Lee Kyeongmin, Cho Eun-Gyung, Choi Youngbo, Kim Yunsik, Lee Jin Hee, Hong Surin
Department of Biotechnology, CHA University, Pocheon 11160, Gyeonggi, Republic of Korea.
Consumer Health 2 Center, CHA Biomedical Research Institute, CHA Bundang Medical Center, CHA University School of Medicine, Seongnam 13496, Gyeonggi, Republic of Korea.
Pharmaceutics. 2025 May 16;17(5):654. doi: 10.3390/pharmaceutics17050654.
: Extracellular vesicles (EVs) are nanoscale, membrane-enclosed structures that play key roles in intercellular communication and biological regulation. Among them, -derived EVs (Lp-EVs) have attracted attention for their anti-inflammatory and anti-aging properties, making them promising candidates for therapeutic and cosmetic use. However, methods for specific detection and quantitative evaluation of Lp-EVs are still limited. This study aims to develop a surface plasmon resonance (SPR)-based sensor system for the precise and selective detection of Lp-EVs. : Anti-p40 antibodies were immobilized on gold thin films to construct an SPR sensing platform. The overexpression of the p40 protein on Lp-EVs was confirmed using flow cytometry and Western blotting. For functional evaluation, Lp-EVs were applied to an artificial skin membrane mounted on a Franz diffusion cell, followed by SPR-based quantification and fluorescence imaging to assess their skin penetration behavior. : The developed SPR sensor demonstrated high specificity and a detection limit of 0.12 µg/mL, with a linear response range from 0.1 to 0.375 µg/mL. It successfully discriminated Lp-EVs from other bacterial EVs. In the skin diffusion assay, Lp-EVs accumulated predominantly in the epidermal layer without penetrating into the dermis, likely due to their negative surface charge and interaction with the hydrophobic epidermal lipid matrix. Fluorescence imaging confirmed this epidermal confinement, which increased over 24 h. : This study presents a sensitive and selective SPR-based platform for detecting Lp-EVs and demonstrates their potential for targeted epidermal delivery. These findings support the use of Lp-EVs in skin-focused therapeutic and cosmetic applications. Future studies will explore strategies such as microneedle-assisted delivery to enhance transdermal penetration and efficacy.
细胞外囊泡(EVs)是纳米级的膜封闭结构,在细胞间通讯和生物调节中发挥关键作用。其中,脂蛋白衍生的细胞外囊泡(Lp-EVs)因其抗炎和抗衰老特性而受到关注,使其成为治疗和美容用途的有前景的候选者。然而,Lp-EVs的特异性检测和定量评估方法仍然有限。本研究旨在开发一种基于表面等离子体共振(SPR)的传感器系统,用于精确和选择性地检测Lp-EVs。:将抗p40抗体固定在金薄膜上,构建SPR传感平台。使用流式细胞术和蛋白质印迹法确认了Lp-EVs上p40蛋白的过表达。为了进行功能评估,将Lp-EVs应用于安装在Franz扩散池上的人工皮肤膜,然后进行基于SPR的定量和荧光成像,以评估它们的皮肤渗透行为。:所开发的SPR传感器显示出高特异性,检测限为0.12μg/mL,线性响应范围为0.1至0.375μg/mL。它成功地将Lp-EVs与其他细菌来源的细胞外囊泡区分开来。在皮肤扩散试验中,Lp-EVs主要积聚在表皮层,未穿透到真皮,这可能是由于它们的表面负电荷以及与疏水性表皮脂质基质的相互作用。荧光成像证实了这种表皮定位,并且在24小时内有所增加。:本研究提出了一种基于SPR的灵敏且选择性的平台,用于检测Lp-EVs,并证明了它们在靶向表皮递送方面的潜力。这些发现支持Lp-EVs在皮肤相关治疗和美容应用中的使用。未来的研究将探索诸如微针辅助递送等策略,以增强透皮渗透和疗效。