Prof. Dr. Martin Kuentz
Prof. Dr. Martin Kuentz
Tätigkeiten an der FHNW
Dozent Pharmatechnologie
Lehre
Martin Kuentz teaches at the School of Life Sciences on the bachelor level a course on industrial processes in the life sciences. This first semester course is mainly about the processes in drug discovery, development, scale-up, and manufacturing of active compounds.
Another course on the bachelor level is about the chemistry and pharmaceutical profiling of active compounds. Martin Kuentz also teaches on special topics in quality management and registration and he takes part in a master module where he lectures on poorly water soluble drugs and on how these compounds can be formulated orally.
Prof. Kuentz has attended several courses in University didactics and gained a certificate from the University of Basel (2008), which is part of the habilitation program.
Profil
Martin Kuentz is since 2007 a professor of pharmaceutical technology at the University of Applied Sciences and Arts Northwestern Switzerland. He leads a research group in the area of Quality by Design of oral dosage forms with a particular focus on lipid-based formulations and oral solid dispersions. Several projects in the research group target a better understanding of oral formulation performance. Particular interests are about gaining insights into the formulation microstructure and to study drug release, which involves in vitro digestion in case of lipid-based systems. Different non-invasive analytical tools are used such as, for example, Raman spectroscopy, UV imaging, ultrasound analysis, and diffusing wave spectroscopy. Pharmaceutical systems are further studied by different surface analytics, e.g. inverse gas chromatography and different imaging techniques. The research group was in several projects making use of mathematical modelling to gain a better understanding of dosage form performance, which should ultimately provide guidance to pharmaceutical scientists.
Prior to his academic assignment, Dr. Kuentz spent almost seven years in pharmaceutical research at F. Hoffmann-La Roche Ltd. in Basel. He was a senior scientist and departmental coordinator of assigned galenical development projects. Prof. Kuentz had among different functions the role of a global contact person in the area of lipid-based drug delivery systems. Martin Kuentz earned his Ph.D. in 1999 in the group of Prof. Leuenberger at the University of Basel (Switzerland), where he also graduated earlier as a pharmacist in 1995.
Prof. Kuentz has published more than 90 research articles in peer-reviewed journals and has given numerous scientific presentations at international congresses.
Prof. Kuentz is a member of the American Association of Pharmaceutical Scientists (AAPS), the “Arbeitsgemeinschaft der Pharmazeutischen Verfahrenstechnik” (APV), the Swiss Society of Industrial Pharmacists (GSIA), and of Catedra Iberoamericana-Suiza de Desarrollo de Medicamentos (CISDEM).
- 2014 IPEC Foundation Best Manuscript of the Year Award, AAPS, San Diego, USA 2014
- Price for the best poster at the 3rd 3. GALENUS WORKSHOP IN GREIFSWALD, Germany 2014
- Best poster award in the category of Pharmaceutical Technology at the Swiss Pharma Science Day (Bern, Switzerland) in the years 2012, 2014, and 2015
The various patents can be inferred from the contribution list in different databases or for example via Google Scholar.
