Pharmaceutical analysis and standardization of noopept tablets

被引:0
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作者
L. N. Grushevskaya
N. I. Avdyunina
B. M. Pyatin
K. V. Alekseev
L. M. Gaevaya
M. S. Sergeeva
M. E. Dudenkova
V. S. Klumova
N. V. Tikhonova
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noopept; tablets; HPLC; chromatography; pharmaceutical analysis; amide; peptide;
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摘要
Procedures for pharmaceutical analysis and standardization of the new nootropic drug noopept in tablets manufactured by direct compression have been developed. The main quality tests were carried out. Ahigh performance liquid chromatography (HPLC) method for quantitative and qualitative analysis of noopept in tablets is developed and applied to determination of impurities, noopept content in tablets, uniformity of dosage, and dissolution rate.
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页码:377 / 380
页数:3
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