Formation of bicalutamide nanodispersion for dissolution rate enhancement
- Author
- CHAN LI1 ; CAIXIA LI1 ; YUAN LE1 ; CHEN, Jian-Feng2
[1] Key Lab for Nanomaterials, Ministry of Education, Beijing University of Chemical Technology, Beijing 100029, China
[2] Research Center of the Ministry of Education for High Gravity Engineering and Technology, Beijing University of Chemical Technology, Beijing 100029, China - Source
International journal of pharmaceutics (Print). 2011, Vol 404, Num 1-2, pp 257-263, 7 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
- Bicalutamide Hydrophilic excipients In vitro dissolution Nanodispersion
- Keyword (fr)
- Anticancéreux Bicalutamide Dissolution Excipient Hydrophilie In vitro Technologie pharmaceutique Antiandrogène Antihormone Composé non stéroïde
- Keyword (en)
- Antineoplastic agent Bicalutamide Dissolution Vehicle(excipient) Hydrophily In vitro Pharmaceutical technology Antiandrogen Antihormone Non steroid compound
- Keyword (es)
- Anticanceroso Bicalutamida Disolución Excipiente(vehiculo) Hidrofilia In vitro Tecnología farmacéutica Antiandrógeno Antihormona Compuesto no esteroide
- 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
- 23817112
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.2010.11.015 
https://dx.doi.org/10.1016/j.ijpharm.2010.11.015
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