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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Materials Map under construction

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)

  • 2022Mass Spectrometry, Structural Analysis, and Anti-Inflammatory Properties of Photo-Cross-Linked Human Albumin Hydrogels.12citations
  • 2021Folic acid-hydrophilic polymer coated mesoporous silica nanoparticles target doxorubicin delivery.18citations
  • 2021Interaction of folate - Linked silica nanoparticles with HeLa cells: Analysis and investigation the effect of polymer length.citations
  • 2016Colloidal stability of gold nanorod solution upon exposure to excised human skin: Effect of surface chemistry and protein adsorption.34citations

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Sharifi, Shahriar
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Dararatana, N.
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Moore, A.
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Em, Lisabeth
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Co-Authors (by relevance)

  • Sharifi, Shahriar
  • Harkins, Shannon
  • Gharibi, Hassan
  • Vegvari, Akos
  • Saei, Amir Ata
  • Dararatana, N.
  • Moore, A.
  • Em, Lisabeth
  • Dahabiyeh, Lina
  • Al-Nadaf, Afaf
  • Jawarneh, S.
  • Nn, Mahmoud
  • Khattabi, Areen
  • Al-Bakri, Amal G.
  • Khalil, Enam
  • Km, Al-Qaoud
  • Am, Alkilany
OrganizationsLocationPeople

article

Folic acid-hydrophilic polymer coated mesoporous silica nanoparticles target doxorubicin delivery.

  • Dahabiyeh, Lina
  • Mahmoud, Nouf
  • Al-Nadaf, Afaf
  • Jawarneh, S.
  • Nn, Mahmoud
Abstract

Mesoporous silica nanoparticles (MSNs) gained significant attention, particularly in the pharmaceutical field. Folic acid (FA) shows marked promise as a targeting agent for its specific interaction with the folate receptor. This receptor is over-expressed on the cell surface of several cancerous cells like breast cancer. Polyethylene glycol (PE), as well as polypropylene glycol (PEG), is used to decorate nanoparticles to improve their biodistribution. Moreover, carboxymethyl beta-cyclodextrin (CM-β-CD), is used as a complexation molecule. In this study, we described the chemical synthesis, in vitro drug release and antiproliferative activity of doxorubicin-loaded/decorated MSNs further coupled with FA in two conditions: chemically bound or as a complex with CM-β-CD. Fourier Transform Infrared Spectroscopy with Transmission Electron Microscopy confirmed the successful surface change. Dynamic Light Scattering confirmed the change in surface characters like zeta potential, polydispersity index (PI), and size. PI improved from 0.58 to 0.23 while the size enlarged from 200 to 348 and 532 nm. Functionalized nanoparticles demonstrated more significant drug entrapment with (97%) while undecorated MSNs only showed (63%). Accordingly, we effectively synthesized FA-PEG2000-MSNs with IC<sub>50</sub>: 0.015 mg/mL targeting HeLa cells. This approach may allow potential applications as a drug delivery system in cancer chemotherapy.HighlightsMesoporous silica nanoparticles (MSNs) with a carboxylic acid or amine surface group can be successfully decorated with long-chain hydrophilic polymer via an amide bond.Carboxymethyl-β-cyclodextrin coupled with long-chain polymer as host to form a complex with targeting molecule folic acid.Folic acid can be anchored directly to a polymer coat.TEM; DLS and FTIR confirmed the surface modification.The drug encapsulation efficiency; cytotoxicity and selectivity of functionalized nanoparticles with PEG and conjugated with FA were the best.Chemical modification has improved cytotoxicity of doxorubicin and selectivity against Hela cells.

Topics
  • nanoparticle
  • impedance spectroscopy
  • surface
  • polymer
  • transmission electron microscopy
  • amine
  • Fourier transform infrared spectroscopy
  • polydispersity
  • dynamic light scattering
  • ion chromatography
  • carboxylic acid