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Poly(l-Lactic Acid)-co-poly(Butylene Adipate) New Block Copolymers for the Preparation of Drug-Loaded Long Acting Injectable Microparticles

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...

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Autores principales: Karava, Vasiliki, Siamidi, Aggeliki, Vlachou, Marilena, Christodoulou, Evi, Bikiaris, Nikolaos D., Zamboulis, Alexandra, Kostoglou, Margaritis, Gounari, Eleni, Barmpalexis, Panagiotis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8308927/
https://www.ncbi.nlm.nih.gov/pubmed/34201567
http://dx.doi.org/10.3390/pharmaceutics13070930
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author Karava, Vasiliki
Siamidi, Aggeliki
Vlachou, Marilena
Christodoulou, Evi
Bikiaris, Nikolaos D.
Zamboulis, Alexandra
Kostoglou, Margaritis
Gounari, Eleni
Barmpalexis, Panagiotis
author_facet Karava, Vasiliki
Siamidi, Aggeliki
Vlachou, Marilena
Christodoulou, Evi
Bikiaris, Nikolaos D.
Zamboulis, Alexandra
Kostoglou, Margaritis
Gounari, Eleni
Barmpalexis, Panagiotis
author_sort Karava, Vasiliki
collection PubMed
description 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.
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spelling pubmed-83089272021-07-25 Poly(l-Lactic Acid)-co-poly(Butylene Adipate) New Block Copolymers for the Preparation of Drug-Loaded Long Acting Injectable Microparticles Karava, Vasiliki Siamidi, Aggeliki Vlachou, Marilena Christodoulou, Evi Bikiaris, Nikolaos D. Zamboulis, Alexandra Kostoglou, Margaritis Gounari, Eleni Barmpalexis, Panagiotis Pharmaceutics Article 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. MDPI 2021-06-23 /pmc/articles/PMC8308927/ /pubmed/34201567 http://dx.doi.org/10.3390/pharmaceutics13070930 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Karava, Vasiliki
Siamidi, Aggeliki
Vlachou, Marilena
Christodoulou, Evi
Bikiaris, Nikolaos D.
Zamboulis, Alexandra
Kostoglou, Margaritis
Gounari, Eleni
Barmpalexis, Panagiotis
Poly(l-Lactic Acid)-co-poly(Butylene Adipate) New Block Copolymers for the Preparation of Drug-Loaded Long Acting Injectable Microparticles
title Poly(l-Lactic Acid)-co-poly(Butylene Adipate) New Block Copolymers for the Preparation of Drug-Loaded Long Acting Injectable Microparticles
title_full Poly(l-Lactic Acid)-co-poly(Butylene Adipate) New Block Copolymers for the Preparation of Drug-Loaded Long Acting Injectable Microparticles
title_fullStr Poly(l-Lactic Acid)-co-poly(Butylene Adipate) New Block Copolymers for the Preparation of Drug-Loaded Long Acting Injectable Microparticles
title_full_unstemmed Poly(l-Lactic Acid)-co-poly(Butylene Adipate) New Block Copolymers for the Preparation of Drug-Loaded Long Acting Injectable Microparticles
title_short Poly(l-Lactic Acid)-co-poly(Butylene Adipate) New Block Copolymers for the Preparation of Drug-Loaded Long Acting Injectable Microparticles
title_sort poly(l-lactic acid)-co-poly(butylene adipate) new block copolymers for the preparation of drug-loaded long acting injectable microparticles
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8308927/
https://www.ncbi.nlm.nih.gov/pubmed/34201567
http://dx.doi.org/10.3390/pharmaceutics13070930
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