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Ex vivo study of telluride nanowires in minigut

  • Yijun Qi
  • , Enzheng Shi
  • , Nathan Peroutka-Bigus
  • , Bryan Bellaire
  • , Michael Wannemuehler
  • , Albert Jergens
  • , Terrence Barrett
  • , Yue Wu
  • , Qun Wang

Producción científica: Articlerevisión exhaustiva

23 Citas (Scopus)

Resumen

Compound semiconductor nanomaterials, such as telluride nanowires, nanorods, and nanoparticles, have many unique properties for wide range of potential applications. The interaction between organoids (a biological system) and telluride nanowires is a crucial research area for human health in terms of its safety concerns. In this study, we demonstrated a case study on Bi 2 Te 3 nanowires. Through live/dead cell viability testing, bright-light image analysis, and surface area calculations, we showed that 50μg/mL Bi 2 Te 3 exerts minimum influence on shrinking crypts and disrupting lumen structure, which causes unhealthy growth. Within this optimal concentration, Bi 2 Te 3 nanowires can stay as a stable and non-toxic material inside the intestine. Unlike the previous studies of the cytotoxicity of Telluride nanomaterials interacting with single type of cells, our research demonstrated the first study of the interactions of engineered Telluride nanomaterials with a real complex gastrointestinal tract system as our primary small intestinal crypts were directly isolated from mice and grew into a self-renewable system with various types of cells and different cell pathways, which has the capability to mimic a fully functional intestinal epithelium layer for a realistic study inside the gastrointestinal tract. Most importantly, we showed that Bi 2 Te 3 nanowires, under infrared exposure, can act as a potential shield to stimulate cell viability and improve cell survivability.

Idioma originalEnglish
Páginas (desde-hasta)978-986
Número de páginas9
PublicaciónJournal of Biomedical Nanotechnology
Volumen14
N.º5
DOI
EstadoPublished - may 2018

Nota bibliográfica

Publisher Copyright:
Copyright © 2018 American Scientific Publishers All rights reserved.

Financiación

vation and further impact on the cells at molecular level are still under investigation, which could be related with Acknowledgments: We thank Tracey Pepper Stewart at the electrical, optical, and therImPa: l20p3ro.5p6er.t2ie4s1.o1f28t hOesne: ThuI,o w24a SMtaatye 2U0n1iv8e 1rs1it:y15B:e2s4sey Microscopy Facility for pro-nanowires. Although the mechanism hCopyright: American Scientific Publishersas not been studied viding equipmentand technologiesfor cell histology imag- yet, sev31eral4243assumptions can be made based oDelivered by Ingentan other ing.WethankCrohn’sandColitisFoundationofAmerica studies. Itissuggestedthatthemechanismofnan- (CCFA) Career Award (No. 348137), PhRMA Foundation otoxicity is related with the generation of reactive oxygen Research Starter Award (No. RSGTMT17), and McGee- species (ROS).42 IR exposure first caused cell inflamma-Wagner Interdisciplinary Research Foundation supported tion, which leads to ROS formations, further caused cell this research. The research was also supported (TAB) by death through free-radical mechanisms. However, telluride NIH (2RO1 DK095662) and VA Merit (1I01CX001353) nanowires are different compared with silicon nanowires. grants. They are thinner, smaller, and have well thermoelectrical and photothermal properties.43 With its thermoelectrical properties, a proper concentration is able to protect our biological system away from IR exposure. The unique shielding effect of nanowires could provide a potential solution for protecting stem cells under radiation or other medical treatment. We thank Tracey Pepper Stewart at Iowa State University Bessey Microscopy Facility for providing equipment and technologies for cell histology imaging. We thank Crohn's and Colitis Foundation of America (CCFA) Career Award (No. 348137), PhRMA Foundation Research Starter Award (No. RSGTMT17), and McGee- Wagner Interdisciplinary Research Foundation supported this research. The research was also supported (TAB) by NIH (2RO1 DK095662) and VA Merit (1I01CX001353) grants.

FinanciadoresNúmero del financiador
Interdisciplinary Research Foundation
PhRMA Foundation Research Starter
Tracey Pepper Stewart at Iowa State University Bessey Microscopy Facility
VA Merit Award1I01CX001353
National Institutes of Health (NIH)2RO1 DK095662
National Institutes of Health (NIH)
Crohn's and Colitis Foundation of America348137
Crohn's and Colitis Foundation of America
Pharmaceutical Research and Manufacturers of America FoundationRSGTMT17
Pharmaceutical Research and Manufacturers of America Foundation

    ODS de las Naciones Unidas

    Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible

    1. Good health and well being
      Good health and well being
    2. Affordable and clean energy
      Affordable and clean energy

    ASJC Scopus subject areas

    • General Medicine

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