Literature DB >> 17613897

An investigation of physicochemical properties of piroxicam liquisolid compacts.

Yousef Javadzadeh1, Mohammad Reza Siahi, Solmaz Asnaashari, Ali Nokhodchi.   

Abstract

The potential of liquisolid systems to improve the dissolution properties of a water-insoluble agent (piroxicam) was investigated. In this study, physicochemical properties of piroxicam liquisolid tablets, effect of aging, and type of the carrier were also investigated. To this end, several liquisolid tablets formulations containing various ratios of drug: solvent and different carriers were prepared. X-ray crystallography, differential scanning calorimetry (DSC), and contact angle measurement were used for evaluation of physicochemical properties of piroxicam. Liquisolid compacts exhibited significantly higher drug dissolution rates, in different dissolution media, than compacts prepared by the direct compression technique. The results showed that enhanced dissolution rate of piroxicam liquisolid tablets was due to an increase in wetting properties and surface area of drug available for dissolution. To investigate the effect of aging on the hardness and dissolution rate of liquisolid compacts, the formulations were stored at 25 degrees C/75% relative humidity for 9 months. The results showed that aging had no significant effect on hardness or dissolution profile of liquisolid tablets. It was shown that Avicel had more liquid retention potential than other carriers, but there were no significant differences in the dissolution profiles between formulations. The results of DSC and X-ray crystallography did not show any changes in crystallinity of the drug and interaction between piroxicam and exipients (Avicel and silica) during the process.

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Year:  2007        PMID: 17613897     DOI: 10.1080/10837450701247574

Source DB:  PubMed          Journal:  Pharm Dev Technol        ISSN: 1083-7450            Impact factor:   3.133


  7 in total

1.  Investigating the use of liquisolid compacts technique to minimize the influence of pH variations on loratadine release.

Authors:  Mazen El-Hammadi; Nisrine Awad
Journal:  AAPS PharmSciTech       Date:  2011-11-19       Impact factor: 3.246

2.  Enhancement of the Oral Bioavailability of Fexofenadine Hydrochloride via Cremophor(®) El-Based Liquisolid Tablets.

Authors:  Soad Ali Yehia; Mohamed Shafik El-Ridi; Mina Ibrahim Tadros; Nolwa Gamal El-Sherif
Journal:  Adv Pharm Bull       Date:  2015-11-30

3.  Piroxicam Loading onto Mesoporous Silicas by Supercritical CO2 Impregnation.

Authors:  Marta Gallo; Luca Serpella; Federica Leone; Luigi Manna; Mauro Banchero; Silvia Ronchetti; Barbara Onida
Journal:  Molecules       Date:  2021-04-25       Impact factor: 4.411

4.  Effect of hydrogen bond formation/replacement on solubility characteristics, gastric permeation and pharmacokinetics of curcumin by application of powder solution technology.

Authors:  Vijay Sharma; Kamla Pathak
Journal:  Acta Pharm Sin B       Date:  2016-06-14       Impact factor: 11.413

5.  Preparation of Microcrystals of Piroxicam Monohydrate by Antisolvent Precipitation via Microfabricated Metallic Membranes with Ordered Pore Arrays.

Authors:  Rahimah Othman; Goran T Vladisavljević; Elena Simone; Zoltan K Nagy; Richard G Holdich
Journal:  Cryst Growth Des       Date:  2017-11-13       Impact factor: 4.076

Review 6.  Liquisolid technique and its applications in pharmaceutics.

Authors:  Mei Lu; Haonan Xing; Jingzheng Jiang; Xiao Chen; Tianzhi Yang; Dongkai Wang; Pingtian Ding
Journal:  Asian J Pharm Sci       Date:  2016-11-04       Impact factor: 6.598

7.  Enhancement of dissolution rate of indomethacin: using liquisolid compacts.

Authors:  Majid Saeedi; Jafar Akbari; Katayoun Morteza-Semnani; Reza Enayati-Fard; Shirin Sar-Reshteh-Dar; Ala Soleymani
Journal:  Iran J Pharm Res       Date:  2011       Impact factor: 1.696

  7 in total

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