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

[Display omitted] 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...

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Veröffentlicht in:International journal of pharmaceutics 2015-08, Vol.491 (1-2), p.198-207
Hauptverfasser: Bartos, Csilla, Ambrus, Rita, Sipos, Péter, Budai-Szűcs, Mária, Csányi, Erzsébet, Gáspár, Róbert, Márki, Árpád, Seres, Adrienn B., Sztojkov-Ivanov, Anita, Horváth, Tamás, Szabó-Révész, Piroska
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container_issue 1-2
container_start_page 198
container_title International journal of pharmaceutics
container_volume 491
creator Bartos, Csilla
Ambrus, Rita
Sipos, Péter
Budai-Szűcs, Mária
Csányi, Erzsébet
Gáspár, Róbert
Márki, Árpád
Seres, Adrienn B.
Sztojkov-Ivanov, Anita
Horváth, Tamás
Szabó-Révész, Piroska
description [Display omitted] 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.
doi_str_mv 10.1016/j.ijpharm.2015.06.046
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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. 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subjects Adhesiveness
Administration, Intranasal
Animals
Anti-Inflammatory Agents, Non-Steroidal - administration & dosage
Anti-Inflammatory Agents, Non-Steroidal - pharmacokinetics
Area Under Curve
AUC
Chemistry, Pharmaceutical
Combined wet milling
Drug Compounding
Excipients - chemistry
Hyaluronic Acid - administration & dosage
Hyaluronic Acid - chemistry
Intranasal formulation
Male
Meloxicam
Membranes, Artificial
Mucoadhesivity
Nanoparticles
Nasal Mucosa - metabolism
Particle Size
Permeability
Polyvinyl Alcohol
Rats
Rats, Sprague-Dawley
Rheology
Solubility
Thiazines - administration & dosage
Thiazines - pharmacokinetics
Thiazoles - administration & dosage
Thiazoles - pharmacokinetics
title Study of sodium hyaluronate-based intranasal formulations containing micro- or nanosized meloxicam particles
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