Visualizing and quantifying drug uptake in skin

C. Evans, K. F. Chan, T. Prow, Sam Osseiran
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引用次数: 2

Abstract

The study of drug uptake, distribution, and activity within skin is a necessary but problematic requirement in the development and translation of compounds from the bench to the bedside. Drug delivery into the skin is highly complex, due in part to the natural barrier function of the stratum corneum in addition to the many different routes of transdermal entry of drugs. Moreover, skin is not uniform throughout the body or across age groups. For example, epidermal thickness changes 30-fold from the thick skin of the fingertips (485 m) to the thin skin of the face and eyelids (17 m).1 Transdermal delivery can occur over a wide range of timescales (from seconds to hours), and the number of potential cellular targets necessitates quantification on the micrometer scale.2 Optical imaging tools are well-suited to meet these challenges, in particular for the uptake of drugs within the first millimeter of skin. Fluorescence, Raman, and nonlinear optical imaging techniques offer subcellular resolution, rapid real-time 3D image acquisition, and the ability to quantitatively analyze imaging data for both pharmacokinetic and pharmacodynamic information. Optical tools are unique in that they also offer the ability to quantify drugs via phenomena that emerge from their structure, including light absorption, fluorescence, and molecular vibrations. This is particularly useful as most pharmaceuticals are small molecules, where modification to include a reporter can completely change the behavior and thus uptake of the compound. Fluorescence imaging methods can be particularly powerful in measuring the uptake and distribution of drugs. We have been developing a topical acne gel, BPX-01, that is currently in a clinical Phase 2b dose-finding study. BPX-01 is an anhydrous hydrophilic topical gel with solubilized minocycline for enhanced cutaneous delivery and bioavailability to target Figure 1. Conventional fluorescence microscopy images of ex vivo human facial skin specimens. (a) Control, and those treated with (b) 1% BPX-01 (a topical acne gel) and (c) 4% BPX-01 at 24 hours. Minocycline fluorescence is shown in red.
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皮肤中药物摄取的可视化和量化
研究药物在皮肤内的吸收、分布和活性是一个必要但有问题的要求,在开发和转化化合物从实验室到床边。药物进入皮肤是非常复杂的,部分原因是角质层的天然屏障功能以及药物经皮进入的许多不同途径。此外,全身或不同年龄层的皮肤并不均匀。例如,从指尖的厚皮肤(485米)到面部和眼睑的薄皮肤(17米),表皮厚度变化了30倍透皮给药可以发生在很宽的时间尺度范围内(从几秒到几小时),潜在细胞靶标的数量需要在微米尺度上进行量化光学成像工具非常适合应对这些挑战,特别是在皮肤的第一毫米内吸收药物。荧光、拉曼和非线性光学成像技术提供亚细胞分辨率、快速实时3D图像采集以及定量分析成像数据的能力,以获得药代动力学和药效学信息。光学工具的独特之处在于,它们还提供了通过从其结构中出现的现象(包括光吸收、荧光和分子振动)来量化药物的能力。这是特别有用的,因为大多数药物都是小分子,其中修改包括一个报告可以完全改变行为,从而吸收化合物。荧光成像方法在测量药物的摄取和分布方面特别有效。我们一直在开发一种局部痤疮凝胶BPX-01,目前正处于临床2b期剂量研究中。BPX-01是一种无水亲水性外用凝胶,可溶解二甲胺四环素,增强皮肤给药和靶向生物利用度。离体人体面部皮肤标本的常规荧光显微镜图像。(a)对照组和(b) 1% BPX-01(一种局部痤疮凝胶)和(c) 4% BPX-01治疗24小时的对照组。米诺环素荧光显示为红色。
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