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Updated: Feb 25, 2026

Taste Exam: A Brief and Validated Test
Published on: August 17, 2018
Early pediatric formulation development with new chemical entities: Opportunities of e-tongue besides human taste
Laura Isabell Immohr1, Angela Dischinger2, Peter Kühl2
1Institute of Pharmaceutics and Biopharmaceutics, Heinrich-Heine-University Duesseldorf, Universitaetsstr. 1, 40225, Duesseldorf, Germany.
Insights
Electronic tongues offer a reproducible, ethical, and cost-effective method for assessing pediatric drug palatability. This instrumental taste assessment complements human studies, aiding in the development of better-tasting new chemical entities (NCEs).
Area of Science:
- Pharmaceutical Sciences
- Sensory Science
- Drug Development
Background:
- Pediatric drug palatability is crucial for therapeutic success, especially for liquid formulations contacting taste buds.
- Ethical considerations and limitations in human taste testing for new chemical entities (NCEs) necessitate alternative assessment methods.
- Electronic tongue (e-tongue) technology offers a potential instrumental approach to characterize drug taste profiles.
Purpose of the Study:
- To demonstrate the implementation and suitability of electronic tongue measurements for assessing pediatric drug palatability.
- To compare in-vitro electronic tongue data with in-vivo human taste assessment results for drug candidates CSE3104 and CSE3165.
- To explore strategies for electronic tongue-guided formulation development, considering excipient effects and formulation comparisons.
Main Methods:
- Comparison of in-vivo human taste data from a Phase 1 clinical study with in-vitro electronic tongue measurements.
- Assessment of bitter taste perception for CSE3104 using electronic tongue technology, correlating with human sensory data.
- Evaluation of CSE3165 taste profiles, including bitterness and sourness, and relating instrumental responses to hedonic descriptors like 'unpleasant'.
Main Results:
- Electronic tongue measurements successfully correlated with human taste perception, accurately assessing the bitterness of CSE3104.
- Increasing concentrations of CSE3165 showed corresponding increases in bitterness values via electronic tongue, aligning with human studies.
- Instrumental assessment of 'unpleasantness' in formulations showed a link to bitterness, and electronic tongue guided development yielded reproducible data.
Conclusions:
- Electronic tongue technology provides a valuable, reproducible, and ethical alternative for characterizing drug palatability in pediatric formulations.
- This instrumental approach can meaningfully interpret taste assessments, especially when human volunteer numbers are limited, reducing time and costs.
- Electronic tongues facilitate formulation development by assessing excipient effects and comparing different drug formulations efficiently.
Abstract:
The palatability of a pediatric drug formulation is one of the key prerequisites for therapeutic success. Liquid formulations are often chosen for pediatric drug products, and they require special attention regarding their taste, as they have direct contact to the taste buds and a relatively long residence time in the oral cavity. For ethical reasons, the role of electronic tongues in the development of oral drug formulations with new chemical entities (NCEs) for pediatric use is growing, however, little is known about the strategies how this instrumental taste assessment can be performed. The present study illustrates two possibilities to combine in-vitro and in-vivo data for the characterization of the palatability of the new drug candidates CSE3104 and CSE3165. As a first step, the implementation and suitability of electronic tongue measurements has been demonstrated by comparison of in-vivo and in-vitro data. In alignment with the taste assessment results during a single-center, double-blinded, randomized, placebo-controlled, single ascending dose (SAD) study in healthy subjects, the bitter taste perception of CSE3104 was assessed with e-tongue measurements. Moreover, the sensor response pattern showed comparable results of the e-tongue measurements to the human taste study of CSE3165: With increasing concentration, the bitterness values were increased. In addition, the human taste pattern showed increasing values for sourness due to higher volumes of the citric acid buffer. Results of the hedonic descriptor "unpleasant" within the human taste assessments could be related to bitterness in the instrumental taste assessment. For the second step in electronic tongue guided formulation development two possibilities are depicted in the article focusing on the effect of different excipients on the formulation on the one hand and on the assessment and comparison of two drug formulations on the other hand. Based on these results, the low number of healthy volunteers for the taste assessment in a Phase 1 study led to a meaningful interpretation, by applying in addition the electronic tongue. Using this instrumental approach led to reproducible data versus the human taste assessment, without ethical concerns, and with a reduction in time and costs.
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