Design and optimization of ganciclovir solid dispersion for improving its bioavailability

• Published in: Drug delivery 2022-12, Vol.29 (1), p.1836-1847
• Main Authors: Gaber, Dalia A., Alnwiser, Manar A., Alotaibi, Nadia L., Almutairi, Rawan A., Alsaeed, Sumaih S., Abdoun, Siham A., Alsubaiyel, Amal M.
• Format: Article
• Language: English
• Subjects: Administration, Oral; Animals; Antiviral Agents; Antiviral drugs; Bioavailability; Biological Availability; Calorimetry, Differential Scanning; cyclodextrin; Drug Carriers - chemistry; factorial design; Ganciclovir; Gancyclovir; nanoparticles; Nanoparticles - chemistry; Particle Size; Permeability; Pharmacokinetics; Rabbits; shellac; solid dispersion; Solubility
• ISSN: 1071-7544; 1521-0464
• DOI: 10.1080/10717544.2022.2083723

Development of new approaches for oral delivery of an existing antiviral drug aimed to enhance its permeability and hence bioavailability. Ganciclovir (GC) is an antiviral drug that belongs to class III in biopharmaceutical classification. The encapsulation of poorly absorbed drugs within nanosized particles offers several characteristics to drug due to their acquired surface properties. In the following study, the solvent evaporation technique was used to incorporate GC, within elegant nanosize particles using cyclodextrin and shellac polymers for enhancing its permeability and release pattern. Formulation variables were optimized using 2 3 full factorial design. The prepared formulations were assessed for yield, particle size, content, and micromeritics behavior. The optimized formula (F6) was identified through differential scanning calorimetry and Fourier transform infrared. In vitro release and stability were also assessed. Pharmacokinetic parameters of optimized nano GC solid dispersion particles (NGCSD-F6) were finally evaluated. The optimized formula (F6) showed a mean particle size of 288.5 ± 20.7 nm, a zeta potential of about 23.87 ± 2.27, and drug content 95.77 ± 2.1%. The in vitro drug release pattern of F6 showed an initial burst release followed by a sustained release over the next 12 h. The optimized formula showed accepted stability upon storage at room and refrigerator temperatures for 6 months with good flowing properties (Carr's index = 18.28 ± 0.44). In vivo pharmacokinetic study in rabbits revealed 2.2 fold increases in the bioavailability of GC compared with commercial convention tablets. The study affords evidence for the success of the solid dispersion technique under specified conditions in improvement of bioavailability of GC.