Back to Search
Start Over
Stealth Iron Oxide Nanoparticles for Organotropic Drug Targeting
- Source :
- Biomacromolecules. 20:1375-1384
- Publication Year :
- 2019
- Publisher :
- American Chemical Society (ACS), 2019.
-
Abstract
- The ability of peculiar iron oxide nanoparticles (IONPs) to evade the immune system was investigated in vivo. The nanomaterial was provided directly into the farming water of zebrafish ( Danio rerio) and the distribution of IONPs and the delivery of oxytetracycline (OTC) was studied evidencing the successful overcoming of the intestinal barrier and the specific and prolonged (28 days) organotropic delivery of OTC to the fish ovary. Noteworthy, no sign of adverse effects was observed. In fish blood, IONPs were able to specifically bind apolipoprotein A1 (Apo A1) and molecular modeling showed the structural analogy between the IONP@Apo A1 nanoconjugate and high-density lipoprotein (HDL). Thus, the preservation of the biological identity of the protein suggests a plausible explanation of the observed overcoming of the intestinal barrier, of the great biocompatibity of the nanomaterial, and of the prolonged drug delivery (benefiting of the lipoprotein transport route). The present study promises novel and unexpected stealth materials in nanomedicine.
- Subjects :
- Polymers and Plastics
Metal Nanoparticles
Bioengineering
02 engineering and technology
Plasma protein binding
010402 general chemistry
Ferric Compounds
01 natural sciences
Mass Spectrometry
Biomaterials
chemistry.chemical_compound
Drug Delivery Systems
In vivo
Materials Chemistry
Animals
Distribution (pharmacology)
Chromatography, High Pressure Liquid
Fishes
021001 nanoscience & nanotechnology
0104 chemical sciences
Cell biology
chemistry
Targeted drug delivery
Blood-Brain Barrier
Lipoprotein transport
Drug delivery
Nanomedicine
0210 nano-technology
Iron oxide nanoparticles
Protein Binding
Subjects
Details
- ISSN :
- 15264602 and 15257797
- Volume :
- 20
- Database :
- OpenAIRE
- Journal :
- Biomacromolecules
- Accession number :
- edsair.doi.dedup.....6f0d93721a362f245133c2d60349bf8c
- Full Text :
- https://doi.org/10.1021/acs.biomac.8b01750