RESUMEN
Increasing industrial contamination necessitates development of sustainable water treatment solutions. Photocatalysis is a green technology utilizing light-activated materials (photocatalysts), which can degrade pollutants into harmless by-products. It is an emergent need to develop a photocatalyst that presents a significant advancement for sustainable water treatment and non-toxic to the environment. This study investigates the photocatalytic activity and in vitro cytotoxicity of a novel hybrid material comprising of alginate, copper oxide (CuO) and graphitic carbon nitride (gC3N4) for methylene blue (MB) degradation. The hybrid material was synthesized by a two-step process: (i) doping of CuO on gC3N4 through co-precipitation method formed CuO-gC3N4 (CG) and (ii) incorporation of CG in the calcium alginate (A) by ionotropic gelation method that is named as ACG. The characteristic features of the synthesized A, CG and ACG were studied using Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD) and thermogravimetric analysis (TGA). The optical characteristic of A, CG and ACG was studied using UV-diffuse reflectance spectroscopy (UV-DRS). The morphology and elemental composition of ACG was evaluated by scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS) and X-ray photoelectron spectroscopy (XPS). To assess the environmental impact of ACG, a two-step approach was employed. First, the photocatalytic activity of ACG under UV-visible light (UV-vis) irradiation for MB degradation was evaluated. ACG exhibited photocatalytic activity by achieving 86.26% of degradation efficiency for MB within 60 min. Second, the in vitro cytotoxicity of ACG, MB and MB degraded products towards tilapia gill cell lines were assessed. By comparing the toxicity of the MB and the secondary products, it is concluded that the overall process leads to a sustainable outcome.
RESUMEN
Lates calcarifer (Bloch) is a potential candidate fish species for culture in marine and brackishwater. A continuous gill cell line was derived from L. calcarifer by the explant culture method and has been passaged for 132 times, in Leibovitz's L-15 medium containing 10% fetal bovine serum (FBS) at 28 °C. The cells showed a rate of recovery between 90 and 95% after being successfully cryopreserved at various passage levels and formed monolayer in 2-3 days without any morphological changes. Immunophenotypic analysis of the SBG cell line revealed that they are of epithelial origin. Polymerase chain reaction assay using mitochondrial 12S rRNA primer specific to L. calcarifer was used to confirm the authenticity of the established gill cell line origin from seabass. The transfection efficiency was evaluated in Seabass Gill (SBG) cell line using pEGFP-N1 and Lipofectamine™ 3000. Transfection efficiency was found to be between 13 and 16%. The cytotoxicity of three different metal detecting probes was evaluated by MTT and Alamar blue assays to determine safe concentration. The result revealed that SBG cell line can be applied for recognition of metals using probes. The current study established, for the first time, a gill-derived cell line (SBG) from Lates calcarifer and its application for the detection of intracellular indium, mercury, and lutetium ions by specific fluorescent probes.
RESUMEN
Danio rerio retinal pigmented epithelial (DrRPE) cell line, derived from the RPE tissue, was established and characterized. The cells were able to grow at a wide range of temperatures from 25°C to 32°C in Leibovitz's L-15 medium. The DrRPE cell line consists of epithelial cells with a diameter of 15-19 µm. The cell line was characterized by mitochondrial 12S rRNA gene, immunocytochemical analysis, and karyotyping. DrRPE cells treated with 10 µM of all-trans-retinol for 24 h readily formed lipid droplets. DrRPE cells were irradiated with narrowband ultraviolet-B (UV-B) radiation at different time periods of 0, 10, 20, and 40 min. The cells were subsequently examined for changes in morphology, cell viability, phagocytotic activity, mitochondrial distribution, nuclei morphology, generation of reactive oxygen species, and expression of apoptotic-related genes p53 and Cas3 by quantitative polymerase chain reaction. The results demonstrate that UV-B radiation can cause a considerable decrease in DrRPE cell viability as well as in phagocytotic activity. In addition, the results demonstrate that UV-B radiation can induce the degradation of mitochondria and DNA in cultured DrRPE cells.
