Detection of DNA damage induced by nanomaterials


Doğan Topal B., Uslu B., Özkan S. A.

Nanoscale Fabrication, Optimization, Scale-up and Biological Aspects of Pharmaceutical Nanotechnology, Alexandru Mihai Grumezescu, Editör, William Andrew Publishing , London, ss.545-577, 2017

  • Yayın Türü: Kitapta Bölüm / Araştırma Kitabı
  • Basım Tarihi: 2017
  • Yayınevi: William Andrew Publishing
  • Basıldığı Şehir: London
  • Sayfa Sayıları: ss.545-577
  • Editörler: Alexandru Mihai Grumezescu, Editör
  • Ankara Üniversitesi Adresli: Evet

Özet

The nanotechnology industry is developing rapidly with promises of significant advantages that will have remarkable economic and scientific influences, applicable to all areas ranging from aerospace engineering to medical healthcare. Because of the beneficial physico-chemical features of nanomaterials, the development and design of novel engineered nanomaterials have been of main importance for industry. A nanomaterial is described as a substance with at least one dimension ,100 nm in size. They could take many different forms such as rods, wires, tubes, or spheres, with more elaborate structures developed, such as nanoonions and nanopeapods (Imasaka et al., 2006; Warner et al., 2008). As nanomaterials become more widely used, human exposure to nanomaterials is inevitable. Their small size could be responsible for adverse biological effects. Nanotoxicology is arising as an important subdiscipline of nanotechnology. Nanotoxicology refers to the study of the interactions of nanostructures with biological systems. An understanding of the relationship between the physical and chemical properties of the nanostructures and their in vivo behavior would provide a fundamental to assess toxic response of the nanostructures (Lewinski et al., 2008; Service, 2003). At lower concentrations, the cellular changes that may emerge, which may not be concluded in cell death but could contribute to human health risks. The most important human health risk is DNA damage induction. The estimated 104 DNA damage events occur in a cell per day caused by exposure to genotoxic substances of environmental origin or endogenously produced. DNA has important biological functions in living systems. Its important biological functions are the primary target molecule for most anticancer therapies in accordance with the cell biology. Exposure to endogenous free radicals and exogenous mutagens has been determined to affect the instability of the genomes. These carcinogens resulted in some degenerative diseases, including cardiovascular disease, Alzheimer’s disease and cancer. By this means, the carcinogenic processes and the cancer risk is associated with high rate of DNA damage and chromosomal defect (Bonassi et al., 2000). Consequently, the detection of DNA damage has become a focus in DNA research fields (Lee et al., 2008; Rawle et al., 2008; Yun et al., 2007). To apply genotoxicity testing and to evaluate the carcinogenic or mutagenic potential of new substances is an important part of preclinical safety testing of new pharmaceuticals, which is a requirement before entering into Phase I/II clinical trials. Assays for the detection of oxidative damaged DNA in cells and animal tissues have been incorporated into the standard battery of nanotoxicology testing methods. This chapter focuses on studies published over the past decade that attempted to detect DNA damage associated with exposure to nanomaterials. Reviewing some selected studies using separation techniques (electrophoresis and high performance liquid chromatography (HPLC)) and electrochemical methods will help improve the current understanding of the potential DNA damages of nanomaterials.