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      Impact of Food and Drink Administration Vehicles on Paediatric Formulation Performance: Part 1—Effects on Solubility of Poorly Soluble Drugs

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          Abstract

          Food and drinks are commonly used to facilitate administration of paediatric medicines to improve palatability and enhance patient compliance. However, the impact of this practice on drug solubility and on oral drug bioavailability is not usually studied. Based on recommended strategies for oral administration of paediatric medicines with food and drink vehicles, the aims of this study were (i) to measure the physicochemical properties of (soft) food and drink vehicles, commonly mixed with paediatric medicines prior to administration, and (ii) to assess the impact of the co-administered vehicles on the solubility of two poorly soluble paediatric drugs. Montelukast (sodium) and mesalazine were selected as the model compounds. Distinct differences were observed between the physicochemical properties ( i.e. pH, surface tension, osmolality, viscosity and buffer capacity) and macronutrient composition ( i.e. fat, sugar and protein content) of the different soft foods and drinks, not only among vehicle type but also within vehicles of the same subtype. Solubility studies of the two model compounds in selected drinks and soft foods resulted in considerably different drug solubility values in each vehicle. The solubility of the drugs was significantly affected by the vehicle physicochemical properties and macronutrient composition, with the solubility of montelukast being driven by the pH, fat and protein content of the vehicles and the solubility of mesalazine by vehicle osmolality, viscosity and sugar content. This vehicle-dependent impact on drug solubility could compromise its bioavailability, and ultimately affect the safety and/or efficacy of the drug and should be taken into consideration during paediatric product development.

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          Most cited references35

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          Experimental design and optimization

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            Estimating drug solubility in the gastrointestinal tract.

            Solubilities measured in water are not always indicative of solubilities in the gastrointestinal tract. The use of aqueous solubility to predict oral drug absorption can therefore lead to very pronounced underestimates of the oral bioavailability, particularly for drugs which are poorly soluble and lipophilic. Mechanisms responsible for enhancing the luminal solubility of such drugs are discussed. Various methods for estimating intra-lumenal solubilities are presented, with emphasis on the two most widely implemented methods: determining solubility in fluids aspirated from the human gastrointestinal tract, and determining solubility in so-called biorelevant media, composed to simulate these fluids. The ability of the biorelevant media to predict solubility in human aspirates and to predict plasma profiles is illustrated with case examples.
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              A NEW APPARATUS FOR MEASURING SURFACE TENSION

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                Author and article information

                Contributors
                n.fotaki@bath.ac.uk
                Journal
                AAPS PharmSciTech
                AAPS PharmSciTech
                AAPS PharmSciTech
                Springer International Publishing (Cham )
                1530-9932
                26 June 2020
                26 June 2020
                July 2020
                : 21
                : 5
                : 177
                Affiliations
                [1 ]GRID grid.7340.0, ISNI 0000 0001 2162 1699, Department of Pharmacy and Pharmacology, , University of Bath, ; Claverton Down, Bath, BA2 7AY UK
                [2 ]GRID grid.417815.e, ISNI 0000 0004 5929 4381, Oral Product Development, Pharmaceutical Technology & Development, Operations, , AstraZeneca, ; Macclesfield, UK
                [3 ]Currently at UCB Pharma, Chemin du Foriest, B-1420 Braine-l’Alleud, Belgium
                Author information
                http://orcid.org/0000-0003-1826-7363
                Article
                1722
                10.1208/s12249-020-01722-z
                7373161
                32592045
                4d811e3c-6349-4dc3-8734-7e3dd2dda592
                © The Author(s) 2020

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 7 May 2020
                : 4 June 2020
                Funding
                Funded by: University of Bath
                Categories
                Research Article
                Custom metadata
                © American Association of Pharmaceutical Scientists 2020

                Pharmacology & Pharmaceutical medicine
                drug manipulation,food,drinks,solubility,physicochemical properties,multivariate analysis,paediatrics

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