Formulation White Papers & Case Studies

  1. Assessing Quality AAV Attributes Including Aggregation And Capsid Load 12/11/2025

    Assessing AAV critical quality attributes (CQAs)—like aggregation and the full-to-empty capsid ratio—is vital for gene therapy safety and efficacy. See how SEC-MALS enables reliable analysis.

  2. Challenges And Solutions In Lyophilization Development For ADCs 12/10/2025

    Successful ADC lyophilization requires a robust, individualized process driven by thermal characterization using DSC and FDM to define the critical parameters for stability and efficient manufacturing.

  3. AOC GMP Manufacture For A FIH Study 12/5/2025

    Successful development of AOCs for FIH studies requires robust GMP processes and efficient scale-up. A key step is careful management of a multi-day conjugation process with vital in-process checks.

  4. AOC Conjugation – mAb With SiRNA 12/5/2025

    See how to overcome risks in mAb-SiRNA conjugation, including disulfide scrambling and SiRNA deconjugation, by using advanced chemical and operational solutions to improve material yield and stability.

  5. The Proven Supplement For CAR-T Solid Tumor Cytotoxicity 12/4/2025

    Optimize cell culture for solid tumor research. Replacing traditional serum can significantly enhance CAR-T cytotoxicity, improve consistency, and streamline the path to GMP-ready workflows.

  6. Quantification Of Total mRNA Content In LNP Complexes 11/21/2025

    Learn how rapid, non-destructive techniques for mRNA quantification in LNPs can improve dosing accuracy, reduce variability, and accelerate decision-making for efficient scale-up and commercialization.

  7. Virus Retention Performance Under Diverse Processing Conditions 11/14/2025

    Virus filtration is robust across a wide range of process parameters, including high protein concentration and flow decay. Discover how retention relies on size exclusion to simplify risk assessment.

  8. Assessing Particle Generation In A Single-Use Mixing System 11/13/2025

    Explore how particle levels remained stable during 24 hours of high-speed mixing, even under extreme temperatures, confirming a system’s suitability for final fill and other particulate-sensitive applications.

  9. Your Guide To Precise And Robust Separation Methods 11/12/2025

    Discover a detailed guide to characterizing GLP-1 receptor agonists that covers advanced LC-MS and SEC-MALS workflows for impurity profiling, stability testing, and aggregate analysis.

  10. Generate CHO-K1 GFP-Expressing Cells For Cell Line Development Workflow 11/7/2025

    Discover a high-efficiency workflow for generating GFP-expressing CHO-K1 clones using automated single-cell dispensing to achieve 93% isolation success and stable expression in under five weeks.