Abstract
A click-chemistry approach to synthesize bioresponsive poly(ethylene glycol acrylate) particles is described. The particles are loaded with a model anticancer drug (doxorubicin, DOX), and undergo simultaneous particle deconstruction and DOX release upon specific activation by the simulated environment of the cellular cytoplasm.
Original language | English |
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Pages (from-to) | 4348-4352 |
Number of pages | 5 |
Journal | Advanced Materials |
Volume | 21 |
Issue number | 43 |
DOIs | |
Publication status | Published - 20 Nov 2009 |
Externally published | Yes |