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New strategy of efficient inhibition of cancer cells by carborane carboxylic acid–CdTe nanocomposites
Abstract Nanoconjugates composed of drug molecules encapsulated in quantum dots (QDs) attract enormous attention due to their promising bioimaging and biomedical applications. Here, the anticancer efficiency of potential pharmacophore agents ( o -carborane (Cb), o -carborane-C-carboxylic acid (Cbac1...
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Published in: | Nanomedicine 2012-08, Vol.8 (6), p.860-869 |
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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: | Abstract Nanoconjugates composed of drug molecules encapsulated in quantum dots (QDs) attract enormous attention due to their promising bioimaging and biomedical applications. Here, the anticancer efficiency of potential pharmacophore agents ( o -carborane (Cb), o -carborane-C-carboxylic acid (Cbac1), and o -carborane-C(1)C(2)-dicarboxylic acid (Cbac2) coupling with cadmium telluride QDs capped with cysteamine (CA-CdTe QDs)) have been explored. Compared with free CA-CdTe QDs, the composites consisting of Cbac1/Cbac2 and safe-dosage QDs can greatly improve the inhibition efficiency toward SMMC-7721 hepatocellular carcinoma cells with the aid of our real-time cell bioelectronic sensing system and the MTT assay. The enhanced cytotoxicity correlates with increased intracellular reactive oxygen species generation and cell apoptosis. Confocal laser scanning fluorescent microscopy shows improved cellular uptake and drug distribution of the Cbac1/Cbac2-CdTe QDs nanoconjugates. This work raises the possibility that the carborane pharmacophore in combination with QDs or other anticancer drugs may be viable for efficient cancer diagnosis and chemotherapy. From the Clinical Editor This team of investigators demonstrates efficient inhibition of cancer cells by carborane carboxylic acid–Cadmium telluride nanodots in cell cultures of hepatocellular carcinoma. Further research is needed to evaluate long-term safety and potential in vivo applicability. |
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ISSN: | 1549-9634 1549-9642 |
DOI: | 10.1016/j.nano.2011.10.011 |