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用于实验性耳鼻咽喉科学的内耳膜模拟物的开发

The Development of Inner Ear Membrane Analog for Experimental Otorhinolaryngology.

作者信息

Riabinin A A, Rogovaya O S, Kryukov A I, Kunelskaya N L, Yanyushkina E S, Mischenko V V, Ilyin M M, Shershunova E A, Voyevodin V V, Nebogatkin S V, Pomanov K I, Vorotelyak E A

机构信息

Research Engineer, Laboratory of Cell Biology; Koltzov Institute of Developmental Biology of the Russian Academy of Sciences, 26 Vavilov St., Moscow, 119334, Russia.

Senior Researcher, Laboratory of Cell Biology; Koltzov Institute of Developmental Biology of the Russian Academy of Sciences, 26 Vavilov St., Moscow, 119334, Russia.

出版信息

Sovrem Tekhnologii Med. 2025;17(3):5-14. doi: 10.17691/stm2025.17.3.01. Epub 2025 Jun 30.

Abstract

UNLABELLED

was to develop and evaluate a model of the human round window membrane (mRWM) of the inner ear that is suitable for representative studies of drug permeation and cytotoxicity.

BIOLOGICAL PART OF THE STUDY

Several substrate options were tested to create the mRWM, including 2 variants of Viscoll collagen membranes (IMTEK, Russia) and a multi-component G-Derm membrane (G-DERM, Russia). In the first variant, only HaCaT epithelial cells were seeded on the membranes, and in the second variant, primary human dermal fibroblasts were seeded together with HaCaT epithelial cells (sequential application). The obtained mRWM were evaluated by morphological criteria using histochemical methods. As a result, the decision was made to use mRWM constructed on Viscoll membranes with the inclusion of both primary fibroblasts and human epithelial cells.

TECHNICAL PART OF THE STUDY

A series of scientific experiments has been performed on the obtained mRWM aimed at studying the permeability and developing modes of electrophysical action on this biological barrier while maintaining its morphological and functional integrity and ensuring accelerated passage of dexamethasone through it. To accelerate the passage of dexamethasone across the mRWM, the electrophysical system initiated targeted iontophoresis of negatively charged dexamethasone molecules in parallel with electroporation of cell membranes in the sample. After the exposure, the residual viability of mRWM was assessed by histochemical staining with calcein and propidium iodide. The change in dexamethasone concentration after passage across the mRWM was assessed using a highly sensitive chromatograph.

CONCLUSION

During the optimization of the mRWM fabrication protocol and the selection of suitable substrate components and cellular material, the model based on a thin Viscoll collagen membrane has been chosen as a substrate and primary human dermal fibroblasts and epithelial cells of the HaCaT line as a cellular material. The obtained experimental samples of mRWM represent a semipermeable membrane with living cells on the surface and are an alternative analog of the native structure, reproducing its geometric and morphofunctional characteristics. In addition, there has been demonstrated a method of using the for preclinical studies of electrophysical devices designed for accelerated passage of target substances through this membrane using electroporative and iontophoretic effects.

摘要

未标注

旨在开发并评估一种适合用于药物渗透和细胞毒性代表性研究的人内耳圆窗膜(mRWM)模型。

研究的生物学部分

测试了几种用于创建mRWM的底物选项,包括Viscoll胶原膜的2种变体(俄罗斯IMTEK公司)和一种多组分G-Derm膜(俄罗斯G-DERM公司)。在第一种变体中,仅将HaCaT上皮细胞接种在膜上,在第二种变体中,将原代人皮肤成纤维细胞与HaCaT上皮细胞一起接种(顺序应用)。使用组织化学方法通过形态学标准评估获得的mRWM。结果,决定使用基于Viscoll膜构建的mRWM,其中包含原代成纤维细胞和人上皮细胞。

研究的技术部分

对获得的mRWM进行了一系列科学实验,旨在研究其渗透性以及对该生物屏障进行电物理作用的方式,同时保持其形态和功能完整性,并确保地塞米松加速通过它。为了加速地塞米松穿过mRWM,电物理系统在对样品中的细胞膜进行电穿孔的同时,启动带负电荷的地塞米松分子的靶向离子导入。暴露后,使用钙黄绿素和碘化丙啶进行组织化学染色评估mRWM的残余活力。使用高灵敏度色谱仪评估地塞米松穿过mRWM后的浓度变化。

结论

在优化mRWM制备方案以及选择合适的底物成分和细胞材料的过程中,已选择基于薄Viscoll胶原膜的模型作为底物,并选择原代人皮肤成纤维细胞和HaCaT系上皮细胞作为细胞材料。获得的mRWM实验样品代表一种表面有活细胞的半透膜,是天然结构的替代类似物,再现了其几何和形态功能特征。此外,还展示了一种使用该模型对旨在通过电穿孔和离子导入作用加速目标物质通过该膜的电物理装置进行临床前研究的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce08/12261290/8f68382ff143/STM-17-3-01-f1.jpg

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