Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Pascal Chalus"'
Autor:
Sonja Peter, Atanas Koulov, Andreas Zerr, Ombeline Danton, Hanns-Christian Mahler, Michael Jahn, Ariane Schröter, Pascal Chalus, Jörg Huwyler
Publikováno v:
Journal of Pharmaceutical Sciences. 110:3410-3417
Leaching of toxic or reactive chemicals from polymeric materials can adversely affect the quality and safety of biopharmaceuticals. It was therefore the aim of the present study to analyze leachables from a disposable clinical administration syringe
Autor:
Franziska Schleinzer, Dennis T. Yang, Dean C. Ripple, Nazar Filonov, Pascal Chalus, Tapan K. Das, Kurt D. Benkstein, Ashwinkumar A. Bhirde, Stefan Romeijn, Fook Chiong Cheong, Sambit R. Kar, Laura A. Philips, Christine Probst, Adam D. Grabarek, Nicole S. Gill, Maciej Jarzebski, Yoen Joo Kim, David L. Duewer, Miguel Saggu, Andrew D. Hollingsworth, Gurusamy Balakrishnan, Judith Hadley, Vikram Kestens, Yannic Ramaye, Anja Matter, Wesley W. Howard, Theodore W. Randolph, Ngoc Do, Jan Kuba Tatarkiewicz, David G. Grier, Heather Anne Wright, Patrick Garidel, Atanas Koulov, Wim Jiskoot, Jared R. Snell, Harshit Khasa
Publikováno v:
J Pharm Sci
Journal of Pharmaceutical Sciences
Journal of Pharmaceutical Sciences
The measurement of polydisperse protein aggregates and particles in biotherapeutics remains a challenge, especially for particles with diameters of ≈ 1 µm and below (sub-micrometer). This paper describes an interlaboratory comparison with the goal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebec099deb60130fdbf19d1d6774ab17
https://europepmc.org/articles/PMC9912188/
https://europepmc.org/articles/PMC9912188/
Autor:
Pascal Chalus, Anja Matter-Schwald, Patrick Favrod, Pauline Heymes, Martin Vogt, Ahmed Besheer, Timothy Pillow, Sergio Mompart Barrenechea, Roman Mathaes, Susanne Joerg, Andrea Kirste, Hanns-Christian Mahler
Publikováno v:
Pharmaceutical Research. 37
Health care professionals can be exposed to hazardous drugs such as cytostatics during preparation of drugs for administration. Closed sytem transfer devices (CSTDs) were introduced to provide protection for healthcare professional against unintended
Autor:
Hanns-Christian Mahler, Dhananjay Jere, Atanas Koulov, Roman Mathaes, Ahmad S. Sediq, Susanne Joerg, Martin Vogt, Anja Matter, Sarah S. Peláez, Maximilian Zaeh, Pascal Chalus
Publikováno v:
Journal of pharmaceutical sciences. 109(9)
Intravitreal (IVT) injection is currently the state of the art for drug delivery to the back of the eye. Drug Products (DP) intended for IVT injections usually pose challenges such as a very low injection volume (e.g. 50 μL) and high injection force
Publikováno v:
Powder Technology. 308:306-317
We derive a simple first order kinetics model for the powder mixing in a bin blender and adapt it to fit the NIR spectra obtained during the real-time mixing. The model is tested on a full drug product formulation mixing consisting of API and multipl
Autor:
Atanas Koulov, Pascal Chalus, Cristina Grigore, Hanns-Christian Mahler, Anja Matter, Carolin Langer, Susanne Joerg, Thomas Lemazurier, Nicolas Marti, Roman Mathaes, Satish K. Singh
Publikováno v:
Journal of pharmaceutical sciences. 109(1)
Glass fogging is a phenomenon occurring in lyophilized drug products and can be described as a thin product layer deposited on the inner surface of the glass container, in the area not covered by the lyo cake itself. It is often considered a cosmetic
Publikováno v:
Journal of pharmaceutical sciences. 108(5)
Physical tablet defects are related to internal structural defects that are not easily assessed by the traditional methods, such as dusting, laminating, or fracturing during appearance, friability, or hardness testing. Also, these methods do not allo
Autor:
Alejandra Nieto, Hanns-Christian Mahler, Michael Adler, Holger Roehl, Pascal Chalus, Helen Brown
Publikováno v:
PDA journal of pharmaceutical science and technology. 70(4)
Container closure integrity (CCI) testing is required by different regulatory authorities in order to provide assurance of tightness of the container closure system against possible contamination, for example, by microorganisms. Microbial ingress CCI
Autor:
Stefanos Karampelas, Michael S. Krzemnicki, Sebastian D. Friess, Pascal Chalus, Henry A. Hänni
Publikováno v:
Gems & Gemology. 46:128-134
Publikováno v:
Analytica Chimica Acta. 591:219-224
The pharmaceutical industry faces increasing regulatory pressure to optimize quality control. Content uniformity is a basic release test for solid dosage forms. To accelerate test throughput and comply with the Food and Drug Administration's process