journal article·2016-11-02

A Facile Strategy to Prepare Hyperbranched Hydroxyl-Rich Polycations for Effective Gene Therapy

Shun Duan, Bingran Yu, Chunxiao Gao, Wei Yuan, Jie Ma, Fu-Jian Xu

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Abstract

For effective gene therapy, nonviral gene carriers with low toxicity and high transfection efficiency are of much importance. In this work, we developed a facile strategy to prepare hyperbranched hydroxyl-rich polycations (denoted by TE) by the one-pot method involving ring-opening reactions between two commonly used reagents, ethylenediamine (ED) with two amino groups and 1,3,5-triglycidyl isocyanurate (TGIC) with three epoxy groups. The hyperbranched TEs with different molecular weights were investigated on their DNA condensation ability, protein absorption property, biocompatibility, transfection efficiency, and in vivo cancer therapy and toxicity. TE exhibited low cytotoxicity and protein absorption property due to the plentiful hydroxyl groups. The optimal transfection efficiency of TE was significantly higher than that of the gold standard polycationic gene carrier branched polyethylenimine (PEI, 25 kDa). Furthermore, TE was applied for in vivo tumor inhibition by the delivery of antioncogene p53, which showed good antitumor efficiency with low adverse effects. The present work provides a new concept for the facile preparation of hyperbranched hydroxyl-rich polycationic carriers with good transfection performances.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: RNA Interference and Gene Delivery · Virus-based gene therapy research · Advanced biosensing and bioanalysis techniques

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

State Key Laboratory of Molecular Oncology, Cancer Institute and Hospital, Chinese Academy of Medical Sciences, Beijing 100021, China

Funding

Ministry of Science and Technology of the People's Republic of China · Beijing University of Chemical Technology · National Natural Science Foundation of China · Collaborative Innovation Center for Cardiovascular Disorders, Capital Medical University

References (39)

Show source-provided references
1. 10.1038/nrclinonc.2015.22810.1038/nrclinonc.2015.228 ↗
2. 10.1038/nrg374210.1038/nrg3742 ↗
3. 10.1016/j.progpolymsci.2010.11.00510.1016/j.progpolymsci.2010.11.005 ↗
4. 10.1038/nrg376310.1038/nrg3763 ↗
5. 10.1016/j.jconrel.2014.05.05510.1016/j.jconrel.2014.05.055 ↗
6. 10.1039/C4TB02106A10.1039/C4TB02106A ↗
7. 10.1021/acsami.6b0161110.1021/acsami.6b01611 ↗
8. 10.1021/acsnano.5b0547010.1021/acsnano.5b05470 ↗
9. 10.1007/s11426-015-5327-810.1007/s11426-015-5327-8 ↗
10. 10.1016/j.biomaterials.2011.03.00310.1016/j.biomaterials.2011.03.003 ↗
11. 10.1021/acs.bioconjchem.5b0057610.1021/acs.bioconjchem.5b00576 ↗
12. 10.1021/bm100309y10.1021/bm100309y ↗
13. 10.1021/am400227710.1021/am4002277 ↗
14. 10.1021/am504617910.1021/am5046179 ↗
15. 10.1021/acsami.6b0169710.1021/acsami.6b01697 ↗
16. 10.1016/j.biomaterials.2011.09.01110.1016/j.biomaterials.2011.09.011 ↗
17. 10.1002/adma.20160231910.1002/adma.201602319 ↗
18. 10.1016/j.actbio.2016.02.03110.1016/j.actbio.2016.02.031 ↗
19. 10.1021/acs.langmuir.5b0240810.1021/acs.langmuir.5b02408 ↗
20. 10.1021/acsami.5b0811910.1021/acsami.5b08119 ↗
21. 10.1039/C5TB01964H10.1039/C5TB01964H ↗
22. 10.1016/j.jconrel.2015.08.00610.1016/j.jconrel.2015.08.006 ↗
23. 10.1039/C5PY01758K10.1039/C5PY01758K ↗
24. 10.1039/C6PY00759G10.1039/C6PY00759G ↗
25. 10.1021/acsami.6b0156110.1021/acsami.6b01561 ↗
26. 10.1016/j.biomaterials.2016.08.02510.1016/j.biomaterials.2016.08.025 ↗
27. 10.1021/ma102419e10.1021/ma102419e ↗
28. 10.1002/adfm.20100017710.1002/adfm.201000177 ↗
29. 10.1021/am504618510.1021/am5046185 ↗
30. 10.1002/jbm.a.3528310.1002/jbm.a.35283 ↗
31. 10.1016/j.biomaterials.2013.03.09210.1016/j.biomaterials.2013.03.092 ↗
32. 10.1021/acs.macromol.5b0186810.1021/acs.macromol.5b01868 ↗
33. 10.1002/smll.20120248510.1002/smll.201202485 ↗
34. 10.1021/nn500857210.1021/nn5008572 ↗
35. 10.1039/C5BM00187K10.1039/C5BM00187K ↗
36. 10.1016/j.addr.2012.07.00410.1016/j.addr.2012.07.004 ↗
37. 10.1016/j.biomaterials.2013.03.08310.1016/j.biomaterials.2013.03.083 ↗
38. 10.1073/pnas.92.16.729710.1073/pnas.92.16.7297 ↗
39. 10.1039/C5BM00046G10.1039/C5BM00046G ↗