Literature DB >> 33959199

Multicomponent crystalline solid forms of aripiprazole produced via hot melt extrusion techniques: An exploratory study.

Arun Butreddy1, Mashan Almutairi1,2, Neeraja Komanduri1, Suresh Bandari1, Feng Zhang3, Michael A Repka1,4.   

Abstract

Multicomponent crystalline solid forms (salts, cocrystals and eutectics) are a promising means of enhancing the dissolution behavior of poorly soluble drugs. The present study demonstrates the development of multicomponent solid forms of aripiprazole (ARP) prepared with succinic acid (SA) and nicotinamide (NA) as coformers using the hot melt extrusion (HME) technique. The HME-processed samples were characterized and analyzed using differential scanning calorimetry (DSC), hot stage microscopy (HSM), Fourier transform infrared (FTIR) spectroscopy, powder X-ray diffraction (PXRD) and scanning electron microscopy (SEM). The DSC and HSM analyses revealed a characteristic single melting temperature in the solid forms, which differed from the melting points of the individual components. The discernible changes in the FTIR (amide C=O stretching) and PXRD results for ARP-SA confirm the formation of new crystalline solid forms. In the case of ARP-NA, these changes were less prominent, without the appearance or disappearance of peaks, suggesting no change in the crystal lattice. The SEM images demonstrated morphological differences between the HME-processed samples and the individual parent components. The in vitro dissolution and microenvironment pH measurement studies revealed that ARP-SA showed a higher dissolution rate, which could be due to the acidic microenvironment pH imparted by the coformer. The observations of the present study demonstrate the applicability of the HME technique for the development of ARP multicomponent solid forms.

Entities:  

Keywords:  Salts; dissolution rate; eutectics; hot melt extrusion; microenvironmental pH

Year:  2021        PMID: 33959199      PMCID: PMC8095679          DOI: 10.1016/j.jddst.2021.102529

Source DB:  PubMed          Journal:  J Drug Deliv Sci Technol        ISSN: 1773-2247            Impact factor:   5.062


  31 in total

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Journal:  Pharm Res       Date:  2012-08-21       Impact factor: 4.200

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Journal:  Mol Pharm       Date:  2019-10-11       Impact factor: 4.939

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Journal:  Mol Pharm       Date:  2017-03-10       Impact factor: 4.939

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Journal:  Int J Pharm       Date:  2012-12-20       Impact factor: 5.875

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Journal:  Eur J Pharm Biopharm       Date:  2018-07-03       Impact factor: 5.571

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