = −10.1 Kcal/mol).</jats:p><jats:p><jats:bold>Conclusion:</jats:bold> Therefore, findings of current study elucidated the therapeutic potential of β-cyclodextrin based nanosponges to be an alternative approach regarding the delivery and solubilization of antitumor drugs.</jats:p>

Topics
  • porous
  • nanocomposite
  • surface
  • melt
  • void