Temperature and pH dually-responsive poly(β-amino ester) nanoparticles for drug delivery
Stimuli-responsive polymers have undoubtedly been of great interest in the past decades due to a variety of their potential applications in biomedical territory. However, their non-degradability limits their in vivo applications. Herein, we report a novel pH and temperature dual-stimuli responsive-p...
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Published in | Chinese journal of polymer science Vol. 35; no. 4; pp. 534 - 546 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Beijing
Chinese Chemical Society and Institute of Chemistry, CAS
01.04.2017
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
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Summary: | Stimuli-responsive polymers have undoubtedly been of great interest in the past decades due to a variety of their potential applications in biomedical territory. However, their non-degradability limits their
in vivo
applications. Herein, we report a novel pH and temperature dual-stimuli responsive-poly(
β
-amino ester). The pH/temperature sensitivities are interrelated and can be easily tuned by changing PEG-diacrylate chain length and the percentage of biamines in the feed ratio. These dual-responsive polymers are very useful in drug delivery. Reaction of methyl ether poly(ethylene glycol) (MPEG) and poly(
β
-amino ester) resulted in an amphiphilic MPEG-PBAE block copolymer which could form nanoparticles by self-assembly. A hydrophobic drug (DOX) was loaded in the self-assembled nanoparticles at low temperature without using organic solvents. The loaded drug was released very slowly and steadily at 37 °C under physiological conditions (pH 7.4), but rapidly released from the micelles in weakly acidic environments (pH 6.4 and 5.0) for intracellular drug release. Thus, these poly(
β
-amino ester) polymers constitute ideal drug carriers since their thermal sensitivity allows the drug loadings without using organic solvent and their pH sensitivity permits fast intracellular drug release. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0256-7679 1439-6203 |
DOI: | 10.1007/s10118-017-1916-7 |