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Expert Perspectives on Enhancing Analytical Methods for Multi-Ingredient Dietary Supplements (MIDS): A Qualitative
Ingyeong Ko1, Hae Jin Park1, Kwang Suk Ko1
1Department of Nutritional Science & Food Management, Ewha Womans University, Seoul 03760, Republic of Korea.
Analyzing multi-ingredient dietary supplements (MIDS) presents challenges due to complex formulations. Industry professionals and experts suggest developing standardized methods and regulatory harmonization for reliable quality control.
Area of Science:
- Analytical Chemistry
- Food Science
- Pharmacology
Background:
- The growing market for multi-ingredient dietary supplements (MIDS) presents significant analytical challenges.
- Complex ingredient interactions and formulation variability complicate quality control and product testing.
Purpose of the Study:
- To investigate the analytical challenges encountered in multi-ingredient dietary supplement (MIDS) testing.
- To explore practical solutions and identify areas for improvement in MIDS quality assurance.
Main Methods:
- Semi-structured focus group interviews were conducted with 33 industry professionals and 10 analytical experts.
- Qualitative data analysis was used to identify obstacles and proposed solutions.
Main Results:
- Key challenges include trace component degradation, ingredient interference, dosage form difficulties, and lack of standardized protocols.
- Industry professionals employ internal, company-specific strategies like raw material substitution and modified analytical procedures.
- Analytical experts recommend matrix-specific pretreatment, optimized extraction, and regulatory harmonization.
Conclusions:
- Current MIDS testing lacks a unified analytical framework, leading to varied internal solutions.
- Standardized methodologies and regulatory harmonization are crucial for enhancing analytical reliability and reproducibility in MIDS analysis.
- The study provides insights for developing robust quality assurance frameworks for MIDS.
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