Abueva Celine Dg, Yoon Sung Ryeong, Carpena Nathaniel T, Ahn Seung Cheol, Chang So-Young, Choi Ji Eun, Lee Min Young, Jung Jae Yun
Beckman Laser Institute Korea, College of Medicine, Dankook University, Cheonan, 31116, Republic of Korea.
Medical Laser Research Center, College of Medicine, Dankook University, Cheonan, 31116, Republic of Korea.
J Nanobiotechnology. 2025 Mar 13;23(1):209. doi: 10.1186/s12951-025-03298-x.
Among nanoparticle platforms, light or photoresponsive nanoparticles have emerged as a promising drug delivery strategy with spatiotemporal control while minimizing off-target effects. The characteristic absorption spectrum of the photoresponsive moiety dictates the wavelength of light needed to activate bond cleavage. However, the low tissue penetration depth limit and short-wavelength ultraviolet (UV) cellular toxicity are considered disadvantageous. This study developed a vestibular ganglion neuron organoid as a model for vestibulopathy. UV and near-infrared (NIR) radiation targeted the inner ear and neural cells, followed by toxicity evaluation. A significantly smaller toxicity of NIR light was confirmed. The photocleavage release of brain-derived neurotrophic factor (BDNF) was used by applying NIR wavelength. The results indicate that polyethylene glycol octamethylene diamine derivative conjugated with leucomethylene blue with an ethanolamine linker nanoparticle can be effectively disassembled and release BDNF when using the 808 nm laser as a trigger. The findings of the cytotoxicity assay suggest that photocleavable nanoparticles (PCNs) and laser irradiation are safe and biocompatible for human-derived and neural progenitor types of cells. Phototriggered BDNF release by NIR laser supported the growth and differentiation of human neural progenitor cells in culture. In addition, the vestibulopathy organoid exhibited a significant regenerative effect. This study harnesses the full potential of NIR laser PCNs to treat vestibular neuropathies.
在纳米颗粒平台中,光或光响应性纳米颗粒已成为一种有前景的药物递送策略,可实现时空控制,同时将脱靶效应降至最低。光响应部分的特征吸收光谱决定了激活键断裂所需的光波长。然而,低组织穿透深度限制和短波长紫外线(UV)细胞毒性被认为是不利的。本研究开发了一种前庭神经节神经元类器官作为前庭病变的模型。紫外线和近红外(NIR)辐射靶向内耳和神经细胞,随后进行毒性评估。证实近红外光的毒性明显较小。通过应用近红外波长来实现脑源性神经营养因子(BDNF)的光裂解释放。结果表明,当使用808nm激光作为触发因素时,与无色亚甲蓝共轭并带有乙醇胺连接体纳米颗粒的聚乙二醇八亚甲基二胺衍生物可以有效地分解并释放BDNF。细胞毒性试验结果表明,光可裂解纳米颗粒(PCNs)和激光照射对人源和神经祖细胞类型是安全且具有生物相容性的。近红外激光触发的BDNF释放在培养中支持了人神经祖细胞的生长和分化。此外,前庭病变类器官表现出显著的再生效应。本研究充分利用了近红外激光PCNs治疗前庭神经病变的全部潜力。