ORCID 0000-0003-2963-2645
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Keine peer-reviewed Inhalte verfügbar
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Peer-reviewedHolm, R., Kuentz, M., Ilie-Spiridon, A.-R., & Griffin, B. T. (2023). Lipid based formulations as supersaturating oral delivery systems. From current to future industrial applications. European Journal of Pharmaceutical Sciences, 189. https://doi.org/10.1016/j.ejps.2023.106556
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Peer-reviewedReppas, C., Kuentz, M., Bauer-Brandl, A., Carlert, S., Dallmann, A., Dietrich, S., Dressman, J., Ejskjaer, L., Frechen, S., Guidetti, M., Holm, R., Holzem, F. L., Karlsson, Ε., Kostewicz, E., Panbachi, S., Paulus, F., Senniksen, M. B., Stillhart, C., Turner, D. B., et al. (2023). Leveraging the use of in vitro and computational methods to support the development of enabling oral drug products. An InPharma commentary. European Journal of Pharmaceutical Sciences, 188. https://doi.org/10.1016/j.ejps.2023.106505
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Peer-reviewedNiederquell, A., Stoyanov, E., & Kuentz, M. (2023). Physiological buffer effects in drug supersaturation - a mechanistic study of hydroxypropyl cellulose as precipitation inhibitor. Journal of Pharmaceutical Sciences, 112(7), 1897–1907. https://doi.org/10.1016/j.xphs.2023.02.013
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Peer-reviewedJouyban-Gharamaleki, V., Martinez, F., Kuentz, M., Rahimpour, E., & Jouyban, A. (2023). Using a laser monitoring technique for dissolution and thermodynamic study of celecoxib in 2-propanol and propylene glycol mixtures. Dissolution Technologies, 30(2), 80–86. https://doi.org/10.14227/dt300223p80
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Peer-reviewedBrokešová, J., Niederquell, A., Kuentz, M., Zámostný, P., Vraníková, B., & Šklubalová, Z. (2023). Corrigendum to “Powder cohesion and energy to break an avalanche. Can we address surface heterogeneity?” [Int. J. Pharm. 626 (2022) 122198]. International Journal of Pharmaceutics, 631. https://doi.org/10.1016/j.ijpharm.2022.122485
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Peer-reviewedMurray, J. D., Lange, J. J., Bennett-Lenane, H., Holm, R., Kuentz, M., O’Dwyer, P. J., & Griffin, B. T. (2023). Advancing algorithmic drug product development. Recommendations for machine learning approaches in drug formulation. European Journal of Pharmaceutical Sciences, 191. https://doi.org/10.1016/j.ejps.2023.106562
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Peer-reviewedNiederquell, A., Vraníková, B., & Kuentz, M. (2023). Study of disordered mesoporous silica regarding intrinsic compound affinity to the carrier and drug-accessible surface area. Molecular Pharmaceutics, 20(12), 6301–6310. https://doi.org/10.1021/acs.molpharmaceut.3c00690
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Peer-reviewedRahimpour, E., Moradi, M., Sheikhi-Sovari, A., Rezaei, H., Rezaei, H., Jouyban-Gharamaleki, V., Kuentz, M., & Jouyban, A. (2023). Comparative drug solubility studies using shake-flask versus a laser-based robotic method. AAPS PharmSciTech, 24(7). https://doi.org/10.1208/s12249-023-02667-9
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Peer-reviewedGuidetti, M., Hilfiker, R., Kuentz, M., Bauer-Brandl, A., & Blatter, F. (2022). Exploring the cocrystal landscape of posaconazole by combining high-throughput screening experimentation with computational chemistry. Crystal Growth & Design, 23(2), 842–852. https://doi.org/10.1021/acs.cgd.2c01072
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Peer-reviewedGuidetti, M., Hilfiker, R., Kuentz, M., Bauer-Brandl, A., & Blatter, F. (2022). Exploring the cocrystal landscape of posaconazole by combining high-throughput screening experimentation with computational chemistry. Crystal Growth & Design, 23(2), 842–852. https://doi.org/10.1021/acs.cgd.2c01072
