Folate receptor mediated intracellular protein delivery using PLL-PEG-FOL conjugate

Sun Hwa Kim, Ji Hoon Jeong, Cheol O. Joe, Tae Gwan Park

Research output: Contribution to journalArticlepeer-review

102 Scopus citations

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 languageEnglish
Pages (from-to)625-634
Number of pages10
JournalJournal of Controlled Release
Volume103
Issue number3
DOIs
StatePublished - Apr 18 2005
Externally publishedYes

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.

FundersFunder number
National Cancer Center02-3-150
Ministerio de Ciencia y TecnologíaM10214000117-02b1500-02110

    Keywords

    • Folate
    • Intracellular protein delivery
    • PLL-PEG-FOL conjugate
    • Targeting

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