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Published on: December 27, 2024
Vitamin C in Infant Formula and Adult/Pediatric Nutritional Formula by Liquid Chromatography with UV Detection:
Esther Campos Giménez1, Frédéric Martin1
1Nestlé Research Center, Vers-chez-les-Blanc, 1000 Lausanne 26, Switzerland.
Insights
This study validated the AOAC INTERNATIONAL First Action Method 2012.22 for quantifying vitamin C in infant formula and nutritional products. The method demonstrated excellent repeatability and reproducibility, meeting established performance standards for reliable nutrient analysis.
Area of Science:
- Analytical Chemistry
- Food Science
- Nutritional Analysis
Background:
- Accurate vitamin C measurement is crucial for infant formula and nutritional products.
- AOAC INTERNATIONAL Method 2012.22 is a liquid chromatography-UV detection technique for vitamin C analysis.
- Validation through collaborative studies ensures method reliability and reproducibility.
Purpose of the Study:
- To determine the repeatability and reproducibility of AOAC INTERNATIONAL First Action Method 2012.22.
- To assess the method's performance against established Standard Method Performance Requirements (SMPR®) 2012.012.
- To recommend the method for Final Action status based on collaborative study results.
Main Methods:
- A collaborative study involving multiple laboratories was conducted in three parts.
- Participants qualified by analyzing practice samples before analyzing 10 blind duplicate samples.
- Method performance was evaluated against SMPR® 2012.012 criteria, including precision and Horwitz ratio.
Main Results:
- Repeatability and reproducibility values were within the SMPR® requirements (1.4-7.3% and 3.2-11.4%, respectively).
- Horwitz ratio values ranged from 0.5 to 1.7, indicating acceptable performance.
- The method successfully quantified vitamin C in infant formula and nutritional products, even with potential sample spoilage.
Conclusions:
- The AOAC INTERNATIONAL First Action Method 2012.22 meets the performance requirements for vitamin C analysis in infant and adult nutritional formulas.
- The collaborative study data supports the recommendation of granting the method Final Action status.
- The validated method provides reliable and reproducible results for nutritional product analysis.
Abstract:
To determine the repeatability and reproducibility values of the AOAC INTERNATIONAL First Action Method 2012.22, Vitamin C in Infant Formula and Adult/Pediatric Nutritional Formula by Liquid Chromatography with UV Detection, a collaborative study was organized. The study was divided into two parts: method setup and qualification of participants (part 1) and collaborative study participation (part 2). During part 1, each laboratory was asked to analyze two practice samples using the aforementioned method. Laboratories that provided results within a range of expected levels were qualified for part 2, where they analyzed 10 samples in blind duplicates. Two of the samples were suspected of spoilage during the test and new cans of the same type of product were analyzed by a subset of laboratories in part 3. The results were compared with Standard Method Performance Requirement (SMPR®) 2012.012 established for vitamin C. The precision results were within the requirements stated in the SMPR: 1.4-7.3% and 3.2-11.4% respectively, for repeatability and reproducibility. Finally, Horwitz ratio values were all <2 (0.5-1.7). The Expert Review Panel for Stakeholder Panel for Infant Formula and Adult Nutritionals Nutrient Methods determined that the data presented met the SMPR and therefore recommended the method be granted Final Action status.
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