Gold nanoparticles surface-functionalized with paclitaxel drug and biotin receptor as theranostic agents for cancer therapy
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文摘
We describe in this study whether the gold nanoparticle (AuNP) surface-functionalized with PEG, biotin, paclitaxel (PTX) and rhodamine B linked beta-cyclodextrinÂ-CD) (AuNP-5?/strong>) can be useful as a theranostic agent for cancer therapy without the cytotoxic effect on normal cells. Prior to surface-functionalizing AuNPs, the cytotoxicity of the nanoparticles was evaluated, followed by their cytocompatibility. PTX, an anti-cancer agent, formed inclusion complexations with ¦Â-CD conjugated AuNPs, and effectively released from the AuNP-2?/strong> surface-functionalized with PEG, beta-cyclodextrin (¦Â-CD) and paclitaxel (PTX) using the intracellular glutathione (GSH) level (10?mm). Two types of AuNP-4 surface-functionalized with PEG and rhodamine B linked ¦Â-CD and AuNP-5 surface-functionalized PEG, biotin and rhodamine B linked ¦Â-CD were used for evaluating their specific interaction on cancer cells such as HeLa, A549 and MG63. These were also tested against normal NIH3T3 cell, determining that the AuNP-5 was more effectively involved with the cancer cells. Confocal laser scanning microscopy (CLSM), fluorescence-activated cell-sorting (FACS) and cell viability analyses showed that the AuNP-5?/strong> plays a significant role in the diagnosis and therapy of the cancer cells, and may be used in theranostic agents.

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