TAT is not capable of transcellular delivery across an intact endothelial monolayer in vitro

Annals of Biomedical Engineering

Volumn 39, Issue 1, 2011, Pages 394-401

  Simon, Melissa J ^a   Kang, Woo Hyeun ^a   Gao, Shan ^a   Banta, Scott ^a   Iii, Barclay Morrison ^a  

^a Columbia University ^*  (United States)

Author keywords

Cell penetrating peptide; Endothelial barrier; TAT peptide; Transcellular delivery

Indexed keywords

BLOOD-BRAIN BARRIER; BRAIN PARENCHYMA; CELL INTEGRITY; CELL-PENETRATING PEPTIDE; DELIVERY VEHICLE; ELECTRICAL RESISTANCES; ENDOTHELIAL BARRIERS; FUSION PROTEINS; GREEN FLUORESCENT PROTEIN; IN-VITRO; POTENTIAL SOLUTIONS; TAT PEPTIDE; TIGHT JUNCTIONS; TRANSCELLULAR DELIVERY; ZONA OCCLUDENS;

DRUG DELIVERY; ELECTRON ENERGY LEVELS; FLUORESCENCE; GLUCOSE; MONOLAYERS; PEPTIDES; SELF ASSEMBLY;

ENDOTHELIAL CELLS;

DRUG CARRIER; TRANSACTIVATOR PROTEIN;

ANIMAL; ARTICLE; BLOOD BRAIN BARRIER; CELL LINE; ENDOTHELIUM CELL; METABOLISM; MOUSE; RAT; SPRAGUE DAWLEY RAT;

ANIMALS; BLOOD-BRAIN BARRIER; CELL LINE; DRUG CARRIERS; ENDOTHELIAL CELLS; GENE PRODUCTS, TAT; MICE; RATS; RATS, SPRAGUE-DAWLEY;

EID: 78650915189     PISSN: 00906964     EISSN: 15739686     Source Type: Journal    
DOI: 10.1007/s10439-010-0144-x     Document Type: Article

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