http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102860988-B

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P17-02
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filingDate 2011-07-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2013-09-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2b07adac0c745030673d16c311969aec
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9787da55efd43c770d22f7c60caba6d5
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publicationDate 2013-09-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102860988-B
titleOfInvention Chymotrypsin composition freeze-dried powder and preparation method thereof
abstract The invention relates to a chymotrypsin preparation, particularly relates to chymotrypsin composition freeze-dried powder and a preparation method thereof. The hymotrypsin composition freeze-dried powder comprises chymotrypsin, dextran 20 and sorbitol, wherein the ratio of chymotrypsin to dextran 20 to sorbitol is 1 million units: 1-1.8g: 0.05-0.6g. The average porosity of the hymotrypsin composition freeze-dried powder is 85-98%. The invention further relates to a preparation method of the hymotrypsin composition freeze-dried powder. The hymotrypsin composition freeze-dried powder disclosed herein has the advantages of full and uniform appearance, high porosity, good re-solubility, high stability, simple prescription, low proportion of pharmaceutic adjuvants, low side effect to human body, safety and reliability. According to the invention, the preparation technology of the hymotrypsin composition freeze-dried powder is further improved, the temperature, liquid volume, and freeze-drying process are improved, and sterilization is conducted twice.
priorityDate 2011-07-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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