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We are analyzing https://link.springer.com/article/10.1007/s11095-010-0073-2.

Title:
Critical Evaluation of Nanoparticle Tracking Analysis (NTA) by NanoSight for the Measurement of Nanoparticles and Protein Aggregates | Pharmaceutical Research
Description:
Purpose To evaluate the nanoparticle tracking analysis (NTA) technique, compare it with dynamic light scattering (DLS) and test its performance in characterizing drug delivery nanoparticles and protein aggregates. Methods Standard polystyrene beads of sizes ranging from 60 to 1,000 nm and physical mixtures thereof were analyzed with NTA and DLS. The influence of different ratios of particle populations was tested. Drug delivery nanoparticles and protein aggregates were analyzed by NTA and DLS. Live monitoring of heat-induced protein aggregation was performed with NTA. Results NTA was shown to accurately analyze the size distribution of monodisperse and polydisperse samples. Sample visualization and individual particle tracking are features that enable a thorough size distribution analysis. The presence of small amounts of large (1,000 nm) particles generally does not compromise the accuracy of NTA measurements, and a broad range of population ratios can easily be detected and accurately sized. NTA proved to be suitable to characterize drug delivery nanoparticles and protein aggregates, complementing DLS. Live monitoring of heat-induced protein aggregation provides information about aggregation kinetics and size of submicron aggregates. Conclusion NTA is a powerful characterization technique that complements DLS and is particularly valuable for analyzing polydisperse nanosized particles and protein aggregates.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Education
  • Science
  • Graphic Design

Content Management System {📝}

What CMS is link.springer.com built with?

Custom-built

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Traffic Estimate {📈}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 5,000,019 visitors per month in the current month.
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How Does Link.springer.com Make Money? {💸}

We see no obvious way the site makes money.

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Keywords {🔍}

nta, dls, size, beads, particles, aggregates, sample, protein, analysis, measurements, number, nanoparticles, article, polystyrene, fig, particle, monodisperse, scattering, distribution, samples, large, concentration, light, obtained, google, scholar, aggregation, drug, sizes, results, smaller, igg, video, panels, software, cas, technique, standard, small, formulation, bead, zave, nanoparticle, mixtures, ratio, table, data, tracking, nanosight, measurement,

Topics {✒️}

/fileadmin/user_upload/sortiment/nanopartikel/nanosight/nanosight_application_review_nta_april_2009_m201b egg l-α-phosphatidyl choline 2-dioleoyl-sn-glycero-3-phospho ethanolamine 2-dioleoyl-3-trimethyl ammonium-propane viton fluoroelastomer o-ring article download pdf epc/dope/dotap molar ratio polystyrene half-micro cuvettes dynamic light-scattering data metal-catalyzed oxidation reaction heat-induced protein aggregation heat-stressed igg formulation film-hydration-rehydration method metal-oxidized insulin formulation filter unit liquid igg1-antibody formulation dynamic light scattering privacy choices/manage cookies low standard deviation default filter factor metal catalyzed oxidation intense light scattering light scattering centers drug delivery technology low micrometer range full size image aggregated protein formulations therapeutic protein products open access drug delivery nanoparticles nanoparticle tracking analysis multiangle light scattering protein heat stress scanning electron microscopy drug delivery system 60-nm/100-nm bead mixture low peak resolution standard polystyrene beads low absorption efficiency approximate particle concentrations protein drug stability individual particle tracking recombinant human insulin 100-nm/400-nm monodisperse beads high standard deviation stressed igg formulation error bars displayed nanoparticle research nanometer size range wim jiskoot

Questions {❓}

  • Can DLS resolve oligomer mixtures?
  • Minimum DLS concentration?
  • Nsf/allfaqbyno/KB000795?

