Kinetic crystallization separation process of the inositol isomers by controlling metastable zones

作者: Kaname Konuki , Izumi Hirasawa

DOI: 10.1016/J.JCRYSGRO.2012.10.017

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摘要: Abstract D-chiro-inositol (DCI) is prepared by the immobilized enzyme reaction which uses myo-inositol (MI) as substrate and conversion rate about 13%. The aim of this study was to develop a separation method for high purity DCI crystals from solution including low only crystallization process. We succeeded in separating 96% water cooling crystallization, but it presumed that scale-up difficult. Although we tried anti-solvent similar were not obtained. Therefore, proposed process controlling metastable zones. desired compound controlled process, because solid–liquid achieved before zone. By using method, 97% yield per batch 50%, actual improved last mother liquor returns into following batch. When repeated, reproduced robustness proved. It expected will be successful, purification could applicable systems such isomers analogs.

参考文章(11)
Ken-ichi Yoshida, Masanori Yamaguchi, Tetsuro Morinaga, Maya Ikeuchi, Masaki Kinehara, Hitoshi Ashida, Genetic Modification of Bacillus subtilis for Production of d-chiro-Inositol, an Investigational Drug Candidate for Treatment of Type 2 Diabetes and Polycystic Ovary Syndrome Applied and Environmental Microbiology. ,vol. 72, pp. 1310- 1315 ,(2006) , 10.1128/AEM.72.2.1310-1315.2006
Sung-Kee Chung, Yong-Uk Kwon, Practical synthesis of all inositol stereoisomers from myo-inositol. Bioorganic & Medicinal Chemistry Letters. ,vol. 9, pp. 2135- 2140 ,(1999) , 10.1016/S0960-894X(99)00348-0
Ken-ichi Yoshida, Masanori Yamaguchi, Tetsuro Morinaga, Masaki Kinehara, Maya Ikeuchi, Hitoshi Ashida, Yasutaro Fujita, myo-Inositol Catabolism in Bacillus subtilis Journal of Biological Chemistry. ,vol. 283, pp. 10415- 10424 ,(2008) , 10.1074/JBC.M708043200
Michael Podeschwa, Oliver Plettenburg, Jochen vom Brocke, Oliver Block, Stephan Adelt, Hans-Josef Altenbach, Stereoselective Synthesis of myo‐, neo‐, L‐chiro, D‐chiro, allo‐, scyllo‐, and epi‐Inositol Systems via Conduritols Prepared from p‐Benzoquinone European Journal of Organic Chemistry. ,vol. 2003, pp. 1958- 1972 ,(2003) , 10.1002/EJOC.200200572
Yoshiaki Takahashi, Hitoshi Nakayama, Keiki Katagiri, Kumi Ichikawa, Nobuhiro Ito, Tomohisa Takita, Tomio Takeuchi, Toshiaki Miyake, Facile and practical synthesis of optically pure 1 d - chiro -inositol from myo -inositol Tetrahedron Letters. ,vol. 42, pp. 1053- 1056 ,(2001) , 10.1016/S0040-4039(00)02178-X
Tie-hua Sun, Douglas B Heimark, Thang Nguygen, Jerry L Nadler, Joseph Larner, Both myo-inositol to chiro-inositol epimerase activities and chiro-inositol to myo-inositol ratios are decreased in tissues of GK type 2 diabetic rats compared to Wistar controls Biochemical and Biophysical Research Communications. ,vol. 293, pp. 1092- 1098 ,(2002) , 10.1016/S0006-291X(02)00313-3
Gianfranco Carlomagno, Vittorio Unfer, Scott Roseff, The D-chiro-inositol paradox in the ovary. Fertility and Sterility. ,vol. 95, pp. 2515- 2516 ,(2011) , 10.1016/J.FERTNSTERT.2011.05.027
John E. Nestler, Daniela J. Jakubowicz, Paula Reamer, Ronald D. Gunn, Geoffrey Allan, Ovulatory and Metabolic Effects of d-Chiro-Inositol in the Polycystic Ovary Syndrome New England Journal of Medicine. ,vol. 340, pp. 1314- 1320 ,(1999) , 10.1056/NEJM199904293401703
Joseph Larner, D-chiro-inositol--its functional role in insulin action and its deficit in insulin resistance. International Journal of Experimental Diabetes Research. ,vol. 3, pp. 47- 60 ,(2002) , 10.1080/15604280212528
Allison S. Kennington, Cynthia R. Hill, James Craig, Clifton Bogardus, Itamar Raz, Heidi K. Ortmeyer, Barbara C. Hansen, Guillermo Romero, Joseph Larner, Low Urinarychiro-Inositol Excretion in Non-Insulin-Dependent Diabetes Mellitus New England Journal of Medicine. ,vol. 323, pp. 373- 378 ,(1990) , 10.1056/NEJM199008093230603