Pisamai Ting

Dr. Pisamai Ting


Research Focus & Metrics

Academic Career Length

6Years (2021-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
1 November 2021 in Journal of Ethnopharmacology
Verified
Journal Article
Closed access
JKJirarat Karinchai
Jirarat Karinchai
PBPhatcharaporn Budluang
Phatcharaporn Budluang
PTPiya Temviriyanukul
Piya Temviriyanukul
PTPisamai Ting
Pisamai Ting
ONOnanong Nuchuchua
Onanong Nuchuchua
Pornsiri PitchakarnPornsiri Pitchakarn
Pornsiri Pitchakarn

8 June 2024 in Nanomaterials
Verified
Journal Article
Open access
PDF file
Pornsiri PitchakarnPornsiri Pitchakarn
Pornsiri Pitchakarn
PTPisamai Ting
Pisamai Ting
PBPensiri Buacheen
Pensiri Buacheen
JKJirarat Karinchai
Jirarat Karinchai
WIwoorawee inthachat
woorawee inthachat
PTPiya Temviriyanukul
Piya Temviriyanukul
Chrysin is hypothesized to possess the ability to prevent different illnesses, such as diabetes, cancer, and neurodegenerative disorders. Nonetheless, chrysin has a low solubility under physiological conditions, resulting in limited bioavailability. In a previous study, we utilized an oil-in-water emulsion system (chrysin-ES or chrysin-NE) to encapsulate chrysin, thereby increasing its bioaccessibility and preserving its antioxidant and anti-Alzheimer’s properties. To promote the chrysin-ES as a supplementary and functional food, it was obligatory to carry out a safety assessment. Cytotoxicity testing showed that chrysin-ES was harmless, with no killing effect on 3T3-L1 (adipocytes), RAW 264.7 (macrophages), HEK293 (kidney cells), and LX-2 (hepatic stellate cells). The acute toxicity evaluation demonstrated that the 50% lethal dose (LD50) for chrysin-ES was greater than 2000 mg/kg BW. Genotoxicity assessments found that chrysin-ES did not induce DNA mutations in vitro or in vivo. Furthermore, chrysin and chrysin-ES exhibited anti-mutagenic properties against PhIP-induced and IQ-induced mutagenesis in the Ames test, while they inhibited urethane-, ethyl methanesulfonate-, mitomycin C-, and N-nitrosomethylurea-mediated mutations in Drosophila. The present study illustrates the safety and anti-genotoxicity properties of chrysin-ES, allowing for the further development of chrysin-based food supplements and nutraceuticals.