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Peer-reviewedWyttenbach, N., Ectors, P., Niederquell, A., & Kuentz, M. (2022). Study and computational modeling of fatty acid effects on drug solubility in lipid-based systems. Journal of Pharmaceutical Sciences, 111(6), 1728–1738. https://doi.org/10.1016/j.xphs.2021.11.023
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Peer-reviewedKuentz, M., Brokesova, J., Slamova, M., Zamostny, P., Koktan, J., Kreicik, L., Svacinova, P., Sklubalova, Z., & Vraníková, B. (2022). Mechanistic study of dissolution enhancement by interactive mixtures of chitosan with meloxicam as model. European Journal of Pharmaceutical Sciences, 169. https://doi.org/10.1016/j.ejps.2021.106087
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Peer-reviewedStoyanov, E., Niederquell, A., & Kuentz, M. (2022). Hydroxypropyl Cellulose for Drug Precipitation Inhibition: From the Potential of Molecular Interactions to Performance Considering Microrheology. Molecular Pharmaceutics, 19(2), 690–703. https://doi.org/10.1021/acs.molpharmaceut.1c00832
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Peer-reviewedKoehl, N., Henze, L., Holm, R., Kuentz, M., Keating, J., De Vijlder, T., Marx, A., & Griffin, B. (2022). Lipophilic salts and lipid-based formulations for bridging the food effect gap of venetoclax. Journal of Pharmaceutical Sciences, 111(1), 164–174. https://doi.org/10.1016/j.xphs.2021.09.008
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Peer-reviewedSvačinová, P., Macho, O., Jarolímová, Ž., Gabrišová, Ľ., Šklubalová, Z., & Kuentz, M. (2022). Evaluation of gravitational consolidation of binary powder mixtures by modified Heckel equation. Powder Technology, 408. https://doi.org/10.1016/j.powtec.2022.117729
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Peer-reviewedBennett-Lenane, H., O’Shea, J., Murray, J., Ilie, A. R., Holm, R., Kuentz, M., & Griffin, B. (2021). Artificial neural networks to predict the apparent degree of supersaturation in supersaturated lipid-based formulations. A pilot study. Pharmaceutics, 13(9). https://doi.org/10.3390/pharmaceutics13091398
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Peer-reviewedKuentz, M., Kronseder, C., Holm, R., Saal, C., & Griffin, B. (2021). Rational selection of bio-enabling oral drug formulations. A PEARRL commentary. Journal of Pharmaceutical Sciences, 110(5), 1921–1930. https://doi.org/10.1016/j.xphs.2021.02.004
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Peer-reviewedKoehl, N., Henze, L., Bennett-Lenane, H., Faisal, W., Price, D. J., Holm, R., Kuentz, M., & Griffin, B. (2021). In Silico, In Vitro, and In Vivo evaluation of precipitation inhibitors in supersaturated lipid-based formulations of venetoclax. Molecular Pharmaceutics, 18(6), 2174–2188. https://doi.org/10.1021/acs.molpharmaceut.0c00645
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Peer-reviewedKuentz, M., Ilie, A. R., Griffin, B., Vertzoni, M., Kolakovic, R., Prudic-Paus, A., Malash, A., Bohets, H., Herman, J., & Holm, R. (2021). Exploring precipitation inhibitors to improve in vivo absorption of cinnarizine from supersaturated lipid-based drug delivery systems. European Journal of Pharmaceutical Sciences, 159. https://doi.org/10.1016/j.ejps.2020.105691
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Peer-reviewedKuentz, M., Vinarov, Z., Bertil, A., Artursson, P., Batchelor, H., Berben, P., Bernkop-Schnürch, A., Butler, J., Ceulemans, J., Davies, N., Dupont, D., Eide Flaten, G., Fotaki, N., Jannin, V., Keemink, J., Kesisoglou, F., Koziolek, M., Augustijns, P., & Griffin, B. (2021). Current challenges and future perspectives in oral absorption research. An opinion of the UNGAP network. Advanced Drug Delivery Reviews, 171, 289–331. https://doi.org/10.1016/j.addr.2021.02.001
