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Extracellular Vesicle Refractive Index Derivation Utilizing Orthogonal Characterization.
Pleet, Michelle L; Cook, Sean; Tang, Vera A; Stack, Emily; Ford, Verity J; Lannigan, Joanne; Do, Ngoc; Wenger, Ellie; Fraikin, Jean-Luc; Jacobson, Steven; Jones, Jennifer C; Welsh, Joshua A.
Afiliação
  • Pleet ML; Viral Immunology Section, Neuroimmunology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland 20892, United States.
  • Cook S; Laboratory of Pathology, Translational Nanobiology Section, Centre for Cancer Research, National Institutes of Health, Bethesda, Maryland 20892, United States.
  • Tang VA; Faculty of Medicine, Department of Biochemistry, Microbiology, and Immunology, University of Ottawa Flow Cytometry & Virometry Core Facility, Ottawa, Ontario K1H 8M5, Canada.
  • Stack E; Viral Immunology Section, Neuroimmunology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland 20892, United States.
  • Ford VJ; Critical Care Medicine Department, Clinical Center, National Institutes of Health, Bethesda, Maryland 20892 United States.
  • Lannigan J; Flow Cytometry Support Services, Alexandria, Virginia 22314, United States.
  • Do N; Spectradyne, Signal Hill, California 90755, United States.
  • Wenger E; Spectradyne, Signal Hill, California 90755, United States.
  • Fraikin JL; Spectradyne, Signal Hill, California 90755, United States.
  • Jacobson S; Viral Immunology Section, Neuroimmunology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland 20892, United States.
  • Jones JC; Laboratory of Pathology, Translational Nanobiology Section, Centre for Cancer Research, National Institutes of Health, Bethesda, Maryland 20892, United States.
  • Welsh JA; Laboratory of Pathology, Translational Nanobiology Section, Centre for Cancer Research, National Institutes of Health, Bethesda, Maryland 20892, United States.
Nano Lett ; 23(20): 9195-9202, 2023 10 25.
Article em En | MEDLINE | ID: mdl-37788377
ABSTRACT
The analysis of small particles, including extracellular vesicles and viruses, is contingent on their ability to scatter sufficient light to be detected. These detection methods include flow cytometry, nanoparticle tracking analysis, and single particle reflective image sensing. To standardize measurements and enable orthogonal comparisons between platforms, a quantifiable limit of detection is required. The main parameters that dictate the amount of light scattered by particles include size, morphology, and refractive index. To date, there has been a lack of accessible techniques for measuring the refractive index of nanoparticles at a single-particle level. Here, we demonstrate two methods of deriving a small particle refractive index using orthogonal measurements with commercially available platforms. These methods can be applied at either a single-particle or population level, enabling the integration of diameter and scattering cross section values to derive the refractive index using Mie theory.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Nanopartículas / Vesículas Extracelulares Limite: Humans Idioma: En Revista: Nano Lett Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Nanopartículas / Vesículas Extracelulares Limite: Humans Idioma: En Revista: Nano Lett Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos