Polysaccharide coated PLA nanoparticles bearing aldehyde groups were prepared by dialysis of DMSO solution of cholesterol hydrophobic-modified dextran polyaldehyde and PLA against water. The average diameter of the nanoparticles was about 160 nm
and the size distribution was nearly homogenous. The nanoparticles were functionalized simultaneously with CD71 and EGFR antibody through the Schiff’s base reaction
and then radiolabeled with 99mTc. After perfused the radiolabeled nanoparticles into tumor-bearing rats through left common carotid artery
the radioactivity in liver
spleen
kidney and brain was measured by scintillation counter. The results showed that less than 2% of nanoparticles were uptaken by the brain due to the uptake of the nanoparticles by the RES system. However
the coupling of transferrin antibody on the nanoparticles facilitated the penetration of nanoparticles across the blood brain barrier
and more specially
compared with monofuctionalized and native nanoparticles
the multifunctionalization enhanced the tumor accumulation of the nanoparticles in vivo.
Abstract
Polysaccharide coated PLA nanoparticles bearing aldehyde groups were prepared by dialysis of DMSO solution of cholesterol hydrophobic-modified dextran polyaldehyde and PLA against water. The average diameter of the nanoparticles was about 160 nm
and the size distribution was nearly homogenous. The nanoparticles were functionalized simultaneously with CD71 and EGFR antibody through the Schiff’s base reaction
and then radiolabeled with 99mTc. After perfused the radiolabeled nanoparticles into tumor-bearing rats through left common carotid artery
the radioactivity in liver
spleen
kidney and brain was measured by scintillation counter. The results showed that less than 2% of nanoparticles were uptaken by the brain due to the uptake of the nanoparticles by the RES system. However
the coupling of transferrin antibody on the nanoparticles facilitated the penetration of nanoparticles across the blood brain barrier
and more specially
compared with monofuctionalized and native nanoparticles
the multifunctionalization enhanced the tumor accumulation of the nanoparticles in vivo.
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