SwePub
Sök i LIBRIS databas

  Extended search

onr:"swepub:oai:DiVA.org:uu-459886"
 

Search: onr:"swepub:oai:DiVA.org:uu-459886" > UNGAP best practice...

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

UNGAP best practice for improving solubility data quality of orally administered drugs

Vertzoni, M. (author)
Natl & Kapodistrian Univ Athens, Dept Pharm, Zografos, Greece.
Alsenz, J. (author)
Roche Pharmaceut Res & Early Dev, Basel, Switzerland.
Augustijns, P. (author)
Katholieke Univ Leuven, Drug Delivery & Disposit, Leuven, Belgium.
show more...
Bauer-Brandl, A. (author)
Univ Southern Denmark, Dept Phys Chem & Pharm, Odense, Denmark.
Bergström, Christel A. S., 1973- (author)
Uppsala universitet,Institutionen för farmaci
Brouwers, J. (author)
Katholieke Univ Leuven, Drug Delivery & Disposit, Leuven, Belgium.
Mullerz, A. (author)
Univ Copenhagen, Dept Pharm, Copenhagen, Denmark.
Perlovich, G. (author)
Russian Acad Sci, Inst Solut Chem, Dept Phys Chem Drugs, Ivanovo, Russia.
Saal, C. (author)
Merck KGaA, Analyt Healthcare, Darmstadt, Germany.
Sugano, K. (author)
Ritsumeikan Univ, Coll Pharmaceut Sci, Kusatsu, Japan.
Reppas, C. (author)
Natl & Kapodistrian Univ Athens, Dept Pharm, Zografos, Greece.
show less...
Natl & Kapodistrian Univ Athens, Dept Pharm, Zografos, Greece Roche Pharmaceut Res & Early Dev, Basel, Switzerland. (creator_code:org_t)
Elsevier, 2022
2022
English.
In: European Journal of Pharmaceutical Sciences. - : Elsevier. - 0928-0987 .- 1879-0720. ; 168
  • Journal article (peer-reviewed)
Abstract Subject headings
Close  
  • An important goal of the European Cooperation in Science and Technology (COST) Action UNGAP (UNder-standing Gastrointestinal Absorption-related Processes, www.ungap.eu) is to improve standardization of methods relating to the study of oral drug absorption. Solubility is a general term that refers to the maximum achievable concentration of a compound dissolved in a liquid medium. For orally administered drugs, relevant information on drug properties is crucial during drug (product) development and at the regulatory level. Collection of reliable and reproducible solubility data requires careful application and understanding of the limitations of the selected experimental method. In addition, the purity of a compound and its solid state form, as well as experimental parameters such as temperature of experimentation, media related factors, and sample handling procedures can affect data quality. In this paper, an international consensus developed by the COST UNGAP network on recommendations for collecting high quality solubility data for the development of orally administered drugs is proposed.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmaceutiska vetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmaceutical Sciences (hsv//eng)

Keyword

Oral drug absorption
Solubility
Terminology
Exerimental Methods
Best Practice
UNGAP

Publication and Content Type

ref (subject category)
art (subject category)

Find in a library

To the university's database

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Search outside SwePub

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Close

Copy and save the link in order to return to this view