Ag NP are effective photothermal agents. A secondary benefit is the differential response of breast cancer cells to Ag NP-induced hyperthermia, due to increased intracellular silver content, compared to non-tumorigenic breast epithelial cells.

Donor-acceptor conjugated polymer nanoparticles and nanofibers, based on Poly[4,4-bis(2-ethylhexyl)-cyclopenta[2,1-b;3,4-b']dithiophene-2,6-diyl-alt22,1,3-benzoselenadiazole-4,7-diyl] (PCPDTBSe), were synthesized using Pluronic F127 as a template. The nanomaterials were compared to previously reported PCPDTBSe nanoparticles, which were synthesized without the use of a template. Our goal was to improve on the aqueous stability and photothermal heating efficiency of the previously synthesized PCPDTBSe nanoparticles by decreasing their size and coating them with a biocompatible surfactant. The pluronic wrapped PCPDTBSe (PW-PCPDTBSe) nanoparticles (40-60 nm) showed excellent aqueous stability compared to the PW-PCPDTBSe nanofibers (d 5 20-60 nm, l 5 200-1000 nm) and previously synthesized PCPDTBSe nanoparticles (150 nm). Under stimulation from 800 nm near infrared light (3 W, 1 min), the PW-PCPDTBSe nanoparticles showed greater heat generation (DT 5 47 C) compared to bare PCPDTBSe nanoparticles and PW-PCPDTBSe nanofibers (DT 5 35 C for both). Cytotoxicity studies determined that both the PW-PCPDTBSe nanoparticles and PW-PCPDTBSe nanofibers displayed no significant toxicity toward either noncancerous small intestinal cells (FHs 74 Int) or colorectal cancer cells (CT26). Photothermal ablation studies confirmed that both the PW-PCPDTBSe nanoparticles and the PW-PCPDTBSe nanofibers can be used as localized photothermal agents to eradicate colorectal cancer cells due to their excellent ablation efficiency (>95% cell death at 15 mg/mL concentration).

The aim of this review is to provide an up-to-date overview of nanoparticles developed for use as photothermal therapy agents (PTT) over the past five years. The main emphasis is on nanoparticles that absorb near infrared (NIR) light for PTT of cancer. Mild hyperthermia, including drug delivery, versus thermal ablation is also discussed. Recent advances in the synthesis of highly anisotropic novel metal nanoparticles for PTT are described. New metals and metal oxide complexes, as well as the use of quantum dots for PTT and as imaging agents are newer areas of development that are explained. This review also highlights current progress in the development of carbon nanoparticles, including reduced graphene oxide for both thermal ablation as well as drug delivery. The review culminates in the recent use electrically conductive polymer nanoparticles for hyperthermia. The advantages and unique features of these contemporary nanoparticles being used for PTT are highlighted. The goal of the present work is to describe the recent evolution of nanoparticles for NIR stimulated PTT, and highlight the innovations and future directions.

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According to the American Cancer Society, breast cancer is the second leading cause of cancer death in the US. Cancerous cells may have inadequate adhesions to the extracellular matrix and adjacent cells. Previous work has suggested that restoring these contacts may negate the cancer phenotype. This work aims to restore those contacts using multi-walled carbon nanotubes (MWNTs). Varying concentrations of carboxylated MWNTs in water, with or without type I collagen, were dried to create a thin film upon which one of three breast cell lines were seeded: cancerous and metastatic MDA- MB-231 cells, cancerous but non-metastatic MCF7 cells, or non-cancerous MCF10A cells. Proliferation, adhesion, scratch and autophagy assays, western blots, and immunochemical staining were used to assess adhesion and E-cadherin expression. Breast cancer cells grown on a MWNT-collagen coated surface displayed increased adhesion and decreased migration which correlated with an increase in E-cadherin. This work suggests an alternative approach to cancer treatment by physically mediating the cells' microenvironment.

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