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Hyperbranched polysiloxysilane nanoparticles: Surface charge control of nonviral gene delivery vectors and nanoprobes
- Source :
- International Journal of Pharmaceutics. 376:141-152
- Publication Year :
- 2009
- Publisher :
- Elsevier BV, 2009.
-
Abstract
- New hyperbranched polysiloxysilane (HBPS) materials containing terminal carboxylic acid and quaternary ammonium groups were designed and synthesized to obtain fluorescent-dye-encapsulated nanoparticles. These polymers exhibited desirable characteristics, including amphiphilicity for nanoparticle formation, and contained various terminal groups for surface-charge control on the nanoparticles or for further bioconjugation for targeted imaging. Nanoprobes composed of polysiloxysilane nanoparticles encapsulating two-photon dyes were also prepared for optical bioimaging with controlled surface charge density (zeta potential) for modulation of cellular uptake. Intracellular delivery of these structurally similar polysiloxysilane nanoparticles, with substantially different surface charges, was investigated using confocal and two-photon fluorescence microscopy as well as flow cytometry. Finally, the use of these nanoparticles as efficient gene delivery vectors was demonstrated by means of in vitro transfection study using beta-galactosidase plasmid and pEGFP-N1 plasmid and the most efficient combination was obtained using HBPS-CN30:70.
- Subjects :
- Siloxanes
Cell Survival
Genetic Vectors
Green Fluorescent Proteins
Pharmaceutical Science
Nanoparticle
Nanoprobe
Nanotechnology
Gene delivery
Transfection
Drug Delivery Systems
Chlorocebus aethiops
Zeta potential
Fluorescence microscope
Animals
Humans
Surface charge
Microparticle
Fluorescent Dyes
Drug Carriers
Bioconjugation
Molecular Structure
Chemistry
Gene Transfer Techniques
beta-Galactosidase
Microscopy, Fluorescence
Models, Chemical
COS Cells
Biophysics
Nanoparticles
HeLa Cells
Plasmids
Subjects
Details
- ISSN :
- 03785173
- Volume :
- 376
- Database :
- OpenAIRE
- Journal :
- International Journal of Pharmaceutics
- Accession number :
- edsair.doi.dedup.....75dc80c913fe70e8bbb0c035534f58b3
- Full Text :
- https://doi.org/10.1016/j.ijpharm.2009.04.023