Size Dependence of Gold Nanorods for Efficient and Rapid Photothermal Therapy.

In recent years, gold nanomaterials have become a hot topic in photothermal tumor therapy due to their unique surface plasmon resonance characteristics. The effectiveness of photothermal therapy is highly dependent on the shape and size of gold nanoparticles. In this work, we investigate the photothermal therapeutic effects of four different sizes of gold nanorods (GNRs). The results show that the uptake of short GNRs with aspect ratios 3.3-3.5 by cells is higher than that of GNRs with aspect ratios 4-5.5. Using a laser with single pulse energy as low as 28 pJ laser for 20 s can induce the death of liver cancer cells co-cultured with short GNRs. Long GNRs required twice the energy to achieve the same therapeutic effect. The dual-temperature model is used to simulate the photothermal response of intracellular clusters irradiated by a laser. It is found that small GNRs are easier to compact because of their morphological characteristics, and the electromagnetic coupling between GNRs is better, which increases the internal field enhancement, resulting in higher local temperature. Compared with a single GNR, GNR clusters are less dependent on polarization and wavelength, which is more conducive to the flexible selection of excitation laser sources.

Photothermal therapy of single cancer cells mediated by naturally created gold nanorod clusters.

Gold nanorods (GNRs) are generally considered to be nontoxic to normal and cancer cells. They are usually accumulated at lysosomes after entering into cells, forming GNR clusters in which strong plasmonic coupling between GNRs is expected. We investigated the photothermal therapy of single cancer cells by exploiting the significantly enhanced two-photon-induced absorption of GNR clusters naturally created in the lysosomes of cancer cells. It was revealed numerically that the plasmonic coupling between GNRs in GNR clusters can effectively enhance the photothermal conversion efficiency. As a result, the thermal damage of single cancer cells can be induced by using pulse energy as low as ~70 pJ. In experiments, the locations of GNR clusters can be accurately determined through the detection of the two-photon-induced luminescence, which is also significantly enhanced, by using a confocal laser scanning microscope. The photothermal therapy was conducted by focusing femtosecond laser light on the targeted GNR clusters, generating bubbles and deforming cell membranes. The photothermal therapy proposed in this work can lead to the rapid and acute injury of single cancer cells. The dependence of the apoptosis time on the pulse energy of femtosecond laser light was also examined. Our findings suggest a novel strategy for the photothermal therapy of single cancer cells with ultralow energy.