AI Article Synopsis

  • Developed a drug delivery system for doxorubicin (DOX) using niosomes made from non-ionic surfactants Brij™ 52, span™ 60, and Solulan™ C24.
  • Used magnetite nanoparticles within the niosomes to enhance DOX loading through a novel remote-loading method.
  • Cytotoxicity tests showed a 22% increase in effectiveness of DOX against A549 cancer cells using this new delivery system.

Article Abstract

The current work deals with developing a suitable drug delivery system of doxorubicin (DOX) for intraperitoneal chemotherapy using niosomes through formulating non-ionic surfactants consisting of Brij™ 52, span™ 60 and Solulan™ C24. Entrapping the magnetite nanoparticles in the hydrophilic parts of niosomes was accompanied with high-efficient DOX loading by the current novel remote-loading method. Cytotoxicity of the prepared formulations was evaluated in vitro against A549 and PC-12 cell lines using the colorimetric WST-1 assay test. The obtained results revealed that, the cytotoxicity of DOX increased up to 22% especially on A549 cells by the current delivery system.

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Source
http://dx.doi.org/10.1080/21691401.2017.1296850DOI Listing

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