Abstract

Recently, photothermal therapy (PTT) has been proved to have great potential in tumor therapy. In the last several years, MoS2, as one novel member of nanomaterials, has been applied into PTT due to its excellent photothermal conversion efficacy. In this work, we applied fluorescence lifetime imaging microscopy (FLIM) techniques into monitoring the PPT-triggered cell death under MoS2 nanosheet treatment. Two types of MoS2 nanosheets (single layer nanosheets and few layer nanosheets) were obtained, both of which exhibited presentable photothermal conversion efficacy, leading to high cell death rates of 4T1 cells (mouse breast cancer cells) under PTT. Next, live cell images of 4T1 cells were obtained via directly labeling the mitochondria with Rodamine123, which were then continuously observed with FLIM technique. FLIM data showed that the fluorescence lifetimes of mitochondria targeting dye in cells treated with each type of MoS2 nanosheets significantly increased during PTT treatment. By contrast, the fluorescence lifetime of the same dye in control cells (without nanomaterials) remained constant after laser irradiation. These findings suggest that FLIM can be of great value in monitoring cell death process during PTT of cancer cells, which could provide dynamic data of the cellular microenvironment at single cell level in multiple biomedical applications.

Highlights

  • IntroductionThe standard methods for measuring the e±ciency of the photothermal therapy (PTT) agents against tumor cells includes biochemical methods such as cytotoxicity assays and microscopy methods such as live and dead cell imaging assays

  • At present, cancer is one of most lethal diseases in the world

  • The morphology of the MoS2 nanosheets was obtained by a transmission electron microscopy (TEM) instrument (JEM-1230 CX, Jeol Ltd, Japan)

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Summary

Introduction

The standard methods for measuring the e±ciency of the PTT agents against tumor cells includes biochemical methods such as cytotoxicity assays and microscopy methods such as live and dead cell imaging assays. These methods could not provide dynamic information of cell death at single cell level or even at subcelluar level. Compared with the above-mentioned methods, °uorescence lifetime imaging microscopy (FLIM) technique has great advantages in monitoring multiple cell physiological processes, including cell growth and cell death, since FLIM can provide real-time images and quantitative subcellular information.[14,15]

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