Photophysical Characterization and In Vitro Evaluation of α-Mangostin-Loaded HDL Mimetic Nano-Complex in LN-229 Glioblastoma Spheroid Model.
Humans
Xanthones
/ chemistry
Glioblastoma
/ drug therapy
Cell Line, Tumor
Nanoparticles
/ chemistry
Lipoproteins, HDL
/ chemistry
Spheroids, Cellular
/ drug effects
Drug Carriers
/ chemistry
Reactive Oxygen Species
/ metabolism
Cell Survival
/ drug effects
Brain Neoplasms
/ drug therapy
Astrocytes
/ metabolism
Antineoplastic Agents
/ pharmacology
Autophagy
/ drug effects
3D spheroid
GBM
LN-229
rHDL
α-mangostin
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
05 Jul 2024
05 Jul 2024
Historique:
received:
06
06
2024
revised:
26
06
2024
accepted:
28
06
2024
medline:
13
7
2024
pubmed:
13
7
2024
entrez:
13
7
2024
Statut:
epublish
Résumé
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.
Identifiants
pubmed: 39000485
pii: ijms25137378
doi: 10.3390/ijms25137378
pii:
doi:
Substances chimiques
Xanthones
0
mangostin
U6RIV93RU1
Lipoproteins, HDL
0
Drug Carriers
0
Reactive Oxygen Species
0
Antineoplastic Agents
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : The National Institutes of Health/National Institute on Aging.
ID : T32 Training Grant in the Neurobiology of Aging and Alzheimer's Disease