Tailoring of Rosuvastatin Calcium and Atenolol Bilayer Tablets for the Management of Hyperlipidemia Associated with Hypertension: A Preclinical Study

• Published in: Pharmaceutics Vol. 14; no. 8; p. 1629
• Main Authors: Elsayed, Mahmoud M. A, Aboelez, Moustafa O, Mohamed, Mohamed S, Mahmoud, Reda A, El-Shenawy, Ahmed A, Mahmoud, Essam A, Al-Karmalawy, Ahmed A, Santali, Eman Y, Alshehri, Sameer, Elsadek, Mahmoud Elkot Mostafa, El Hamd, Mohamed A, Ramadan, Abd El hakim
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 01-08-2022; MDPI
• Subjects: Atenolol; Atherosclerosis; bilayer tablets; Bioavailability; Cardiovascular disease; Chemical properties; Dosage and administration; Drug therapy; Drug therapy, Combination; Drugs; factorial design; Hyperlipidemia; Hypertension; Investigations; Lactose; Metabolism; Methods; Obesity; Pharmaceuticals; Production processes; Rosuvastatin; rosuvastatin calcium; Sodium; Spectrum analysis; Tablets (Medicine); Egypt; Cairo Egypt; Mumbai India; United States > US; Japan; India
• ISSN: 1999-4923; 1999-4923
• DOI: 10.3390/pharmaceutics14081629

Hyperlipidemia is still the leading cause of heart disease in patients with hypertension. The purpose of this study is to make rosuvastatin calcium (ROS) and atenolol (AT) bilayer tablets to treat coexisting dyslipidemia and hypertension with a single product. ROS was chosen for the immediate-release layer of the constructed tablets, whereas AT was chosen for the sustained-release layer. The solid dispersion of ROS with sorbitol (1:3 w/w) was utilized in the immediate-release layer while hydroxypropyl methylcellulose (HPMC), ethylcellulose (EC), and sodium bicarbonate were incorporated into the floating sustained-release layer. The concentrations of HPMC and EC were optimized by employing 32 full factorial designs to sustain AT release. The bilayer tablets were prepared by the direct compression method. The immediate-release layer revealed that 92.34 ± 2.27% of ROS was released within 60 min at a pH of 1.2. The second sustained-release layer of the bilayer tablets exhibited delayed release of AT (96.65 ± 3.36% within 12 h) under the same conditions. The release of ROS and AT from the prepared tablets was found to obey the non-Fickian diffusion and mixed models (zero-order, Higuchi and Korsmeyer–Peppas), respectively. Preclinical studies using rabbit models investigated the impact of ROS/AT tablets on lipid profiles and blood pressure. A high-fat diet was used to induce obesity in rabbits. Bilayer ROS/AT tablets had a remarkable effect on decreasing the lipid profiles, slowing weight gain, and lowering blood pressure to normal levels when compared to the control group.