Cytotoxic effects of TCPs were assessed with the LDH release assay. PMNs were first treated with the indicated concentrations of IVE25 or GKY25 for 1 hr at 37 °C on a 96-well flat-bottom plate. The supernatants were then used for LDH assay according to manufacturer’s instructions. Absorbance readings at 490 and 680 nm were acquired using the Cytation 3 Cell-Imaging Multi-Mode reader (Research Instruments, USA). LDH activity was determined by subtracting absorbance reading at 680 nm from the reading at 490 nm (A490 − A680). Per cent cytotoxicity was calculated as below:
Do you have any questions about this protocol?
Post your question to gather feedback from the community. We will also invite the authors of this article to respond.