Karava Vasiliki, Siamidi Aggeliki, Vlachou Marilena, Christodoulou Evi, Bikiaris Nikolaos D, Zamboulis Alexandra, Kostoglou Margaritis, Gounari Eleni, Barmpalexis Panagiotis
Department of Pharmacy, Section of Pharmaceutical Technology, Zografou Campus, National and Kapodistrian University of Athens, 15784 Athens, Greece.
Department of Chemistry, Laboratory of Polymer Chemistry and Technology, Aristotle University of Thessaloniki, 54124 Thessaloniki, Greece.
Pharmaceutics. 2021 Jun 23;13(7):930. doi: 10.3390/pharmaceutics13070930.
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 /) 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.
本研究评估了新合成的聚(L-乳酸)-共聚(己二酸丁二酯)(PLA/PBAd)嵌段共聚物作为微载体用于制备载阿立哌唑(ARI)长效注射剂(LAI)制剂的情况。各种PLA与PBAd比例(95/5、90/10、75/25和50/50)对共聚物酶促水解的影响表明,随着PBAd含量的增加,侵蚀速率加快,而细胞毒性研究表明所有制备的生物材料均无毒性。扫描电子显微镜(SEM)图像显示形成了形状良好的球形微球,其外表面光滑且无颗粒团聚,而差示扫描量热法(DSC)和粉末X射线衍射(pXRD)数据表明,共聚物中PBAd的存在有利于ARI的非晶化。傅里叶变换红外光谱(FTIR)显示PLA和PBAd部分之间形成了新的酯键,而微球制剂分析表明不存在分子药物-聚酯基质相互作用。体外溶出研究表明,长达30天具有高度可调的双相缓释特性,这表明合成的共聚物有潜力作为有前景的LAI制剂,可在较长时间内维持持续的治疗水平。最后,还测试了几种经验模型和机理模型对实验释放数据的拟合能力。