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

Author:

Kapic Ammar1ORCID,Sabnis Nirupama1ORCID,Dossou Akpedje S.1ORCID,Chavez Jose2,Ceresa Luca2,Gryczynski Zygmunt2,Fudala Rafal1,Dickerman Rob3,Bunnell Bruce A.1ORCID,Lacko Andras G.1

Affiliation:

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

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

3. Department of Spine Surgery, Neurological and Spine Surgeon, 5575 Frisco Square Blvd, Frisco, TX 75093, USA

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.

Funder

The Peggy Dickerman Brain Cancer Research Fund

The Virginia Kincaid Foundation

Wheels for Wellness, Fort Worth

Cancer Prevention and Research Institute of Texas

T32 Training Grant in the Neurobiology of Aging and Alzheimer’s Disease from the National Institutes of Health/National Institute on Aging

Publisher

MDPI AG

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