Physicochemical, in silico and in vivo evaluation of a danazol-β-cyclodextrin complex
- Author
- JADHAV, G. S1 ; VAVIA, P. R1
[1] Pharmaceutical Division, Mumbai University Institute of Chemical Technology, N. P. Marg, Matunga, Mumbai 400019, India - Source
International journal of pharmaceutics. 2008, Vol 352, Num 1-2, pp 5-16, 12 p ; ref : 3/4 p
- CODEN
- IJPHDE
- ISSN
- 0378-5173
- Scientific domain
- Pharmacology drugs
- Publisher
- Elsevier, Amsterdam
- Publication country
- Netherlands
- Document type
- Article
- Language
- English
- Author keyword
- Antiovulatory activity Danazol Molecular modeling Solubility β-Cyclodextrin
- Keyword (fr)
- Composé inclusion Danazol Evaluation In silico In vivo Modélisation Solubilité Technologie pharmaceutique β-Cyclodextrine Androgène Antagoniste Cyclodextrine Gonadotrophine Oligoside Propriété physicochimique
- Keyword (en)
- Inclusion compound Danazol Evaluation In silico In vivo Modeling Solubility Pharmaceutical technology β-Cyclodextrin Androgen Antagonist Cyclodextrin Gonadotropin Oligosaccharide Physicochemical properties
- Keyword (es)
- Compuesto inclusión Danazol Evaluación In silico In vivo Modelización Solubilidad Tecnología farmacéutica β-Ciclodextrina Andrógeno Antagonista Ciclodextrina Gonadotropina Oligósido Propiedad fisicoquímica
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B02 Pharmacology. Drug treatments / 002B02A General pharmacology / 002B02A03 Pharmaceutical technology. Pharmaceutical industry
- Discipline
- General pharmacology
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 20184970
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1016/j.ijpharm.2007.10.005 
https://dx.doi.org/10.1016/j.ijpharm.2007.10.005
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