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Development of multifunctional hyaluronan-coated nanoparticles for imaging and drug delivery to cancer cells.


ABSTRACT: Currently, there is high interest in developing multifunctional theranostic platforms for cancer monitoring and chemotherapy. Herein, we report hyaluronan (HA)-coated superparamagnetic iron oxide nanoparticles (HA-SPION) as a promising system for targeted imaging and drug delivery. When incubated with cancer cells, HA-SPIONs were rapidly taken up and the internalization of HA-SPION by cancer cells was much higher than the NPs without HA coating. The high magnetic relaxivity of HA-SPION coupled with enhanced uptake enabled magnetic resonance imaging of cancer cells. Furthermore, doxorubicin (DOX) was attached onto the nanoparticles through an acid responsive linker. While HA-SPION was not toxic to cells, DOX-HA-SPION was much more potent than free DOX to kill not only drug-sensitive but also multi-drug-resistant cancer cells. This was attributed to differential uptake mechanisms and cellular distributions of free DOX and DOX-HA-SPION in cancer cells.

SUBMITTER: El-Dakdouki MH 

PROVIDER: S-EPMC5475368 | biostudies-literature | 2012 Apr

REPOSITORIES: biostudies-literature

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Development of multifunctional hyaluronan-coated nanoparticles for imaging and drug delivery to cancer cells.

El-Dakdouki Mohammad H MH   Zhu David C DC   El-Boubbou Kheireddine K   Kamat Medha M   Chen Jianjun J   Li Wei W   Huang Xuefei X  

Biomacromolecules 20120313 4


Currently, there is high interest in developing multifunctional theranostic platforms for cancer monitoring and chemotherapy. Herein, we report hyaluronan (HA)-coated superparamagnetic iron oxide nanoparticles (HA-SPION) as a promising system for targeted imaging and drug delivery. When incubated with cancer cells, HA-SPIONs were rapidly taken up and the internalization of HA-SPION by cancer cells was much higher than the NPs without HA coating. The high magnetic relaxivity of HA-SPION coupled w  ...[more]

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