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Naji, M. |
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Motta, Antonella |
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Aletan, Dirar |
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Mohamed, Tarek |
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Ertürk, Emre |
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Taccardi, Nicola |
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Kononenko, Denys |
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Petrov, R. H. | Madrid |
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Alshaaer, Mazen | Brussels |
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Bih, L. |
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Casati, R. |
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Muller, Hermance |
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Kočí, Jan | Prague |
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Šuljagić, Marija |
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Kalteremidou, Kalliopi-Artemi | Brussels |
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Azam, Siraj |
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Ospanova, Alyiya |
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Blanpain, Bart |
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Ali, M. A. |
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Popa, V. |
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Rančić, M. |
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Ollier, Nadège |
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Azevedo, Nuno Monteiro |
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Landes, Michael |
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Rignanese, Gian-Marco |
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Lamprou, Dimitrios A.
Queen's University Belfast
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (22/22 displayed)
- 2023Combining microfluidics and coaxial 3D-bioprinting for the manufacturing of diabetic wound healing dressingscitations
- 2023Combining microfluidics and coaxial 3D-bioprinting for the manufacturing of diabetic wound healing dressingscitations
- 2023Urethane dimethacrylate-based photopolymerizable resins for stereolithography 3D printing: a physicochemical characterisation and biocompatibility evaluationcitations
- 20223D bioprinted scaffolds for diabetic wound healing applicationscitations
- 2022Stereolithography 3D printed implants: a preliminary investigation as potential local drug delivery systems to the earcitations
- 2022High spatial resolution ToF-SIMS imaging and image analysis strategies to monitor and quantify early phase separation in amorphous solid dispersionscitations
- 2022Fused deposition modeling 3D printing proof of concept study for personalised inner ear therapycitations
- 2021Fused deposition modelling for the development of drug loaded cardiovascular prosthesiscitations
- 2021Microfluidics Technology for the Design and Formulation of Nanomedicinescitations
- 2021Optimization of FDM 3D printing process parameters to produce haemodialysis curcumin-loaded vascular graftscitations
- 2021Microfluidics technology for the design and formulation of nanomedicinescitations
- 20203D printing of drug-loaded thermoplastic polyurethane meshes: A potential material for soft tissue reinforcement in vaginal surgerycitations
- 20193D printed microneedle patches using stereolithography (SLA) for intradermal insulin deliverycitations
- 2017Fabrication and characterisation of drug-loaded electrospun polymeric nanofibers for controlled release in hernia repaircitations
- 2017A novel methodology to study polymodal particle size distributions produced during continuous wet granulationcitations
- 2017Probing polydopamine adhesion to protein and polymer films : microscopic and spectroscopic evaluation
- 2017Isatin thiosemicarbazones promote honeycomb structure formation in spin-coated polymer films: concentration effect and release studiescitations
- 2017Probing polydopamine adhesion to protein and polymer films: microscopic and spectroscopic evaluationcitations
- 2016A novel hot-melt extrusion formulation of albendazole for increasing dissolution propertiescitations
- 2016Isatin thiosemicarbazone-blended polymer films for biomedical applications : surface morphology, characterisation and preliminary biological assessmentcitations
- 2014The degradative effects of germicidal light on flexible endoscope material
- 2012Polymer templating of supercooled indomethacin for polymorph selectioncitations
Places of action
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article
A novel methodology to study polymodal particle size distributions produced during continuous wet granulation
Abstract
It is important during powder granulation to obtain particles of a homogeneous size especially in critical situations such as pharmaceutical manufacture. To date, homogeneity of particle size distribution has been defined by the use of the d50 combined with the span of the particle size distribution, which has been found ineffective for polymodal particle size distributions. This work focuses on demonstrating the limitations of the span parameter to quantify homogeneity and proposes a novel improved metric based on the transformation of a typical particle size distribution curve into a homogeneity factor which can vary from 0 to 100%. The potential of this method as a characterisation tool has been demonstrated through its application to the production of granules using two different materials. The workspace of an 11 mm twin screw granulator was defined for two common excipients (α-lactose monohydrate and microcrystalline cellulose). Homogeneity of the obtained granules varied dramatically from 0 to 95 % in the same workspace, allowing identification of critical process parameters (e.g. feed rate, liquid/solid ratio, torque velocities). In addition it defined the operational conditions required to produce the most homogeneous product within the range 5 μm – 2.2 mm from both materials.