Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz

Logo MUG-Forschungsportal

Gewählte Publikation:

SHR Neuro Krebs Kardio Lipid Stoffw Microb

Millotti, G; Perera, G; Vigl, C; Pickl, K; Sinner, FM; Bernkop-Schnürch, A.
The use of chitosan-6-mercaptonicotinic acid nanoparticles for oral peptide drug delivery.
Drug Deliv. 2011; 18(3): 190-197. Doi: 10.3109/10717544.2010.522611
Web of Science PubMed FullText FullText_MUG

 

Co-Autor*innen der Med Uni Graz
Sinner Frank Michael
Altmetrics:

Dimensions Citations:

Plum Analytics:

Scite (citation analytics):

Abstract:
The aim of this study was to develop a novel nanoparticulate formulation and test its potential for oral peptide drug delivery. Chitosan-6-mercaptonicotinic acid is a novel thiolated chitosan with strong mucoadhesive properties. Nanoparticles were developed by an ionic gellation method. The obtained particles were characterized in terms of mucoadhesion, stability, toxicity, and in vitro release. Human insulin (HI) was chosen as a model peptide drug, incorporated in the particles and orally administered to rats. Human insulin was quantified in the blood by means of ELISA. The size of the obtained particles was in the range of 200-300 nm and the zeta potential was determined to be +8-+23 depending on the amount of thiol groups attached on the polymer. After 3 h of incubation up to 60% of the thiolated chitosan nanoparticles remained attached to the mucosa in contrast to 20% of unmodified chitosan particles. The AUC of HI after oral administration of thiolated chitosan nanoparticles was 4-fold improved compared to unmodified chitosan nanoparticles. Due to these improvements, chitosan-6-mercaptonicotinic acid nanoparticles are promising vehicles for oral delivery of peptide drugs.
Find related publications in this database (using NLM MeSH Indexing)
Adhesiveness -
Administration, Oral -
Animals -
Area Under Curve -
Caco-2 Cells -
Chitosan - analogs & derivatives
Chitosan - chemistry
Chitosan - toxicity
Drug Carriers - chemistry
Drug Carriers - toxicity
Drug Delivery Systems -
Drug Stability -
Enzyme-Linked Immunosorbent Assay -
Humans -
Insulin - administration & dosage
Insulin - pharmacokinetics
Insulin - toxicity
Male -
Nanoparticles -
Particle Size -
Rats -
Rats, Sprague-Dawley -
Sulfhydryl Compounds - chemistry
Sulfhydryl Compounds - toxicity

Find related publications in this database (Keywords)
Thiomers
nanoparticles
mucoadhesion
in vivo insulin delivery
toxicity
© Med Uni Graz Impressum