Zhang Jikai, Bahar Duygu, Ong Hui Ling, Arnold Peter, Zhang Meng, Jiang Yunhong, Tao Ran, Haworth Luke, Yang Xin, Brain Chelsea, Rahmati Mohammad, Torun Hamdi, Wu Qiang, Luo Jingting, Fu Yong-Qing
Faculty of Engineering and Environment, Northumbria University, Newcastle Upon Tyne, Newcastle, NE1 8ST, UK.
Hub for Biotechnology in the Built Environment, Department of Applied Sciences, Faculty of Health and Life Sciences, Northumbria University at Newcastle, Newcastle Upon Tyne, NE1 8ST, UK.
Drug Deliv Transl Res. 2025 Apr;15(4):1363-1375. doi: 10.1007/s13346-024-01682-y. Epub 2024 Aug 6.
Transdermal drug delivery provides therapeutic benefits over enteric or injection delivery because its transdermal routes provide more consistent concentrations of drug and avoid issues of drugs affecting kidneys and liver functions. Many technologies have been evaluated to enhance drug delivery through the relatively impervious epidermal layer of the skin. However, precise delivery of large hydrophilic molecules is still a great challenge even though microneedles or other energized (such as electrical, thermal, or ultrasonic) patches have been used, which are often difficult to be integrated into small wearable devices. This study developed a flexible surface acoustic wave (SAW) patch platform to facilitate transdermal delivery of macromolecules with fluorescein isothiocyanates up to 2000 kDa. Two surrogates of human skin were used to evaluate SAW based energized devices, i.e., delivering dextran through agarose gels and across stratum corneum of pig skin into the epidermis. Results showed that the 2000 kDa fluorescent molecules have been delivered up to 1.1 mm in agarose gel, and the fluorescent molecules from 4 to 2000 kDa have been delivered up to 100 µm and 25 µm in porcine skin tissue, respectively. Mechanical agitation, localised streaming, and acousto-thermal effect generated on the skin surface were identified as the main mechanisms for promoting drug transdermal transportation, although micro/nanoscale acoustic cavitation induced by SAWs could also have its contribution. SAW enhanced transdermal drug delivery is dependent on the combined effects of wave frequency and intensity, duration of applied acoustic waves, temperature, and drug molecules molecular weights.
经皮给药相对于肠道给药或注射给药具有治疗优势,因为其经皮途径能使药物浓度更稳定,并避免药物影响肝肾功能的问题。人们已经评估了许多技术,以增强药物透过相对致密的皮肤表皮层的递送。然而,即使使用了微针或其他能量激发(如电、热或超声)贴片,精确递送大的亲水分子仍然是一个巨大的挑战,这些贴片通常难以集成到小型可穿戴设备中。本研究开发了一种柔性表面声波(SAW)贴片平台,以促进高达2000 kDa的异硫氰酸荧光素大分子的经皮递送。使用两种人类皮肤替代物来评估基于SAW的能量激发装置,即通过琼脂糖凝胶递送葡聚糖并穿过猪皮肤的角质层进入表皮。结果表明,2000 kDa的荧光分子在琼脂糖凝胶中的递送深度可达1.1 mm,4至2000 kDa的荧光分子在猪皮肤组织中的递送深度分别可达100 µm和25 µm。皮肤表面产生的机械搅拌、局部流动和声热效应被确定为促进药物经皮运输的主要机制,尽管SAW诱导的微/纳米级声空化也可能有其作用。SAW增强的经皮给药取决于波频率和强度、施加声波的持续时间、温度以及药物分子分子量的综合作用。