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石墨烯生物传感器在人类干细胞治疗效力分析中的优势。

Advantages of Graphene Biosensors for Human Stem Cell Therapy Potency Assays.

机构信息

Faculty of Medical Engineering, University Politehnica of Bucharest, Gh. Polizu 1-7, 011061 Bucharest, Romania.

Advanced Polymer Materials Group, University Politehnica of Bucharest, Gh. Polizu 1-7, 011061 Bucharest, Romania.

出版信息

Biomed Res Int. 2018 May 29;2018:1676851. doi: 10.1155/2018/1676851. eCollection 2018.

Abstract

Regenerative medicine is challenged by the need to conform to rigorous guidelines for establishing safe and effective development and translation of stem cell-based therapies. Counteracting widespread concerns regarding unproven cell therapies, stringent cell-based assays seek not only to avoid harm but also to enhance quality and efficacy. Potency indicates that the cells are functionally fit for purpose before they are administered to the patient. It is a paramount quantitative critical quality attribute serving as a decisive release criterion. Given a broad range of stem cell types and therapeutic contexts the potency assay often comprises one of the most demanding hurdles for release of a cell therapy medicinal product. With need for improved biomarker assessment and expedited measurement, recent advances in graphene-based biosensors suggest that they are poised to be valuable platforms for accelerating potency assay development. Among several potential advantages, they offer versatility for sensitive measurement of a broad range of potential biomarker types, cell biocompatibility for direct measurement, and small sample sufficiency, plus ease of use and point-of-care applicability.

摘要

再生医学面临着需要符合严格的指导方针,以确保安全有效的开发和转化基于干细胞的疗法。为了应对人们对未经证实的细胞疗法的广泛担忧,严格的基于细胞的检测不仅旨在避免伤害,还旨在提高质量和疗效。效力表明,在将细胞施用于患者之前,细胞在功能上适合于特定用途。它是一个至关重要的定量关键质量属性,是决定性的放行标准。鉴于广泛的干细胞类型和治疗环境,效力检测通常是放行细胞治疗药物产品的最具挑战性的障碍之一。由于需要改进生物标志物评估和加速测量,基于石墨烯的生物传感器的最新进展表明,它们有望成为加速效力检测开发的有价值的平台。在几个潜在优势中,它们提供了广泛的潜在生物标志物类型的敏感测量的多功能性、用于直接测量的细胞生物相容性以及小样本量的充足性,加上易于使用和即时应用的便利性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58cf/5996421/3b093ae8ea9b/BMRI2018-1676851.001.jpg

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