发明授权
- 专利标题: Process for the production of immunobiological preparations applicable in the diagnosis, prevention and/or treatment of Candida guilliermondii infections
- 专利标题(中): 用于生产适用于诊断,预防和/或治疗念珠菌感染的免疫生物制剂的方法
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申请号: US319711申请日: 1981-11-09
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公开(公告)号: US4678748A公开(公告)日: 1987-07-07
- 发明人: Pal Sutka , Klara Sutka
- 申请人: Pal Sutka , Klara Sutka
- 专利权人: Pal Sutka,Klara Sutka
- 当前专利权人: Pal Sutka,Klara Sutka
- 主分类号: A61K36/064
- IPC分类号: A61K36/064 ; A61K39/00 ; A61K39/395 ; C12N1/16 ; C12P1/02 ; C12P21/00 ; C12Q1/04 ; G01N33/569
摘要:
The invention relates to a process for the production of new immunobiological preparations for the diagnosis, prophylaxis and/or treatment of Candida guilliermondii infections. According to the invention one proceeds as follows:(a) a Candida guilliermondii strain is propagated under aerobic conditions at 24-42.degree. C. on a culture medium containing assimilable carbon and nitrogen sources, the resulting population(s) is (are) maintained under identical conditions for a prolonged period, therafter the fungus cells are separated from the culture, washed, ruptured mechanically, extracted, the extract is treated with a polar organic solvent, and the resulting precipitate is converted into an immunobiological preparation either as such or after further purification, or(b) a Candida guilliermondii strain is cultivated for 48-72 hours under aerobic conditions at 24.degree.-42.degree. C. on a culture medium containing assimilable carbon and nitrogen sources, the resulting culture is optionally propagated further to produce two or three new populations, then the fungus cells are separated from the culture, washed, ruptured mechanically, extracted, then, if desired, a polar organic solvent is added to the extract, and the resulting precipitate is converted into an immunobiological preparation either as such or after further purification, or(c) a Candida guilliermondii strain is cultivated for 48-72 hours under aerobic conditions at 24.degree.-42.degree. C. on a culture medium containing assimilable carbon and nitrogen sources, then the culture is killed, the killed cells are separated and converted then into an immunobiological preparation either as such or after purification.
公开/授权文献
- US6154231A Suction recovery of ink jet recording apparatus 公开/授权日:2000-11-28
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