Solubility Enhancement Solid Dispersion Fenofibric Acid HPMC and Their Physicochemical Characterization
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Abstract
Fenofibric acid is a water-soluble antihyperlipidemia drug, and the solubility of fenofibric acid is 162.5 µg/mL.1 Solid dispersion systems are aimed to improve the solubility of poorly soluble active pharmaceutical ingredients. This study aimed to formulate and characterization fenofibric acid-hydroxypropyl methylcellulose (HPMC) solid dispersion. The solid dispersion of fenofibric acid was prepared using the solvent evaporation method. The ratios of fenofibric acid and HPMC were F1 (1:1), F2 (1:3) and F3 (1:5). The formulated products were subjected to various physicochemical characterisation using X-ray diffractograms, DSC thermograms, SEM and FTIR, including particle size distribution and solubility test. The physicochemical characterisation showed the specific characteristics of the solid dispersions. X-ray diffractograms, DSC thermograms and SEM photographs indicated that fenofibric acid was amorphous and trapped in the HPMC matrix. FTIR test results show no new functional groups indicating no chemical interaction between the active pharmaceutical ingredients and the matrix. SEM results show that the solid dispersion system was morphologically different from pure fenofibric acid and the physical mixture. The solubility of fenofibrate acid was 42.33 µg/mL while the solubility of solid dispersion F3 ratio 1:3 was 113.25 µg/mL. The solubility of fenofibrate acid solid dispersion with HPMC 1:3 ratio is 2.68 times greater than that of pure fenofibrate acid.
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References
Kim KS, Kim JH, Jin SG, Kim DW, Kim DS, Kim JO, Yong CS, Cho KH, Li DX, Woo JS, Choi HG. Effect of magnesium carbonate on the solubility, dissolution and oral bioavailability of fenofibric acid powder as an alkalising solubilizer. Arch Pharm Res. 2016; 39(4):531–538. https://doi.org/10.1007/s12272-015-0701-9
Alagona P. Fenofibric acid: A new fibrate approved for use in combination with statin for the treatment of mixed dyslipidemia. Vasc Health Risk Manag. 2010; 6(1):351–362.
Zhu T, Ansquer JC, Kelly MT, Sleep DJ, Pradhan RS. Comparison of the gastrointestinal absorption and bioavailability of fenofibrate and fenofibric acid in humans. J . Clin Pharm. 2010; 50(8):914–921. https://doi.org/10.1177/0091270009354995
Tsume Y, Mudie DM, Langguth P, Amidon GE, Amidon GL. The Biopharmaceutics Classification System: Subclasses for in vivo predictive dissolution (IPD) methodology and IVIVC. Eur J.Pharm Sci. 2014; 57(1), 152–163. https://doi.org/10.1016/j.ejps.2014.01.009
Chavda PV and Soniwala M. Biological Classification System (BCS); with a New Perspective. MOJ Bioequiv Bioavailab. 2017; 3(4):108–109. https://doi.org/10.15406/mojbb.2017.03.00043
Richards D. Drug development and regulation. Med. 2008; 36(7):369–376. https://doi.org/10.1016/j.mpmed.2008.04.007
Anggraini D, Salsabila H, Umar S, Aldi Y, Zaini E. Preparation and Characterization of a Eutectic Mixture of Fenofibric Acid and Nicotinic Acid and Evaluatuion of In Vivo Antihyperlipidemic Activity. Sci Technol Ind. 2022; 7(4):514–521. https://doi.org/10.26554/sti.2022.7.4.514-521
Anggraini D, Umar S, Arifin H, Zaini E. Dissolution rate enhancement and physicochemical characterization of a fenofibric acid–nicotinamide eutectic mixture. Trop J Nat Prod Res. 2021; 5(9):1614–1618. https://doi.org/10.26538/tjnpr/v5i9.14
Anggraini D, Firmansyah F, Novita, G, Audia RA. Improving the Solubility of Fenofibric Acid via Multicomponent Crystal Formation with Theobromine Coformer. Trop J Nat Prod Res. 2024; 8(4):6901–6905. https://doi.org/10.26538/tjnpr/v8i4.21
Zaini E, Wahyuni F, Salsabila H, Anggraini D, Yuliandra Y, Lucida H. Eutectic mixture of fenofibric acid and syringic acid: Improvement of dissolution rate and its antihyperlipidemic activity. Chem Select. 2023; 8(20): e202300044.
Vo CL, Park C, Lee BJ. Current trends and future perspectives of solid dispersions containing poorly water-soluble drugs. Eur J Pharm Biopharm. 2013; 85(3 PART B):799–813. https://doi.org/10.1016/j.ejpb.2013.09.007
Burdock GA. Safety assessment of hydroxypropyl methylcellulose as a food ingredient. Food Chem Toxicol. 2007; 45(12):2341–2351. https://doi.org/10.1016/j.fct.2007.07.011
Banahan S, Byrne D. Methods of particle size determination – A review. Innopharm Technol. 2019; 1: 1–25.
Huang Y and Dai WG. Fundamental aspects of solid dispersion technology for poorly soluble drugs. B Acta Pharm Sin. 2014; 4(1):18–25. https://doi.org/10.1016/j.apsb.2013.11.001
Baird JA, Taylor LS. Evaluation of amorphous solid dispersion properties using thermal analysis techniques. Adv Drug Deliv Rev. 2012; 64(5):396–421. https://doi.org/10.1016/j.addr.2011.07.009
Kong Y and Hay JN. The enthalpy of fusion and degree of crystallinity of polymers as measured by DSC. Eur Polym J. 2003; 39(8):1721–1727. https://doi.org/10.1016/S0014-3057(03)00054-5
Fitriani L, Afriyanti I, Ismed F, Zaini E. Solid dispersion of usnic acid–HPMC 2910 prepared by spray drying and freeze-drying techniques. Orient J Chem. 2018; 34(4):2083–2088. https://doi.org/10.13005/ojc/3404048
Kumar A. Fourier transform infrared spectroscopy: Data interpretation and applications in structure elucidation and analysis of small molecules and nanostructures, Data Processing Handbook for Complex Biological Data Sources. Elsevier HS J. 2019. 77-96 p.
Chadha K, Karan M, Chadha R, Bhalla Y, Vasisht K. Is Failure of Cocrystallization Actually a Failure? Eutectic Formation in Cocrystal Screening of Hesperetin. J Pharm Sci. 2017; 106(8):2026–2036.