Zobrazeno 1 - 5
of 5
pro vyhledávání: '"I. A. Builova"'
Autor:
O. V. Gunar, I. A. Builova
Publikováno v:
Pharmaceutical Chemistry Journal. 55:308-311
The present study focuses on the use of surfactants (SA) in quality control of solid dosage forms. Features of the dissolution of solid dosage forms and factors affecting the extraction of microorganisms from drug samples are discussed. The propertie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::335826c3d8c67a2ae623a20c84347c9e
https://doi.org/10.1007/s11094-021-02417-w
https://doi.org/10.1007/s11094-021-02417-w
Publikováno v:
Pharmaceutical Chemistry Journal
The possibility of reducing the sample size for microbiological examination of some pharmaceutical substances is considered. Trypticase-soy agar was evaluated for the ability to detect yeast and mold fungi and to isolate the minimal amount of certain
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a345ffbd3e77cf99c1a29f8e2b3aa65
https://pubmed.ncbi.nlm.nih.gov/34873351
https://pubmed.ncbi.nlm.nih.gov/34873351
Publikováno v:
Farmaciya (Pharmacy). 68
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::24a71165068d628e935919306f4c12f6
https://doi.org/10.29296/25419218-2019-07-01
https://doi.org/10.29296/25419218-2019-07-01
Autor:
I. A. Builova, O. V. Gunar
Publikováno v:
Pharmaceutical Chemistry Journal. 50:108-113
A new approach to microbiological analysis of several pharmaceuticals, in particular, those that can be used in manufacturing sterile medical products, is presented. The proposed approach was verified using a series of 23 samples of various products,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::26f508366710441f8c4382c9111ae629
https://doi.org/10.1007/s11094-016-1406-1
https://doi.org/10.1007/s11094-016-1406-1
Autor:
I. A. Builova, O. V. Gunar
Publikováno v:
Pharmaceutical Chemistry Journal. 51:68-70
We present here the results of validation of qualitative microbiological methods, particularly a modified method for determining the microbiological purity of medicines. The parameters required for validating qualitative microbiological methods and c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::97fa015aaaa5540aa6c37696e9e5063f
https://doi.org/10.1007/s11094-017-1560-0
https://doi.org/10.1007/s11094-017-1560-0