Polymer(Korea), Vol.29, No.2, 135-139, March, 2005
유전자 전달체로서 폴리(에틸렌 글리콜) 및 폴레이트로 수식된 폴리(에틸렌 이민)의 합성
Preparation of PEG-Folate-graft-Polyethylenimine as a Gene Carrier
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초록
본 연구에서는 세포 독성을 감소시키고 in vivo에서 표적화를 향상시키기 위하여 methoxypoly(ethylene glycol) (mPEG) 및 folate가 도입된 poly(ethylene imine) (PEI)를 합성하였다. Folate 의 카복실 그룹을 EDC/NHS으로 활성화시킨 후 mPEG-PEI의 아민기와의 반응으로 PEG-folate-graft-PEI를 합성하였다. 합성된 고분자의 화학적 구조는 1H-NMR과 FT-IR을 이용하여 확인하였다. 합성된 고분자와 DNA가 정전기적 인력에 의해 완전한 복합체의 형성을 확인하기 위해 여러 가지 N/P charge 비율로 agarose gel 전기영동 및 형광을 측정하였고, 2 이상의 N/P charge 비율에서 완전한 복합체를 형성함을 확인하였다. 복합체의 크기는 광산란장치 및 AFM으로부터 100~300 nm임을 관찰하였다. 이러한 결과들로부터 합성된 양이온성 고분자와 DNA가 복합체를 잘 이루어지는 것을 관찰하였고 유전자 전달체로서의 가능성을 평가하고자 하였다.
In this study, poly(ethylene imine) (PEI) modified by methoxypoly(ethylene glycol) (mPEG) and folate as a gene carrier was synthesized to decrease cytotoxicity and to improve in vivo targeting. mPEG was modified by glutaric anhydride (GA) to endow carboxylic end group, followed by the activation reaction with EDC (N-ethyl-N'-(3-dimethyl-with the amines of PEI to give mPEG graft PEI. The mPEG-folate-graft-PEI was synthesized by the reaction of mPEG-PEI with folate pre-activated by EDC/NHS. The obtained copolymers were characterized by 1H-NMR and FT-IR. Gelretardation assay and fluorescence measurement indicated that DNA formed th ecomplexes with the synthesized copolymers above N/P charge ratio 2. The size of complexes was ranging from 100 nm to 300 nm. In conclusion, we confirmed that the synthesized copolymer have the possibility as a DNA carrier.
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