Advanced Sample Processing for Research

Course Objectives
The purpose of this article is to be able to:
  1. Describe the principles of advanced biospecimen processing and their role in ensuring the accuracy, reproducibility, and integrity of research data.
  2. Explain the key differences between plasma and serum separation methods, as well as their impact on downstream analytical testing and data interpretation.
  3. Identify the procedures and best practices for specialized sample processing, including PBMC isolation and nucleic acid extraction, with attention to maintaining specimen viability and purity. 
  4. Discuss the importance of standardization and documentation in maintaining consistency across multi-site studies and collaborative research environments.
  5. Apply advanced quality control and chain-of-custody practices to support ethical, reproducible, and high-quality research outcomes.
Course Content
Course Creator: Kristen Moylan BSPH, CCRC
Total CE Hours: 1 Credit Hour
Pace Course #:586-2516-25

Outline:
  • Foundations of Advanced Biospecimen Processing and Research Integrity
    • Environmental conditions and manipulation impacts
    • Reproducibility
    • Documentation and traceability
    • Case study application 
  • Differentiating Plasma and Serum in Advanced Sample Processing
    • Plasma vs Serum
    • Pre-analytical handling
    • Multi-site consistency
      • Variables
      • Phlebotomist’s role
  • Standardization and Reproducibility in Multi-Site Research Studies
    • Unified protocols
    • QC
    • Data documentation
    • Communication
  • Documentation, Quality Control, and Chain-of-Custody in Advanced Sample Processing
    • Documentation at point of collection
    • QC measures
    • Chain of custody
  • Applying Quality Assurance and Best Practices for Reproducible Research
    • Adherence to standardized procedures
    • Quality checks
      • instrument calibration 
      • reagent verification
      • proficiency testing
    • Best practices

References: 

  1. Carter, E. (2023, August 22). Risks of Delayed Centrifugation in Blood Sample Processing: Impact on Test Results and Patient Safety. Needle.Tube - Diagnostic Lab Supplies, Great Prices, Fast Delivery, Blood Collection Needles, Blood Collection Tubes, Infusion Needles. https://www.needle.tube/resources-8/risks-of-delayed-centrifugation-in-blood-sample-processing-impact-on-test-results-and-patient-safety
  2. Ezzelle, J., Rodriguez-Chavez, I. R., Darden, J. M., Stirewalt, M., Kunwar, N., Hitchcock, R., Walter, T., & D’Souza, M. P. (2008). Guidelines on good clinical laboratory practice: Bridging operations between research and clinical research laboratories. Journal of Pharmaceutical and Biomedical Analysis, 46(1), 18–29. https://doi.org/10.1016/j.jpba.2007.10.010
  3. Foster, B. (2024, November 5). A Guide to DNA and RNA Quantification and Quality. Genomics Research from Technology Networks; Technology Networks. https://www.technologynetworks.com/genomics/articles/a-guide-to-dna-and-rna-quantification-and-quality-392900
  4. Hedayati, M., Razavi, S. A., Boroomand, S., & Kheradmand Kia, S. (2020). The impact of pre‐analytical variations on biochemical analytes stability: A systematic review. Journal of Clinical Laboratory Analysis, 34(12). https://doi.org/10.1002/jcla.23551
  5. Jaquet, V., Wallerich, S., Voegeli, S., Demeter Túrós, Eduardo Calero Viloria, & Attila Becskei. (2022). Determinants of the temperature adaptation of mRNA degradation. Nucleic Acid Research, 50(2), 1092–1110. https://doi.org/10.1093/nar/gkab1261
  6. Lodge, A. (2020, November 2). Ask A Scientist: What’s the Difference Between Serum and Plasma? Charles River. https://www.criver.com/eureka/ask-scientist-whats-difference-between-serum-and-plasma
  7. Mathew, J., Varacallo, M., & Sankar, P. (2023, April 24). Physiology, blood plasma. Nih.gov; StatPearls Publishing. https://www.ncbi.nlm.nih.gov/books/NBK531504/
  8. PBMC Analysis: Isolation, Counting & Characterization | Revvity. (2025). Revvity.com. https://www.revvity.com/ask/peripheral-blood-mononuclear-cells-pbmcs