Abstract
In the present research, the thermophysical properties of phytosterols were investigated by thermogravimetry (TG) and differential scanning calorimetry (DSC) in the range of 300–800 K. As a result, the areas of their thermal stability were established. The thermodynamic characteristics of melting and crystallization have been determined. For one of the samples, the specific heat was studied in the range 260–570 K. Comparison of the present results with the data available in the literature was carried out. The dependence of thermophysical properties on the composition and nature of phytosterols has been concluded.
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References
Demonty I, Ras RT, Van Der Knaap HCM, Duchateau GSMJE, Meijer L, Zock PL, et al. Continuous dose-response relationship of the LDL-cholesterol-lowering effect of phytosterol intake. J Nutr. 2009;139:271–84. https://doi.org/10.3945/jn.108.095125.
Wester I. Cholesterol-lowering effect of plant sterols. Eur J Lipid Sci Technol. 2000;102:37–44. https://doi.org/10.1002/(sici)1438-9312(200001)102:1%3C37::aid-ejlt37%3E3.0.co;2-1.
Fernandes P, Cabral JMS. Phytosterols: Applications and recovery methods. Bioresour Technol. 2007;98:2335–50. https://doi.org/10.1016/j.biortech.2006.10.006.
Bot A. Phytosterols. Encycl Food Chem. 2018;54:225–8. https://doi.org/10.1016/B978-0-08-100596-5.21626-0.
Vaikousi H, Lazaridou A, Biliaderis CG, Zawistowski J. Phase transitions, solubility, and crystallization kinetics of phytosterols and phytosterol-oil blends. J Agric Food Chem. 2007;55:1790–8. https://doi.org/10.1021/jf0624289.
Oja V, Chen X, Hajaligol MR, Chan WG. Sublimation thermodynamic parameters for cholesterol, ergosterol, β-Sitosterol, and stigmasterol. J Chem Eng Data. 2009;54:730–4.
Moreno-Calvo E, Temelli F, Cordoba A, Masciocchi N, Veciana J, Ventosa N. A new microcrystalline phytosterol polymorph generated using CO2-expanded solvents. Cryst Growth Des. 2014;14:58–68. https://doi.org/10.1021/cg401068n.
Mel’nikov SM, Ten-Hoorn JWMS, Bertrand B. Can cholesterol absorption be reduced by phytosterols and phytostanols via a cocrystallization mechanism? Chem Phys Lipids. 2004;127:15–33. https://doi.org/10.1016/j.chemphyslip.2003.08.007.
Acevedo NC, Franchetti D. Analysis of co-crystallized free phytosterols with triacylglycerols as a functional food ingredient. Food Res Int. 2016;85:104–12.
Kawachi H, Tanaka R, Hirano M, Igarashi K, Ooshima H. Crystallization of β-sitosterol using a water-immiscible solvent hexane. J Chem Eng Japan. 2006;39:869–75. https://doi.org/10.1252/jcej.39.869.
Christiansen LI, Rantanen JT, Von Bonsdorff AK, Karjalainen MA, Yliruusi JK. A novel method of producing a microcrystalline β-sitosterol suspension in oil. Eur J Pharm Sci. 2002;15:261–9. https://doi.org/10.1016/S0928-0987(01)00223-8.
Nekrasova VB. Obtaining and using biologically active and related products from sulfate soap. Dr Eng Sci Diss. 2006;25:168.
Barriuso B, Ansorena D, Astiasarán I. Oxysterols formation: A review of a multifactorial process. J Steroid Biochem Mol Biol. 2017;169:39–45. https://doi.org/10.1016/j.jsbmb.2016.02.027.
Rudzińska M, Przybylski R, Wąsowicz E. Products formed during thermo-oxidative degradation of phytosterols. JAOCS, J Am Oil Chem Soc. 2009;86:651–62. https://doi.org/10.1007/s11746-009-1397-0.
Rudzinska M, Przybylski R, Zhao YY, Curtis JM. Sitosterol thermo-oxidative degradation leads to the formation of dimers, trimers and oligomers: A study using combined size exclusion chromatography/mass spectrometry. Lipids. 2010;45:549–58. https://doi.org/10.1007/s11745-010-3433-0.
Gost R. 56340–2015. Organic liquids. Determination of water by coulometric Karl Fischer titration. Moscow Standartinform Publ. 2019;9:15.
Laakso PH. Determination of plant stanols and plant sterols in phytosterol enriched foods with a gas chromatographic-flame ionization detection method: NMKL collaborative study. J AOAC Int. 2014;97:1097–108. https://doi.org/10.5740/jaoacint.14-011.
Rossi L, Ten-Hoorn JWMS, Melnikov SM, Velikov KP. Colloidal phytosterols: Synthesis, characterization and bioaccessibility. Soft Matter. 2010;6:928–36.
Hohne GWH, Hemminger WF, Flammersheim HF. Differential scanning calorimetry. Berlin Heidelberg: Springer-Verlag; 2003.
Drebushchak VA. Calibration coefficient of a heat-flow DSC. Part II. Optimal calibration procedure. J Therm Anal Calorim. 2005;79:213–8. https://doi.org/10.1007/s10973-004-0586-1.
Razuvaev GA, Latyaeva VN, Mar’in VP, Vyshinskaya LI, Korneva SP, Andrianov YA, et al. Thermal decomposition of organo-bielemental vanadium compounds Cp2V(ER3) (ER3 - GeEt3, SnEt3, CH2SiMe3, SeGeEt3). J Organomet Chem. 1982;225:233–44. https://doi.org/10.1016/S0022-328X(00)86826-6.
Acknowledgements
The authors would like to thank the Shared Use Equipment Center for high–precision measuring in photonics (VNIIOFI) for NIR spectra and the Common Use Centre “New Materials and Resource-saving Technologies” (Research Institute for Chemistry of UNN) for XRPD measurements.
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Korshunov, A.O., Markin, A.V., Kushnir, S.R. et al. Thermophysical properties of phytosterols. J Therm Anal Calorim 147, 14175–14182 (2022). https://doi.org/10.1007/s10973-022-11618-8
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DOI: https://doi.org/10.1007/s10973-022-11618-8