Biosynthesis of silver nanoparticles using tea leaf extract (camellia sinensis) for photocatalyst and antibacterial effect.

Silver nanoparticles (C. AgNPs) are synthesized by the biological reduction method using extracts from green tea leaves (Camellia Sinensis) collected from tea hills at an altitude of 100 m above the ground. The chemicals present in the tea leaf extract act as reducing agents used to reduce Ag+ ions to silver atoms to form C. AgNPs in the solution. In this work, we optimized the C. AgNPs synthesis process by investigating the influence of reaction parameters such as concentration of tea leaf extract (1 ppm-50 ppm), reaction temperature (30 °C-60 °C), reaction time (5 min-100 min), and reaction rate (400 rpm-800 rpm) through absorption UV-Vis spectroscopy, TEM transmission electron microscopy, and spectroscopy X-ray. Organic compounds in tea leaf extract are detected by NMR measurement. The functional groups on the C. AgNPs are shown on the Fourier transform infrared (FTIR) spectrum. The C. AgNPs are used to degrade MB dye at 10 ppm concentration based on the photocatalytic effect using a 6500 K white light source. The C. AgNPs have also been studied for their antibacterial activity on two bacteria, Pseudomonas aeruginosa (P.A) and Staphylococcus aureus (S.A), while a positive control is Ampicillin 50 mg/ml and a negative control is H2O. The results reveal that the C. AgNPs with diameters in the range of 25 nm-55 nm degrade 10 ppm MB dye after 1 h with photodegradation efficiency up to 96 %. The antibacterial ability of C. AgNPs against both bacteria is good, even superior to that of Ampicillin. Furthermore, the particle synthesis efficiency and therefore the antibacterial activity as well as the photodegradation effect of C. AgNPs are higher than previously reported. At the same time, using green tea leaf extract to synthesize C. AgNPs creates environmentally friendly products. These useful behaviors are the potential to increase the scope and applicability of C. AgNPs, especially for biomedical applications in the near future.

Anti-cancer activity of Marsdenialongise A, a new C21 steroidal glycoside isolated from Marsdenia longipes W.T. Wang (Apocynaceae).

C21 steroidal glycosides are a group of natural compounds with biological activities such as anti-cancer, anti-microbial, and anti-viral properties. In this study, we isolated and determined the structure of a new C21 steroidal glycoside, named Marsdenialongise A from Marsdenia longipes W.T. Wang, using nuclear magnetic resonance spectroscopy and mass spectra data. Marsdenialongise A is a derivative of tenacigenin B and was isolated for the first time from a plant. The inhibitory effect of Marsdenialongise A on cancer cells was evaluated through MTT and cell migration assays, cell cycle, and apoptosis analyses. The results of the MTT assay showed that Marsdenialongise A reduces the cell viability of cancer cells, with the AGS cell line being more sensitive than other cell lines, with an IC50 value of 5.69 µM (for 48 h of treatment). Marsdenialongise A also exhibited an ability to prevent the migration of cancer cells in AGS cells. Further analysis using flow cytometry has revealed that Marsdenialongise A is capable of inducing cell cycle arrest and apoptosis. The overexpression of reactive oxygen species (ROS) production induced by Marsdenialongise A can be considered a cause that leads to the influence on the cell cycle and apoptosis of cancer cells. Thus, Marsdenialongise A can be considered a potential anti-cancer agent.