Document Type

Article

Rights

This item is available under a Creative Commons License for non-commercial use only

Disciplines

Organic Chemistry, Physical chemistry

Publication Details

Journal of Inclusion Phenomena and Macrocyclic Chemistry, 81(1-2), 85-94.

Abstract

Many chemotherapeutic drugs are therapeutically non-selective and do not distinguish between healthy cells and tumour cells which can result in severe side effects and toxicity. Drug delivery systems can be used to target specific cells and therefore may eliminate many of the side effects, increasing drug efficiency and efficacy, and controlling drug release. One possible strategy for targeted drug delivery is to use unique molecular markers such as folate receptors in cancer cells. In this work the cytotoxicity of a novel cyclodextrin-folate conjugate, 6-deoxy-6-[(1-(-2amino)ethylamino)folate-β-cyclodextrin (CDEnFA) was studied using the MTT assay and the MCF-7 (Breast), HeLa (Cervical), A549 (Lung cancer) and BEAS-2B (normal Lung) cell lines.

The MTT assay showed that the drug delivery vehicle CDEnFA is not cytotoxic towards the cell lines studied even towards the normal BEAS-2B cell line and therefore it is expected that it is safe for medical use. The inclusion complex CDEnFA:MTX has superior cytotoxic activity towards all of the cancer cell lines studied compared to the drug MTX alone and CDEnFA:MTX is four times less cytotoxic than the drug towards the normal cell line. The observed toxicity is attributed solely to MTX since CDEnFA did not exhibit significant cytotoxicity. These results also suggest that the drug remains bioactive even after inclusion in the CD cavity. The cytotoxicity trend observed for CDEnFA:MTX in this study is MCF-7 (Breast) > A549 (Lung) > HeLa (Cervical) > BEAS-2B (normal Lung).

DOI

10.1007/s10847-014-0436-0

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