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Magnetoelectric nanoparticles for delivery of antitumor peptides into glioblastoma cells by magnetic fields.


ABSTRACT: AIM:We studied externally controlled anticancer effects of binding tumor growth inhibiting synthetic peptides to magnetoelectric nanoparticles (MENs) on treatment of glioblastomas. METHODS:Hydrothermally synthesized 30-nm MENs had the core-shell composition of CoFe2O4@BaTiO3. Molecules of growth hormone-releasing hormone antagonist of the MIA class (MIA690) were chemically bound to MENs. In vitro experiments utilized human glioblastoma cells (U-87MG) and human brain microvascular endothelial cells. RESULTS:The studies demonstrated externally controlled high-efficacy binding of MIA690 to MENs, targeted specificity to glioblastoma cells and on-demand release of the peptide by application of d.c. and a.c. magnetic fields, respectively. CONCLUSION:The results support the use of MENs as an effective drug delivery carrier for growth hormone-releasing hormone antagonists in the treatment of human glioblastomas.

SUBMITTER: Stewart TS 

PROVIDER: S-EPMC5810849 | biostudies-literature | 2018 Feb

REPOSITORIES: biostudies-literature

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Magnetoelectric nanoparticles for delivery of antitumor peptides into glioblastoma cells by magnetic fields.

Stewart Tiffanie S TS   Nagesetti Abhignyan A   Guduru Rakesh R   Liang Ping P   Stimphil Emmanuel E   Hadjikhani Ali A   Salgueiro Luis L   Horstmyer Jeffrey J   Cai Renzhi R   Schally Andrew A   Khizroev Sakhrat S  

Nanomedicine (London, England) 20180118 4


<h4>Aim</h4>We studied externally controlled anticancer effects of binding tumor growth inhibiting synthetic peptides to magnetoelectric nanoparticles (MENs) on treatment of glioblastomas.<h4>Methods</h4>Hydrothermally synthesized 30-nm MENs had the core-shell composition of CoFe<sub>2</sub>O<sub>4</sub>@BaTiO<sub>3</sub>. Molecules of growth hormone-releasing hormone antagonist of the MIA class (MIA690) were chemically bound to MENs. In vitro experiments utilized human glioblastoma cells (U-87M  ...[more]

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