Polyamidoamine dendron-bearing lipid assemblies: Their morphologies and gene transfection ability

Author:

Iwashita Shinki1,Hiramatsu Yoshie1,Otani Takayuki1,Amano Chie1,Hirai Masahiko1,Oie Kazunori1,Yuba Eiji2,Kono Kenji2,Miyamoto Masaaki34,Igarashi Koichi1

Affiliation:

1. R&D Division, Katayama Chemical Industries Co. Ltd., 4-1-7 Ina, Minoh, Osaka 562-0015, Japan

2. Department of Applied Chemistry, Graduate School of Engineering, Osaka Prefecture University, 1-1 Gakuen-cho, Sakai, Osaka 599-8531, Japan

3. Department of Biology, Graduate School of Science, Kobe University, 1-1 Rokkodai-cho, Kobe 657-8501, Japan

4. Center for Supports to Research and Education Activities, Kobe University, 1-1 Rokkodai-cho, Kobe 567-8501, Japan

Abstract

Assembly morphology made from lipids is controlled by the balance between the polar headgroup and the hydrophobic tails. In this study, we showed the various generations of polyamidoamine dendron-bearing lipids could form various assembly morphologies. Furthermore, the effect of the assembly morphologies made from dendron-bearing lipids for transfection abilities were examined. We synthesized three novel dendron-bearing lipids, DL-U2-G1 (G1), DL-U2-G2 (G2), and DL-U2-G3 (G3), which included first, second, and third generation polyamidoamine dendrons, respectively. Transmission electron microscopy showed that lipoplexes (complexes with cationic lipids and plasmid DNA) comprising G1 had multilamellar structures. G2 presented as aggregates of cubic particles and G3 exhibited clusters of spherical micelles. The ability to form complexes with plasmid DNA was in the decreasing order G3 > G2 > G1; calcein release from endosomes was in the order G3 > G2, G1; and transfection activity followed the order G1 > G2, G3. Interaction of the lipoplexes with heparin suggests that G3 had a lower level of plasmid DNA dissociation from lipoplexes than G1 in vitro. These results suggest that the size of the DL-U2 headgroup determines assembly morphology and that the structure markedly affects transfection activity.

Publisher

SAGE Publications

Subject

Biomedical Engineering,Biomaterials

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