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Ionizable drug delivery systems for efficient and selective gene therapy.
Zhang, Yu-Qi; Guo, Ran-Ran; Chen, Yong-Hu; Li, Tian-Cheng; Du, Wen-Zhen; Xiang, Rong-Wu; Guan, Ji-Bin; Li, Yu-Peng; Huang, Yuan-Yu; Yu, Zhi-Qiang; Cai, Yin; Zhang, Peng; Ling, Gui-Xia.
Afiliação
  • Zhang YQ; Faculty of Medical Device, Shenyang Pharmaceutical University, Shenyang, 110016, Liaoning, China.
  • Guo RR; Wuya College of Innovation, Shenyang Pharmaceutical University, Shenyang, 110016, Liaoning, China.
  • Chen YH; School of Pharmacy, Yanbian University, Yanji, 133002, Jilin, China.
  • Li TC; School of Pharmacy, Shenyang Pharmaceutical University, Shenyang, 110016, Liaoning, China.
  • Du WZ; Wuya College of Innovation, Shenyang Pharmaceutical University, Shenyang, 110016, Liaoning, China.
  • Xiang RW; Faculty of Medical Device, Shenyang Pharmaceutical University, Shenyang, 110016, Liaoning, China.
  • Guan JB; Masonic Cancer Center, University of Minnesota, Minneapolis, MN, 55455, USA.
  • Li YP; Masonic Cancer Center and Department of Medicinal Chemistry, University of Minnesota, Minneapolis, MN, 55455, USA.
  • Huang YY; Advanced Research Institute of Multidisciplinary Science; School of Life Science; School of Medical Technology; Key Laboratory of Molecular Medicine and Biotherapy; Key Laboratory of Medical Molecule Science and Pharmaceutics Engineering, Beijing Institute of Technology, Beijing, 100081, China.
  • Yu ZQ; Department of Laboratory Medicine, Dongguan Institute of Clinical Cancer Research, Affiliated Dongguan Hospital, Southern Medical University, Dongguan, 523018, Guangdong, China.
  • Cai Y; Department of Health Technology and Informatics, The Hong Kong Polytechnic University, Hong Kong, Hong Kong SAR, China.
  • Zhang P; Wuya College of Innovation, Shenyang Pharmaceutical University, Shenyang, 110016, Liaoning, China. zhangpengspu@163.com.
  • Ling GX; Faculty of Medical Device, Shenyang Pharmaceutical University, Shenyang, 110016, Liaoning, China. pharlab@163.com.
Mil Med Res ; 10(1): 9, 2023 02 27.
Article em En | MEDLINE | ID: mdl-36843103
Gene therapy has shown great potential to treat various diseases by repairing the abnormal gene function. However, a great challenge in bringing the nucleic acid formulations to the market is the safe and effective delivery to the specific tissues and cells. To be excited, the development of ionizable drug delivery systems (IDDSs) has promoted a great breakthrough as evidenced by the approval of the BNT162b2 vaccine for prevention of coronavirus disease 2019 (COVID-19) in 2021. Compared with conventional cationic gene vectors, IDDSs can decrease the toxicity of carriers to cell membranes, and increase cellular uptake and endosomal escape of nucleic acids by their unique pH-responsive structures. Despite the progress, there remain necessary requirements for designing more efficient IDDSs for precise gene therapy. Herein, we systematically classify the IDDSs and summarize the characteristics and advantages of IDDSs in order to explore the underlying design mechanisms. The delivery mechanisms and therapeutic applications of IDDSs are comprehensively reviewed for the delivery of pDNA and four kinds of RNA. In particular, organ selecting considerations and high-throughput screening are highlighted to explore efficiently multifunctional ionizable nanomaterials with superior gene delivery capacity. We anticipate providing references for researchers to rationally design more efficient and accurate targeted gene delivery systems in the future, and indicate ideas for developing next generation gene vectors.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ácidos Nucleicos / COVID-19 Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ácidos Nucleicos / COVID-19 Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article