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Matthias Manne Knopp
Matthias Manne Knopp
Principal Scientist, Bioneer A/S
Verified email at bioneer.dk - Homepage
Title
Cited by
Cited by
Year
Comparative study of different methods for the prediction of drug–polymer solubility
MM Knopp, L Tajber, Y Tian, NE Olesen, DS Jones, A Kozyra, K Lobmann, ...
Molecular pharmaceutics 12 (9), 3408-3419, 2015
1502015
Precipitation of a poorly soluble model drug during in vitro lipolysis: characterization and dissolution of the precipitate
PJ Sassene, MM Knopp, JZ Hesselkilde, V Koradia, A Larsen, T Rades, ...
Journal of pharmaceutical sciences 99 (12), 4982-4991, 2010
1492010
Influence of polymer molecular weight on drug–polymer solubility: a comparison between experimentally determined solubility in PVP and prediction derived from solubility in monomer
MM Knopp, NE Olesen, P Holm, P Langguth, R Holm, T Rades
Journal of pharmaceutical sciences 104 (9), 2905-2912, 2015
1182015
Recent advances and potential applications of modulated differential scanning calorimetry (mDSC) in drug development
MM Knopp, K Löbmann, DP Elder, T Rades, R Holm
European Journal of Pharmaceutical Sciences 87, 164-173, 2016
772016
Influence of polymer molecular weight on in vitro dissolution behavior and in vivo performance of celecoxib: PVP amorphous solid dispersions
MM Knopp, JH Nguyen, C Becker, NM Francke, EB Jørgensen, P Holm, ...
European Journal of Pharmaceutics and Biopharmaceutics 101, 145-151, 2016
762016
The role interplay between mesoporous silica pore volume and surface area and their effect on drug loading capacity
CG Bavnhøj, MM Knopp, CM Madsen, K Löbmann
International journal of pharmaceutics: X 1, 100008, 2019
682019
Influence of PVP/VA copolymer composition on drug–polymer solubility
MB Rask, MM Knopp, NE Olesen, R Holm, T Rades
European journal of pharmaceutical sciences 85, 10-17, 2016
672016
Comparison of two DSC-based methods to predict drug-polymer solubility
MB Rask, MM Knopp, NE Olesen, R Holm, T Rades
International Journal of Pharmaceutics 540 (1-2), 98-105, 2018
602018
Effect of polymer type and drug dose on the in vitro and in vivo behavior of amorphous solid dispersions
MM Knopp, N Chourak, F Khan, J Wendelboe, P Langguth, T Rades, ...
European journal of pharmaceutics and biopharmaceutics 105, 106-114, 2016
572016
Effect of amorphous phase separation and crystallization on the in vitro and in vivo performance of an amorphous solid dispersion
MM Knopp, J Wendelboe, R Holm, T Rades
European Journal of Pharmaceutics and Biopharmaceutics 130, 290-295, 2018
462018
Quantification of microwave-induced amorphization of celecoxib in PVP tablets using transmission Raman spectroscopy
M Edinger, MM Knopp, H Kerdoncuff, J Rantanen, T Rades, K Löbmann
European Journal of Pharmaceutical Sciences 117, 62-67, 2018
432018
Evaluation of drug–polymer solubility curves through formal statistical analysis: comparison of preparation techniques
MM Knopp, NE Olesen, P Holm, K Löbmann, R Holm, P Langguth, ...
Journal of pharmaceutical sciences 104 (1), 44-51, 2015
432015
A promising new method to estimate drug-polymer solubility at room temperature
MM Knopp, N Gannon, I Porsch, MB Rask, NE Olesen, P Langguth, ...
Journal of pharmaceutical sciences 105 (9), 2621-2624, 2016
412016
Influence of Copolymer Composition on In Vitro and In Vivo Performance of Celecoxib-PVP/VA Amorphous Solid Dispersions
MM Knopp, JH Nguyen, H Mu, P Langguth, T Rades, R Holm
The AAPS journal 18, 416-423, 2016
382016
Impact of drug loading in mesoporous silica-amorphous formulations on the physical stability of drugs with high recrystallization tendency
RS Antonino, M Ruggiero, Z Song, TL Nascimento, EM Lima, A Bohr, ...
International Journal of Pharmaceutics: X 1, 100026, 2019
332019
A fast and reliable DSC-based method to determine the monomolecular loading capacity of drugs with good glass-forming ability in mesoporous silica
NJ Hempel, K Brede, NE Olesen, N Genina, MM Knopp, K Löbmann
International Journal of Pharmaceutics 544 (1), 153-157, 2018
312018
The influence of drug and polymer particle size on the in situ amorphization using microwave irradiation
NJ Hempel, MM Knopp, R Berthelsen, JA Zeitler, K Löbmann
European Journal of Pharmaceutics and Biopharmaceutics 149, 77-84, 2020
292020
Importance of in vitro dissolution conditions for the in vivo predictability of an amorphous solid dispersion containing a pH-sensitive carrier
J Wendelboe, MM Knopp, F Khan, N Chourak, T Rades, R Holm
International Journal of Pharmaceutics 531 (1), 324-331, 2017
182017
Statistical analysis of a method to predict drug–polymer miscibility
MM Knopp, NE Olesen, Y Huang, R Holm, T Rades
Journal of Pharmaceutical Sciences 105 (1), 362-367, 2016
182016
The influence of temperature and viscosity of polyethylene glycol on the rate of microwave-induced in situ amorphization of celecoxib
NJ Hempel, T Dao, MM Knopp, R Berthelsen, K Löbmann
Molecules 26 (1), 110, 2020
172020
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