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Solid and liquid state characterization of tetrahydrocurcumin using XRPD, FT-IR, DSC, TGA, LC-MS, GC-MS, and NMR and its biological activities
- Source :
- Journal of Pharmaceutical Analysis, Vol 10, Iss 4, Pp 334-345 (2020), Journal of Pharmaceutical Analysis
- Publication Year :
- 2020
- Publisher :
- Elsevier, 2020.
-
Abstract
- Tetrahydrocurcumin (THC) is one of the major metabolites of curcumin (CUR), an ancient bioactive natural polyphenolic compound. This research article describes both the solid and liquid state characterization of THC using advanced spectroscopic and thermo-analytical techniques. Anti-inflammatory, anti-oxidant, and neuroprotective activities of THC were investigated using in vitro cell lines. Liquid chromatography-mass spectrometry analysis revealed that our sample comprised 95.15% THC, 0.51% tetrahydrodemethoxycurcumin (THDC), 3.40% hexahydrocurcumin, and 0.94% octahydrocurcumin. Gas chromatography-mass spectrometry analysis indicated the presence of 96.68% THC and 3.32% THDC. THC in solution existed as keto-enol tautomers in three different forms at different retention time, but the enol form was found to be dominant, which was also supported by nuclear magnetic resonance analysis. THC was thermally stable up to 335.55 °C. THC exhibited more suppression of cytokines (TNF-α, IL-1β, and MIP-1α) than CUR in a concentration-dependent manner in mouse splenocytes, while NK-cell and phagocytosis activity was increased in macrophages. THC showed a significant reduction of free radicals (LPO) along with improved antioxidant enzymes (SOD and catalase) and increased free radical scavenging activity against ABTS+ radicals in HepG2 cells. THC displayed higher protection capability than CUR from oxidative stress and neuronal damage by improving cell viability against H2O2 induced HepG2 cells and MPP+ induced SH-SY5Y cells, respectively, in a concentration-dependent manner. Thus, a variation of the biological activities of THC might rely on its keto-enol form and the presence of other THC analogs as impurities. The present study could be advantageous for further research on THC for better understanding its physicochemical properties and biological variation.<br />Graphical abstract Image 1<br />Highlights • Solid and liquid state characterization of THC using advanced analytical techniques. • THC existed in 3 different forms viz. one keto form, two enol forms in solution. • THC was found to be thermally more stable than curcumin. • THC exhibited significant suppression of proinflammatory cytokines, increased NK cells and phagocytosis activities. • THC showed higher total anti-oxidant activity and neuroprotective activity than curcumin.
- Subjects :
- Antioxidant
medicine.medical_treatment
Radical
Pharmaceutical Science
02 engineering and technology
Pharmacy
01 natural sciences
Analytical Chemistry
chemistry.chemical_compound
Keto-enol tautomer
Liquid chromatography–mass spectrometry
Spectroscopic and thermal analysis
Drug Discovery
mental disorders
Electrochemistry
medicine
Liquid chromatography-mass spectrometry
Spectroscopy
ABTS
Chromatography
biology
organic chemicals
010401 analytical chemistry
lcsh:RM1-950
021001 nanoscience & nanotechnology
0104 chemical sciences
lcsh:Therapeutics. Pharmacology
chemistry
Catalase
Polyphenol
Curcumin
biology.protein
Original Article
Gas chromatography–mass spectrometry
Tetrahydrocurcumin
Anti-inflammatory
0210 nano-technology
Subjects
Details
- Language :
- English
- ISSN :
- 20951779
- Volume :
- 10
- Issue :
- 4
- Database :
- OpenAIRE
- Journal :
- Journal of Pharmaceutical Analysis
- Accession number :
- edsair.doi.dedup.....495822e7f4a04a1f7c78b05be1cd3f6f