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原位形成 PLGA 植入物:朝着毒性更低的溶剂发展。

In-situ forming PLGA implants: Towards less toxic solvents.

机构信息

Univ. Lille, Inserm, CHU Lille, U1008, F-59000 Lille, France; Univ. Lille, CNRS, INRAE, Centrale Lille, UMR 8207 UMET, F-59000 Lille, France.

Univ. Lille, CNRS, INRAE, Centrale Lille, UMR 8207 UMET, F-59000 Lille, France.

出版信息

Int J Pharm. 2024 May 25;657:124121. doi: 10.1016/j.ijpharm.2024.124121. Epub 2024 Apr 15.

Abstract

In-situ forming poly(lactic-co-glycolic acid) (PLGA) implants offer a great potential for controlled drug delivery for a variety of applications, e.g. periodontitis treatment. The polymer is dissolved in a water-miscible solvent. The drug is dissolved or dispersed in this solution. Upon contact with aqueous body fluids, the solvent diffuses into the surrounding tissue and water penetrates into the formulation. Consequently, PLGA precipitates, trapping the drug. Often, N-methyl-2-pyrrolidine (NMP) is used as a water-miscible solvent. However, parenteral administration of NMP raises toxicity concerns. The aim of this study was to identify less toxic alternative solvent systems for in-situ forming PLGA implants. Various blends of polyethylene glycol 400 (PEG 400), triethyl citrate (TEC) and ethanol were used to prepare liquid formulations containing PLGA, ibuprofen (as an anti-inflammatory drug) and/or chlorhexidine dihydrochloride (as an antiseptic agent). Implant formation and drug release kinetics were monitored upon exposure to phosphate buffer pH 6.8 at 37 °C. Furthermore, the syringeability of the liquids, antimicrobial activity of the implants, and dynamic changes in the latter's wet mass and pH of the release medium were studied. Importantly, 85:10:5 and 60:30:10 PEG 400:TEC:ethanol blends provided good syringeability and allowed for rapid implant formation. The latter controlled ibuprofen and chlorhexidine release over several weeks and assured efficient antimicrobial activity. Interestingly, fundamental differences were observed concerning the underlying release mechanisms of the two drugs: Ibuprofen was dissolved in the solvent mixtures and partially leached out together with the solvents during implant formation, resulting in relatively pronounced burst effects. In contrast, chlorhexidine dihydrochloride was dispersed in the liquids in the form of tiny particles, which were effectively trapped by precipitating PLGA during implant formation, leading to initial lag-phases for drug release.

摘要

原位形成的聚(乳酸-共-乙醇酸)(PLGA)植入物为各种应用(例如牙周炎治疗)的药物控制释放提供了巨大的潜力。聚合物溶解在可与水混溶的溶剂中。药物溶解或分散在该溶液中。与水性体液接触时,溶剂扩散到周围组织中,水渗透到制剂中。因此,PLGA 沉淀,捕获药物。通常,N-甲基-2-吡咯烷酮(NMP)用作可与水混溶的溶剂。然而,NMP 的 体 内 给 药 会 引 起 毒 性 关 注。本研究的目的是确定用于原位形成 PLGA 植入物的毒性较低的替代溶剂系统。使用各种聚乙二醇 400(PEG 400)、柠檬酸三乙酯(TEC)和乙醇的混合物来制备含有 PLGA、布洛芬(作为抗炎药)和/或盐酸洗必泰(作为防腐剂)的液体制剂。在 37°C 下暴露于 pH 6.8 的磷酸盐缓冲液中时,监测植入物的形成和药物释放动力学。此外,研究了液体的可注射性、植入物的抗菌活性以及后者湿重和释放介质 pH 的动态变化。重要的是,85:10:5 和 60:30:10 的 PEG 400:TEC:乙醇混合物提供了良好的可注射性,并允许快速形成植入物。后者控制布洛芬和洗必泰在数周内释放,并确保有效的抗菌活性。有趣的是,观察到两种药物的基本释放机制存在差异:布洛芬溶解在溶剂混合物中,并在植入物形成过程中与溶剂一起部分浸出,导致相对明显的突释效应。相比之下,盐酸洗必泰以微小颗粒的形式分散在液体中,在植入物形成过程中有效地被沉淀的 PLGA 捕获,导致药物释放的初始滞后期。

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