Jan Henrik Finke

Dr. Jan Henrik Finke

Institute for Particle Technology, Technische Universität Braunschweig, 38104 Braunschweig, Germany
orcid

Research Focus & Metrics

Academic Career Length

17Years (2010-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 May 2018 in European Journal of Pharmaceutics and Biopharmaceutics
Verified
Journal Article
Closed access
KGKatrin Göke
Katrin Göke
TLThomas Lorenz
Thomas Lorenz
ARAlexandros Repanas
Alexandros Repanas
FSFrederic Schneider
Frederic Schneider
DSDenise Steiner
Denise Steiner
Arno KwadeArno Kwade
Arno Kwade


1 April 2021 in International Journal of Pharmaceutics
Verified
Journal Article
Closed access
IWIsabell Wünsch
Isabell Wünsch
Jan Henrik FinkeJan Henrik Finke
Jan Henrik Finke
EJEdgar John
Edgar John
MJMichael Juhnke
Michael Juhnke
Arno KwadeArno Kwade
Arno Kwade

1 March 2020 in Advanced Powder Technology
Verified
Journal Article
Closed access
RCRamon Cabiscol
Ramon Cabiscol
HSHao Shi
Hao Shi
IWIsabell Wünsch
Isabell Wünsch
VMVanessa Magnanimo
Vanessa Magnanimo
Jan Henrik FinkeJan Henrik Finke
Jan Henrik Finke
Arno KwadeArno Kwade
Arno Kwade

15 March 2019 in Pharmaceutics
Verified
Journal Article
Open access
PDF file
IWIsabell Wünsch
Isabell Wünsch
Jan Henrik FinkeJan Henrik Finke
Jan Henrik Finke
EJEdgar John
Edgar John
MJMichael Juhnke
Michael Juhnke
Arno KwadeArno Kwade
Arno Kwade
In-die compression analysis is an effective method for the characterization of powder compressibility. However, physically unreasonable apparent solid fractions above one or apparent in-die porosities below zero are often calculated for higher compression stresses. One important reason for this is the neglect of solid compressibility and hence the assumption of a constant solid density. In this work, the solid compressibility of four pharmaceutical powders with different deformation behaviour is characterized using mercury porosimetry. The derived bulk moduli are applied for the calculation of in-die porosities. The change of in-die porosity due to the consideration of solid compressibility is for instance up to 4% for microcrystalline cellulose at a compression stress of 400 MPa and thus cannot be neglected for the calculation of in-die porosities. However, solid compressibility and further uncertainties from, for example the measured solid density and from the displacement sensors, are difficult or only partially accessible. Therefore, a mathematic term for the calculation of physically reasonable in-die porosities is introduced. This term can be used for the extension of common mathematical models, such as the models of Heckel and of Cooper & Eaton. Additionally, an extended in-die compression function is introduced to precisely describe the entire range of in-die porosity curves and to enable the successful differentiation and quantification of the compression behaviour of the investigated pharmaceutical powders.

25 February 2011 in Chemical Engineering & Technology
Verified
Journal Article
Closed access
PDF file
TGT. Gothsch
T. Gothsch
Jan Henrik FinkeJan Henrik Finke
Jan Henrik Finke
SBS. Beinert
S. Beinert
CLC. Lesche
C. Lesche
JSJ. Schur
J. Schur
Arno KwadeArno Kwade
Arno Kwade