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Optimization of a combined wet milling process in order to produce poly(vinyl alcohol) stabilized nanosuspension.
Bartos, Csaba; Jójárt-Laczkovich, Orsolya; Katona, Gábor; Budai-Szucs, Mária; Ambrus, Rita; Bocsik, Alexandra; Gróf, Ilona; Deli, Mária Anna; Szabó-Révész, Piroska.
Afiliação
  • Bartos C; Faculty of Pharmacy, Institute of Pharmaceutical Technology and Regulatory Affairs, University of Szeged, Szeged, Hungary.
  • Jójárt-Laczkovich O; Faculty of Pharmacy, Institute of Pharmaceutical Technology and Regulatory Affairs, University of Szeged, Szeged, Hungary.
  • Katona G; Faculty of Pharmacy, Institute of Pharmaceutical Technology and Regulatory Affairs, University of Szeged, Szeged, Hungary.
  • Budai-Szucs M; Faculty of Pharmacy, Institute of Pharmaceutical Technology and Regulatory Affairs, University of Szeged, Szeged, Hungary.
  • Ambrus R; Faculty of Pharmacy, Institute of Pharmaceutical Technology and Regulatory Affairs, University of Szeged, Szeged, Hungary.
  • Bocsik A; Institute of Biophysics, Biological Research Centre, Hungarian Academy of Sciences, Szeged, Hungary.
  • Gróf I; Institute of Biophysics, Biological Research Centre, Hungarian Academy of Sciences, Szeged, Hungary.
  • Deli MA; Institute of Biophysics, Biological Research Centre, Hungarian Academy of Sciences, Szeged, Hungary.
  • Szabó-Révész P; Faculty of Pharmacy, Institute of Pharmaceutical Technology and Regulatory Affairs, University of Szeged, Szeged, Hungary.
Drug Des Devel Ther ; 12: 1567-1580, 2018.
Article em En | MEDLINE | ID: mdl-29910603
ABSTRACT

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 11 (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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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Álcool de Polivinil / Tiazinas / Tiazóis / Tecnologia Farmacêutica Idioma: En Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Hungria

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Álcool de Polivinil / Tiazinas / Tiazóis / Tecnologia Farmacêutica Idioma: En Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Hungria