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| Content Provider | Royal Society of Chemistry (RSC) |
|---|---|
| Author | Cao, Youjia Liu, Keliang Yan, Yu Zhang, Hongkai Liu, Xiaozhou Guo, Miao Yan, Husheng |
| Copyright Year | 2010 |
| Abstract | Nanocarriers with multilayer core–shell architecture were prepared by coating a superparamagnetic Fe3O4 core with a triblock copolymer. The first block of the copolymer formed the biocompatible outermost shell of the nanocarrier. The second block that contains amino groups and hydrophobic moiety formed the inner shell. The third block bound tightly onto the Fe3O4 core. Chlorambucil (an anticancer agent) and indomethacin (an anti-inflammation agent), each containing a carboxyl group and a hydrophobic moiety, were loaded into the amino-group-containing inner shell by a combination of ionic and hydrophobic interactions. The release rate of the loaded drugs was slow at pH 7.4, mimicking the blood environment, whereas the release rate increased significantly at acidic pH, mimicking the intracellular conditions in the endosome/lysosome. This can be attributed to the disruption of the ionic bond caused by protonation of the carboxylate anion of the drugs and the swelling of the inner shell caused by protonation of the amino groups. |
| Starting Page | 434 |
| Ending Page | 441 |
| Page Count | 8 |
| File Format | HTM / HTML PDF |
| ISSN | 20403364 |
| Volume Number | 2 |
| Issue Number | 3 |
| Journal | Nanoscale |
| DOI | 10.1039/b9nr00244h |
| Language | English |
| Publisher | Royal Society of Chemistry |
| Access Restriction | Open |
| Subject Keyword | Chlorambucil Carboxylic acid Indometacin Lysosome PH Biocompatibility Ion Superparamagnetism Copolymer Hydrophobe Endosome Ionic bonding |
| Content Type | Text |
| Resource Type | Article |
| Subject | Nanoscience and Nanotechnology |
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