Literature DB >> 26142244

Study of sodium hyaluronate-based intranasal formulations containing micro- or nanosized meloxicam particles.

Csilla Bartos1, Rita Ambrus2, Péter Sipos2, Mária Budai-Szűcs2, Erzsébet Csányi2, Róbert Gáspár3, Árpád Márki3, Adrienn B Seres3, Anita Sztojkov-Ivanov3, Tamás Horváth2, Piroska Szabó-Révész4.   

Abstract

This article reports on the micro- and nanonization of meloxicam (MEL) with the aim of developing pre-dispersions as intermediates for the design of intranasal formulations. As a new approach, combined wet milling technology was developed in order to reduce the particle size of the MEL. Different milling times resulted in micro- or nanosized MEL in the pre-dispersions with polyvinyl alcohol as stabilizer agent, which were directly used for preparing intranasal liquid formulations with the addition of sodium hyaluronate as mucoadhesive agent. Reduction of the MEL particle size into the nano range led to increased saturation solubility and dissolution velocities, and increased adhesiveness to surfaces as compared with microsized MEL particles. A linear correlation was demonstrated between the specific surface area of MEL and the AUC. The in vitro and in vivo studies indicated that the longer residence time and the uniform distribution of nano MEL spray throughout an artificial membrane and the nasal mucosa resulted in better diffusion and a higher AUC. Nanosized MEL may be suggested for the development of an innovative dosage form with a different dose of the drug, as a possible administration route for pain management.
Copyright © 2015 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  AUC; Combined wet milling; Intranasal formulation; Meloxicam; Mucoadhesivity; Permeability

Mesh:

Substances:

Year:  2015        PMID: 26142244     DOI: 10.1016/j.ijpharm.2015.06.046

Source DB:  PubMed          Journal:  Int J Pharm        ISSN: 0378-5173            Impact factor:   5.875


  11 in total

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4.  Investigation of Absorption Routes of Meloxicam and Its Salt Form from Intranasal Delivery Systems.

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9.  Comparison of Modern In Vitro Permeability Methods with the Aim of Investigation Nasal Dosage Forms.

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10.  Structure and Fate of Nanoparticles Designed for the Nasal Delivery of Poorly Soluble Drugs.

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