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Peer-reviewedGuimaraes, M., Kuentz, M., Vertzoni, M., & Fotaki, N. (2021). Evaluating pediatric and adult simulated fluids solubility. Abraham solvation parameters and multivariate analysis. Pharmaceutical Research, 38, 1889–1896. https://doi.org/10.1007/s11095-021-03123-8
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Peer-reviewedKuentz, M. (2020). Synergistic Computational Modeling Approaches as Team Players in the Game of Solubility Predictions. Journal of Pharmaceutical Sciences, 110(1), 22–34. https://doi.org/10.1016/j.xphs.2020.10.068
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Peer-reviewedIlie, A. R., & Kuentz, M. (2020). Toward simplified oral lipid-based drug delivery using mono-/di-glycerides as single component excipients. Drug Development and Industrial Pharmacy, 46(12), 2051–2060. https://doi.org/10.1080/03639045.2020.1843475
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Peer-reviewedVraníková, B., Niederquell, A., & Kuentz, M. (2020). Relevance of the theoretical critical pore radius in mesoporous silica for fast crystallizing drugs. International Journal of Pharmaceutics, 591. https://doi.org/10.1016/j.ijpharm.2020.120019
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Peer-reviewedTrpělková, Ž., & Kuentz, M. (2020). Introduction of the energy to break an avalanche as a promising parameter for powder flowability prediction. Powder Technology, 375, 33–41. https://doi.org/10.1016/j.powtec.2020.07.095
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Peer-reviewedKoehl, N., & Kuentz, M. (2020). Exploring the Impact of Surfactant Type and Digestion: Highly Digestible Surfactants Improve Oral Bioavailability of Nilotinib. Molecular Pharmaceutics, 17(9), 3202–3213. https://doi.org/10.1021/acs.molpharmaceut.0c00305
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Peer-reviewedO’Dwyer, P. J., & Kuentz, M. (2020). Novel Biphasic Lipolysis Method To Predict in Vivo Performance of Lipid-Based Formulations. Molecular Pharmaceutics, 17(9), 3342–3352. https://doi.org/10.1021/acs.molpharmaceut.0c00427.
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Peer-reviewedIlie, A. R., & Kuentz, M. (2020). Exploring impact of supersaturated lipid-based drug delivery systems of celecoxib on in vitro permeation across Permeapad Ⓡ membrane and in vivo absorption. European Journal of Pharmaceutical Sciences, 152. https://doi.org/10.1016/j.ejps.2020.105452
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Peer-reviewedKoehl, N., & Kuentz, M. (2020). Supersaturated Lipid-Based Formulations to Enhance the Oral Bioavailability of Venetoclax. Pharmaceutics, 12(6), 564. https://doi.org/10.3390/pharmaceutics12060564
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Peer-reviewedKoehl, N., & Kuentz, M. (2020). Chase Dosing of Lipid Formulations to Enhance Oral Bioavailability of Nilotinib in Rats. Pharmaceutical Research, 37(7), 124. https://doi.org/10.1007/s11095-020-02841-9
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Peer-reviewedWyttenbach, N., Niederquell, A., & Kuentz, M. (2020). Machine Estimation of Drug Melting Properties and Influence on Solubility Prediction. Molecular Pharmaceutics, 17(7), 2660–2671. https://doi.org/10.1021/acs.molpharmaceut.0c00355
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Peer-reviewedJouyban, K., & Kuentz, M. (2020). Solubility of 5-aminosalicylic acid in N-methyl-2-pyrrolidone + water mixtures at various temperatures. Journal of Molecular Liquids, 310. https://doi.org/10.1016/j.molliq.2020.113143
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Peer-reviewedJankovic, S., & Kuentz, M. (2020). Broadband Diffusing Wave Spectroscopy Reveals Microstructuring of Polymer–Drug System. Crystal Growth & Design, 3957–3967. https://doi.org/10.1021/acs.cgd.0c00267
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Peer-reviewedBarzegar-Jalali, M., & Kuentz, M. (2020). Solubility of ketoconazole in 1,4-dioxane + water mixtures at T = (293.2 to 313.2) K. Journal of Molecular Liquids, 306. https://doi.org/10.1016/j.molliq.2020.112830
