(+)-Dihydromyricetin 정제를 위한 분별침전공정 개선
Improvement of the Fractional Precipitation Process for the Purification of (+)-Dihydromyricetin
2
조회
0
다운로드
5
인용
0
참고문헌
키워드
초록
Fractional precipitation is a simple method for purifying (+)-dihydromyricetin extracted from biomass. However, the fractionalprecipitation process has been inherently problematic due to the lengthy precipitation time that is required. The fractional precipitationtime was shortened and (+)-dihydromyricetin yield was improved by increasing the surface area per working volume(S/V) of the reacting solution through the addition of a cation exchange resin (Amberlite 200, Amberlite IR 120Na, Amberlite IR120H, or Amberlite IRC 50). Most of the (+)-dihydromyricetin (>90%) could be obtained after about 16 h of fractional precipitationusing Amberlite 200. Since high-purity (+)-dihydromyricetin can be obtained at a high yield and the precipitation time canbe reduced by increasing the surface area available for precipitation, this improved method is expected to minimize solventusage and the size and complexity of the high performance liquid chromatography operation required for (+)-dihydromyricetinpurification.
Abstract
Fractional precipitation is a simple method for purifying (+)-dihydromyricetin extracted from biomass. However, the fractionalprecipitation process has been inherently problematic due to the lengthy precipitation time that is required. The fractional precipitationtime was shortened and (+)-dihydromyricetin yield was improved by increasing the surface area per working volume(S/V) of the reacting solution through the addition of a cation exchange resin (Amberlite 200, Amberlite IR 120Na, Amberlite IR120H, or Amberlite IRC 50). Most of the (+)-dihydromyricetin (>90%) could be obtained after about 16 h of fractional precipitationusing Amberlite 200. Since high-purity (+)-dihydromyricetin can be obtained at a high yield and the precipitation time canbe reduced by increasing the surface area available for precipitation, this improved method is expected to minimize solventusage and the size and complexity of the high performance liquid chromatography operation required for (+)-dihydromyricetinpurification.
참고문헌 (24)
- An SW, "Comparison of hepatic detoxification activity and reducing serum alcohol concentration of Hovenia dulsis Thunb and Alnus japonica Steud", Korean J. Medicinal Crop. Sci, 7, pp.263~268 (1999)
- Cho EB, "Enhanced dissolution of megestrol acetate microcrystals prepared by antisolvent precipitation process using hydrophilic additives", Int. J. Pharm, 396, pp.91~98 (2010)
- Dong Y, "Preparation and characterization of spironolactone nanoparticles by antisolvent precipitation", Int. J. Pharm, 375, pp.84~88 (2009)
- Du Q, "Purification of (+)-dihydromyricetin from leaves extract of Ampelopsis grossedentata using high-speed countercurrent chromatograph with scaleup triple columns", J. Chromatogr. A, 973, pp.217~220 (2002)
- Han MG, "Development of a micelle-fractional precipitation hybrid process for the pre-purification of paclitaxel from plant cell cultures", Process Biochem, 45, pp.1368~1374 (2010)
- Hase K, "Effect of Hovenia dulcis on lipopolysaccharide-induced liver injury in chronic alcohol-fed rats", J. Trad. Med, 14, pp.28~33 (1997)
- 김진현, "Precipitation characteristics of paclitaxel in solvent systems with different ion exchange resins", The Korean Journal of Chemical Engineering, 30(10), pp.1954~1959 (2013), 한국화학공학회[DOI]
- Kang I, "Effect of reactor type on the purification efficiency of paclitaxel in the increased surface area fractional precipitation process", Sep. Puri. Technol, 99, pp.14~19 (2012)
- Kim WS, "Principles and applications of crystallization technology", KIC News, 10, pp.9~24 (2007)
- 김우식, "Bioproduct 분리를 위한 결정화 연구 동향", KSBB Journal, 20(3), pp.164~176 (2005), 한국생물공학회
- 이지연, "표면적이 증가된 분별침전에 의한 paclitaxel의 입자 크기 감소", 한국미생물·생명공학회지, 40(2), pp.157~162 (2012), 한국미생물·생명공학회[DOI]
- Lee JY, "Evaluation of the effect of crude extract purity and pure paclitaxel content on the increased surface area fractional precipitation process for the purification of paclitaxel", Process Biochem, 47, pp.2388~2397 (2012)
- Kang-Hee Lee, "Development and Optimization of Fractional Precipitation for the Pre-purification of (+)-Dihydromyricetin", Biotechnology and Bioprocess Engineering, 13(3), pp.274~278 (2008), 한국생물공학회
- Lee MK, "Biological activities of Hovenia dulcis Thunb", Korean J. Medicinal Crop. Sci, 7, pp.185~192 (1999)
- Pyo SH, "Efficient purification and morphology characterization of paclitaxel from cell cultures of Taxus chinensis", J. Chem. Technol. Biotechnol, 79, pp.1162~1168 (2005)
- Sakai K, "Effect of water extracts of crude drugs in decreasing blood alcohol concentrations in rats", Chem. Pharm. Bull, 35, pp.4597~4604 (1987)
- Sim HA, "Evaluation of a high surface area acetone", pentane precipitation process for the purification of paclitaxel from plant cell cultures, 2012, pp.89, 112~116
- Song X, "Preparation and application of dihydromyricetin", CN Patent 1,288,892, ~ (2001)
- Yeo SD, "Recrystallization of sulfathiazole and chlorpropamide using the supercritical fluid antisolvent process", J. Supercrit. Fluids, 25, pp.143~154 (2003)
- Yohsikawa M, "Four methyl-migrated 16,17-seco-dammarane triterpene glycosides from chines natural Medicine, Hovenia semen seu fructus, the seeds and fruit of Hovenia dulcis Thunb", Chem. Pharm. Bull, 44, pp.1736~1743 (1996)
- Yohsikawa M, "Bioactive constituents of Chinese natural medicines. III. Absolute stereostructures of new dihydroflavonols, hovenitins I, II, and III, isolated from hoveniae semen seu fructus, the seed and fruit of Hovenia dulcis Thunb. (Rhamnaceae): Inhibitory effect on alcohol-induced muscular relaxation and hepatoprotective activity", Yakugaku Zasshi, 117, pp.108~118 (1997)
- Yoo SM, "Recovery and pre-purification of (+)-dihydromyricetin from Hovenia dulcis", Process Biochem, 41, pp.567~570 (2006)
- Zhang HX, "Micronization of atorvastatin calcium by antisolvent precipitation process", Int. J. Pharm, 374, pp.106~113 (2009)
- Zhang Y, "Process for preparing dihydromyricetin from Porcelain ampelopsis", ~, pp.CN Patent 1,393,443 (2003)
