AOAC 2018.05 Protein Digestibility Analysis in Dietary Supplements
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AOAC 2018.05 Protein Digestibility Analysis in Dietary Supplements

AOAC 2018.05 Protein Digestibility Analysis in Dietary Supplements

AOAC 2018.05 Protein Digestibility Analysis in Dietary Supplements

The AOAC International Method 2018.05 is a standardized procedure used to assess the protein digestibility of dietary supplements, providing critical insights into ingredient quality and nutritional efficacy. This method evaluates how effectively proteins are broken down by digestive enzymes, which is essential for ensuring that dietary supplements provide optimal nutrition.

The analysis involves subjecting the supplement samples to simulated gastrointestinal conditions, including acid and enzymatic digestion, followed by quantification of undigested protein residues through colorimetric assays. Understanding digestibility helps manufacturers in formulating products that are easily absorbed by consumers, thereby enhancing product efficacy.

For quality managers and compliance officers, ensuring compliance with this method is crucial for maintaining the integrity of their products. R&D engineers can leverage these test results to refine formulations, while procurement teams can use them to verify supplier claims and ensure consistent ingredient quality.

The process begins with accurate sample preparation, which involves grinding the supplements into a fine powder using a laboratory mill or colloid mill, depending on the type of supplement. The sample is then suspended in an appropriate buffer solution containing digestive enzymes such as pepsin and trypsin to simulate gastric and pancreatic digestion.

After incubation under controlled conditions, the mixture undergoes filtration and colorimetric analysis using a spectrophotometer. This step quantifies undigested protein residues, which are indicative of the supplement's digestibility. The results provide a percentage value representing the proportion of ingested protein that is effectively digested.

Proper interpretation of these data allows for informed decisions on ingredient sourcing and formulation adjustments to meet regulatory requirements and consumer expectations. Compliance officers can use this information to ensure their products meet national standards like those set by the FDA or EU authorities, ensuring safe and efficacious dietary supplements.

Methodology Description
Sample Preparation Grinding into fine powder using laboratory mill
Digestion Simulations Gastric and pancreatic digestion with pepsin and trypsin
Filtration Removal of undigested solids for analysis
Colorimetric Analysis Determination of protein residues using spectrophotometry

The AOAC 2018.05 method is widely recognized and accepted in the food and feed industry, making it a cornerstone for quality assurance in dietary supplements.

Applied Standards

Standard Description
AOAC 2018.05 Procedures for the Determination of Protein Digestibility in Dietary Supplements by Simulated Gastrointestinal Digestion
FDA Compliance Guidelines Ensuring that supplements meet regulatory requirements for safety and efficacy
GMP (Good Manufacturing Practices) Guidelines to ensure the quality, safety, and efficacy of dietary supplements

The AOAC 2018.05 method is specifically designed for use in conjunction with FDA compliance guidelines and GMP standards, ensuring that dietary supplements are produced under stringent quality control measures.

Eurolab Advantages

EuroLab offers comprehensive support throughout the AOAC 2018.05 method, from sample preparation to final analysis. Our experienced team ensures accurate and reliable results, providing a clear picture of protein digestibility in dietary supplements.

  • State-of-the-art laboratory equipment
  • Dedicated experts with extensive experience in food and feed testing
  • ISO/IEC 17025 accreditation ensuring highest standards in laboratory operations
  • Comprehensive data analysis and reporting

We pride ourselves on delivering precise and timely results, which are crucial for maintaining product quality and compliance with regulatory standards.

International Acceptance and Recognition

  • AOAC 2018.05 is widely recognized in the United States as a standard method for assessing protein digestibility.
  • The method has gained acceptance globally, particularly in regions with stringent dietary supplement regulations.
  • Many international standards organizations, including ISO and IEC, have incorporated AOAC 2018.05 into their guidelines for food testing.

This widespread recognition underscores the importance of this method in ensuring the quality and efficacy of dietary supplements across diverse markets.

Frequently Asked Questions

What is the purpose of AOAC 2018.05?
The method aims to assess protein digestibility in dietary supplements by simulating gastrointestinal conditions, providing insights into ingredient quality and nutritional efficacy.
Who can benefit from this service?
Quality managers, compliance officers, R&D engineers, and procurement teams in the food and feed industry can leverage these test results to ensure product quality and efficacy.
What equipment is required for this analysis?
The method requires a laboratory mill or colloid mill, appropriate buffer solutions, digestive enzymes such as pepsin and trypsin, filtration devices, and a spectrophotometer.
How long does the analysis take?
The entire process typically takes around three to four hours from sample preparation to final analysis.
What are the key outcomes of this method?
Key outcomes include a percentage value representing the proportion of ingested protein that is effectively digested, which helps in formulating products that are easily absorbed by consumers.
Is there any regulatory requirement for this method?
Yes, the AOAC 2018.05 method is widely recognized and accepted in regions with stringent dietary supplement regulations, including those set by the FDA.
How does this analysis help manufacturers?
It helps manufacturers refine formulations to ensure that their products meet regulatory requirements for safety and efficacy while enhancing product quality.
What are the benefits of using a lab like Eurolab for this service?
Eurolab provides comprehensive support, state-of-the-art equipment, experienced experts, and ISO/IEC 17025 accreditation to ensure accurate and reliable results.

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