Stimuli‐Responsive Dendritic Supramolecular Vector for Tumor‐Specific Gene Delivery

Author:

Ouyang Xumei123,Gao Dongruo14,Shen Jie135,Zhou Yichen1,Gao Ying13,Lv Yuanyuan134,Wang Qiwen6,Yu Guocan7ORCID,Chu Paul K.5

Affiliation:

1. Key Laboratory of Novel Targets and Drug Study for Neural Repair of Zhejiang Province School of Medicine Hangzhou City University Hangzhou 310015 China

2. Guangdong Provincial Key Laboratory of Tumor Interventional Diagnosis and Treatment Zhuhai Institute of Translational Medicine Zhuhai People's Hospital Affiliated with Jinan University Jinan University Zhuhai Guangdong 519000 China

3. Institute of Pharmaceutics, College of Pharmaceutical Sciences Zhejiang University Hangzhou 310058 China

4. College of Chemical and Biological Engineering Zhejiang University Zhejiang Hangzhou 310027 China

5. Department of Physics Department of Materials Science and Engineering, and Department of Biomedical Engineering City University of Hong Kong Tat Chee Avenue Kowloon Hong Kong China

6. Department of Cardiology The First Affiliated Hospital School of Medicine Zhejiang University Hangzhou 310003 China

7. Key Laboratory of Bioorganic Phosphorus Chemistry & Chemical Biology Department of Chemistry Tsinghua University Beijing 100084 China

Abstract

To simplify the preparation of dendritic materials, host–guest molecular recognition and self‐assembly are utilized to form a supramolecular dendritic gene vector (DNCVP). DNCVP is constructed from an amino dendron‐conjugated naphthol, viologen containing pH‐sensitive hydrazone‐bond‐linked PEG, and CB[8] with a molar ratio of 1:1:1. The pH‐ and reducing‐sensitivity of DNCVP is verified, and the stimuli‐responsive capacity enables the vector tumor targeting gene delivery ability. Owing to the protection of surface PEG, the supramolecular engineering endows the delivery vector with low cytotoxicity and good biocompatibility that are confirmed by the MTT assay. The excellent delivery ability of genes is investigated by in vitro transfection of pEGFP, pGL3, and silencing of siGAPDH. In vivo studies demonstrate promoted tumor accumulation of genes mediated by the dual‐responsive DNCVP and the transfection efficiency at the tumor site is greatly improved benefiting from the dynamic nature of noncovalent interactions. This study reveals DNCVP is a promising supramolecular dendritic gene delivery vector, providing a sophisticated strategy for precise gene therapy.

Funder

National Natural Science Foundation of China

Health and Medical Research Fund

Publisher

Wiley

Subject

General Medicine

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