Physicochemical characterization and molecular modeling study of host–guest systems of aripiprazole and functionalized cyclodextrins

Author:

Tănase Ionuț-Mihai,Sbârcea Laura,Ledeți Adriana,Vlase Gabriela,Barvinschi Paul,Văruţ Renata-Maria,Dragomirescu Anca,Axente Carmen,Ledeți Ionuț

Publisher

Springer Science and Business Media LLC

Reference49 articles.

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2. Casey AB, Canal CE. Classics in chemical neuroscience: aripiprazole. ACS Chem Neurosci. 2017;8(6):1135–46.

3. Abdelbary AA, Elshafeey AH, El-Nabarawi M, Elassasy A, Li X, Jasti B. Comparative in vivo evaluation of aripiprazole coprecipitate, nanoparticles and marketed tablets in healthy human volunteers and in vitro-in vivo correlation. Curr Trends Biotechnol Pharm. 2011;5(4):1397–409.

4. Silki, Sinha VR. Enhancement of in vivo efficacy and oral bioavailability of aripiprazole with solid lipid nanoparticles. AAPS PharmSciTech. 2018;19(3):1264–73.

5. Brittain HG. Aripiprazole: polymorphs and solvatomorphs. In: Brittain HG, editor. Profile of drug substances, excipients and related metodology, vol. 37. Amsterdam: Esevier; 2012. p. 1–29.

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