Preparation and Evaluation of Antihypercholesterolemic Activity of Atorvastatin Calcium-Maleic Acid Co-Amorphous Solids
Abstract
Atorvastatin calcium is a statin drug used for antihypercholesterolemic. The oral bioavailability of atorvastatin calcium is relatively low because it is poorly soluble in water. The low oral bioavailability of the drug causes a decrease in its therapeutic effectiveness. This study aimed to increase the solubility of atorvastatin calcium through the formation of co-amorphous solids and evaluate its activity as antihypercholesterolemic. Atorvastatin calcium was prepared into co-amorphous solids with a maleic acid coformer using the spray drying method. Solids characterization was carried out using Powder X-Ray Diffraction (PXRD), Differential Scanning Calorimetry (DSC), Fourier Transforms Infra Red (FTIR), and Scanning Electronic Microscopy (SEM). The solubility test was carried out using the shaking method, while the evaluation of antihypercholesterolemic was carried out in vivo in experimental animals. The results of the analysis of diffractograms, thermograms, FTIR spectra, and micrograph images showed that the atorvastatin calcium-maleic acid solids prepared by spray drying were a co-amorphous solid. The atorvastatin calcium-maleic acid co-amorphous solids had a greater solubility in water (p<0.05) when compared to pure atorvastatin calcium. However, the in vivo antihypercholesterolemic activity results in experimental animals showed that the cholesterol-lowering activity of the atorvastatin calcium-maleic acid co-amorphous solidswas not significantly different (p>0.05) with pure atorvastatin calcium. This phenomenon is thought to be because atorvastatin calcium from co-amorphous solids in solution is more present as a charged fraction, affecting the permeability and absorption process.
References
Ashwini, A. B., A. A. Satish, and J. G. Anil (2021). Solubility enhancement of atorvastatin calcium by solid dispersion using skimmed milk powder. Journal of Pharmaceutical Sciences and Research, 13(6); 365-368
Brake, K., A. Gumireddy, A. Tiwari, H. Chauhan, and D. Kumari (2017). In vivo studies for drug development via oral delivery: challenges, animal models and techniques. Pharmaceutica Analytica Acta, 08(9);1-11
Chavan, R. B., R. Thipparaboina, D. Kumar, and N. R. Shastri (2016). Co amorphous systems: A product development perspective. International Journal of Pharmaceutics, 515(1-2); 403-415
Djamil, R., D. Rahmat, S. Zaidan, and M. N. Latifah (2020). Anticholesterol activity of okra fruit extract (Abelmoschus esculentus (L) Moench) and its nanoemulsion in vivo. Pharmacognosy Journal, 12(2); 316-320
Dressman, J.B., C. Reppas (2000). In vitro-in vivo correlations for lipophilic, poorly water-soluble drugs. European Journal of Pharmaceutical Sciences, 11; S73–80
Karagianni, A., K. Kachrimanis, and I. Nikolakakis (2018). Co-amorphous solid dispersions for solubility and absorption improvement of drugs: composition, preparation, characterization and formulations for oral delivery. Pharmaceutics, 10(98)
Kwon, J., B. R. Giri, E. S. Song, J. G. Bae, J. Lee, and D. W. Kim (2019). Spray-dried amorphous solid dispersions of atorvastatin calcium for improved supersaturation and oral bioavailability. Pharmaceutics, 11(461)
Kurniawan, M. F., and M. Audita (2021). Formulation, evaluation of physical properties, anti-cholesterol activity from Ficus carica L. leaves extract tablet. Science and Technology Indonesia, 6(4); 285–295
Labib, S., and M. Nasr (2021). Formulation and evaluation of atorvastatin calcium nanocrystals containing p-glycoprotein inhibitors for enhancing oral delivery. International Journal of Current Pharmaceutical Research, 13(3); 19-23
Lee, H. L., J. M. Vasoya, M. D. Cirqueira, K. L.Yeh, T. Lee, and A. T. Serajuddin (2017). Continuous preparation of 1:1 haloperidol-maleic acid salt by a novel solvent-free method using a twin screw melt extruder. Molecular Pharmaceutics, 14(4); 1278-1291
Lemsi, M., H. Galai, M. R. Louhaichi, H. Fessi, and R. Kalfat (2017). Amorphization of atorvastatin calcium by mechanical process: characterization and stabilization within polymeric matrix. Journal of Pharmaceutical Innovation, 12(3); 216-225
Renuka, S. K. Singh, M. Gulati, and R. Narang (2017). Stable amorphous binary systems of glipizide and atorvastatin powders with enhanced dissolution profiles: formulation and characterization. Pharmaceutical Development and Technology, 22(1); 13–25
Rohniani, S., A. Yugatama, B.B. Suryadi, L.F. Felicitas, A. Ainurofiq, and F. Prihapsara (2020). Evaluation of compared dissolution profile of atorvastatin tablets in markets. Journal of Advanced Pharmacy Education and Research, 10(1); 107–115.
Samsodien, H., M. Bapoo, T. I. Doom, Z. Harneker, A. S. Lou, I. C. Scheepers, A. B. Sonday, and B. Geldenhuys (2017). FTIR, dissolution and anti-viral activity of nevirapine co-crystals. Pharmaceutica Analytica Acta, 8(9)
Shaker, M. A. (2018). Dissolution and bioavailability enhancement of atorvastatin: gelucire semi-solid binary system. Journal of Drug Delivery Science and Technology, 43; 178-184
Sharma, M., and I. Mehta (2019). Surface stabilized atorvastatin nanocrystals with improved bioavailability, safety and antihyperlipidemic potential. Scientific Reports, 9; 16105
Shi, Q., S. M. Moinuddin, and T. Cai (2019). Advances in coamorphous drug delivery systems. Acta Pharmaceutica Sinica B, 9(1); 19–35
Sugita, K., N. Takata, and E. Yonemochi (2021). Dose-dependent solubility–permeability interplay for poorly soluble drugs under non-sink conditions. Pharmaceutics, 13(323)
Trivedi, H. R., D. S. Borkar, and P. K. Puranik (2020). Experimental design approach for development of cocrystals and immediate release cocrystal tablet of atorvastatin calcium for enhancement of solubility and dissolution. Journal of Research in Pharmacy, 24(5); 720-737
Wahjuningsih, S. B., H. Haslina, and M. Marsono (2018). Hypolipidaemic effects of high resistant starch sago and red bean flour- based analog rice on diabetic rats. Materia socio-medica, 30(4); 232–239
Wairkar, S., and R. S. Gaud (2019). Development and characterization of microstructured, spray-dried co-amorphous mixture of antidiabetic agents stabilized by silicate. AAPS PharmSciTech, 20(141)
Wicaksono, Y., D. Setyawan, S. Siswandono, and T. A. Siswoyo (2019). Preparation and characterization of a novel cocrystal of atorvastatin calcium with succinic acid coformer. Indonesian Journal of Chemistry, 19(3); 660 – 667
Wicaksono, Y., V. A. Rosidi, S. Y. Saragih, L. S. Fauziah, and D. Setyawan (2021). Preparation of spray dried coamorphous solids to improve the solubility and dissolution rate of atorvastatin calcium. Jurnal Teknologi, 83(2); 77–83
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