聚乙二醇化紫杉醇纳米药物面临三维限制:细胞毒性与细胞行为
PEGylated Paclitaxel Nanomedicine Meets 3D Confinement: Cytotoxicity and Cell Behaviors.
作者信息
Lin Wenhai, Xu Yuanhao, Hong Xiao, Pang Stella W
机构信息
Department of Electrical Engineering, City University of Hong Kong, Hong Kong, China.
Centre for Biosystems, Neuroscience, and Nanotechnology, City University of Hong Kong, Hong Kong, China.
出版信息
J Funct Biomater. 2023 Jun 15;14(6):322. doi: 10.3390/jfb14060322.
Investigating the effect of nanomedicines on cancer cell behavior in three-dimensional (3D) platforms is beneficial for evaluating and developing novel antitumor nanomedicines in vitro. While the cytotoxicity of nanomedicines on cancer cells has been widely studied on two-dimensional flat surfaces, there is little work using 3D confinement to assess their effects. This study aims to address this gap by applying PEGylated paclitaxel nanoparticles (PEG-PTX NPs) for the first time to treat nasopharyngeal carcinoma (NPC43) cells in 3D confinement consisting of microwells with different sizes and a glass cover. The cytotoxicity of the small molecule drug paclitaxel (PTX) and PEG-PTX NPs was studied in microwells with sizes of 50 × 50, 100 × 100, and 150 × 150 μm both with and without a concealed top cover. The impact of microwell confinement with varying sizes and concealment on the cytotoxicity of PTX and PEG-PTX NPs was analyzed by assessing NPC43 cell viability, migration speed, and cell morphology following treatment. Overall, microwell isolation was found to suppress drug cytotoxicity, and differences were observed in the time-dependent effects of PTX and PEG-PTX NPs on NPC43 cells in isolated and concealed microenvironments. These results not only demonstrate the effect of 3D confinement on nanomedicine cytotoxicity and cell behaviors but also provide a novel method to screen anticancer drugs and evaluate cell behaviors in vitro.
研究纳米药物在三维(3D)平台上对癌细胞行为的影响,有利于在体外评估和开发新型抗肿瘤纳米药物。虽然纳米药物对癌细胞的细胞毒性已在二维平面上得到广泛研究,但利用3D受限环境评估其效果的工作却很少。本研究旨在填补这一空白,首次应用聚乙二醇化紫杉醇纳米粒(PEG-PTX NPs)在由不同尺寸微孔和玻璃盖组成的3D受限环境中治疗鼻咽癌(NPC43)细胞。在有和没有隐蔽顶盖的50×50、100×100和150×150μm尺寸的微孔中研究了小分子药物紫杉醇(PTX)和PEG-PTX NPs的细胞毒性。通过评估处理后NPC43细胞的活力、迁移速度和细胞形态,分析了不同尺寸和隐蔽性的微孔受限环境对PTX和PEG-PTX NPs细胞毒性的影响。总体而言,发现微孔隔离会抑制药物细胞毒性,并且在隔离和隐蔽微环境中观察到PTX和PEG-PTX NPs对NPC43细胞的时间依赖性效应存在差异。这些结果不仅证明了3D受限环境对纳米药物细胞毒性和细胞行为的影响,还提供了一种在体外筛选抗癌药物和评估细胞行为的新方法。