4.6 Article

&ITIn vitro&IT toxic effects of reduced graphene oxide nanosheets on lung cancer cells

期刊

NANOTECHNOLOGY
卷 28, 期 50, 页码 -

出版社

IOP PUBLISHING LTD
DOI: 10.1088/1361-6528/aa95a8

关键词

necrosis; apoptosis; toxicity; cell viability; reduced graphene oxide nanosheets

资金

  1. FORCE Cancer Charity United Kingdom [50703]
  2. EPSRC project on Data Driven Surrogate-Assisted Evolutionary Fluid Dynamic Optimisation, University of Exeter, United Kingdom [EP/M017869/1]
  3. Higher Committee for Education Development (HCED), Iraq
  4. EPSRC Centre for Doctoral Training in Metamaterials, XM2 the University Of Exeter EX4, United Kingdom [EP/L015331/1]
  5. EPSRC [EP/M017869/1, EP/M017915/1] Funding Source: UKRI
  6. Engineering and Physical Sciences Research Council [EP/M017869/1, 1636743] Funding Source: researchfish

向作者/读者索取更多资源

The intriguing properties of reduced graphene oxide (rGO) have paved the way for a number of potential biomedical applications such as drug delivery, tissue engineering, gene delivery and bio-sensing. Over the last decade, there have been escalating concerns regarding the possible toxic effects, behaviour and fate of rGO in living systems and environments. This paper reports on integrative chemical-biological interactions of rGO with lung cancer cells, i.e. A549 and SKMES-1, to determine its potential toxicological impacts on them, as a function of its concentration. Cell viability, early and late apoptosis and necrosis were measured to determine oxidative stress potential, and induction of apoptosis for the first time by comparing two lung cancer cells. We also showed the general trend between cell death rates and concentrations for different cell types using a Gaussian process regression model. At low concentrations, rGO was shown to significantly produce late apoptosis and necrosis rather than early apoptotic events, suggesting that it was able to disintegrate the cellular membranes in a dose dependent manner. For the toxicity exposures undertaken, late apoptosis and necrosis occurred, which was most likely resultant from limited bioavailability of unmodified rGO in lung cancer cells.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据