EL-Badry, M., Mahmoud, O., Fathalla, D., EL-Gendy, G. (2024). Development and characterization of nanostructure lipid carrier for anti-hepatitis-C virus drug. Journal of Advanced Biomedical and Pharmaceutical Sciences, 7(1), 18-25. doi: 10.21608/jabps.2023.234602.1202
Mahmoud EL-Badry; Ominia Ali Mahmoud; Dina Fathalla; Gamal EL-Gendy. "Development and characterization of nanostructure lipid carrier for anti-hepatitis-C virus drug". Journal of Advanced Biomedical and Pharmaceutical Sciences, 7, 1, 2024, 18-25. doi: 10.21608/jabps.2023.234602.1202
EL-Badry, M., Mahmoud, O., Fathalla, D., EL-Gendy, G. (2024). 'Development and characterization of nanostructure lipid carrier for anti-hepatitis-C virus drug', Journal of Advanced Biomedical and Pharmaceutical Sciences, 7(1), pp. 18-25. doi: 10.21608/jabps.2023.234602.1202
EL-Badry, M., Mahmoud, O., Fathalla, D., EL-Gendy, G. Development and characterization of nanostructure lipid carrier for anti-hepatitis-C virus drug. Journal of Advanced Biomedical and Pharmaceutical Sciences, 2024; 7(1): 18-25. doi: 10.21608/jabps.2023.234602.1202
Development and characterization of nanostructure lipid carrier for anti-hepatitis-C virus drug
1Dept of Pharmaceutics
Faculty of Pharmacy
Assiut University
2Department of pharmaceutics, Faculty of pharmacy, Sohag University
3Faculty of Pharmacy, Assiut university
4Department of Pharmaceutics, Faculty of pharmacy, Assiut University
Abstract
Abstract
Velpatasvir (VLP) as, a medication used to treat hepatitis-C virus (HCV). It has a very low oral bioavailability (25%). The aim of the current work is to prepare VLP loaded nanostructured lipid carriers (VLP-NLCs) as a potential way to enhance VLP aqueous solubility and bioavailability and increase its efficacy. The preparation of VLP-NLCs was carried out using the emulsification - solvent evaporation method, followed by ultrasonication. The prepared nanocarrier was examined for its particle size, zeta potential, entrapment efficiency and in-vitro drug release of the selected formula. VLP-NLCs displayed narrow size distribution, spherical morphologies that were nanosized (105 ± 2.3 nm), and significant drug entrapment efficiencies (> 80%). Particle size ranged between 105 ± 2.3 to 1399 ± 2.8 nm and zeta potential between -14.6 ± 0.2 to -46.0 ± 1.1 mV. High entrapping efficiency was obtained due to incorporation of liquid lipid. The In Vitro release showed prolonged time dependent release. NLC 6 had the best results among the eight prepared formulae. These findings show that NLC is a potential carrier to improve the solubility of drug and enhance its bioavailability.
View on SCiNiTO
Top