Cytotoxic study in the treatment of tetracycline by using magnetic Fe3O4–PAMAM–antibody complexes
- 1. Fuzhou University, College of Chemical Engineering (China)
- 2. Fuzhou University, College of Chemistry (China)
Description
Antibiotics are widely used as drugs to treat human and animal diseases. However, the widespread use of antibiotics has induced environmental contamination by antibiotics and development of resistant bacteria. There thus a need for advanced methods to remove antibiotics, e.g. from natural waters. Here we used the concept that antigens and antibodies bind specifically to remove tetracycline. Magnetic Fe3O4–polyamidoamine(PAMAM)–antibody complexes were synthesized to remove tetracycline at optimum pH and temperature. In vitro cytotoxicity of tetracycline/treated solutions was evaluated in human skin fibroblasts (HSF) cells by using MTT dye assay, along with flow cytometry study for cell cycle distributions and cell apoptosis. The results show that the toxicity of tetracycline solutions was highly reduced after treatment by magnetic Fe3O4–PAMAM–antibody complexes, and the survival rate of the cells was increased. The tetracycline may induce the disintegration of the nucleosomes of the HSF cells and eventually lead to the cell apoptosis. The results show that the method of removing tetracycline has higher biosafety.
Additional details
Identifiers
Publishing Information
- Journal Title
- Environmental Chemistry Letters (Internet)
- Journal Volume
- 17
- Journal Issue
- 1
- Journal Page Range
- p. 543-549
- ISSN
- 1610-3661
INIS
- Country of Publication
- Germany
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 54111173
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE; S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- ANTIBODIES; ANTIGENS; APOPTOSIS; BACTERIA; CELL CYCLE; CONTAMINATION; DISEASES; DISTRIBUTION; DYES; FERRITES; FIBROBLASTS; HUMANS; IRON OXIDES; NUCLEOSOMES; PH VALUE; SKIN; TETRACYCLINES; TOXICITY
- Descriptors DEC
- ANIMAL CELLS; ANIMALS; ANTIBIOTICS; ANTI-INFECTIVE AGENTS; BODY; CHALCOGENIDES; CHROMATIN; CONNECTIVE TISSUE CELLS; DRUGS; FERRIMAGNETIC MATERIALS; IRON COMPOUNDS; MAGNETIC MATERIALS; MAMMALS; MATERIALS; MICROORGANISMS; ORGANIC COMPOUNDS; ORGANS; OXIDES; OXYGEN COMPOUNDS; PRIMATES; SOMATIC CELLS; TRANSITION ELEMENT COMPOUNDS; VERTEBRATES
Optional Information
- Copyright
- Copyright (c) 2019 Springer Nature Switzerland AG