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Olanzapine loaded cationic solid lipid nanoparticles for oral lymphatic delivery

  • At: 2011 FIP Congress in Hyderabad (India)
  • Type: Poster
  • By: JAWAHAR, Natarajan (JSS College of Pharmacy, Ootacamund, India)
  • Co-author(s): Sumeet, Sood (JSS College of pharmacy, Ootacamund, India)
    Meyyanathan, Subramanya nainar (Jss college of pharmacy, Ootacamund, India)
    Gowthamarajan, Kuppusamy (Jss college of pharmacy, Ootacamund, India)
    Suresh, Bhojraj (Jss university, Mysore, India)
  • Abstract:

    Olanzapine, a lipophilic antipsychotic drug, has poor oral bioavailability (~57%) due to first-pass effect. Also the dosing has to be repeated several times a day and wide varieties of side effects are associated with the current dosage forms of the drug. In this work, Solid Lipid Nanoparticles (SLNs) of Olanzapine were developed using lipids

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Last update 4 October 2019

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