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Multifunctional receptor-targeted nanocomplexes for the delivery of therapeutic nucleic acids to the Brain
被引:44
作者:
Kenny, Gavin D.
[1
,2
,3
]
Bienemann, Alison S.
[4
]
Tagalakis, Aristides D.
[1
]
Pugh, John A.
[5
]
Welser, Katharina
[6
]
Campbell, Frederick
[6
]
Tabor, Alethea B.
[6
]
Hailes, Helen C.
[6
]
Gill, Steven S.
[4
]
Lythgoe, Mark F.
[2
,3
]
McLeod, Cameron W.
[5
]
White, Edward A.
[4
]
Hart, Stephen L.
[1
]
机构:
[1] UCL Inst Child Hlth, Mol Immunol Unit, London WC1N 1EH, England
[2] UCL, Ctr Adv Biomed Imaging, Dept Med, London WC1E 6DD, England
[3] UCL, Inst Child Hlth, London WC1E 6DD, England
[4] Univ Bristol, Funct Neurosurg Res Grp, Southmead Hosp, Sch Clin Sci,AMBI Labs, Bristol BS10 5NB, Avon, England
[5] Univ Sheffield, Ctr Analyt Sci, Sheffield S10 2TN, S Yorkshire, England
[6] UCL, Dept Chem, London WC1H 0AJ, England
基金:
英国工程与自然科学研究理事会;
关键词:
Gene therapy;
Magnetic resonance imaging (MRI);
Nanoparticles;
Convection enhanced delivery (CEO);
Peptide;
CONVECTION-ENHANCED DELIVERY;
SMALL INTERFERING RNA;
GENE DELIVERY;
ANTISENSE OLIGONUCLEOTIDES;
LIPID NANOPARTICLES;
MALIGNANT GLIOMAS;
DRUG-RESISTANCE;
IN-VITRO;
LIPOSOMES;
CANCER;
D O I:
10.1016/j.biomaterials.2013.07.081
中图分类号:
R318 [生物医学工程];
学科分类号:
0831 ;
摘要:
Convection enhanced delivery (CED) is a method of direct injection to the brain that can achieve widespread dispersal of therapeutics, including gene therapies, from a single dose. Non-viral, nanocomplexes are of interest as vectors for gene therapy in the brain, but it is essential that administration should achieve maximal dispersal to minimise the number of injections required. We hypothesised that anionic nanocomplexes administered by CED should disperse more widely in rat brains than cationics of similar size, which bind electrostatically to cell-surface anionic moieties such as proteoglycans, limiting their spread. Anionic, receptor-targeted nanocomplexes (RTN) containing a neurotensin-targeting peptide were prepared with plasmid DNA and compared with cationic RTNs for dispersal and transfection efficiency. Both RTNs were labelled with gadolinium for localisation in the brain by MRI and in brain sections by LA-ICP-MS, as well as with rhodamine fluorophore for detection by fluorescence microscopy. MRI distribution studies confirmed that the anionic RTNs dispersed more widely than cationic RTNs, particularly in the corpus callosum. Gene expression levels from anionic formulations were similar to those of cationic RTNs. Thus, anionic RTN formulations can achieve both widespread dispersal and effective gene expression in brains after administration of a single dose by CED. (C) 2013 The Authors. Published by Elsevier Ltd. All rights reserved.
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页码:9190 / 9200
页数:11
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