Pharma Excipients
Inorganic Chemicals
The effect of filler particle size on API homogeneity of controlled release formulations via…
Abstract
Previous research has shown that controlled release (CR) formulations with hydrox- ypropyl methylcellulose (HPMC) as hydrophilic matrix former produced via twin-screw wet granulation (TSWG) yield granules with an inhomogeneous active pharmaceutical ingredient (API) distribution (Denduyver…
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Achieving tunable and interconnected porosity of biomimetic apatite scaffolds through Pickering…
Abstract
Synthetic apatitic calcium phosphates are widely used to develop biomaterial devices due to their excellent biological properties. The aim of this study was to develop nanocrystalline apatitic calcium phosphates (NCA) bioceramics with tunable porosity (size of pores, total porosity…
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Complemental Hard Modeling in Raman spectroscopy – A case study on titanium dioxide-free coating…
Abstract
Tablets are coated for taste or odor modification, for modified release profiles or as a protective layer to increase the stability. Here, titanium dioxide is frequently added as a coating component due to its opaque properties. Furthermore, its Raman activity makes it an integral part…
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Development and Evaluation of Lactose-Free Single-Unit and Multiple-Unit Preparations of a BCS Class…
Abstract
Background/Objectives: The aim of the present study was to develop lactose-free formulations of rivaroxaban, a novel oral anticoagulant used for the treatment and prevention of blood clotting. As a BCS Class II drug, rivaroxaban is characterized by poor solubility in aqueous media, posing…
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Influence of multiple compression phases during tableting of spray dried Saccharomyces cerevisiae on…
Abstract
The viability of probiotic microorganisms is essential for their health-promoting effects and must be preserved in the best possible way during the production of the final dosage form, such as tablets. This applies to both drying and tableting. Saccharomyces cerevisiae is spray-dried…
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In silico formulation optimization and particle engineering of pharmaceutical products using a…
Abstract
Pharmaceutical drug dosage forms are critical for ensuring the effective and safe delivery of active pharmaceutical ingredients to patients. However, traditional formulation development often relies on extensive lab and animal experimentation, which can be time-consuming and costly.…
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Advancements in Colon-Targeted Drug Delivery: A Comprehensive Review on Recent Techniques with…
Abstract
This review investigates the progression and effectiveness of colon-targeted drug delivery systems, offering a comprehensive understanding of the colon's anatomy and physiological environment. Recognizing the distinctive features of the colon is crucial for successfully formulating…
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Data-driven insights into the characteristics of liquisolid systems based on the machine learning…
Abstract
Liquisolid systems (LS) represent a formulation approach where liquid drug or its dispersion is transformed into a powder with good flowability and compactibility, leading to enhanced drug dissolution and bioavailability. Many research groups have focused on the preparation and…
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Mechanical properties of tablets: direct compression vs. twin-screw melt granulation with PEG 8000
This poster was presented at the DDF Summit Conference 2024 by Valentyn MOHYLYUK, Zoltán Márk HORVÁTH, Kirils KUKULS, Liga LAUBERTE, Artūrs PAULAUSKS from Rīga Stradiņš University:
Introduction
Replacing batch wet granulation with twin-screw melt extruder as a continuous solventless process is…
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Calcium phosphate microcapsules for paediatric drug delivery
This poster was presented by Galvita at EuPFI 2024 in Rotterdam
Introduction
Modern drug delivery needs to use novel multifunctional materials for developing medicinal products and new therapies. Porous particles attract a lot of attention as promising drug delivery systems. Functions of porous…
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