Formulation Optimization and Real-Time Size Monitoring in the Semi-Continuous Production of Edaravone-Loaded Lipid-Based Nanocarriers Using the Microfluidizer® Technology: Part 2.

IF 4.7 3区 医学 Q1 PHARMACOLOGY & PHARMACY
Christina Glader, Ramona Jeitler, Yan Wang, Jesús Alberto Afonso Urich, Carolin Tetyczka, Philippe Caisse, Steve Mesite, Vanessa Bourgeaux, Johannes Khinast, Eva Roblegg
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Abstract

Recently, we established a semi-continuous top-down process enabling the solvent-free production of drug-free lipid-based nanosystems. In this study, the applicability of the established process line to drug-loaded nanosystems was evaluated, focusing on whether process parameters require adjustment upon drug incorporation. Edaravone was selected as a model drug and encapsulated in nanostructured lipid carriers (NLC) composed of Precirol® ATO 5 or Gelucire® 43/01 as solid lipids, combined with Labrafac™ Lipophile WL 1349 or Capryol® 90 as liquid lipids, as well as in nanoemulsions (NEs) consisting solely of the liquid lipids. Integration of the NanoFlowSizer enabled real-time size monitoring via spatially resolved dynamic light scattering (SR-DLS) during Microfluidizer® processing and allowed detection of potential formulation instabilities caused by altered intermolecular interactions following drug incorporation. Design of Experiments (DoE) was employed to optimize encapsulation efficiency (EE%) and loading capacity (LC%). Initial lipid screening revealed superior compatibility of Labrafac™ Lipophile WL 1349 over Capryol® 90 with both solid lipids and edaravone. Gelucire®-based NLC achieved EE% and LC% up to 47% and 0.9%, respectively, while Labrafac™-based NEs reached 86% EE% and 1.7% LC%. Higher drug concentrations (2%) led to increased NLC sizes compared to lower concentrations (0.8%). Lipid type was identified as the most influential formulation parameter, while the solid to liquid lipid ratio and drug concentration had minor effects. Combining inline and offline SR-DLS measurements enabled early detection of subtle instabilities such as micelle formation and particle agglomeration, outperforming conventional offline DLS. Overall, the findings underscore the versatility and robustness of the semi-continuous, solvent-free production line with integrated SR-DLS as a powerful platform for the efficient development of lipid-based nanocarriers with improved drug loading, stability, and process control.

使用微流化器®技术半连续生产依达拉奉负载脂基纳米载体的配方优化和实时尺寸监测:第2部分。
最近,我们建立了一种半连续自上而下的工艺,使无溶剂生产无药物脂基纳米系统成为可能。在本研究中,评估了所建立的工艺线对载药纳米系统的适用性,重点是在药物掺入时是否需要调整工艺参数。选择依德拉奉作为模型药物,并将其封装在纳米结构脂质载体(NLC)中,该纳米结构脂质载体由Precirol®ATO 5或Gelucire®43/01作为固体脂质,与Labrafac™亲脂剂WL 1349或Capryol®90作为液体脂质,以及仅由液体脂质组成的纳米乳液(NEs)中。在Microfluidizer®处理过程中,NanoFlowSizer的集成通过空间分辨动态光散射(SR-DLS)实现了实时尺寸监测,并允许检测药物掺入后分子间相互作用改变引起的潜在配方不稳定性。采用实验设计(DoE)优化包封效率(EE%)和负载能力(LC%)。最初的脂质筛选显示Labrafac™亲脂剂WL 1349优于Capryol®90与固体脂质和依达拉奉的相容性。基于Gelucire®的NLC分别达到47%和0.9%的EE%和LC%,而基于Labrafac™的NEs达到86%的EE%和1.7%的LC%。与较低浓度(0.8%)相比,较高的药物浓度(2%)导致NLC大小增加。脂质类型是影响最大的处方参数,而料液脂比和药物浓度对其影响较小。结合在线和离线SR-DLS测量,可以早期检测细微的不稳定性,如胶束形成和颗粒团聚,优于传统的离线DLS。总的来说,研究结果强调了半连续、无溶剂生产线的多功能性和稳健性,该生产线集成了SR-DLS,作为高效开发脂基纳米载体的强大平台,具有改进的药物负载、稳定性和过程控制。
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来源期刊
CiteScore
9.60
自引率
2.20%
发文量
248
审稿时长
50 days
期刊介绍: The journal publishes research articles, review articles and scientific commentaries on all aspects of the pharmaceutical sciences with emphasis on conceptual novelty and scientific quality. The Editors welcome articles in this multidisciplinary field, with a focus on topics relevant for drug discovery and development. More specifically, the Journal publishes reports on medicinal chemistry, pharmacology, drug absorption and metabolism, pharmacokinetics and pharmacodynamics, pharmaceutical and biomedical analysis, drug delivery (including gene delivery), drug targeting, pharmaceutical technology, pharmaceutical biotechnology and clinical drug evaluation. The journal will typically not give priority to manuscripts focusing primarily on organic synthesis, natural products, adaptation of analytical approaches, or discussions pertaining to drug policy making. Scientific commentaries and review articles are generally by invitation only or by consent of the Editors. Proceedings of scientific meetings may be published as special issues or supplements to the Journal.
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