Affiliations 

  • 1 Laboratory Fundamental of Pharmaceutics, Faculty of Pharmacy, Universiti Teknologi MARA, Selangor Darul Ehsan, Malaysia; Pharmaceutical and Life Sciences Core, Universiti Teknologi MARA, Shah Alam, Selangor Darul Ehsan, Malaysia
  • 2 Pharmaceutical and Life Sciences Core, Universiti Teknologi MARA, Shah Alam, Selangor Darul Ehsan, Malaysia
J Adv Pharm Technol Res, 2016 Jul-Sep;7(3):80-6.
PMID: 27429926 DOI: 10.4103/2231-4040.184589

Abstract

Categorized as a Biopharmaceutics Classification System Class II drugs, atorvastatin (ATV) exhibits low aqueous solubility and bioavailability thus presenting an obstacle and great challenge to formulation researchers. Numerous studies are available in regard to the solubility enhancement of ATV, but very few actually describe this phenomenon in terms of thermodynamics and the solute-solvent interaction. Arginine (ARG) is an amino acid that has been reported to enhance the solubility of the highly insoluble wheat protein gluten through hydrogen bonding and π electron-cation interaction. To our knowledge, ARG has never been investigated as a solubility enhancement agent of aqueous insoluble drugs. Thus, this study aimed to elucidate the solute-solvent and solute-cosolute interactions and derive thermodynamic parameters that bolstered the solubility of ATV in the presence of ARG. We examined the electrolytic conductance and densities of ATV-ARG binary system covering the temperature ranging from 298.15 K to 313.15 K. Conductometric and volumetric parameters such as limiting molar conductance, association constants, limiting partial molar volumes, and expansibility values were calculated. Additionally, thermodynamic parameters (ΔG(0), ΔH(0), ΔS(0), and Es) involved in the association process of the solute in the aqueous solution of ARG were also determined.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.