EN 25260 Macrolide Profiling in Dairy Powders

EN 25260 Macrolide Profiling in Dairy Powders

EN 25260 Macrolide Profiling in Dairy Powders

The European standard EN 25260 provides a method for the profiling of macrolides in dairy powders, ensuring the safety and quality of food products. This standard is crucial in the detection and quantification of macrolides, particularly erythromycin, clarithromycin, and azithromycin, which are commonly used veterinary drugs. These residues can accumulate in animal tissues and subsequently transfer to milk, leading to their presence in dairy powders if not controlled.

Dairy powder is a processed product derived from dried milk solids. Its production involves the removal of water content while preserving essential nutrients. Due to the drying process, macrolide residues may concentrate more than they would be found in fresh milk. This makes it imperative for manufacturers and regulators to monitor these residues closely.

The EN 25260 method utilizes liquid chromatography with tandem mass spectrometry (LC-MS/MS) as its primary analytical technique. LC-MS/MS allows for high sensitivity and specificity, making it ideal for detecting trace amounts of macrolides even in complex matrices like dairy powders.

The testing process involves several steps:

  • Sample preparation: This includes the extraction of macrolides from the sample using appropriate solvents followed by cleanup to remove interfering substances.
  • Liquid chromatography separation: The extracted components are separated based on their chemical properties and molecular weight.
  • Tandem mass spectrometry detection: Each compound is identified through its unique fragmentation pattern, allowing for positive identification of macrolides present in the sample.

The acceptance criteria for this test are stringent to ensure compliance with international regulations. Samples must meet predefined limits set by standards such as EN 25260 and EU directives. Compliance ensures that dairy powders do not contain harmful levels of macrolide residues, thereby protecting consumer health.

Understanding the implications of macrolides in dairy powders is critical for quality managers, compliance officers, R&D engineers, and procurement teams involved in food safety and product development. Regular monitoring using EN 25260 helps maintain high standards of hygiene and safety in the production of dairy powders.

By adhering to this standard, manufacturers can demonstrate their commitment to food safety, which is essential for maintaining consumer trust and regulatory compliance. This proactive approach not only protects public health but also ensures that products meet international quality benchmarks.

Scope and Methodology

The scope of EN 25260 focuses on the analysis of macrolides in dairy powders, specifically targeting erythromycin, clarithromycin, and azithromycin. The methodology described in this standard provides a robust framework for laboratories to perform accurate and reliable testing.

The first step is sample preparation, which involves extracting macrolides from the sample matrix using an optimized solvent system followed by cleanup techniques like solid-phase extraction (SPE). This ensures that only the target compounds are present for analysis. The extracted analytes are then subjected to liquid chromatography separation on a suitable column.

Upon completion of the LC separation, the eluted components enter the mass spectrometer where they undergo tandem MS analysis. The characteristic fragmentation patterns generated by each macrolide serve as the basis for identification and quantification. Quantitation is performed using calibration curves prepared with known concentrations of the target compounds.

The standard also includes quality control measures such as spiked samples to ensure method reliability and reproducibility. These controls help verify that the analytical procedure consistently yields accurate results under various conditions.

Finally, reporting should include detailed information on sample identity, test parameters, analyte concentrations, and compliance with regulatory limits set by relevant standards like EN 25260 and EU regulations. This comprehensive approach ensures transparency and traceability throughout the testing process.

Eurolab Advantages

Eurolab offers unparalleled expertise in food safety testing, leveraging its extensive experience across various sectors including pharmaceuticals, chemicals, and environmental monitoring. Our team of highly qualified scientists ensures that each test conducted meets the highest standards of accuracy and reliability.

We employ state-of-the-art instrumentation, including advanced LC-MS/MS systems, to deliver precise results every time. Our laboratories are equipped with everything needed for complete testing cycles from sample preparation through final analysis. This comprehensive setup allows us to provide end-to-end services tailored to our clients' needs.

Our commitment to quality is further reflected in our ISO 17025 accreditation, which guarantees that all tests performed comply with internationally recognized standards. We adhere strictly to these guidelines ensuring consistent and accurate results across different batches or samples tested within the same batch.

In addition to technical proficiency, Eurolab prioritizes client satisfaction by offering fast turnaround times without compromising on quality. Our experienced staff provides detailed reports along with actionable insights based on our findings. This proactive approach helps clients make informed decisions regarding product safety and regulatory compliance.

Why Choose This Test

  • Comprehensive Analysis: Detects multiple macrolides including erythromycin, clarithromycin, and azithromycin simultaneously.
  • High Sensitivity: Capable of identifying even trace amounts of macrolide residues in complex matrices like dairy powders.
  • Regulatory Compliance: Ensures adherence to international standards such as EN 25260 and EU directives on veterinary drug residue limits.
  • Precision and Reliability: Utilizes advanced LC-MS/MS technology for accurate quantification of macrolides.
  • Client-Focused Services: Offers fast turnaround times while maintaining high-quality standards. Detailed reports provide actionable insights to clients.
  • Expertise and Experience: Our team consists of highly skilled scientists with extensive experience in food safety testing.
What is the purpose of EN 25260 Macrolide Profiling?
The primary purpose of EN 25260 is to ensure that dairy powders do not contain harmful levels of macrolide residues, thereby protecting consumer health and ensuring compliance with international regulations.
How does Eurolab ensure the accuracy of its tests?
Eurolab ensures accuracy through the use of state-of-the-art LC-MS/MS instrumentation, adherence to ISO 17025 accreditation standards, and implementation of rigorous quality control measures.
What are the key steps in sample preparation?
Key steps include extraction of macrolides using optimized solvents followed by cleanup procedures like solid-phase extraction to ensure only target compounds enter further analysis.
How long does it take for results?
Turnaround times vary depending on the complexity of the sample but typically range from a few days up to two weeks, ensuring that clients receive timely reports.
Can you provide additional support beyond testing?
Yes, Eurolab offers comprehensive support including detailed reporting with actionable insights and assistance in interpreting results for informed decision-making.
Are there any specific instruments used during the process?
Advanced LC-MS/MS systems are utilized to ensure precise quantification of macrolides. These high-performance instruments form a crucial part of our testing capabilities.
What standards does this service comply with?
This service complies with EN 25260 and EU directives regarding veterinary drug residue limits in food products.
How often should testing be conducted?
Testing frequency depends on specific regulatory requirements, but periodic monitoring is recommended to maintain consistent compliance with international standards.

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