Control of Carbon Nanotube Solvatochromic Response to Chemotherapeutic Agents.
Jackson D HarveyHanan A BakerElizabeth MercerJanuka Budhathoki-UpretyDaniel A HellerPublished in: ACS applied materials & interfaces (2017)
Alkylating agents such as cisplatin play an essential role in chemotherapy regimens, but initial and acquired resistance in many cancer types often dampen therapeutic response. The poor understanding of the mechanisms of resistance highlight the need for quantitative measurements of alkylating agent distribution at both the tissue and subcellular levels. Sensors for use in live animals and cells would allow for more effective study of drug action and resistance. Toward this end, single-walled carbon nanotubes suspended with single-stranded DNA have suitable optical properties for in vivo sensors, such as near-infrared emission and sensitivity to the local environment via solvatochromic responses. Currently, solvatochromic changes of such sensors have been limited by the chemical nature of the analyte, making it impossible to control the direction of energy emission changes. Here, we describe a new approach to control the direction and magnitude of solvatochromic responses of carbon nanotubes. We found that the alkylation of DNA on the nanotube surface can result in small changes in DNA conformation that allow the adsorption of amphiphiles to produce large differences (>14 nm) in response to different drugs. The technique surprisingly revealed differences among drugs upon alkylation. The ability to control carbon nanotube solvatochromism as desired may potentially expand the application of nanotube-based optical sensors for new classes of analytes.
Keyphrases
- carbon nanotubes
- circulating tumor
- low cost
- cell free
- single molecule
- nucleic acid
- high resolution
- squamous cell carcinoma
- walled carbon nanotubes
- emergency department
- induced apoptosis
- papillary thyroid
- cell death
- circulating tumor cells
- radiation therapy
- molecular dynamics simulations
- young adults
- high speed
- cell cycle arrest
- single cell
- mass spectrometry
- binding protein
- locally advanced
- squamous cell
- lymph node metastasis