Table 2.
Research of inhaled siRNA formulations for respiratory infections.
| Disease | Target | Administration | Delivery System | Ref. |
|---|---|---|---|---|
| Influenza | Nucleoprotein | Intranasal administration |
Chitosan nanoparticles | [31] |
| Influenza | Nucleoprotein, acidic polymerase |
Intranasal administration |
Oligofectamine | [32] |
| H1N1 | Nucleoprotein, acidic polymerase |
Inhalation | PH-responsive peptides | [33] |
| RSV | N-protein | Intranasal administration |
Naked siRNA | [34] |
| RSV | RSV-protein | Intranasal administration |
Naked siRNA | [35] |
| RSV | NSP1 | Intranasal administration |
Chitosan nanoparticles | [36] |
| Pneumonia | TNF-α | Intratracheal delivery |
RC-NCs | [30] |
| Tuberculosis | TGFβ1 | Inhalation | Naked siRNA | [37] |
| Tuberculosis | XCL1 | Oro-tracheal administration |
Naked siRNA | [29] |
Notes: RC, an inflammation-sheddable, charge-reversal pro-peptide of RAGE-binding peptide (RBP); NCs, nanocomplexes.