发明名称 |
A MIXTURE OF MEDICAMENT QUALITY CONTROL “0.1 G SUBLINGUAL GLYCINE TABLETS” AND METHOD FOR PREPARING THEREOF |
摘要 |
The invention relates to chemico-pharmaceutical industry, more definite to a mixture for a medicament quality control “0.1 g. sublingual glycine tablets” and a method for preparing thereof. The method comprises a mixture preparing by dissolving 2.5 g. of tablets crushed to powder in 250 ml of purified water and measuring light-scattering using a spectrophotometer with wave length 700±2 nm in a cuvette with 10 mm layer thickness respective to the purified water. The dilution of the 2.5 g. of tablets are carried out at 37°C during 20 min. in an device for determining dilution using an impeller mixer at 150 rev/min. After the dilution the mixture is maintained for 10 minutes, then 4 ml is sampled for determining light scattering . The quality control mixture comprises the ratio 100:1 between water and the crushed powder tablet comprising 0.101 g. microcapsules of non-sintered crystals of aminoacetic acid coated with a polymeric methylcellulose film of MC-100 grade, and 0.001 magnesium stearate. The light scanning coefficient compared to the purified water is within between 50 to 70% at the wave length 700±2 nm for 4 ml mixture at 10 mm layer thickness. |
申请公布号 |
EA007615(B1) |
申请公布日期 |
2006.12.29 |
申请号 |
EA20060000147 |
申请日期 |
2005.12.16 |
申请人 |
NON-COMMERCIAL ENTERPRISE "SCIENTIFIC-RESEARCH INSTITUTE OF CITOCHEMISTRY AND MOLECULAR PHARMACOLOGY" |
发明人 |
KOMISSAROVA IRINA, ALEXEEVNA;SOLDATENKOVA TATIANA, DMITRIEVNA;GUDKOVA YULIYA, VASILIEVNA;KONDRASHEVA TATIANA, TIKHONOVNA;BURBENSKAYA NATALIA, MIKHAILOVNA |
分类号 |
G01N21/17;A61K31/195;G01N1/38 |
主分类号 |
G01N21/17 |
代理机构 |
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