2013
DOI: 10.1016/j.gene.2013.03.055
|View full text |Cite
|
Sign up to set email alerts
|

Ability of plasmid DNA complexed with histidinylated lPEI and lPEI to cross in vitro lung and muscle vascular endothelial barriers

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
6
0

Year Published

2013
2013
2023
2023

Publication Types

Select...
5
2

Relationship

0
7

Authors

Journals

citations
Cited by 10 publications
(6 citation statements)
references
References 56 publications
0
6
0
Order By: Relevance
“…MCEC are a frequently used in vitro cell system 11,12,[16][17][18][19] . Though they showed endothelial cell-like behavior in in vitro assays, MCEC apparently lost key endothelial cell characteristics in their gene expression program.…”
Section: Discussionmentioning
confidence: 99%
“…MCEC are a frequently used in vitro cell system 11,12,[16][17][18][19] . Though they showed endothelial cell-like behavior in in vitro assays, MCEC apparently lost key endothelial cell characteristics in their gene expression program.…”
Section: Discussionmentioning
confidence: 99%
“…Building on the proton sponge hypothesis, histidines or other imidazole derivatives with a p K a of around 6 have been incorporated into polymers such as polylysine, PEI, or dendrimers to increase their endosomal buffer capacity. Various reports demonstrate the beneficial effects of these buffering units on transfection efficiency …”
Section: Cationic Core Polymersmentioning
confidence: 99%
“…As reported in the literature, branched PEI is a well‐known cytotoxic molecule in most cell types related to its direct interaction with plasma membrane molecules, and forms a precipitation on the cell surface 32 . Safer alternatives of PEI could be designed for in vivo administrations because of its beneficial activities on a wide range of advanced biological applications, including nonviral gene, 26 DNA, nucleic acid, and drug delivery, 33 transfection efficiency, 13 and especially significant antimicrobial activity 12 . Polyplex forms of PEI containing DNA, lipids or different biomolecules reduce the toxicity of branched PEI thanks to the lower cationic charge density of the polyplex form 14 .…”
Section: Resultsmentioning
confidence: 99%
“…12 However, the high toxicity of PEI limits its direct use to inhibit bactericidal, fungal or viral growth, especially in human contact application areas. 12 To overcome this less biocompatibility effect, preparation of complex form PEI with various biomacromolecules such as DNA, 13 lipids, 14 and phenolic compounds. 15 Sahiner and Demirci 16 reported that synthesis of betainized PEI microgels was the most feasible approach in design of more compatible PEI-based material.…”
Section: Introductionmentioning
confidence: 99%