Enhanced Nasal Delivery of Luteinizing Hormone Releasing Hormone Agonist Buserelin by Oleic Acid Solubilized and Stabilized in Hydroxy propyl-β-cyclodextrin

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Abstract

The potential use of three 2-hydroxypropyl ether derivatives of cyclodextrins (HP-α-, HP-β-and HP-y-CyDs) as biocompatible solubilizers and stabilizers for oleic acid, a lipophilic absorption enhancer, was assessed in the nasal absorption of buserelin, an agonist of luteinizing hormone-releasing hormone, in rats. HP-CyDs increased the aqueous solubility of oleic acid and protected it against oxidation through the formation of inclusion complexes with the efficacy increasing in the order: HP-y-CyD«HP-α-CyD

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Abe, K., Irie, T., & Uekama, K. (1995). Enhanced Nasal Delivery of Luteinizing Hormone Releasing Hormone Agonist Buserelin by Oleic Acid Solubilized and Stabilized in Hydroxy propyl-β-cyclodextrin. Chemical and Pharmaceutical Bulletin, 43(12), 2232–2237. https://doi.org/10.1248/cpb.43.2232

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