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Peer-reviewedAgha, E. M. H., & Kuentz, M. (2020). Solubility of mesalazine in {1-propanol/water} mixtures at different temperatures. Journal of Molecular Liquids, 301. https://doi.org/10.1016/j.molliq.2019.112436
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Peer-reviewedMoradi, M., & Kuentz, M. (2020). Solubility of 5-aminosalicylic acid in {N-methyl-2-pyrrolidone + ethanol} mixtures at T = (293.2 to 313.2) K. Journal of Molecular Liquids, 306. https://doi.org/10.1016/j.molliq.2020.112774
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Peer-reviewedJouyban-Gharamaleki, V., & Kuentz, M. (2020). A laser monitoring technique for determination of mesalazine solubility in propylene glycol and ethanol mixtures at various temperatures. Journal of Molecular Liquids, 304. https://doi.org/10.1016/j.molliq.2020.112714
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Peer-reviewedVraníková, B., Niederquell, A., Ditzinger, F., & Kuentz, M. (2020). Mechanistic aspects of drug loading in liquisolid systems with hydrophilic lipid-based mixtures. International Journal of Pharmaceutics, 578, 1–11. https://doi.org/10.1016/j.ijpharm.2020.119099
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Peer-reviewedIlie, A. R., & Kuentz, M. (2020). Supersaturated lipid-based drug delivery systems - exploring impact of lipid composition type and drug properties on supersaturability and physical stability. Drug Development and Industrial Pharmacy, 1–29. https://doi.org/10.1080/03639045.2020.1721526
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Peer-reviewedPrice, D. J., Nair, A., Becker-Baldus, J., Glaubitz, C., Kuentz, M., Dressman, J., & Saal, C. (2020). Incorporation of HPMCAS during loading of glibenclamide onto mesoporous silica improves dissolution and inhibits precipitation. European Journal of Pharmaceutical Sciences. https://doi.org/10.1016/j.ejps.2019.105113
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Peer-reviewedDitzinger, F., Wieland, R., Statelova, M., Vertzoni, M., Holm, R., & Kuentz, M. (2020). In Vivo Performance of Innovative Polyelectrolyte Matrices for Hot Melt Extrusion of Amorphous Drug Systems. Molecular Pharmaceutics, 17(8), 3053–3061. https://doi.org/10.1021/acs.molpharmaceut.0c00485
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Peer-reviewedDitzinger, F., Price, D. J., Nair, A., Becker-Baldus, J., Glaubitz, C., Dressman, J., Saal, C., & Kuentz, M. (2019). Opportunities for Successful Stabilization of Poor Glass-Forming Drugs: A Stability-Based Comparison of Mesoporous Silica Versus Hot Melt Extrusion Technologies. Pharmaceutics, 11(11), 577. https://doi.org/10.3390/pharmaceutics11110577
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Peer-reviewedAlsenz, J., & Kuentz, M. (2019). From Quantum Chemistry to Prediction of Drug Solubility in Glycerides. Molecular Pharmaceutics, 16(11), 4661–4669. https://doi.org/10.1021/acs.molpharmaceut.9b00801
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Peer-reviewedLitou, C., & Kuentz, M. (2019). Combining biorelevant in vitro and in silico tools to simulate and better understand the in vivo performance of a nano-sized formulation of aprepitant in the fasted and fed states. European Journal of Pharmaceutical Sciences. https://doi.org/10.1016/j.ejps.2019.105031
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Peer-reviewedGong, Y., Niederquell, A., & Kuentz, M. (2019). Ultra-sub-stoichiometric “Dynamic” Bioconjugation Reduces Viscosity by Disrupting Immunoglobulin Oligomerization. Biomacromolecules, 20(9), 3557–3565. https://doi.org/10.1021/acs.biomac.9b00867
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Peer-reviewedAbreu-Villela, R., & Kuentz, M. (2019). Benefits of Fractal Approaches in Solid Dosage Form Development. Pharmaceutical Research, 36(11), 156. https://doi.org/10.1007/s11095-019-2685-5
