Using drug-excipient interactions for siRNA delivery☆

Autor: Katharina Bruno
Jazyk: angličtina
Rok vydání: 2011
Předmět:
CPP
cell penetrating peptide

Small interfering RNA
Time Factors
Drug Evaluation
Preclinical

Pharmaceutical Science
MW
molecular weight

Small hairpin RNA
chemistry.chemical_compound
Drug excipient
Drug Delivery Systems
RNA interference
DLS
Dynamic light scattering

RISC
RNA-induced silencing complex

TNF-α
Tumor necrosis factor-α

IL
Interleukin

shRNA
small hairpin RNA

RNA
Small Interfering

media_common
Clinical Trials as Topic
VEGF
Vascular Endothelial Growth Factor

ds
double-stranded

mRNA
messenger RNA

PLGA
RNAi
RNA interference

AMD
age related macular degeneration

RNA Interference
ITC
Isothermal titration calorimetry

Delivery
TLR
Toll-like receptor

Drug
bPEI
branched PEI

Aptamer
media_common.quotation_subject
N/P ratio
Nitrogen to Phosphor ratio

Static Electricity
PEI
Polyethyleneimine

Nanotechnology
Article
Excipients
SAXS
Small angle X-ray scattering

Bp
base-pairs

STR-R8
stearyl octaarginine

i.v.
intravenous

Animals
Humans
TEM
transmission electron microscopy

D5W
5% (w/v) glucose in water

Clinic
PEG
polyethylene glycol

PAMAM
poly(amidoamine)

DD
deacetylation degree

technology
industry
and agriculture

RNA

half-life

AFM
atomic force microscopy

chemistry
Formulation
siRNA
small interfering RNA

siRNA
RNAi
CDP
Cyclodextrin-containing polymers

Biophysics
R8
octaarginine

RES
reticuloendothelial system

ApoB
Apolipoprotein B
Zdroj: Advanced Drug Delivery Reviews
ISSN: 1872-8294
0169-409X
Popis: SiRNA is the trigger of RNA interference, a mechanism discovered in the late 1990s. To release the therapeutic potential of this versatile but large and fragile molecule, excipients are used which either interact by electrostatic interaction, passively encapsulate siRNA or are covalently attached to enable specific and safe delivery of the drug substance. Controlling the delicate balance between protective complexation and release of siRNA at the right point and time is done by understanding excipients-siRNA interactions. These can be lipids, polymers such as PEI, PLGA, Chitosans, Cyclodextrins, as well as aptamers and peptides. This review describes the mechanisms of interaction of the most commonly used siRNA delivery vehicles, and looks at the results of their clinical and preclinical studies.
Databáze: OpenAIRE