Literature DB >> 16621418

Physicochemical characterization of meloxicam-mannitol binary systems.

Parya Reisi Nassab1, Róbert Rajkó, Piroska Szabó-Révész.   

Abstract

The dissolution behaviour of drugs remains one of the most challenging aspects in formulation development. The anti-inflammatory drug, meloxicam (ME) has poor water solubility. The object of this experiment was to improve the rate of dissolution of meloxicam in capsule form. In order to achieve this, mannitol was used as a carrier in different ratios, in physical mixtures and melted forms. Mannitol, a sugar alcohol, is a cheap and readily available excipient. Differential scanning calorimetry (DSC) and X-ray diffractometry were used to investigate the characteristics of meloxicam-mannitol binary systems. Multivariate curve resolution (MCR) as a chemometric method was applied to interpret the X-ray diffractograms. This is believed to be the first published use of this reasoning for this interpretation. According to the results, the amount of mannitol and the particle size of ME were important factors in the rate of dissolution. To the perfect dissolution of ME, the melt technology was used which resulted in mixed crystals. This technology was made by 10 parts of mannitol and 1 part of ME2 with about 6 microm in average particle size. The interaction (adhesion) between mannitol and ME for physical mixtures was not enough to the perfect dissolution.

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Year:  2006        PMID: 16621418     DOI: 10.1016/j.jpba.2006.02.055

Source DB:  PubMed          Journal:  J Pharm Biomed Anal        ISSN: 0731-7085            Impact factor:   3.935


  4 in total

1.  Development and characterization of enteric-coated immediate-release pellets of aceclofenac by extrusion/spheronization technique using kappa-carrageenan as a pelletizing agent.

Authors:  Vaishali A Kilor; Nidhi P Sapkal; Jasmine G Awari; Bharti D Shewale
Journal:  AAPS PharmSciTech       Date:  2010-03-03       Impact factor: 3.246

2.  Development of meloxicam salts with improved dissolution and pharmacokinetic behaviors in rats with impaired gastric motility.

Authors:  Masanori Ochi; Ryo Inoue; Yukinori Yamauchi; Shizuo Yamada; Satomi Onoue
Journal:  Pharm Res       Date:  2012-09-15       Impact factor: 4.200

Review 3.  The Role of Functional Excipients in Solid Oral Dosage Forms to Overcome Poor Drug Dissolution and Bioavailability.

Authors:  Jannes van der Merwe; Jan Steenekamp; Dewald Steyn; Josias Hamman
Journal:  Pharmaceutics       Date:  2020-04-25       Impact factor: 6.321

4.  Smartcrystals for Efficient Dissolution of Poorly Water-Soluble Meloxicam.

Authors:  Rita Ambrus; Areen Alshweiat; Piroska Szabó-Révész; Csilla Bartos; Ildikó Csóka
Journal:  Pharmaceutics       Date:  2022-01-21       Impact factor: 6.321

  4 in total

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