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

• Main Authors: Bartos C (Author), Jójárt-Laczkovich O (Author), Katona G (Author), Budai-Szűcs M (Author), Ambrus R (Author), Bocsik A (Author), Gróf I (Author), Deli MA (Author), Szabó-Révész P (Author)
• Format: Book
• Published: Dove Medical Press, 2018-05-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Summary

Csaba Bartos,1 Orsolya Jójárt-Laczkovich,1 Gábor Katona,1 Mária Budai-Szűcs,1 Rita Ambrus,1 Alexandra Bocsik,2 Ilona Gróf,2 Mária Anna Deli,2 Piroska Szabó-Révész1 1Faculty of Pharmacy, Institute of Pharmaceutical Technology and Regulatory Affairs, University of Szeged, Szeged, Hungary; 2Institute of Biophysics, Biological Research Centre, Hungarian Academy of Sciences, Szeged, Hungary 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. Keywords: nanonization, meloxicam, milled dispersion, milling efficiency, zeta potential, intermediate product

Item Description

1177-8881