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The performance of attapulgite hybrids combined with MTX and Au nanoparticles
Methotrexate (MTX) conjugated with attapulgite clay (ATP), ATP/MTX, was successfully synthesized by using MTX as a guest molecule and natural ATP as a kind of drug carrier, where MTX was intercalated and adsorbed onto the channel and surface of ATP in acidic aqueous solution. Furthermore, Au nanopar...
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Published in: | The Journal of physics and chemistry of solids 2019-01, Vol.124, p.73-80 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Methotrexate (MTX) conjugated with attapulgite clay (ATP), ATP/MTX, was successfully synthesized by using MTX as a guest molecule and natural ATP as a kind of drug carrier, where MTX was intercalated and adsorbed onto the channel and surface of ATP in acidic aqueous solution. Furthermore, Au nanoparticles were bound onto the surface of ATP to form tubelike ATP-Au nanocomposites by electrostatic force. These nanocomposites exhibit similar localized surface plasmon resonance absorption characteristics to those of Au nanorods with a longitudinal absorption mode that shifts to the near-infrared (NIR) region (∼670 nm). The results indicated that the addition of MTX had no effect on the morphology of ATP, and the drug-loading efficiency of ATP was measured as 22.36%. Results of MTT bioassay and cell morphology analysis revealed that while ATP did not kill human cervical cancer cells (Hela), ATP/MTX nanocomposites had a good inhibitory effect on them.
•The nanocomposite of methotrexate (MTX)-based attapulgite clay (ATP) was prepared via adsorption of MTX onto the channel and surface of ATP in an acidic aqueous solution.•Using electrostatic interaction, Au nanoparticles were conjugated onto the surface of ATP to form tubelike ATP-Au nanocomposites.•In vitro cytotoxicity tests showed that MTX-based ATP exhibited superior anticancer efficacy compared with free drug. |
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ISSN: | 0022-3697 1879-2553 |
DOI: | 10.1016/j.jpcs.2018.06.017 |