Your browser doesn't support javascript.
loading
Investigation of Absorption Routes of Meloxicam and Its Salt Form from Intranasal Delivery Systems.
Bartos, Csilla; Ambrus, Rita; Kovács, Anita; Gáspár, Róbert; Sztojkov-Ivanov, Anita; Márki, Árpád; Janáky, Tamás; Tömösi, Ferenc; Kecskeméti, Gábor; Szabó-Révész, Piroska.
Afiliación
  • Bartos C; Institute of Pharmaceutical Technology and Regulatory Affairs, University of Szeged, Eötvös u. 6, H-6720 Szeged, Hungary. bartoscsilla@pharm.u-szeged.hu.
  • Ambrus R; Institute of Pharmaceutical Technology and Regulatory Affairs, University of Szeged, Eötvös u. 6, H-6720 Szeged, Hungary. arita@pharm.u-szeged.hu.
  • Kovács A; Institute of Pharmaceutical Technology and Regulatory Affairs, University of Szeged, Eötvös u. 6, H-6720 Szeged, Hungary. anita.kovacs@pharm.u-szeged.hu.
  • Gáspár R; Department of Pharmacodynamics and Biopharmacy, University of Szeged, Eötvös u. 6, H-6720 Szeged, Hungary. gaspar@pharm.u-szeged.hu.
  • Sztojkov-Ivanov A; Department of Pharmacodynamics and Biopharmacy, University of Szeged, Eötvös u. 6, H-6720 Szeged, Hungary. Anita@gmail.com.
  • Márki Á; Department of Pharmacodynamics and Biopharmacy, University of Szeged, Eötvös u. 6, H-6720 Szeged, Hungary. marki@pharm.u-szeged.hu.
  • Janáky T; Department of Medical Chemistry, University of Szeged, Dóm tér 8, H-6720 Szeged, Hungary. janaky.tamas@med.u-szeged.hu.
  • Tömösi F; Department of Medical Chemistry, University of Szeged, Dóm tér 8, H-6720 Szeged, Hungary. tomosi.ferenc@med.u-szeged.hu.
  • Kecskeméti G; Department of Medical Chemistry, University of Szeged, Dóm tér 8, H-6720 Szeged, Hungary. kecskemeti.gabor@med.u-szeged.hu.
  • Szabó-Révész P; Institute of Pharmaceutical Technology and Regulatory Affairs, University of Szeged, Eötvös u. 6, H-6720 Szeged, Hungary. bartoscsilla@pharm.u-szeged.hu.
Molecules ; 23(4)2018 Mar 28.
Article en En | MEDLINE | ID: mdl-29597330
The aim of this article was to study the trans-epithelial absorption to reach the blood and to target the brain by axonal transport using nasal formulations with nanonized meloxicam (nano MEL spray) and its salt form known as meloxicam potassium monohydrate (MELP spray). The physicochemical properties and the mucoadhesivity of nasal formulations were controlled. In vitro and in vivo studies were carried out. These forms were first investigated in "nose-to-brain" relation. It was found that the in vitro study and in vivo study did not show any significant correlation. In vitro experiments demonstrated faster dissolution rate and higher diffusion of MELP from the spray compared with the nano MEL spray. The administration of the nano MEL spray resulted in faster absorption and constant plasma concentration of the drug after five minutes of administration as compared to MELP. The axonal transport of the drug was justified. MEL appeared in the brain tissues after the first five minutes of administration in the case of both spray forms, but its amount was too small in comparison with the total plasma concentration. The application of the nano MEL spray resulted in the same AUC in the brain as the intravenous injection. The "nose-to-blood" results predicted the nasal applicability of MEL and MELP in pain management. The "nose-to-brain" pathway requires further study.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Tiazinas / Tiazoles / Sistemas de Liberación de Medicamentos / Absorción Nasal Límite: Animals Idioma: En Revista: Molecules Asunto de la revista: BIOLOGIA Año: 2018 Tipo del documento: Article País de afiliación: Hungria Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Tiazinas / Tiazoles / Sistemas de Liberación de Medicamentos / Absorción Nasal Límite: Animals Idioma: En Revista: Molecules Asunto de la revista: BIOLOGIA Año: 2018 Tipo del documento: Article País de afiliación: Hungria Pais de publicación: Suiza