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Lipofection - The delivery of DNA into cells using liposomes is called lipofection. Liposomes are small vesicles prepared from a suitable lipid. Initially, nonionic lipids were used for preparing liposomes so that DNA had to be introduced within the vesicles following specific encapsidation procedures.

The use of cationic lipids for the construction of liposomes is a distinct advantage as DNA spontaneously and efficiently complexes with these liposomes making encapsidation procedures unnecessary.

The cationic liposomes have a single lipid bilayer membrane (unilamellar), and they bind to the cells efficiently. Probably they fuse with the plasma membrane and, thereby, deliver the DNA (complexed with them) into the cells, which brings about transfection.

Considerable work has been done on lipofection due to its potential application for targetting genes to specific human tissues for gene therapy. Usually, liposomes are prepared by dispersion of a phospholipid like phosphatidyl choline (PC) in water by mechanical methods, like sonication, which tend to destroy DNA. DNA of upto 1 kb has been incorporated into small sonicated liposomes. However, some other techniques allow the entrapment of large DNA sequences into liposomes.

Liposomes prepared by the above approaches are phagocytosed by the cell. The phagocytosis vesicles thus produced ordinarily fuse with lysosomes leading to DNA degradation and low transfection frequencies. The use of cationic liposomes to which DNA binds on the outside by electrostatic attraction has been quite successful.

These liposomes cause perturbations in plasma membrane due to which they fuse and the DNA enters into the cytoplasm. Cationic liposomes are available commercially (marketed as 'Lipofectin' by Gibco-BRL).

Lipofection is the method of choice for transfection of mammalian cells in vitro. It has also been used to deliver DNA into live animals by direct injection or intravenous injection.