Institute of Medicine, Chung Shan Medical University, Taichung 40201, Taiwan.
Department of Neurosurgery, Changhua Christian Hospital, Changhua 50006, Taiwan.
Cells. 2022 Jul 11;11(14):2172. doi: 10.3390/cells11142172.
n-butylidenephthalide (BP) has been verified as having the superior characteristic of cancer cell toxicity. Furthermore, gold (Au) nanoparticles are biocompatible materials, as well as effective carriers for delivering bio-active molecules for cancer therapeutics. In the present research, Au nanoparticles were first conjugated with polyethylene glycol (PEG), and then cross-linked with BP to obtain PEG-Au-BP nanodrugs. The physicochemical properties were characterized through ultraviolet-visible spectroscopy (UV-Vis), Fourier-transform infrared spectroscopy (FTIR), and dynamic light scattering (DLS) to confirm the combination of PEG, Au, and BP. In addition, both the size and structure of Au nanoparticles were observed through scanning electron microscopy (SEM) and transmission electron microscopy (TEM), where the size of Au corresponded to the results of DLS assay. Through in vitro assessments, non-transformed BAEC and DBTRG human glioma cells were treated with PEG-Au-BP drugs to investigate the tumor-cell selective cytotoxicity, cell uptake efficiency, and mechanism of endocytic routes. According to the results of MTT assay, PEG-Au-BP was able to significantly inhibit DBTRG brain cancer cell proliferation. Additionally, cell uptake efficiency and potential cellular transportation in both BAEC and DBTRG cell lines were observed to be significantly higher at 2 and 24 h. Moreover, the mechanisms of endocytosis, clathrin-mediated endocytosis, and cell autophagy were explored and determined to be favorable routes for BAEC and DBTRG cells to absorb PEG-Au-BP nanodrugs. Next, the cell progression and apoptosis of DBTRG cells after PEG-Au-BP treatment was investigated by flow cytometry. The results show that PEG-Au-BP could remarkably regulate the DBTRG cell cycle at the Sub-G1 phase, as well as induce more apoptotic cells. The expression of apoptotic-related proteins in DBTRG cells was determined through Western blotting assay. After treatment with PEG-Au-BP, the apoptotic cascade proteins p21, Bax, and Act-caspase-3 were all significantly expressed in DBTRG brain cancer cells. Through in vivo assessments, the tissue morphology and particle distribution in a mouse model were examined after a retro-orbital sinus injection containing PEG-Au-BP nanodrugs. The results demonstrate tissue integrity in the brain (forebrain, cerebellum, and midbrain), heart, liver, spleen, lung, and kidney, as they did not show significant destruction due to PEG-Au-BP treatment. Simultaneously, the extended retention period for PEG-Au-BP nanodrugs was discovered, particularly in brain tissue. The above findings identify PEG-Au-BP as a potential nanodrug for brain cancer therapies.
正丁烯基苯酞(BP)已被证实具有优异的癌细胞毒性特征。此外,金(Au)纳米粒子是生物相容性材料,也是将生物活性分子递送至癌症治疗的有效载体。在本研究中,首先将 Au 纳米粒子与聚乙二醇(PEG)缀合,然后与 BP 交联,得到 PEG-Au-BP 纳米药物。通过紫外可见分光光度法(UV-Vis)、傅里叶变换红外光谱(FTIR)和动态光散射(DLS)对其理化性质进行了表征,以确认 PEG、Au 和 BP 的结合。此外,通过扫描电子显微镜(SEM)和透射电子显微镜(TEM)观察了 Au 纳米粒子的大小和结构,Au 的大小与 DLS 测定结果相对应。通过体外评估,用 PEG-Au-BP 药物处理非转化的 BAEC 和 DBTRG 人神经胶质瘤细胞,以研究肿瘤细胞的选择性细胞毒性、细胞摄取效率和内吞途径的机制。根据 MTT 测定的结果,PEG-Au-BP 能够显著抑制 DBTRG 脑癌细胞的增殖。此外,在 BAEC 和 DBTRG 细胞系中,在 2 和 24 小时时观察到细胞摄取效率和潜在的细胞转运明显更高。此外,还探讨并确定了内吞作用、网格蛋白介导的内吞作用和细胞自噬的机制,这些机制有利于 BAEC 和 DBTRG 细胞吸收 PEG-Au-BP 纳米药物。接下来,通过流式细胞术研究了 DBTRG 细胞在 PEG-Au-BP 处理后的细胞进展和凋亡情况。结果表明,PEG-Au-BP 可以显著调节 DBTRG 细胞在 Sub-G1 期的细胞周期,并诱导更多的凋亡细胞。通过 Western blot 测定法确定了 DBTRG 细胞中凋亡相关蛋白的表达。用 PEG-Au-BP 处理后,凋亡级联蛋白 p21、Bax 和 Act-caspase-3 在 DBTRG 脑癌细胞中均明显表达。通过体内评估,在含有 PEG-Au-BP 纳米药物的眶后窦注射后,检查了小鼠模型中的组织形态和颗粒分布。结果表明,在脑(前脑、小脑和中脑)、心脏、肝脏、脾脏、肺和肾脏中组织完整性没有因 PEG-Au-BP 治疗而受到明显破坏。同时,发现 PEG-Au-BP 纳米药物的保留时间延长,特别是在脑组织中。上述发现表明 PEG-Au-BP 是一种有潜力的用于脑癌治疗的纳米药物。