基于分离乳清蛋白的微凝胶靶向小鼠肾脏递送方案。

IF 1 Q3 BIOLOGY
Oksana A Mayorova, Mariia S Saveleva, Daria A Terentyeva, Olga I Gusliakova, Olga A Sindeeva
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引用次数: 0

摘要

每年,慢性肾脏疾病的病例数量都在增加,延迟开始适当的治疗可能导致肾衰竭,这需要定期透析或移植。用于治疗肾脏疾病的强化全身治疗通常会对其他虚弱的器官产生负面影响,因此确保药物直接靶向递送到肾脏并最大限度地减少全身副作用至关重要。为了降低药物的毒性和减少剂量,人们正在开发创新的给药方法,例如微型靶向给药系统,它确保了胶囊化药物直接在器官内的高效分布。在最近的一篇文章中,我们提出了用分离乳清蛋白(WPI)稳定的创新乳化微凝胶,专门设计用于靶向药物递送到肾脏。我们的稳定性研究表明,这些微凝胶在72小时后开始降解,这种降解表现出时间依赖性。此外,通过尾静脉静脉给药的微凝胶悬浮液在肝脏和肾脏中选择性积累了5天。作为我们研究的一部分,我们提出了从分离乳清蛋白中合成乳状微凝胶的方案。本文提供了前驱体制备过程的全面概述,以及乳液体系随时间稳定性的深入研究。该方案还包括将乳状微凝胶悬浮液注射到小鼠尾静脉中,以评估其生物相容性和潜在的治疗效果。本方案概述了在实验的每个阶段应考虑的预防措施和重要的细微差别。•本协议提供了详细的说明,合成荧光标记的乳液微凝胶使用粘接乳清蛋白分离,允许复制这一过程。•该协议详细描述了如何准备共聚焦显微镜样品。•我们正在探索一种通过光学显微镜分析乳化液液滴大小来研究乳化液微凝胶稳定性的方法。•我们指导将悬浮液注入小鼠尾静脉,然后可视化微凝胶的体内生物分布。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Protocol of Whey Protein Isolate-Based Microgel Targeted Delivery in Mouse Kidney.

Every year, there is an increase in the number of cases of chronic kidney disease, and a delay in the initiation of adequate treatment can lead to kidney failure, which requires regular dialysis or transplantation. Intensive systemic therapy used to treat kidney diseases often has a negative impact on other weakened organs, making it crucial to ensure targeted delivery of medications directly to the kidneys and to minimize systemic side effects. In order to reduce the toxicity of medications and decrease dosages, innovative delivery methods are being developed, such as micro-sized targeted delivery systems, which ensure highly effective distribution of encapsulated drugs directly within the organs. In a recent article, we presented innovative emulsified microgels stabilized with whey protein isolate (WPI), specifically designed for targeted drug delivery to the kidneys. Our stability studies revealed that these microgels start to degrade after 72 h, with this degradation exhibiting a time-dependent profile. Furthermore, intravenous administration of the microgel suspension through the tail vein showed significant selective accumulation in both the liver and kidneys over a duration of 5 days. As part of our research, we present the protocol for synthesizing emulsion microgels derived from whey protein isolate. This article provides a comprehensive overview of the procedures for precursor preparation, along with an in-depth investigation of the emulsion system's stability over time. The protocol also includes the injection of an emulsion microgel suspension into the tail vein of mice, enabling the evaluation of their biocompatibility and potential therapeutic efficacy. This protocol outlines the precautions and important nuances that should be considered at each stage of the experiment. Key features • This protocol provides detailed instructions on the synthesis of fluorescently labeled emulsion microgels using mucoadhesive whey protein isolate, allowing the replication of this process. • The protocol describes in detail how to prepare samples for confocal microscopy. • We are exploring a method to study the stability of emulsion microgels by analyzing the size of emulsion droplets using optical microscopy. • We provide guidance on the administration of suspension into the tail vein of mice, followed by visualization of the microgels' body biodistribution.

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