## Abstract Following bolus intravenous injection of disopyramide in eight normal volunteers the renal clearance of the drug appeared to fall with time. In the first two hours after injection renal clearance had a mean value of 89Β·0 ml min^β1^ and fell to 29Β·4 ml min^β1^ between 48 and 72 h. In a
Mechanism of naked DNA clearance after intravenous injection
β Scribed by Feng Liu; Lisa M. Shollenberger; Christine C. Conwell; Xing Yuan; Leaf Huang
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 476 KB
- Volume
- 9
- Category
- Article
- ISSN
- 1099-498X
- DOI
- 10.1002/jgm.1054
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
Background
Injection of naked DNA has been viewed as a safer alternative to current gene delivery systems; however, the rate of clearance from the circulation has been a constant barrier in developing these methods. Naked DNA after intravenous (i.v.) injection will be taken up by the liver and depredated by serum nucleases.
Materials and methods
Our study examines the mechanisms involved in clearance of naked DNA by each compartment, the blood and the liver, in an in vivo mouse model. Confocal microscopy and transmission electron microscopy were employed to identify the type of cells taking up DNA and the barrier to DNA access to hepatocytes, respectively.
Results
Our data showed the liver could take up over 50% of 5 Β΅g perfused pDNA, with a maximum 25 Β΅g of pDNA during a single pass, and a slower clearance rate compared to that of liver uptake. It was demonstrated that naked DNA is primarily taken up by the liver endothelial cells and this endothelial barrier to transfection could be overcome by manually massaging the liver, which enlarges the fenestrae.
Conclusions
This study clarifies the mechanism by which naked DNA is eliminated from the circulation after i.v. injection, focusing on the role of both the liver and blood compartments in vivo (i.e. mouse). With this knowledge, we can more clearly understand the mechanism of naked DNA clearance and develop more efficient strategies for DNA transfer in vivo. Copyright Β© 2007 John Wiley & Sons, Ltd.
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