Revisiting nanoparticle technology for blood-brain barrier transport: Unfolding at the endothelial gate improves the fate of transferrin receptor-targeted liposomes

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• 作者：Kasper Bendix Johnsen ; Torben Moos ; ^{tmoos@hst.aau.dk" class="auth_mail" title="E-mail the corresponding author}
• 关键词：6-OHDA ; 6-hydroxydopamine ; ABC ; ATP-binding cassette ; ATP ; adenosine triphosphate ; BBB ; blood&ndash ; brain barrier ; BCEC ; brain capillary endothelial cell ; bFGF ; basic fibroblast growth factor ; CHE ; cholesteryl hexadecyl ether ; CNS ; central nervous system ; CSF ; cerebrospinal fluid ; Da ; Dalton ; DMT1 ; divalent metal transporter 1 ; DNA ; deoxyribonucleic acid ; DOTAP ; 1 ; 2-dioleoyl-3-trimethylammonium-propane ; DPPC ; 1 ; 2-dipalmitoyl-sn-glycero-3-phosphocholine ; DSPC ; 1 ; 2-distearoyl-sn-glycero-3-phosphoc
• 刊名：Journal of Controlled Release
• 出版年：2016
• 出版时间：28 January 2016
• 年：2016
• 卷：222
• 期：Complete
• 页码：32-46
• 全文大小：1430 K

文摘

An unmet need exists for therapeutic compounds to traverse the brain capillary endothelial cells that denote the blood–brain barrier (BBB) to deliver effective treatment to the diseased brain. The use of nanoparticle technology for targeted delivery to the brain implies that targeted liposomes encapsulating a drug of interest will undergo receptor-mediated uptake and transport through the BBB with a subsequent unfolding of the liposomal content inside the brain, hence revealing drug release to adjacent drug-demanding neurons. As transferrin receptors (TfRs) are present on brain capillary endothelial, but not on endothelial cells elsewhere in the body, the use of TfR-targeted liposomes — colloidal particulates with a phospholipid bilayer membrane — remains the most relevant strategy to obtain efficient drug delivery to the brain. However, many studies have failed to provide sufficient quantitative data to proof passage of the BBB and significant appearance of drugs inside the brain parenchyma. Here, we critically evaluate the current evidence on the use of TfR-targeted liposomes for brain drug delivery based on a thorough investigation of all available studies within this research field. We focus on issues with respect to experimental design and data analysis that may provide an explanation to conflicting reports, and we discuss possible explanations for the current lack of sufficient transcytosis across the BBB for implementation in the design of TfR-targeted liposomes. We finally provide a list of suggestions for strategies to obtain substantial uptake and transport of drug carriers at the BBB with a concomitant transport of therapeutics into the brain.