Enhancing the in vivo stability of polycation gene carriers by using PEGylated hyaluronic acid as a shielding system

Author:

Liu Jiaxue1,Bao Xiaoli2,Kolesnik Irina3,Jia Boyan1,Yu Zihan4,Xing Caiyun4,Huang Jiawen4,Gu Tingting4,Shao Xiaotong5,Kletskov Alexey6,Kritchenkov Andreii S.6,Potkin Vladimir3,Li Wenliang1

Affiliation:

1. Jilin Collaborative Innovation Center for Antibody Engineering, Jilin Medical University, Jilin, China

2. Norman Bethune Health Science Center, Jilin University, Jilin, China

3. Institute of Physical Organic Chemistry of National Academy of Sciences of Belarus, 13 Surganov Str., 220072, Minsk, Belarus

4. School of Pharmacy, Jilin Medical University, Jilin, China

5. School of Medical Laboratory, Jilin Medical University, Jilin, China

6. Peoples’ Friendship University of Russia (RUDN University), Miklukho-Maklaya St. 6, Moscow, 117198, Russian Federation

Abstract

Abstract To increase the in vivo stability of cationic gene carriers and avoid the adverse effects of their positive charge, we synthesized a new shielding material by conjugating low molecular weight polyethylene glycol (PEG) to a hyaluronic acid (HA) core. The HA-PEG conjugate assembled with the positively charged complex, forming a protective layer through electrostatic interactions. DNA/polyetherimide/HA-PEG (DNA/PEI/HA-PEG) nanoparticles had higher stability than both DNA/polyethyleneimine (DNA/PEI) and DNA/PEI/HA complexes. Furthermore, DNA/PEI/HA-PEG nanoparticles also showed a diminished nonspecific response toward serum proteins in vivo. The in vivo transfection efficiency was also enhanced by the low cytotoxicity and the improved stability; therefore, this material might be promising for use in gene delivery applications.

Publisher

Compuscript, Ltd.

Subject

General Earth and Planetary Sciences,General Environmental Science

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