Liposomes and Lipid Disks Traverse the BBB and BBTB As Intact Forms As Revealed by Two-step Förster Resonance Energy Transfer Imaging
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The blood-brain barrier (BBB) and the blood-brain tumor barrier (BBTB) prevent drug and nano-drug delivery systems from entering the brain. However, ligand-mediated nano-drug delivery systems have significantly enhanced the therapeutic treatment of glioma. In this study we investigated the mechanism especially the integrity of liposomes and lipid disks while traversing the BBB and BBTB both and . Fluorophores (DiO, DiI and DiD) were loaded into liposomes and lipid disks to form Förster resonance energy transfer (FRET) nano-drug delivery systems. Using brain capillary endothelial cells as a BBB model, we show that liposomes and disks are present in the cytoplasm as their intact forms and traverse the BBB with a ratio of 0.68‰ and 1.67‰, respectively. Using human umbilical vein endothelial cells as BBTB model, liposomes and disks remained intact and traversed the BBTB with a ratio of 2.31‰ and 8.32‰ at 3 h. imaging and immunohistochemical results revealed that liposomes and disks could traverse the BBB and BBTB as intact forms. In conclusion, these observations explain in part the mechanism by which nano-drug delivery systems increase the therapeutic treatment of glioma.
Lubitz L, Haffner M, Rieger H, Leneweit G Pharmaceutics. 2024; 16(9).
PMID: 39339149 PMC: 11434700. DOI: 10.3390/pharmaceutics16091112.
Lubitz L, Haffner M, Rieger H, Leneweit G Biomedicines. 2024; 12(9).
PMID: 39335648 PMC: 11430759. DOI: 10.3390/biomedicines12092135.
Chen X, Luo J, Song M, Pan L, Qu Z, Huang B Front Aging Neurosci. 2024; 16:1342366.
PMID: 38389560 PMC: 10882099. DOI: 10.3389/fnagi.2024.1342366.
Targeted gene delivery to the brain using CDX-modified chitosan nanoparticles.
Sepasi T, Bani F, Rahbarghazi R, Ebrahimi-Kalan A, Sadeghi M, Alamolhoda S Bioimpacts. 2023; 13(2):133-144.
PMID: 37193076 PMC: 10182443. DOI: 10.34172/bi.2022.23876.
Tang Y, Gao J, Wang T, Zhang Q, Wang A, Huang M Acta Pharm Sin B. 2022; 12(4):2043-2056.
PMID: 35847504 PMC: 9279712. DOI: 10.1016/j.apsb.2021.09.029.