Particle flowability and compactibility are the two critical process parameters tested when a pharmaceutical material is formulated for a tabletting process. These behavioral descriptions are strongly affected by geometrical, physical, chemical and mechanical particle properties, as well as operational conditions. The property influences are broadly known in a qualitative sense, but have largely escaped fundamental quantitative description. Various measurement methods have been separately developed for each of these properties which provide comparative indices to assist in process and formulation design. This paper seeks to establish the connections between interparticle van der Waals force and both flowability and compactibility, and therefore also the inter-relations between the two apparently distinct properties. Paracetamol and the excipients often associated with it for tabletting are used as test materials to provide an initial validation of the theoretical development. These powders are well-characterized and known to be particularly difficult with respect to flowability and compactibility.
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http://dx.doi.org/10.1016/j.ijpharm.2004.05.001 | DOI Listing |
Materials (Basel)
December 2024
Faculty of Architecture and Civil Engineering, TU Dortmund University, 44227 Dortmund, Germany.
Industrial and construction wastes make up about half of all world wastes. In order to reduce their negative impact on the environment, it is possible to use part of them for concrete production. Using experimental-statistical modeling techniques, the combined effect of brick powder, recycling sand, and alkaline activator on fresh and hardened properties of self-compacting concrete for the production of textile-reinforced concrete was investigated.
View Article and Find Full Text PDFInt J Pharm
December 2024
Evelo Biosciences, Cambridge, MA 02139, USA. Electronic address:
Interest in oral delivery of biological drug products, commonly prepared through lyophilization, is surging. Typically, low solid content solutions are employed for lyophilization to enhance mass transfer and minimize drying time. Yet, this approach often results in lyophilized powders with low bulk density and poor flowability, challenging downstream processing steps that are required for oral product development.
View Article and Find Full Text PDFInt J Pharm
January 2025
School of Chemical Engineering, The University of Birmingham, Edgbaston, Birmingham B15 2TT, UK.
High shear wet granulation (HSWG) is widely used in tablet manufacturing mainly because of its advantages in improving flowability, powder handling, process run time, size distribution, and preventing segregation. In-line process analytical technology measurements are essential in capturing detailed particle dynamics and presenting real-time data to uncover the complexity of the HSWG process and ultimately for process control. This study is to find relationships between Lenterra in-line measurements and granule properties and tablet properties.
View Article and Find Full Text PDFAAPS PharmSciTech
November 2024
Key Laboratory of Modern Preparation of TCM, Ministry of Education, Institute for Advanced Study, Jiangxi University of Chinese Medicine, Nanchang, 330004, People's Republic of China.
This study investigates the improvements in direct compaction powder properties achieved through particle design using laboratory and pilot-scale spray dryers. Hydroxypropyl methylcellulose and polyvinylpyrrolidone were used as modifying agent, which have low hygroscopicity and surface tension, good flowability, and excellent compactibility. Ammonium bicarbonate and sodium bicarbonate were used as pore-forming agents, and the composite particles were prepared using laboratory and pilot-scale spray dryers.
View Article and Find Full Text PDFPharmaceutics
November 2024
Department of Pharmaceutical Technology and Cosmetology, Faculty of Pharmacy, University of Belgrade, Vojvode Stepe 450, 11221 Belgrade, Serbia.
: Improving the production rates of modern tablet presses places ever greater demands on the performance of excipients. Although co-processing has emerged as a promising solution, there is still a lack of directly compressible excipients for modified-release formulations. The aim of the present study was to address this issue by investigating the potential of novel co-processed excipients for the manufacture of modified-release tablets containing ibuprofen.
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