Biomolecular Sciences Research Centre, Sheffield Hallam University, Howard Street, Sheffield S1 1WB, UK.
PerkinElmer AES (UK) Ltd., Chalfont Road, Seer Green, Beaconsfield HP9 2FX, UK.
Cells. 2023 Dec 21;13(1):24. doi: 10.3390/cells13010024.
Extracellular vesicles (EVs) are lipid bilayer structures released by all cells that mediate cell-to-cell communication via the transfer of bioactive cargo. Because of the natural origin of EVs, their efficient uptake by recipient cells, capacity to stabilize and transport biomolecules and their potential for cell/tissue targeting and preferential uptake by cancer cells, they have enormous potential for bioengineering into improved and targeted drug delivery systems. In this work, we investigated the use of laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) as a tool to measure the loading of platinum-based chemotherapeutic agents. The EV loading of oxaliplatin via co-incubation was demonstrated, and LA-ICP-MS imaging showed greater efficiency of delivery to colorectal cancer cells compared to free oxaliplatin, leading to enhanced cytotoxic effect. Further, the impact of EV co-loading with a porphyrin (C5SHU, known as 'C5') photosensitizer on oxaliplatin delivery was assessed. Fluorescence analysis using nano-flow cytometry showed dose-dependent EV loading as well as a trend towards the loading of larger particles. Exposure of OXA-C5-EV-treated colorectal cancer cells to light indicated that delivery was enhanced by both light exposure and porphyrins, with a synergistic effect on cell viability observed between oxaliplatin, EVs and light exposure after the delivery of the co-loaded EVs. In summary, this work demonstrates the utility of LA-ICP-MS and mass spectrometry imaging in assessing the loading efficiency and cellular delivery of platinum-based therapeutics, which would also be suitable for agents containing other elements, confirms that EVs are more efficient at delivery compared to free drugs, and describes the use of light exposure in optimizing delivery and therapeutic effects of EV-mediated drug delivery both in combination and independently of porphyrin-based photosensitizers.
细胞外囊泡 (EVs) 是所有细胞释放的脂质双层结构,通过传递生物活性货物来介导细胞间通讯。由于 EVs 的天然来源,它们被受体细胞有效摄取的能力、稳定和运输生物分子的能力以及它们对细胞/组织的靶向能力和对癌细胞的优先摄取能力,使它们在生物工程中具有巨大的潜力,可以转化为改进的、靶向的药物输送系统。在这项工作中,我们研究了使用激光烧蚀电感耦合等离子体质谱法 (LA-ICP-MS) 作为测量铂类化疗药物负载的工具。通过共孵育证明了奥沙利铂对 EV 的加载,并且 LA-ICP-MS 成像显示与游离奥沙利铂相比,向结直肠癌细胞的递送效率更高,导致细胞毒性增强。此外,还评估了 EV 与卟啉 (C5SHU,称为 'C5') 光敏剂共加载对奥沙利铂递送的影响。使用纳米流式细胞术进行荧光分析表明 EV 负载呈剂量依赖性,并且有负载更大颗粒的趋势。用光照射载有 OXA-C5-EV 的结直肠癌细胞表明,光暴露和卟啉都增强了递送,在共加载 EV 递送后,观察到奥沙利铂、EV 和光暴露之间的细胞活力存在协同作用。总之,这项工作证明了 LA-ICP-MS 和质谱成像在评估基于铂的治疗剂的负载效率和细胞递送方面的实用性,这也适用于含有其他元素的制剂,证实与游离药物相比,EV 更有效地递送,并且描述了在单独或与基于卟啉的光敏剂联合使用时,用光照射来优化 EV 介导的药物递送的递送和治疗效果。