Skip to the main content

Original scientific paper

https://doi.org/10.15255/KUI.2025.035

Evaluation of the Solubility Profiles of Hypolipidemic Drugs

Nemanja Turković orcid id orcid.org/0000-0002-3320-2966 ; University of Montenegro, Faculty of Medicine, Kruševac bb, 81 000 Podgorica, Montenegro *
Branka Ivković orcid id orcid.org/0000-0001-7350-3483 ; Faculty of Pharmacy, Department of Pharmaceutical Chemistry, University of Belgrade, Vojvode Stepe 450, 11 221 Belgrade, Serbia
Jasmina Šljivić ; Faculty of Pharmacy, University “Bijeljina” Bijeljina, Pavlovića put 024, 76 300 Bijeljina, Bosnia & Herzegovina
Jasna Savić orcid id orcid.org/0009-0005-1872-9902 ; The Academy of Applied Studies Polytechnic, Katarine Ambrozić 3, 11 120 Belgrade, Serbia
Milena Turković ; The Health Institution of the Pharmacy of Montenegro “Montefarm”, Ankarski bulevar 3, 81 000 Podgorica, Montenegro

* Corresponding author.


Full text: english pdf 637 Kb

page 365-374

downloads: 0

cite


Abstract

Hypolipidemic agents represent an important class of drugs used in the treatment of hyperlipoproteinemia. Statins are reversible, competitive inhibitors of 3-hydroxy-3-methylglutaryl-coenzyme A reductase, ezetimibe selectively inhibits intestinal and biliary absorption of cholesterol by blocking Niemann-Pick C1-like protein, while fibrates act as agonists of the peroxisome proliferator-activated receptor alpha nuclear receptor. Drug solubility is a critical parameter influencing bioavailability and therapeutic efficacy, particularly in orally administered formulations. This is of special importance for hypolipidemic agents such as simvastatin, atorvastatin, and fenofibrate, which are widely used in the treatment of hyperlipidemia.
In this study, an HPLC method was developed and validated for determining the solubility of these three drugs. Method validation confirmed specificity, linearity, and precision. Solubility was assessed in four media of varying pH values (1.2, 4.5, 6.8, and 7.4) at 37 °C, employing a Zorbax Eclipse C18 column (5 µm, 150 × 4.6 mm), with a mobile phase consisting of acetonitrile and 0.1 % phosphoric acid, and UV detection at 242 nm.
The results enabled solubility characterisation based on the dose number, which, in combination with literature-derived logP (partition coefficient) values, facilitated the Biopharmaceutics Classification System (BCS) categorisation of the investigated drugs. These findings provide valuable guidance for the design of new pharmaceutical formulations containing simvastatin, atorvastatin, or fenofibrate, as well as the optimisation of existing ones.

Keywords

hypolipidemic drugs; solubility; HPLC; BCS classification; bioavailability

Hrčak ID:

346447

URI

https://hrcak.srce.hr/346447

Publication date:

17.7.2026.

Article data in other languages: croatian

Visits: 0 *