Abstract
The amount of water in therapeutic nanoparticles (NPs) is of great importance to the pharmaceutical industry, as water content reflects the volume occupied by the solid components. For example, certain biomolecules, such as mRNA, can undergo conformational change or degradation when exposed to water. Using static light scattering (SLS) and dynamic light scattering (DLS), we estimated the water content of NPs, including extruded liposomes of two different sizes and polystyrene (PS) Latex NPs. In addition, we used small-angle neutron scattering (SANS) to independently access the water content of the samples. The water content of NPs estimated by SLS/DLS was systematically higher than that from SANS. The discrepancy is most likely attributed to the larger radius determined by DLS, in contrast to the SANS-derived radius observed by SANS. However, because of low accessibility to the neutron facilities, we validate the combined SLS/DLS to be a reasonable alternative to SANS for determining the water (or solvent) content of NPs.
Original language | English |
---|---|
Pages (from-to) | 227-235 |
Number of pages | 9 |
Journal | Langmuir |
Volume | 39 |
Issue number | 1 |
DOIs | |
State | Published - Jan 10 2023 |
Funding
H.L.S. and J.K. were supported through the Scientific User Facilities Division of the DOE Office of Basic Energy Sciences under US DOE Contract No. DE-AC05-00OR22725. Neutron scattering studies performed on CG-3 Bio-SANS (IPTS-28955.1) and S.V.P are supported by the Office of Biological and Environmental Research funded Center for Structural Molecular Biology (CSMB) under Contract FWP ERKP291, using the High Flux Isotope Reactor supported by the Scientific User Facilities Division, Office of Basic Energy Sciences, U.S. Department of Energy. The SANS/SAXS data were fitted utilizing the SasView 4.2.2 application, originally developed under NSF award DMR-0520547. SasView contains code developed with funding from the European Union’s Horizon 2020 research and innovation programme under the SINE2020 project, grant agreement No. 654000. This manuscript has been coauthored by UT-Battelle, LLC, under Contract No. DE-AC05- 00OR22725 with the U.S. Department of Energy. The United States Government retains and the publisher, by accepting the article for publication, acknowledges that the United States Government retains a non-exclusive, paid-up, irrevocable, world-wide license to publish or reproduce the published form of this manuscript, or allow others to do so, for United States Government purposes. The Department of Energy will provide public access to these results of federally sponsored research in accordance with the DOE Public Access Plan ( http://energy.gov/downloads/doe-public-access-plan ). Acknowledgments
Funders | Funder number |
---|---|
Office of Biological and Environmental Research funded Center for Structural Molecular Biology | |
Scientific User Facilities Division | |
National Science Foundation | DMR-0520547 |
U.S. Department of Energy | DE-AC05-00OR22725, IPTS-28955.1 |
Basic Energy Sciences | |
Horizon 2020 Framework Programme | 654000 |
Canadian Society for Molecular Biosciences | FWP ERKP291 |
UT-Battelle | DE-AC05- 00OR22725 |