| Literature DB >> 30582802 |
Valentina Brega1, Federica Scaletti2, Xianzhi Zhang2, Li-Sheng Wang2, Prudence Li3, Qiaobing Xu3, Vincent M Rotello2, Samuel W Thomas1.
Abstract
We report the synthesis of amphiphilic polymers featuring lipophilic stearyl chains and hydrophilic poly(ethylene glycol) polymers that are connected through singlet oxygen-cleavable alkoxyanthracene linkers. These amphiphilic polymers assembled in water to form micelles with diameters of ∼20 nm. Reaction of the alkoxyanthracene linkers with light and O2 cleaved the ether C-O bonds, resulting in formation of the corresponding 9,10-anthraquinone derivatives and concomitant disruption of the micelles. These micelles were loaded with the chemotherapeutic agent doxorubicin, which was efficiently released upon photo-oxidation. The drug-loaded reactive micelles were effective at killing cancer cells in vitro upon irradiation at 365 nm, functioning through both doxorubicin release and photodynamic mechanisms.Entities:
Keywords: amphiphilic polymers; doxorubicin; drug delivery; light-responsive materials; self-assembly
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Year: 2019 PMID: 30582802 PMCID: PMC6623983 DOI: 10.1021/acsami.8b18099
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229