Multi-Analytical Framework to Assess the In Vitro Swallowability of Solid Oral Dosage Forms Targeting Patient Acceptability and Adherence

A lack of effective intervention in addressing patient non-adherence and the acceptability of solid oral dosage forms combined with the clinical consequences of swallowing problems in an ageing world population highlight the need for developing methods to study the swallowability of tablets. Due to...

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Main Authors: Abdul Latif Ershad (Author), Ali Rajabi-Siahboomi (Author), Shahrzad Missaghi (Author), Daniel Kirby (Author), Afzal Rahman Mohammed (Author)
Format: Book
Published: MDPI AG, 2021-03-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Abdul Latif Ershad  |e author 
700 1 0 |a Ali Rajabi-Siahboomi  |e author 
700 1 0 |a Shahrzad Missaghi  |e author 
700 1 0 |a Daniel Kirby  |e author 
700 1 0 |a Afzal Rahman Mohammed  |e author 
245 0 0 |a Multi-Analytical Framework to Assess the In Vitro Swallowability of Solid Oral Dosage Forms Targeting Patient Acceptability and Adherence 
260 |b MDPI AG,   |c 2021-03-01T00:00:00Z. 
500 |a 10.3390/pharmaceutics13030411 
500 |a 1999-4923 
520 |a A lack of effective intervention in addressing patient non-adherence and the acceptability of solid oral dosage forms combined with the clinical consequences of swallowing problems in an ageing world population highlight the need for developing methods to study the swallowability of tablets. Due to the absence of suitable techniques, this study developed various in vitro analytical tools to assess physical properties governing the swallowing process of tablets by mimicking static and dynamic stages of time-independent oral transitioning events. Non-anatomical models with oral mucosa-mimicking surfaces were developed to assess the swallowability of tablets; an SLA 3D printed in vitro oral apparatus derived the coefficient of sliding friction and a friction sledge for a modified tensometer measured the shear adhesion profile. Film coat hydration and in vitro wettability was evaluated using a high-speed recording camera that provided quantitative measurements of micro-thickness changes, simulating static in vivo tablet-mucosa oral processing stages with artificial saliva. In order to ascertain the discriminatory power and validate the multianalytical framework, a range of commonly available tablet coating solutions and new compositions developed in our lab were comparatively evaluated according to a quantitative swallowability index that describes the mathematical relationship between the critical physical forces governing swallowability. This study showed that the absence of a film coat significantly impeded the ease of tablet gliding properties and formed chalky residues caused by immediate tablet surface erosion. Novel gelatin- and λ-carrageenan-based film coats exhibited an enhanced lubricity, lesser resistance to tangential motion, and reduced stickiness than polyvinyl alcohol (PVA)-PEG graft copolymer, hydroxypropyl methylcellulose (HPMC), and PVA-coated tablets; however, Opadry<sup>®</sup> EZ possessed the lowest friction-adhesion profile at 1.53 a.u., with the lowest work of adhesion profile at 1.28 J/mm<sup>2</sup>. For the first time, the in vitro analytical framework in this study provides a fast, cost-effective, and repeatable swallowability ranking method to screen the in vitro swallowability of solid oral medicines in an effort to aid formulators and the pharmaceutical industry to develop easy-to-swallow formulations. 
546 |a EN 
690 |a film coating 
690 |a solid oral dosage forms 
690 |a in vitro swallowability 
690 |a dysphagia 
690 |a adherence 
690 |a acceptability 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Pharmaceutics, Vol 13, Iss 3, p 411 (2021) 
787 0 |n https://www.mdpi.com/1999-4923/13/3/411 
787 0 |n https://doaj.org/toc/1999-4923 
856 4 1 |u https://doaj.org/article/eea653ccddf14e5b973d77097a00f39f  |z Connect to this object online.