Ivermectin-induced cell death of cervical cancer cells in vitro a consequence of precipitate formation in culture media
The anthelmintic ivermectin has been reported to possess anticancer and antiviral efficacy. However, the effective concentrations reported in vitro are near the predicted aqueous solubility limit for this hydrophobic drug. We observed that ivermectin-induced cell death in two cervical cancer cell li...
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| Published in: | Toxicology and applied pharmacology Vol. 449; p. 116073 |
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| Main Authors: | , , , , , |
| Format: | Journal Article |
| Language: | English |
| Published: |
United States
Elsevier Inc
15-08-2022
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| Subjects: | |
| Online Access: | Get full text |
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| Summary: | The anthelmintic ivermectin has been reported to possess anticancer and antiviral efficacy. However, the effective concentrations reported in vitro are near the predicted aqueous solubility limit for this hydrophobic drug. We observed that ivermectin-induced cell death in two cervical cancer cell lines correlated with the formation of solid ivermectin aggregates in both serum-free and serum-supplemented culture media. Filtration of ivermectin particles >0.2 μm abolished these cytolytic effects in both cell lines. An inhibitory effect on cell proliferation persisted for filtered solutions, but only for ivermectin concentrations higher than reported to be clinically attainable in humans. In addition to the importance of distinguishing between free and bound drug in solution, our data emphasize the importance of acknowledging the likely solubility limit of hydrophobic drugs when assessing their in vitro cytotoxicity.
•Hydrophobic ivermectin precipitates in culture media within concentration range reported cytotoxic in vitro•Ivermectin-induced cell death in vitro dependent on formation of solid aggregates of >0.2 μm size•Poor evidence for in vitro cytoxicity of ivermectin clinically relevant concentrations |
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| Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
| ISSN: | 0041-008X 1096-0333 |
| DOI: | 10.1016/j.taap.2022.116073 |