Title
Controllable Self-Assembly Of Nanoparticles For Specific Delivery Of Multiple Therapeutic Molecules To Cancer Cells Using Rna Nanotechnology
Abstract
By utilizing RNA nanotechnology, we engineered both therapeutic siRNA and a receptor-binding RNA aptamer into individual pRNAs of phi29's motor. The RNA building block harboring siRNA or other therapeutic molecules was fabricated subsequently into a trimer through the interaction of engineered right and left interlocking RNA loops. The incubation of the protein-free nanoscale particles containing the receptor-binding aptamer or other ligands resulted in the binding and co-entry of the trivalent therapeutic particles into cells, subsequently modulating the apoptosis of cancer cells and leukemia model lymphocytes in cell culture and animal trials. The use of such antigenicity-free 20-40 nm particles holds promise for the repeated long-term treatment of chronic diseases. © 2005 American Chemical Society.
Publication Date
9-1-2005
Publication Title
Nano Letters
Volume
5
Issue
9
Number of Pages
1797-1808
Document Type
Article
Personal Identifier
scopus
DOI Link
https://doi.org/10.1021/nl051264s
Copyright Status
Unknown
Socpus ID
24944565527 (Scopus)
Source API URL
https://api.elsevier.com/content/abstract/scopus_id/24944565527
STARS Citation
Khaled, Annette; Guo, Songchuan; and Li, Feng, "Controllable Self-Assembly Of Nanoparticles For Specific Delivery Of Multiple Therapeutic Molecules To Cancer Cells Using Rna Nanotechnology" (2005). Scopus Export 2000s. 3768.
https://stars.library.ucf.edu/scopus2000/3768