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通过机械测试对可注射性进行量化

The Quantification of Injectability by Mechanical Testing.

作者信息

Robinson Thomas E, Hughes Erik A B, Eisenstein Neil M, Grover Liam M, Cox Sophie C

机构信息

School of Chemical Engineering, University of Birmingham;

School of Chemical Engineering, University of Birmingham.

出版信息

J Vis Exp. 2020 May 13(159). doi: 10.3791/61417.

Abstract

Injectable biomaterials are becoming increasingly popular for the minimally invasive delivery of drugs and cells. These materials are typically more viscous than traditional aqueous injections and may be semi-solid, therefore, their injectability cannot be assumed. This protocol describes a method to objectively assess the injectability of these materials using a standard mechanical tester. The syringe plunger is compressed by the crosshead at a set rate, and the force is measured. The maximum or plateau force value can then be used for comparison between samples, or to an absolute force limit. This protocol can be used with any material, and any syringe and needle size or geometry. The results obtained may be used to make decisions about formulations, syringe and needle sizes early in the translational process. Further, the effects of altering formulations on injectability may be quantified, and the optimum time to inject temporally changing materials determined. This method is also suitable as a reproducible way to examine the effects of injection on a material, to study phenomena such as self-healing and filter pressing or study the effects of injection on cells. This protocol is faster and more directly applicable to injectability than rotational rheology, and requires minimal post processing to obtain key values for direct comparisons.

摘要

可注射生物材料在药物和细胞的微创递送方面越来越受欢迎。这些材料通常比传统的水性注射剂更粘稠,可能是半固体,因此,不能想当然地认为它们具有可注射性。本方案描述了一种使用标准机械测试仪客观评估这些材料可注射性的方法。注射器柱塞由十字头以设定速率压缩,并测量力。然后,最大或平台力值可用于样品之间的比较,或与绝对力极限进行比较。本方案可用于任何材料,以及任何注射器和针头尺寸或几何形状。所获得的结果可用于在转化过程的早期对配方、注射器和针头尺寸做出决策。此外,可以量化改变配方对可注射性的影响,并确定注射随时间变化的材料的最佳时间。该方法也适合作为一种可重复的方式来检查注射对材料的影响,研究诸如自愈和压滤等现象,或研究注射对细胞的影响。与旋转流变学相比,该方案用于评估可注射性更快、更直接,并且需要最少的后处理来获得用于直接比较的关键值。

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