Literature DB >> 33944661

Ethanol-assisted kneading of apigenin with arginine for enhanced dissolution rate of apigenin: development of rapidly disintegrating tablets.

Fatma A Kassem1, Abdelaziz E Abdelaziz1, Gamal M El Maghraby2.   

Abstract

Apigenin is a natural flavonoid which is claimed to have many pharmacological activities ranging from simple anti-inflammatory to anticancer action. However, poor dissolution slowed the advancement of this drug through the development pipelines. The objective of this work was to probe ethanol-aided kneading of apigenin with arginine as a new strategy for enhanced dissolution rate. The work was extended to develop rapidly disintegrating tablets of apigenin. Apigenin was mixed with increasing molar ratios of arginine before ethanol-aided kneading. The resulting products were examined using Fourier transform infrared spectroscopy, differential scanning calorimetry, and X-ray diffraction in addition to probing the dissolution characteristics of apigenin. The analytical techniques highlighted the existence of new crystalline species with a possibility of salt formation. The recorded alterations in the crystalline properties were associated with a significant enhancement in the dissolution rate of apigenin. The presence of arginine did not have any negative effect of the cytotoxic power of apigenin. Optimum formulation was successfully prepared as rapidly disintegrating tablets which showed fast liberation of apigenin. The study introduced arginine as a potential excipient for enhanced dissolution of apigenin after ethanol-assisted kneading.

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Keywords:  Salt formation; amino acids; apigenin; cytotoxicity; dispersible tablets; wet co-grinding

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Year:  2021        PMID: 33944661     DOI: 10.1080/10837450.2021.1922441

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


  1 in total

1.  Formulation of Apigenin-Cyclodextrin-Chitosan Ternary Complex: Physicochemical Characterization, In Vitro and In Vivo Studies.

Authors:  Mohammed Jafar; Mohammed Saifuddin Khalid; Hajer Alghamdi; Mohd Amir; Sarah Aon Al Makki; Ohud Saud Alotaibi; Afnan Ali Al Rmais; Syed Sarim Imam; Sultan Alshehri; Sadaf Jamal Gilani
Journal:  AAPS PharmSciTech       Date:  2022-02-10       Impact factor: 3.246

  1 in total

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