Additionally, DC-Chol was found to have a four-fold reduction in

Additionally, DC-Chol was found to have a four-fold reduction in cytotoxicity versus Lipofectin in some

cell lines [24]. In contrast to cationic liposomes containing fully charged quaternary amines (e.g. DOTMA and DOTAP), DC-Chol, in a 1:1 lipid ratio with DOPE, contains a tertiary amine that is charged on 50% of the liposome surface at pH 7.4 [45]. This feature is thought to reduce the aggregation of lipoplexes leading to higher transgene HA-1077 mw expression [46]. The reduction in overall lipoplex charge can also aid in DNA dissociation during Inhibitors,research,lifescience,medical gene delivery [41], which has been proven to be necessary for successful transfection [42]. 3.2. Multivalent Cationic Lipids 3.2.1. DOSPA (see Figure 6) Figure 6 The structure of DOSPA. 2,3-dioleyloxy-N-[2(sperminecarboxamido)ethyl]-N,N-dimethyl-l-propanaminium trifluoroacetate, or DOSPA, is another cationic lipid synthesized as a derivative of DOTMA. The structure is similar to DOTMA except Inhibitors,research,lifescience,medical for a spermine group which is bound via a peptide bond to the hydrophobic chains.

This cationic lipid, used with the neutral helper lipid DOPE at a 3:1 ratio, is commercially available as the transfection reagent Lipofectamine. In general, the addition of the spermine functional group allows for a more efficient packing of DNA in terms of liposome size. The efficient condensation is possibly due Inhibitors,research,lifescience,medical to the many ammonium groups in spermine. It has been shown that spermine can interact via hydrogen bonds with the bases of DNA in such a way as to be attracted on one strand and wind around the major groove to interact with complementary bases of the opposite strand [47]. 3.2.2.

Inhibitors,research,lifescience,medical DOGS (see Figure 7) Figure 7 The structure of DOGS. Di-octadecyl-amido-glycyl-spermine, or DOGS, has a structure similar to DOSPA; both molecules have a multivalent spermine head group and two 18-carbon alkyl chains. However, the chains in DOGS are saturated, are linked to the head group through a peptide bond, and lack a quaternary amine. DOGS is commercially available under the name Transfectam. This lipid has been Inhibitors,research,lifescience,medical used to transfect many cell lines, with transgene expression levels more than 10-fold greater than those seen following calcium phosphate transfections [25]. In addition, Behr et al. showed that not only was DOGS very effective in delivering the CAT reporter plasmid, but it was also associated with no noticeable cytotoxicity [25]. Much like the multivalent cationic lipid DOSPA, DOGS is very 17-DMAG (Alvespimycin) HCl efficient at binding and packing DNA, a result of the spermine head group that so closely associates with DNA [25]. Characterization of the head group of DOGS was determined to facilitate not only efficient condensation of DNA but also buffering of the endosomal compartment, which was thought to protect the delivered DNA from degradation by pH-sensitive nucleases [36]. DOGS is a multifaceted molecule in terms of buffering capacity. At pH values lower than 4.

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