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Peer-reviewedBoyd, B. J., & Kuentz, M. (2019). Successful oral delivery of poorly water-soluble drugs both depends on the intraluminal behavior of drugs and of appropriate advanced drug delivery systems. European Journal of Pharmaceutical Sciences, 137. https://doi.org/10.1016/j.ejps.2019.104967
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Peer-reviewedDitzinger, F., Price, D. J., Ilie, A. R., Koehl, N., Jankovic, S., Tsakiridou, G., Aleandri, S., Kalantzi, L., Holm, R., Nair, A., Saal, C., Griffin, B., & Kuentz, M. (2019). Lipophilicity and hydrophobicity considerations in bio-enabling oral formulations approaches | a PEARRL review. Journal of Pharmacy and Pharmacology, 71(4), 464–482. https://doi.org/10.1111/jphp.12984
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Peer-reviewedTrpělková, Ž., & Kuentz, M. (2019). Predicting the Angle of Internal Friction from Simple Dynamic Consolidation Using Lactose Grades as Model. Journal of Pharmaceutical Innovation. https://doi.org/10.1007/s12247-019-09387-3
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Peer-reviewedKuentz, M. (2019). Calculation of drug-polymer mixing enthalpy as a new screening method of precipitation inhibitors for supersaturating pharmaceutical formulations. European Journal of Pharmaceutical Sciences, 132, 142–156. https://doi.org/10.1016/j.ejps.2019.03.006
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Peer-reviewedKoehl, N., & Kuentz, M. (2019). New Insights into Using Lipid Based Suspensions for ‘Brick Dust’ Molecules: Case Study of Nilotinib. Pharmaceutical Research, 36. https://doi.org/10.1007/s11095-019-2590-y
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Peer-reviewedNiederquell, A., & Kuentz, M. (2019). Partial Solvation Parameters of Drugs as a New Thermodynamic Tool for Pharmaceutics. Pharmaceutics, 11(1). https://doi.org/10.3390/pharmaceutics11010017
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Peer-reviewedJankovic, S., Imanidis, G., & Kuentz, M. (2019). Biphasic drug release testing coupled with diffusing wave spectroscopy for mechanistic understanding of solid dispersion performance. European Journal of Pharmaceutical Sciences. https://doi.org/10.1016/j.ejps.2019.105001
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Peer-reviewedDitzinger, F., Scherer, U. M., Schönenberger, M., Holm, R., & Kuentz, M. (2019). Modified Polymer Matrix in Pharmaceutical Hot Melt Extrusion by Molecular Interactions with a Carboxylic Coformer. Molecular Pharmaceutics, 16(1), 141–150. https://doi.org/10.1021/acs.molpharmaceut.8b00920
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Peer-reviewedNiederquell, A., & Kuentz, M. (2019). A Relative Permittivity Approach for Fast Drug Solubility Screening of Solvents and Excipients in Lipid-Based Delivery. Journal of Pharmaceutical Sciences, 108(10), 3457–3460. https://doi.org/10.1016/j.xphs.2019.06.014
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Peer-reviewedDitzinger, F., Dejoie, C., Sisak Jung, D., & Kuentz, M. (2019). Polyelectrolytes in Hot Melt Extrusion: A Combined Solvent-Based and Interacting Additive Technique for Solid Dispersions. Pharmaceutics, 11(4), 174. https://doi.org/10.3390/pharmaceutics11040174
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Peer-reviewedKuentz, M., Abreu-Villela, R., Schönenberger, M., & Caraballo, I. (2018). Early stages of drug crystallization from amorphous solid dispersion via fractal analysis based on chemical imaging. European Journal of Pharmaceutics and Biopharmaceutics, 133, 122–130. https://doi.org/10.1016/j.ejpb.2018.10.007
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Peer-reviewedKuentz, M. (2018). Drug supersaturation during formulation digestion, including real-time analytical approaches. Advanced Drug Delivery Reviews. https://doi.org/10.1016/j.addr.2018.11.003
