Abstract
Functionalized cyclodextrin molecules assemble into a wide variety of superstructures in solution, which are of interest for drug delivery and other nanomaterial and biomaterial applications. Here we use a combined simulation and experimental approach to probe the coassembly of siRNA and cationic cyclodextrin (c-CD) derivatives into a highly stable gene delivery nanostructure. The c-CD form supramolecular structures via interdigitation of their aliphatic tails, analogous to the formation of lipid bilayers and micelles. The native conformation of siRNA is preserved by the encapsulating c-CD superstructure in an extensive hydrogen-bonding network between the positively charged side arms of c-CD and the negatively charged siRNA backbone. The stability of the complexation is confirmed using isothermal titration calorimetry, and the experimental/simulation codesign methodology opens new avenues for creation of highly engineerable gene delivery vectors.
Original language | English |
---|---|
Pages (from-to) | 1358-1366 |
Number of pages | 9 |
Journal | Molecular Pharmaceutics |
Volume | 16 |
Issue number | 3 |
DOIs | |
Publication status | Published - 4 Mar 2019 |
Keywords
- cyclodextrin
- gene delivery
- molecular dynamics
- self-assembly
- siRNA