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Optimization of a combined wet milling process in order to produce poly(vinyl alcohol) stabilized nanosuspension

PURPOSE: The article reports a wet milling process, where the planetary ball mill was combined with pearl milling technology to reach nanosize range of meloxicam (Mel; 100–500 nm). The main purpose was to increase the dissolution rate and extent of a poorly water-soluble Mel as nonsteroidal anti-inf...

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Autores principales: Bartos, Csaba, Jójárt-Laczkovich, Orsolya, Katona, Gábor, Budai-Szűcs, Mária, Ambrus, Rita, Bocsik, Alexandra, Gróf, Ilona, Deli, Mária Anna, Szabó-Révész, Piroska
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5987755/
https://www.ncbi.nlm.nih.gov/pubmed/29910603
http://dx.doi.org/10.2147/DDDT.S159965
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author Bartos, Csaba
Jójárt-Laczkovich, Orsolya
Katona, Gábor
Budai-Szűcs, Mária
Ambrus, Rita
Bocsik, Alexandra
Gróf, Ilona
Deli, Mária Anna
Szabó-Révész, Piroska
author_facet Bartos, Csaba
Jójárt-Laczkovich, Orsolya
Katona, Gábor
Budai-Szűcs, Mária
Ambrus, Rita
Bocsik, Alexandra
Gróf, Ilona
Deli, Mária Anna
Szabó-Révész, Piroska
author_sort Bartos, Csaba
collection PubMed
description PURPOSE: The article reports a wet milling process, where the planetary ball mill was combined with pearl milling technology to reach nanosize range of meloxicam (Mel; 100–500 nm). The main purpose was to increase the dissolution rate and extent of a poorly water-soluble Mel as nonsteroidal anti-inflammatory drug as well as to study its permeability across cultured intestinal epithelial cell layers. METHODS: Viscosity of milled dispersion and particle size distribution and zeta potential of Mel were investigated and differential scanning calorimeter and X-ray powder diffractometer were used to analyse the structure of the suspended Mel. Finally in vitro dissolution test and in vitro cell culture studies were made. RESULTS: It was found that the ratio of predispersion and pearls 1:1 (w/w) resulted in the most effective grinding system (200-fold particle size reduction in one step) with optimized process parameters, 437 rpm and 43 min. Nanosuspension (1% Mel and 0.5% poly[vinyl alcohol]) as an intermediate product showed a stable system with 2 weeks of holding time. This optimized nanosuspension enhanced the penetration of Mel across cultured intestinal epithelial cell layers without toxic effects. CONCLUSION: The dissolution rate of Mel from the poly(vinyl alcohol) stabilized nanosuspension justified its applicability in the design of innovative per oral dosage form (capsule) in order to ensure/give a rapid analgesia.
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spelling pubmed-59877552018-06-15 Optimization of a combined wet milling process in order to produce poly(vinyl alcohol) stabilized nanosuspension Bartos, Csaba Jójárt-Laczkovich, Orsolya Katona, Gábor Budai-Szűcs, Mária Ambrus, Rita Bocsik, Alexandra Gróf, Ilona Deli, Mária Anna Szabó-Révész, Piroska Drug Des Devel Ther Original Research PURPOSE: The article reports a wet milling process, where the planetary ball mill was combined with pearl milling technology to reach nanosize range of meloxicam (Mel; 100–500 nm). The main purpose was to increase the dissolution rate and extent of a poorly water-soluble Mel as nonsteroidal anti-inflammatory drug as well as to study its permeability across cultured intestinal epithelial cell layers. METHODS: Viscosity of milled dispersion and particle size distribution and zeta potential of Mel were investigated and differential scanning calorimeter and X-ray powder diffractometer were used to analyse the structure of the suspended Mel. Finally in vitro dissolution test and in vitro cell culture studies were made. RESULTS: It was found that the ratio of predispersion and pearls 1:1 (w/w) resulted in the most effective grinding system (200-fold particle size reduction in one step) with optimized process parameters, 437 rpm and 43 min. Nanosuspension (1% Mel and 0.5% poly[vinyl alcohol]) as an intermediate product showed a stable system with 2 weeks of holding time. This optimized nanosuspension enhanced the penetration of Mel across cultured intestinal epithelial cell layers without toxic effects. CONCLUSION: The dissolution rate of Mel from the poly(vinyl alcohol) stabilized nanosuspension justified its applicability in the design of innovative per oral dosage form (capsule) in order to ensure/give a rapid analgesia. Dove Medical Press 2018-05-31 /pmc/articles/PMC5987755/ /pubmed/29910603 http://dx.doi.org/10.2147/DDDT.S159965 Text en © 2018 Bartos et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Bartos, Csaba
Jójárt-Laczkovich, Orsolya
Katona, Gábor
Budai-Szűcs, Mária
Ambrus, Rita
Bocsik, Alexandra
Gróf, Ilona
Deli, Mária Anna
Szabó-Révész, Piroska
Optimization of a combined wet milling process in order to produce poly(vinyl alcohol) stabilized nanosuspension
title Optimization of a combined wet milling process in order to produce poly(vinyl alcohol) stabilized nanosuspension
title_full Optimization of a combined wet milling process in order to produce poly(vinyl alcohol) stabilized nanosuspension
title_fullStr Optimization of a combined wet milling process in order to produce poly(vinyl alcohol) stabilized nanosuspension
title_full_unstemmed Optimization of a combined wet milling process in order to produce poly(vinyl alcohol) stabilized nanosuspension
title_short Optimization of a combined wet milling process in order to produce poly(vinyl alcohol) stabilized nanosuspension
title_sort optimization of a combined wet milling process in order to produce poly(vinyl alcohol) stabilized nanosuspension
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5987755/
https://www.ncbi.nlm.nih.gov/pubmed/29910603
http://dx.doi.org/10.2147/DDDT.S159965
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