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Peer-reviewedJankovic, S., Kuentz, M., & Aleandri, S. (2018). Towards a better understanding of solid dispersions in aqueous environment by a fluorescence quenching approach. International Journal of Pharmaceutics, 550(1-2). https://doi.org/doi.org/10.1016/j.ijpharm.2018.08.029
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Peer-reviewedDitzinger, F., Price, D., Ilie, A. R., Koehl, N., Jankovic, S., Tsakiridou, G., Aleandri, S., Kalantzi, L., Holm, R., Nair, A., Saal, C., Griffin, B., & Kuentz, M. (2018). Lipophilicity and hydrophobicity considerations in bio‐enabling oral formulations approaches – a PEARRL review. Journal of Pharmacy and Pharmacology, 71. https://doi.org/10.1111/jphp.12984
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Peer-reviewedJankovic, S., Tsakiridou, G., Ditzinger, F., Koehl, N., Price, D., Ilie, A. R., Kalantzi, L., Kimpe, K., Holm, R., Nair, A., Griffin, B., Saal, C., & Kuentz, M. (2018). Application of the solubility parameter concept to assist with oral delivery of poorly water-soluble drugs – a PEARRL review. Journal of Pharmacy and Pharmacology, 71(4). https://doi.org/10.1111/jphp.12948
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Peer-reviewedNiederquell, A., Wyttenbach, N., & Kuentz, M. (2018). New prediction methods for solubility parameters based on molecular sigma profiles using pharmaceutical materials. International Journal of Pharmaceuticals, 546(1-2), 137–144. https://doi.org/10.1016/j.ijpharm.2018.05.033
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Peer-reviewedO’Dwyer, P. J., Litou, C., Box, K. J., Dressman, J., Kostewicz, E. S., Kuentz, M., & Reppas, C. (2018). In vitro methods to assess drug precipitation in the fasted small intestine – a PEARRL review. Journal of Pharmacy and Pharmacology, 71. https://doi.org/10.1111/jphp.12951
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Peer-reviewedPrice, D. J., Ditzinger, F., Koehl, N., Jankovic, S., Tsakiridou, G., Nair, A., Holm, R., Kuentz, M., Dressman, J., & Saal, C. (2018). Approaches to increase mechanistic understanding and aid in the selection of precipitation inhibitors for supersaturating formulations – a PEARRL review. Journal of Pharmacy and Pharmacology, 71. https://doi.org/10.1111/jphp.12927
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Peer-reviewedSaal, W., Wyttenbach, N., Alsenz, J., & Kuentz, M. (2018). Interactions of dimethylaminoethyl methacrylate copolymer with non-acidic drugs demonstrated high solubilization in vitro and pronounced sustained release. European Journal of Pharmaceutics and Biopharmaceutics, 125, 68–75. https://doi.org/10.1016/j.ejpb.2018.01.006
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Peer-reviewedAleandri, S., Schönenberger, M., Niederquell, A., & Kuentz, M. (2018). Temperature-Induced Surface Effects on Drug Nanosuspensions. Pharmaceutical Research, 35(69). https://doi.org/10.1007/s11095-017-2300-6.
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Peer-reviewedAbreu-Villela, R., Adler, C., Caraballo, I., & Kuentz, M. (2018). Electron microscopy/energy dispersive X-ray spectroscopy of drug distribution in solid dispersions and interpretation by multifractal geometry. Journal of Pharmaceutical and Biomedical Analysis, 150, 241–247. https://doi.org/10.1016/j.jpba.2017.12.020
Kontakt
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Prof. Dr. Martin Kuentz
- Dozent Pharmatechnologie
- Telefonnummer
- +41 61 228 56 42 (Direkt)
- bWFydGluLmt1ZW50ekBmaG53LmNo
- Hochschule für Life Sciences FHNW
Institut für Pharma Technology
Hofackerstrasse 30
4132 Muttenz
Institut für Pharma Technology
Fachhochschule Nordwestschweiz FHNW
Hochschule für Life Sciences
Institut für Pharma Technology
Hofackerstrasse 30
4132 Muttenz
- Telefon
- +41 61 228 56 36
- Z2Vvcmdpb3MuaW1hbmlkaXNAZmhudy5jaA==