“…These methods consist of electroporation, serving as an efficient gene delivery system [ 45 ], electrofusion [ 46 ], microinjection [ 47 ], transfection [ 48 ], liposome-mediated drug delivery [ 49 ], the fusion of cell ghost [ 50 ], cell-penetrating peptides to deliver therapeutic proteins and oligonucleotides [ 51 ], osmotic lysis [ 52 ] and laser pulses for the delivery of therapeutics into cells [ 53 ] or by glass beads [ 54 ]. As an example, mouse L cells grown in suspension culture could be rendered permeable to exogenous deoxynucleoside triphosphates by a cold shock in a slightly hypotonic buffer system containing 0.01 M Tris-HCl pH 7.8, 0.25 M sucrose, 1 mM EDTA, 30 mM 2-mercaptoethanol and 4 mM MgCl 2 [ 6 , 7 , 8 ].…”