Responsive Sensory Evaluation to Develop Flexible Taste-Masked Paediatric Primaquine Tablets against Malaria for Low-Resource Settings

Author:

Ranmal Sejal R.1ORCID,Lavarde Marc2ORCID,Wallon Elodie2,Issa Samar2ORCID,Taylor Walter R.34,Nguyen Ngoc Pouplin Julie L. A.5,Tuleu Catherine1ORCID,Pensé-Lhéritier Anne-Marie2ORCID

Affiliation:

1. UCL School of Pharmacy, University College London, 29–39 Brunswick Square, London WC1N 1AX, UK

2. Ecole de Biologie Industrielle—EBI, UPR EBInnov®, 49 Avenue des Genottes CS90009, 95895 Cergy, France

3. Mahidol Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, 420/60 Rajvithi Road, Bangkok 10400, Thailand

4. Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford OX1 3SY, UK

5. Reseau Medicaments et Developpement (ReMeD), 21bis Avenue du Commandant l’Herminier, 44600 Saint-Nazaire, France

Abstract

Primaquine is an important antimalarial drug for malaria transmission blocking and radical cure, but it is not currently available in child-friendly formulations in appropriate doses. Adult-strength tablets are often crushed and dissolved in water to obtain the required dose, which exposes the drug’s bitter taste. As part of the developing paediatric primaquine (DPP) project, this study adopted a responsive sensory pharmaceutics approach by integrating real-time formulation development and pre-clinical taste assessment to develop palatable, flavour-infused primaquine tablets. A design of experiment (DoE) approach was used to screen different taste-masking agents and excipient blends with trained, expert sensory assessors, with quinine hydrochloride as a model bitter tastant. The taste-masking efficacy of selected prototype formulation blends was validated with naïve assessors using the highest 15 mg primaquine dose. The mean bitterness intensity rating, measured on a discrete 11-point scale, was halved from 7.04 for the unflavoured control to 2.74–3.70 for the formulation blends. Sucralose had the biggest impact on bitterness suppression and improving palatability. Two different flavouring systems have been developed, and their acceptability in paediatric patients will be assessed as part of upcoming validation field clinical trials in Africa.

Funder

European Union

Publisher

MDPI AG

Subject

Pharmaceutical Science

Reference44 articles.

1. (2023). WHO Guidelines for Malaria (Standard No. WHO/UCN/GMP/2023.01).

2. World Health Organization (2022). World Malaria Report 2022, World Health Organization.

3. Safety of age-dosed, single low-dose primaquine in children with glucose-6-phosphate dehydrogenase deficiency who are infected with Plasmodium falciparum in Uganda and the Democratic Republic of the Congo: A randomised, double-blind, placebo-controlled, non-inferiority trial;Taylor;Lancet Infect. Dis.,2023

4. Development of weight and age-based dosing of daily primaquine for radical cure of vivax malaria;Taylor;Malar. J.,2021

5. World Health Organization (2023, March 05). 21st Invitation to Manufacturers of Antimalarial Medicines to Submit an Expression of Interest (EOI) for Product Evaluation to the WHO Prequalification Unit (PQT). Available online: https://extranet.who.int/pqweb/sites/default/files/documents/EOI-MalariaV21_0.pdf.

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