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A potential non-invasive glioblastoma treatment: Nose-to-brain delivery of farnesylthiosalicylic acid incorporated hybrid nanoparticles.

Abstract
New drug delivery systems are highly needed in research and clinical area to effectively treat gliomas by reaching a high antineoplastic drug concentration at the target site without damaging healthy tissues. Intranasal (IN) administration, an alternative route for non-invasive drug delivery to the brain, bypasses the blood-brain-barrier (BBB) and eliminates systemic side effects. This study evaluated the antitumor efficacy of farnesylthiosalicylic acid (FTA) loaded (lipid-cationic) lipid-PEG-PLGA hybrid nanoparticles (HNPs) after IN application in rats. FTA loaded HNPs were prepared, characterized and evaluated for cytotoxicity. Rat glioma 2 (RG2) cells were implanted unilaterally into the right striatum of female Wistar rats. 10days later, glioma bearing rats received either no treatment, or 5 repeated doses of 500μM freshly prepared FTA loaded HNPs via IN or intravenous (IV) application. Pre-treatment and post-treatment tumor sizes were determined with MRI. After a treatment period of 5days, IN applied FTA loaded HNPs achieved a significant decrease of 55.7% in tumor area, equal to IV applied FTA loaded HNPs. Herewith, we showed the potential utility of IN application of FTA loaded HNPs as a non-invasive approach in glioblastoma treatment.
AuthorsEmine Sekerdag, Sevda Lüle, Sibel Bozdağ Pehlivan, Naile Öztürk, Aslı Kara, Abbas Kaffashi, Imran Vural, Ilkay Işıkay, Burҫin Yavuz, Kader Karlı Oguz, Figen Söylemezoğlu, Yasemin Gürsoy-Özdemir, Melike Mut
JournalJournal of controlled release : official journal of the Controlled Release Society (J Control Release) Vol. 261 Pg. 187-198 (09 10 2017) ISSN: 1873-4995 [Electronic] Netherlands
PMID28684169 (Publication Type: Journal Article)
CopyrightCopyright © 2017 Elsevier B.V. All rights reserved.
Chemical References
  • Antineoplastic Agents
  • Drug Carriers
  • Lipids
  • Polyesters
  • Salicylates
  • farnesylthiosalicylic acid
  • polyethylene glycol-poly(lactide-co-glycolide)
  • Polyethylene Glycols
  • Farnesol
Topics
  • Administration, Intranasal
  • Animals
  • Antineoplastic Agents (administration & dosage, pharmacology)
  • Blood-Brain Barrier (metabolism)
  • Brain Neoplasms (diagnostic imaging, drug therapy)
  • Drug Carriers (chemistry)
  • Drug Delivery Systems
  • Farnesol (administration & dosage, analogs & derivatives, pharmacology)
  • Female
  • Glioblastoma (diagnostic imaging, drug therapy)
  • Lipids (chemistry)
  • Magnetic Resonance Imaging
  • Nanoparticles
  • Polyesters (chemistry)
  • Polyethylene Glycols (chemistry)
  • Rats
  • Rats, Wistar
  • Salicylates (administration & dosage, pharmacology)
  • Treatment Outcome

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