Literature DB >> 28359817

Solubility and thermodynamics of apremilast in different mono solvents: Determination, correlation and molecular interactions.

Faiyaz Shakeel1, Nazrul Haq2, Fars K Alanazi2, Ibrahim A Alsarra2.   

Abstract

The solubility data of recently launched poorly soluble antipsoriatic drug apremilast (APM) in any mono solvent or cosolvent mixtures with respect to temperature are not available in literature. Hence, in this research work, the solubility of APM in twelve different mono solvents namely "water, methanol, ethanol, isopropanol (IPA), ethylene glycol (EG), propylene glycol (PG), 1-butanol, 2-butanol, ethyl acetate (EA), dimethyl sulfoxide (DMSO), polyethylene glycol-400 (PEG-400) and Transcutol®" was determined at temperatures "T=298.2K to 318.2K" and pressure "p=0.1 MPa". Eexperimental solubilities of APM in mole fraction were determined by a static equilibrium method using high performance liquid chromatography at 254nm. Experimental solubilities of APM in mole fraction were correlated well with "Van't Hoff and Apelblat models". The solubilities of APM in mole fraction were recorded highest in DMSO (9.91×10-2), followed by EA (2.54×10-2), Transcutol (2.51×10-2), PEG-400 (2.16×10-2),PG (4.01×10-3), EG (1.61×10-3), IPA (4.96×10-4), 1-butanol (4.18×10-4), 2-butanol (3.91×10-4), methanol (2.25×10-4), ethanol (2.20×10-4) and water (1.29×10-6) at "T=318.2K" and similar results were also obtained at each temperature evaluated. The molecular interactions between solute and solvent molecules were evaluated by the determination of activity coefficients. Based on activity coefficients, the higher solute-solvents molecular interactions were recorded in APM-DMSO, APM-EA, APM-Transcutol and APM-PEG-400 in comparison with other combination of solute and solvents. "Apparent standard thermodynamic parameters" of APM indicated an "endothermic and entropy-driven dissolution" of APM in all mono solvents evaluated. Based on these results, APM was proposed as freely soluble in DMSO, EA and Transcutol, sparingly soluble in PEG0-400, slightly soluble in methanol, ethanol, IPA, EG, PG, 1-butanol and 2-butanol and practically insoluble in water. Hence, DMSO, EA and Transcutol were selected as the best solvents and water and ethanol were selected as the anti-solvents for APM.
Copyright © 2017 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Activity coefficient; Antipsoriatic arthritis; Apremilast; Dissolution thermodynamics; Mono solvent; Solubility

Mesh:

Substances:

Year:  2017        PMID: 28359817     DOI: 10.1016/j.ijpharm.2017.03.067

Source DB:  PubMed          Journal:  Int J Pharm        ISSN: 0378-5173            Impact factor:   5.875


  4 in total

1.  Correlation of Solubility Thermodynamics of Glibenclamide with Recrystallization and In Vitro Release Profile.

Authors:  Ravi Maharjan; Junoh Jeong; Ripesh Bhujel; Min-Soo Kim; Hyo-Kyung Han; Nam Ah Kim; Seong Hoon Jeong
Journal:  Molecules       Date:  2022-02-18       Impact factor: 4.411

2.  Self-Nanoemulsifying Drug Delivery System (SNEDDS) of Apremilast: In Vitro Evaluation and Pharmacokinetics Studies.

Authors:  Ahad S Abushal; Fadilah S Aleanizy; Fulwah Y Alqahtani; Faiyaz Shakeel; Muzaffar Iqbal; Nazrul Haq; Ibrahim A Alsarra
Journal:  Molecules       Date:  2022-05-11       Impact factor: 4.927

3.  Effect of Penetration Enhancers and Safety on the Transdermal Delivery of Apremilast in Skin.

Authors:  Paulo Sarango-Granda; Lupe Carolina Espinoza; Natalia Díaz-Garrido; Helen Alvarado; María J Rodríguez-Lagunas; Laura Baldomá; Ana Calpena
Journal:  Pharmaceutics       Date:  2022-05-07       Impact factor: 6.525

4.  Thermodynamic Solubility Profile of Temozolomide in Different Commonly Used Pharmaceutical Solvents.

Authors:  Abdul Ahad; Faiyaz Shakeel; Mohammad Raish; Ajaz Ahmad; Yousef A Bin Jardan; Fahad I Al-Jenoobi; Abdullah M Al-Mohizea
Journal:  Molecules       Date:  2022-02-21       Impact factor: 4.411

  4 in total

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