Hyperbranched PEG-based supramolecular nanoparticles for acid-responsive targeted drug delivery.
Xiaofei Chen, Xuemei Yao, Chunran Wang, Li Chen, Xuesi Chen
Index: Biomater. Sci. 3 , 870-8, (2015)
Full Text: HTML
Abstract
Herein, hyperbranched poly(ethylene glycol)-based supramolecular nanoparticles with pH-sensitive properties were designed and used for targeted drug delivery. Via host-guest recognition between benzimidazole anchored poly(ethylene glycol)-hyperbranched polyglycerol (PEG-HPG-BM) and folic acid modified CD (FA-CD), targeted supramolecular nanoparticles (TSNs) were fabricated. At neutral aqueous conditions TSNs could load the model drug DOX. While under intracellular acidic conditions the loaded-drug would be released due to the protonation of BM. This protonation allowed the supramolecular nanoparticles to expand or even disassemble, which showes the pH-dependent property. The introduction of the active targeting FA molecule and the specific interactions with the receptor of HeLa cells means that DOX-loaded TSNs show a significantly improved anticancer efficacy. In vitro drug release assays and intracellular experiments confirmed that TSNs had an obvious pH-sensitive property and remarkably improved anticancer effects, which hold great potential for further biomedical applications such as anticancer drug delivery.
Related Compounds
Related Articles:
Permeation of Dopamine Sulfate through the Blood-Brain Barrier.
2015-01-01
[PLoS ONE 10 , e0133904, (2015)]
Lipophilic prodrugs of nucleoside triphosphates as biochemical probes and potential antivirals.
2015-01-01
[Nat. Commun. 6 , 8716, (2015)]
2015-11-13
[Eur. J. Med. Chem. 105 , 63-79, (2015)]
2015-09-01
[Bioorg. Med. Chem. 23 , 5402-9, (2015)]
2015-08-01
[Pharm. Res. 32 , 2713-26, (2015)]