| Literature DB >> 34201567 |
Vasiliki Karava1, Aggeliki Siamidi1, Marilena Vlachou1, Evi Christodoulou2, Nikolaos D Bikiaris2, Alexandra Zamboulis2, Margaritis Kostoglou3, Eleni Gounari4,5, Panagiotis Barmpalexis6.
Abstract
The present study evaluates the use of newly synthesized poly(l-lactic acid)-co-poly(butylene adipate) (PLA/PBAd) block copolymers as microcarriers for the preparation of aripiprazole (ARI)-loaded long acting injectable (LAI) formulations. The effect of various PLA to PBAd ratios (95/5, 90/10, 75/25 and 50/50 w/w) on the enzymatic hydrolysis of the copolymers showed increasing erosion rates by increasing the PBAd content, while cytotoxicity studies revealed non-toxicity for all prepared biomaterials. SEM images showed the formation of well-shaped, spherical MPs with a smooth exterior surface and no particle's agglomeration, while DSC and pXRD data revealed that the presence of PBAd in the copolymers favors the amorphization of ARI. FTIR spectroscopy showed the formation of new ester bonds between the PLA and PBAd parts, while analysis of the MP formulations showed no molecular drug-polyester matrix interactions. In vitro dissolution studies suggested a highly tunable biphasic extended release, for up to 30 days, indicating the potential of the synthesized copolymers to act as promising LAI formulations, which will maintain a continuous therapeutic level for an extended time period. Lastly, several empirical and mechanistic models were also tested, with respect to their ability to fit the experimental release data.Entities:
Keywords: aripiprazole; block copolymers; long acting injectables; microparticles; poly(butylene adipate); poly(l-lactic acid); sustained release
Year: 2021 PMID: 34201567 DOI: 10.3390/pharmaceutics13070930
Source DB: PubMed Journal: Pharmaceutics ISSN: 1999-4923 Impact factor: 6.321