Advanced biophysical characterization can accelerate the development of emerging drug modalities like liposomes and lipid nanoparticles (LNPs). Cryogenic electron microscopy (cryo-EM) is widely employed to assess liposome lamellarity and LNP morphology but the technique has low data throughput. Small Angle X-ray Scattering (SAXS) offers complementary size and shape information of nanoparticles in solution with higher throughput, especially when combined with robotics-enabled automated sampling. In this webinar, we show how we correlated cryo-EM imaging with SAXS measurements to enable SAXS as a rapid screening tool in pharmaceutical process and formulation development for liposomes and LNPs.
The utility of SAXS in pharmaceutical development
How SAXS is applied to liposome and LNP characterization
Model fitting of SAXS liposome data using SaSView
Current trends and limitations in fitting and modeling of SAXS LNP data