Dual pH-Responsive Polymer Nanogels with a Core–Shell Structure for Improved Cell Association
Source abstract
Abstract
We report the fabrication of polymer nanogels with a pH-responsive core and a pH-sheddable shell and investigate the pH-dependent cell association of the pH-responsive polymer nanogels. The pH-responsive core composed of poly(2-diisopropylaminoethyl methacrylate) (PDPA) with a pKa ≈ 6.2 was synthesized by using polymerization in emulsion droplets. The pH-sheddable poly(ethylene glycol) (PEG) shell was coated on the amine-modified PDPA nanogels by an acid-degradable amide bond. The PEG shell is cleavable in response to the acidic tumor microenvironment, and subsequently, the surface charge of the nanogels can be reversed, which effectively enhances cellular association of these nanogels. The reported pH-responsive polymer nanogels provide a promising way for the better understanding of bio−nano interactions and potentially enrich the application of therapeutic delivery for cancer therapy.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Nanoparticle-Based Drug Delivery · Hydrogels: synthesis, properties, applications · RNA Interference and Gene Delivery
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Key Laboratory of Colloid and Interface Chemistry of the Ministry of Education, School of Chemistry and Chemical Engineering, Shandong University, Jinan, Shandong 250100, China
State Key Laboratory of Microbial Technology, Shandong University, Qingdao, Shandong 266237, China
Funding
Ministry of Education of the People's Republic of China · National Natural Science Foundation of China
References (33)
Show source-provided references
1. 10.1038/nrd450310.1038/nrd4503 ↗
2. 10.1002/anie.20161081910.1002/anie.201610819 ↗
3. 10.1002/adma.20130336010.1002/adma.201303360 ↗
4. 10.1002/adma.20160662810.1002/adma.201606628 ↗
5. 10.1002/adma.20140155410.1002/adma.201401554 ↗
6. 10.1021/acsnano.6b0087010.1021/acsnano.6b00870 ↗
7. 10.1016/j.ijpharm.2014.05.03210.1016/j.ijpharm.2014.05.032 ↗
8. 10.1002/anie.20090267210.1002/anie.200902672 ↗
9. 10.1016/s1359-6446(05)03575-010.1016/s1359-6446(05)03575-0 ↗
10. 10.1021/bm501713910.1021/bm5017139 ↗
11. 10.1021/nn506157810.1021/nn5061578 ↗
12. 10.1002/adma.20140275310.1002/adma.201402753 ↗
13. 10.1021/acs.biomac.6b0053710.1021/acs.biomac.6b00537 ↗
14. 10.1002/adhm.20180160710.1002/adhm.201801607 ↗
15. 10.1021/acs.langmuir.8b0211710.1021/acs.langmuir.8b02117 ↗
16. 10.1016/j.chempr.2018.07.00210.1016/j.chempr.2018.07.002 ↗
17. 10.1021/acs.accounts.8b0019510.1021/acs.accounts.8b00195 ↗
18. 10.1016/j.biomaterials.2015.12.01410.1016/j.biomaterials.2015.12.014 ↗
19. 10.1002/anie.20090721010.1002/anie.200907210 ↗
20. 10.1073/pnas.152208011310.1073/pnas.1522080113 ↗
21. 10.1016/j.polymer.2007.04.01110.1016/j.polymer.2007.04.011 ↗
22. 10.1002/jbm.a.3404810.1002/jbm.a.34048 ↗
23. 10.1021/mp400738710.1021/mp4007387 ↗
24. 10.1002/anie.20150950710.1002/anie.201509507 ↗
25. 10.1039/c8py00579f10.1039/c8py00579f ↗
26. 10.1021/nl071542i10.1021/nl071542i ↗
27. 10.1016/j.polymer.2010.06.01010.1016/j.polymer.2010.06.010 ↗
28. 10.1021/nn203503h10.1021/nn203503h ↗
29. 10.1038/nnano.2011.16610.1038/nnano.2011.166 ↗
30. 10.1002/adhm.20120011210.1002/adhm.201200112 ↗
31. 10.1039/c3py00849e10.1039/c3py00849e ↗
32. 10.1021/nn204240b10.1021/nn204240b ↗
33. 10.2147/ijn.s3448910.2147/ijn.s34489 ↗