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. 2011 Apr 18;12(5):329–340. doi: 10.1038/nrg2968

Table 2.

Methods for the delivery of RNAi triggers to cells and tissues

Species/formulation Packaging capacity Applications and considerations Refs*
Viral vector
Adenovirus Up to ~35 kb, usually <10 kb dsDNA vector with large packaging capacity, transient expression, highly immunogenic 76,77
Adeno-associated virus (AAV) ~4.5 kb ssDNA vector, small packaging capacity, mildly immunogenic, lasting expression in nondividing cells, capsid pseudotyping/engineering facilitates specific cell-targeting 82,91,103,108
Lentivirus Up to 13.5 kb (larger inserts will decrease titre) RNA vector, integration competent and incompetent forms available, less immunogenic than adenovirus or AAV, envelope pseudotyping facilitates cell targeting, clinical production more difficult than for adenovirus or AAV 83,84,85,86,87,88,140,155
Herpes simplex virus 150kb DNA vector, episomal, lasting expression, immunogenic 119
Bacterial vector species
Escherichia coli, S. Typhymurium§ Delivery of short hairpin RNA or small interfering RNA to gut tissue 73,74,75
Non-viral formulations ||
Nanoparticle Self-assembling, may target specific receptors, requires technical expertise to prepare 59
Stable nucleic acid lipid particle (SNALP) Stable for systemic delivery, broad cell-type delivery 51
Aptamer Targeting of specific receptors, requires sophisticated screening to develop 53
Cholesterol Stable for systemic delivery, broad cell-type delivery 46
*Representative references.
Bacterial minicells can carry plasmids, short interfering RNAs or drugs.
§Salmonella enterica subsp. enterica serovar Typhimurium.
||The nucleic acids in non-viral carriers can be any size from small oligonucleotides to large artificial chromosomes.