Developing methodology to evaluate the oral sensory features of pharmaceutical tablet coatings

Acceptability of medicines is critical for effective pharmacotherapy. The aim of this study was to investigate the oral sensory properties of tablet coatings to determine how mouthfeel can improve acceptability. A randomised double-blind study was performed in 84 adult volunteers (51% ≥55 years). Each participant received 4 placebo tablets (3 coated and 1 uncoated) to evaluate (i) ease of swallowing and (ii) palatability. Visual analogue scales (VAS) were used to capture sensory parameters. Acceptability was assessed using the following parameters: ease of swallowing; amount of water taken with the tablet; rank order of preference; roughness; adhesiveness and slipperiness. Ease of swallowing was determined to be the most sensitive measure of acceptance. The best coating was the one that was reported to be the most slippery and smooth. The presence of a coating improved ease of swallowing, mouthfeel and overall palatability. This study demonstrates that slippery coatings improve acceptability of tablets. The study also demonstrates the value of VAS to measure the sensory attributes of coated tablets

Single-Polymer Composites (SPCs) : Status and Future Trends

Preparation, properties and applications of single-polymer composites (SPCs), representing an emerging family within the polymeric composite materials, have been surveyed. SPCs were classified in respect to their composition (one- and two-constituents), and preforms (non-consolidated and consolidated). SPCs composed of amorphous or semicrystalline matrices and semicrystalline reinforcements were considered. Methods to widen the temperature difference between the matrix- and reinforcement-giving materials of the same polymer (one-constituent) or same polymer type (two-constituent approach) have been introduced and discussed. Special attention was paid to the unsolved questions related to the interface/interphase in SPCs. It was emphasized that the development of SPCs is fuelled by the need of engineering parts in different applications which have low density and “ultimate” recyclability (i.e. reprocessing via remelting). Recent development of SPCs is supported by novel preform preparation, consolidation and production possibilities

Impact of immediate release film coating on the disintegration process of tablets

Pharmaceutical tablets are often coated with a layer of polymeric material to protect the drug from environmental degradation, facilitate the packaging process, and enhance patient compliance. However, the detailed effects of such coating layers on drug release are not well understood. To investigate this, flat-faced pure microcrystalline cellulose tablets with a diameter of 13 mm and a thickness between 1.5 mm to 1.6 mm were directly compressed, and a film coating layer with a thickness of 80 μm to 120 μm was applied to one face of these tablets. This tablet geometry and immediate release film coating were chosen as a model system to understand how the film coating interacts with the tablet core. The coating hydration and dissolution process was studied using terahertz pulsed imaging, while optical coherence tomography was used to capture further details on the swelling process of the polymer in the coated tablet. The study investigated the film coating polymer dissolution process and found the gelling of dissolving polymer restricted the capillary liquid transport in the core. These findings can help predict the dissolution of film coating within the typical range of thickness (30 μm to 40 μm) and potentially be extended to understand modified release coating formulations

On the morphology of advanced polymer-fibres and their composites

SIGLEAvailable from British Library Document Supply Centre-DSC:DXN018988 / BLDSC - British Library Document Supply CentreGBUnited Kingdo

Impact of Immediate Release Film Coating on the Disintegration Process of Tablets

Pharmaceutical tablets are often coated with a layer of polymeric material to protect the drug from environmental degradation, facilitate the packaging process, and enhance patient compliance. However, the detailed effects of such coating layers on drug release are not well understood. To investigate this, flat-faced pure microcrystalline cellulose tablets with a diameter of 13 mm and a thickness between 1.5-1.6 mm were directly compressed, and a film coating layer with a thickness of 80-120 μm was applied to one face of these tablets. This tablet geometry and immediate release film coating were chosen as a model system to understand how the film coating interacts with the tablet core. The coating hydration and dissolution process was studied using terahertz pulsed imaging, while optical coherence tomography was used to capture further details on the swelling process of the polymer in the coated tablet. The study investigated the film coating polymer dissolution process and found the gelling of dissolving polymer restricted the capillary liquid transport in the core. These findings can help predict the dissolution of film coating within the typical range of thickness (30-40 μm) and potentially be extended to understand modified release coating formulations

Morphology and crystallization kinetics of dilute binary blends of two monodisperse n-alkanes with a length ratio of two

The crystallization kinetics and morphologies of dilute binary blends of the monodisperse alkane n-C122H246 in n-C246H494 and vice versa have been investigated. With a molecular length ratio close to two, this pair of n-alkanes does not produce permanent cilia when once-folded C246H494 molecules cocrystallize with extended chains of C122H246. In this condition, the supplementary splaying of adjacent dominant lamellae and the consequently more spherulitic textures, which are present in previous blends for which a longer guest molecule gives permanent cilia, are absent, although other features of blend crystallization remain. Specifically, the isothermal radial growth rate is constant for cocrystallizing blends, although less than for their pure hosts, but becomes nonlinear with cellulation when C122H246 forms a segregated population within extended-chain C246H494. Increased nucleation in the blends give smaller scale textures than for the host materials, but the presence of a second component reduces splaying and thereby disfavors spherulitic growth