猪皮肤的体内、原位和离体比较,用于微注射阵列穿透深度、递送效率和弹性模量评估。

Jonathan C. J. Wei, Ian D. Cartmill, M. Kendall, M. Crichton
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引用次数: 2

摘要

随着可穿戴技术的发展,皮肤和设备的界面特性变得更加重要。出于研发目的,猪皮通常用于评估设备性能,但体内、原位和离体猪皮机械性能之间的差异可能会在技术开发过程中误导研究人员。在这项研究中,我们研究了有灌注和无灌注时(体内组织与体外组织)机械性能的显著变化。本研究的设备重点是皮肤靶向纳米疫苗微针设备,用于评估由于不同组织条件导致的关键皮肤接触参数(穿透深度和递送效率)的变化。用荧光或14C放射性标记的制剂包被贴片,用于体内和死后4小时的时间点的穿透深度和递送效率定量。血液循环立即停止后,微针的平均穿透深度从~100μm下降到~55μm(~45%)。由于尸僵导致的下层组织硬化,然后在4小时的时间点将穿透深度增加到~100μm,与体内相比差异不大(p=0.0595)。在这个时间点,也观察到制剂进入皮肤的最高递送效率(在皮肤中测量的剂量,不包括皮肤和贴片表面的剩余剂量)为~25%,高于体内的~2%。本文获得的数据促进了医疗设备的开发,强调了在评估尸体原型时需要考虑状态和肌肉组织。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In vivo, in situ and ex vivo comparison of porcine skin for microprojection array penetration depth, delivery efficiency and elastic modulus assessment.
With the development of wearable technologies, the interfacial properties of skin and devices have become much more important. For research and development purposes, porcine skin is often used to evaluate device performance, but the differences between in vivo, in situ and ex vivo porcine skin mechanical properties can potentially misdirect investigators during the development of their technology. In this study, we investigated the significant changes to mechanical properties with and without perfusion (in vivo versus in vitro tissue). The device focus for this study was a skin-targeting Nanopatch vaccine microneedle device, employed to assess the variance to key skin engagement parameters - penetration depth and delivery efficiency - due to different tissue conditions. The patches were coated with fluorescent or 14C radiolabelled formulations for penetration depth and delivery efficiency quantification in vivo, and at time points up to 4 h post mortem. An immediate cessation of blood circulation saw mean microneedle penetration depth fell from ∼100 μm to ∼55 μm (∼45%). Stiffening of underlying tissues as a result of rigor mortis then augmented the penetration depths at the 4 h timepoint back to ∼100 μm, insignificantly different (p = 0.0595) when compared with in vivo. The highest delivery efficiency of formulation into the skin (dose measured in the skin excluding leftover dose on skin and patch surfaces) was also observed at this time point of ∼25%, up from ∼2% in vivo. Data obtained herein progresses medical device development, highlighting the need to consider the state and muscle tissues when evaluating prototypes on cadavers.
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