Abstract
Antisense oligonucleotides with base sequence complementary to a specific RNA or DNA seem to provide a promising new tool for the therapy of viral diseases and of cancer. They offer the exciting potential of selectively modulating the expression of an individual gene (Hélène and Toulmé, 1990). The oligonucleotides have been used successfully in cell culture to inhibit the expression of specific HIV genes (Agrawal et al, 1988; Goodchild et al, 1988; Lisziewicz et al, 1988) and there is now widespread interest in extending the use of antisense compounds in the in vivo setting (Bayever et al, 1993; Wahlestedt et al, 1993). However, before the therapeutic potential of antisense compounds can be fullfilled, it will be necessary to overcome significant problems relating to their poor stability and their ability to reach their intracellular target.
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Ropert, C., Malvy, C., Couvreur, P. (1996). pH Sensitive Liposomes as Efficient Carriers for Intracellular Delivery of Oligonucleotides. In: Gregoriadis, G., McCormack, B. (eds) Targeting of Drugs 5. NATO ASI Series, vol 290. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-6405-8_16
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DOI: https://doi.org/10.1007/978-1-4615-6405-8_16
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