Insights into 2D and 3D cell culture models for nanoparticle-based drug delivery to glioblastoma

被引:0
作者
Dabkeviciute, Girstaute [1 ]
Petrikaite, Vilma [1 ,2 ]
机构
[1] Vilnius Univ, Inst Biotechnol, Life Sci Ctr, Sauletekio Al 7, LT-10257 Vilnius, Lithuania
[2] Lithuanian Univ Hlth Sci, Inst Cardiol, Lab Drug Targets Histopathol, Sukileliu Ave 13, LT-50162 Kaunas, Lithuania
关键词
Glioblastoma; Nanoparticles; Drug delivery; Blood-brain barrier; Tumor microenvironment; BRAIN-BARRIER MODEL; ENDOTHELIAL-CELLS; PHASE-II; SURFACE MODIFICATION; BASEMENT-MEMBRANE; MULTICENTER TRIAL; LINES; MICROENVIRONMENT; EXPRESSION; INVASIVENESS;
D O I
10.1016/j.bcp.2025.116931
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Glioblastoma (GBM) remains a formidable challenge due to its aggressive nature, protected location within the brain, and resistance to conventional treatments. Its complex tumor microenvironment (TME), coupled with the blood-brain barrier (BBB), hinders drug delivery leading to poor treatment outcomes. Nanoparticles (NPs) offer a promising solution, as they can improve the pharmacokinetic properties of anticancer agents. By functionalizing NPs with targeting molecules, researchers aim to enhance drug concentration in the brain. However, developing effective NP-based therapies requires robust in vitro models that accurately capture the complexities of GBM. Two-dimensional (2D) and three-dimensional (3D) cell culture models provide a versatile platform for studying NP-cell interactions. By customizing cell types, incorporating TME components, and adjusting flow conditions, researchers can tailor these models to specific research questions. While 2D models offer a simpler starting point, 3D models, such as multicellular spheroids and organoids, can more accurately replicate the complex TME, including the BBB and tumor heterogeneity. These models enable a more comprehensive evaluation of NP efficacy and safety, ultimately accelerating drug development and reducing reliance on animal testing.
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页数:16
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