Critical View on the Qualification of Electronic Tongues Regarding Their Performance in the Development of Peroral Drug Formulations with Bitter Ingredients

Author:

Steiner Denise1ORCID,Meyer Alexander2,Immohr Laura Isabell3,Pein-Hackelbusch Miriam2ORCID

Affiliation:

1. Institute of Pharmaceutical Technology and Biopharmaceutics, University of Muenster, Corrensstraße 48, 48149 Muenster, Germany

2. Institute for Life Science Technologies (ILT.NRW), Ostwestfalen-Lippe University of Applied Sciences and Arts, Campusallee 12, 32657 Lemgo, Germany

3. NextPharma Germany Bidco GmbH, Hildebrandstrasse 12, 37081 Goettingen, Germany

Abstract

In this review, we aim to highlight the advantages, challenges, and limitations of electronic tongues (e-tongues) in pharmaceutical drug development. The authors, therefore, critically evaluated the performance of e-tongues regarding their qualification to assess peroral formulations containing bitter active pharmaceutical ingredients. A literature search using the keywords ‘electronic’, ‘tongue’, ‘bitter’, and ‘drug’ in a Web of Science search was therefore initially conducted. Reviewing the publications of the past decade, and further literature where necessary, allowed the authors to discuss whether and how e-tongues perform as expected and whether they have the potential to become a standard tool in drug development. Specifically highlighted are the expectations an e-tongue should meet. Further, a brief insight into the technologies of the utilized e-tongues is given. Reliable protocols were found that enable (i) the qualified performance of e-tongue instruments from an analytical perspective, (ii) proper taste-masking assessments, and (iii) under certain circumstances, the evaluation of bitterness.

Publisher

MDPI AG

Reference150 articles.

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2. Council of the European Union, European Parliament (2006). Regulation (EC) No. 1901/2006 on medicinal products for pediatric use and amending Regulation (EEC) No 1768/92, Directive 2001/20/EC, Directive 2001/83/EC and Regulation (EC) No 726/2004. Regulation (EC) No. 1901/2006 2006. Off. J. Eur. Union, L378, 1–31.

3. Preference for pharmaceutical formulation and treatment process attributes;Stewart;Patient Prefer. Adherence,2016

4. Proposed tool to compare and assess the applicability of taste assessment techniques for pharmaceuticals;Clapham;J. Pharm. Sci.,2022

5. Early pediatric formulation development with new chemical entities: Opportunities of e-tongue besides human taste assessment;Immohr;Int. J. Pharm.,2017

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