Cross-linked low molecular weight glycopeptide-mediated gene delivery:: Relationship between DNA metabolic stability and the level of transient gene expression in vivo

DNA co-condensates were formed by reacting [I-125]DNA with an admixture of a high-mannose glycopeptide (Man9-CWK18) and either of two poly (ethylene glycol) peptides (PEG-VS-CWK18 or PEG-SS-CWK18) followed by crosslinking with 6-50 mol equiv of glutaraldehyde. [I-125]DNA co-condensates were administered intravenously in mice to determine the influence of peptide DNA formulation parameters on specific targeting to Kupffer cells. Optimal targeting to Kupffer cells required the combined use of 50 mol % Man9-CVTK18 and PEG-CWK18 to mediate specific recognition by the mannose receptor to Kupffer cells. The cellular uptake of cross-linked Man9-CWK18/PEG-CWK18 DNA co-condensates was receptor mediated since Kupffer cell targeting was inhibited by pre-administration of Man-bovine serum albumin (BSA) but not BSA. An optimized formulation targeted 60% of the dose to the liver, with 80% of the liver-targeted DNA localized to Kupffer cells. Crosslinking with either 6, 15, or 50 mol equiv of glutaraldehyde led to a corresponding decrease in the metabolism rate of DNA in liver as measured by half-live- of 4, 6, and 39 h, respectively. Tail vein dosing of 50 mug of DNA co-condensates cross-linked with 6 mol equiv of glutaraldehyde produced detectable levels of human al-antitrypsin in blood after 12 h, which peaked at day six and persisted for 10 days. The level of human alpha (1)-antitrypsin was elevated two-fold each day when dosing with DNA co-condensates cross-linked with 15 mol equiv of glutaraldehyde, revealing a correlation between the metabolic stability of the DNA in liver and level of gene expression. In addition to possessing greater metabolic stability, DNA co-condensates cross-linked with 50 mol equiv of glutaraldehyde, but lacking a targeting ligand, avoided rapid liver uptake and possessed a prolonged pharmacokinetic half-life, providing insight into a means to target DNA condensates to peripheral tissues. (C) 2001 Wiley-Liss, Inc. and the American Pharmaceutical Association.