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基于 α-倒捻子素载脂蛋白 mimetic 纳米复合物的光物理特性表征及其在 LN-229 神经胶质瘤球体模型中的体外评价

Photophysical Characterization and In Vitro Evaluation of α-Mangostin-Loaded HDL Mimetic Nano-Complex in LN-229 Glioblastoma Spheroid Model.

机构信息

Lipoprotein Drug Delivery Research Laboratory, Department of Microbiology, Immunology & Genetics, University of North Texas Health Science Center, Fort Worth, TX 76107, USA.

College of Science and Engineering, Texas Christian University, Fort Worth, TX 76109, USA.

出版信息

Int J Mol Sci. 2024 Jul 5;25(13):7378. doi: 10.3390/ijms25137378.

Abstract

Cytotoxic activity has been reported for the xanthone α-mangostin (AMN) against Glioblastoma multiforme (GBM), an aggressive malignant brain cancer with a poor prognosis. Recognizing that AMN's high degree of hydrophobicity is likely to limit its systemic administration, we formulated AMN using reconstituted high-density lipoprotein (rHDL) nanoparticles. The photophysical characteristics of the formulation, including fluorescence lifetime and steady-state anisotropy, indicated that AMN was successfully incorporated into the rHDL nanoparticles. To our knowledge, this is the first report on the fluorescent characteristics of AMN with an HDL-based drug carrier. Cytotoxicity studies in a 2D culture and 3D spheroid model of LN-229 GBM cells and normal human astrocytes showed an enhanced therapeutic index with the rHDL-AMN formulation compared to the unincorporated AMN and Temozolomide, a standard GBM chemotherapy agent. Furthermore, treatment with the rHDL-AMN facilitated a dose-dependent upregulation of autophagy and reactive oxygen species generation to a greater extent in LN-229 cells compared to astrocytes, indicating the reduced off-target toxicity of this novel formulation. These studies indicate the potential therapeutic benefits to GBM patients via selective targeting using the rHDL-AMN formulation.

摘要

已经有报道称,针对多形性胶质母细胞瘤(GBM),一种预后不良的侵袭性恶性脑癌,酮基紫檀芪(AMN)具有细胞毒性。鉴于 AMN 的高度疏水性很可能限制其全身给药,我们使用重建的高密度脂蛋白(rHDL)纳米颗粒来制备 AMN。制剂的光物理特性,包括荧光寿命和稳态各向异性,表明 AMN 已成功掺入 rHDL 纳米颗粒中。据我们所知,这是关于基于 HDL 的药物载体的 AMN 荧光特性的首次报道。在 LN-229 GBM 细胞的 2D 培养和 3D 球体模型中的细胞毒性研究表明,与未掺入的 AMN 和替莫唑胺(一种标准的 GBM 化疗药物)相比,rHDL-AMN 制剂具有更高的治疗指数。此外,与星形胶质细胞相比,rHDL-AMN 处理更能剂量依赖性地上调自噬和活性氧的产生,表明这种新型制剂的脱靶毒性降低。这些研究表明,通过使用 rHDL-AMN 制剂进行选择性靶向,可能会为 GBM 患者带来治疗益处。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21e2/11242846/9b1d000caba6/ijms-25-07378-g001.jpg

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