Abstract
To develop a receptor-mediated intracellular delivery system that can transport therapeutic proteins or other bioactive macromolecules into a specific cell, a di-block copolymer conjugate, poly(l-lysine)-poly(ethylene glycol)-folate (PLL-PEG-FOL), was synthesized. The PLL-PEG-FOL conjugate was physically complexed with fluorescein isothiocyanate conjugated bovine serum albumin (FITC-BSA) in an aqueous phase by ionic interactions. Cellular uptake of PLL-PEG-FOL/FITC-BSA complexes was greatly enhanced against a folate receptor over-expressing cell line (KB cells) compared to a folate receptor deficient cell line (A549 cells). The presence of an excess amount of free folate (1 mM) in the medium inhibited the intracellular delivery of PLL-PEG-FOL/FITC-BSA complexes. This suggests that the enhanced cellular uptake of FITC-BSA by KB cells in a specific manner was attributed to folate receptor-mediated endocytosis of the complexes having folate moieties on the surface. The PLL-PEG-FOL di-block copolymer could be potentially applied for intracellular delivery of a wide range of other biological active agents that have negative charges on the surface.
Original language | English |
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Pages (from-to) | 625-634 |
Number of pages | 10 |
Journal | Journal of Controlled Release |
Volume | 103 |
Issue number | 3 |
DOIs | |
State | Published - Apr 18 2005 |
Externally published | Yes |
Funding
This study was supported by the grants from the National Cancer Center (02-3-150) and the Ministry of Science and Technology (M10214000117-02b1500-02110), Republic of Korea.
Funders | Funder number |
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National Cancer Center | 02-3-150 |
Ministerio de Ciencia y Tecnología | M10214000117-02b1500-02110 |
Keywords
- Folate
- Intracellular protein delivery
- PLL-PEG-FOL conjugate
- Targeting