Isabell Wünsch

Ms. Isabell Wünsch

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Research Focus & Metrics

Academic Career Length

8Years (2019-Present)

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

Representative Publications

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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.

31 March 2020 in Pharmaceutics
Verified
Journal Article
Open access
PDF file
IWIsabell Wünsch
Isabell Wünsch
IFIrene Friesen
Irene Friesen
DPDaniel Puckhaber
Daniel Puckhaber
TSThomas Schlegel
Thomas Schlegel
Jan Henrik FinkeJan Henrik Finke
Jan Henrik Finke
Compaction simulators are frequently used in the formulation and process development of tablets, bringing about the advantages of flexibility, low material consumption, and high instrumentation to generate the most possible process understanding. However, their capability of resembling general aspects of rotary press compaction and their precision in simulating or mimicking sub-processes such as feeding and filling need to be systematically studied. The effect of material deformation behavior, blend composition, and feeding on tensile strength and simulation precision as compared with rotary presses of different scales is evaluated in this study. Generally, good simulation performance was found for the studied compaction simulator. Compaction profile-sensitivity was demonstrated for highly visco-plastic materials while shear-sensitivity in feeding was demonstrated for lubricated blends of ductile particles. Strategies for the compensation of both in compaction simulator experiments are presented by careful investigation of the compaction stress over time profiles and introduction of a compaction simulator-adapted shear number approach to account for differences in layout and operation mode between compaction simulator and rotary press, respectively. These approaches support the general aim of this study to provide a more straightforward determination of scaling process parameters between rotary press and compaction simulator and facilitate a quicker and more reliable process transfer.