Schema {🗺️}

WebPage:
      mainEntity:
         headline:Critical Evaluation of Nanoparticle Tracking Analysis (NTA) by NanoSight for the Measurement of Nanoparticles and Protein Aggregates
         description:To evaluate the nanoparticle tracking analysis (NTA) technique, compare it with dynamic light scattering (DLS) and test its performance in characterizing drug delivery nanoparticles and protein aggregates. Standard polystyrene beads of sizes ranging from 60 to 1,000 nm and physical mixtures thereof were analyzed with NTA and DLS. The influence of different ratios of particle populations was tested. Drug delivery nanoparticles and protein aggregates were analyzed by NTA and DLS. Live monitoring of heat-induced protein aggregation was performed with NTA. NTA was shown to accurately analyze the size distribution of monodisperse and polydisperse samples. Sample visualization and individual particle tracking are features that enable a thorough size distribution analysis. The presence of small amounts of large (1,000 nm) particles generally does not compromise the accuracy of NTA measurements, and a broad range of population ratios can easily be detected and accurately sized. NTA proved to be suitable to characterize drug delivery nanoparticles and protein aggregates, complementing DLS. Live monitoring of heat-induced protein aggregation provides information about aggregation kinetics and size of submicron aggregates. NTA is a powerful characterization technique that complements DLS and is particularly valuable for analyzing polydisperse nanosized particles and protein aggregates.
         datePublished:2010-03-04T00:00:00Z
         dateModified:2010-03-04T00:00:00Z
         pageStart:796
         pageEnd:810
         license:https://creativecommons.org/licenses/by-nc/2.0
         sameAs:https://doi.org/10.1007/s11095-010-0073-2
         keywords:
            dynamic light scattering
            liposomes
            nanoparticles
            nanoparticle tracking analysis
            protein aggregates
            Pharmacology/Toxicology
            Pharmacy
            Biochemistry
            general
            Medical Law
            Biomedical Engineering and Bioengineering
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                        name:Division of Drug Delivery Technology, Leiden/Amsterdam Center for Drug Research, Leiden University, Leiden, The Netherlands
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                        name:Division of Drug Delivery Technology, Leiden/Amsterdam Center for Drug Research, Leiden University, Leiden, The Netherlands
                        type:PostalAddress
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               name:Wim Jiskoot
               affiliation:
                     name:Leiden University
                     address:
                        name:Division of Drug Delivery Technology, Leiden/Amsterdam Center for Drug Research, Leiden University, Leiden, The Netherlands
                        type:PostalAddress
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      headline:Critical Evaluation of Nanoparticle Tracking Analysis (NTA) by NanoSight for the Measurement of Nanoparticles and Protein Aggregates
      description:To evaluate the nanoparticle tracking analysis (NTA) technique, compare it with dynamic light scattering (DLS) and test its performance in characterizing drug delivery nanoparticles and protein aggregates. Standard polystyrene beads of sizes ranging from 60 to 1,000 nm and physical mixtures thereof were analyzed with NTA and DLS. The influence of different ratios of particle populations was tested. Drug delivery nanoparticles and protein aggregates were analyzed by NTA and DLS. Live monitoring of heat-induced protein aggregation was performed with NTA. NTA was shown to accurately analyze the size distribution of monodisperse and polydisperse samples. Sample visualization and individual particle tracking are features that enable a thorough size distribution analysis. The presence of small amounts of large (1,000 nm) particles generally does not compromise the accuracy of NTA measurements, and a broad range of population ratios can easily be detected and accurately sized. NTA proved to be suitable to characterize drug delivery nanoparticles and protein aggregates, complementing DLS. Live monitoring of heat-induced protein aggregation provides information about aggregation kinetics and size of submicron aggregates. NTA is a powerful characterization technique that complements DLS and is particularly valuable for analyzing polydisperse nanosized particles and protein aggregates.
      datePublished:2010-03-04T00:00:00Z
      dateModified:2010-03-04T00:00:00Z
      pageStart:796
      pageEnd:810
      license:https://creativecommons.org/licenses/by-nc/2.0
      sameAs:https://doi.org/10.1007/s11095-010-0073-2
      keywords:
         dynamic light scattering
         liposomes
         nanoparticles
         nanoparticle tracking analysis
         protein aggregates
         Pharmacology/Toxicology
         Pharmacy
         Biochemistry
         general
         Medical Law
         Biomedical Engineering and Bioengineering
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            1573-904X
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         name:Springer US
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                     type:PostalAddress
                  type:Organization
                  name:Utrecht University
                  address:
                     name:Department of Pharmaceutics, Utrecht Institute for Pharmaceutical Sciences (UIPS), Utrecht University, Utrecht, The Netherlands
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Andrea Hawe
            affiliation:
                  name:Leiden University
                  address:
                     name:Division of Drug Delivery Technology, Leiden/Amsterdam Center for Drug Research, Leiden University, Leiden, The Netherlands
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Wim Jiskoot
            affiliation:
                  name:Leiden University
                  address:
                     name:Division of Drug Delivery Technology, Leiden/Amsterdam Center for Drug Research, Leiden University, Leiden, The Netherlands
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         name:Department of Pharmaceutics, Utrecht Institute for Pharmaceutical Sciences (UIPS), Utrecht University, Utrecht, The Netherlands
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      name:Leiden University
      address:
         name:Division of Drug Delivery Technology, Leiden/Amsterdam Center for Drug Research, Leiden University, Leiden, The Netherlands
         type:PostalAddress
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            name:Leiden University
            address:
               name:Division of Drug Delivery Technology, Leiden/Amsterdam Center for Drug Research, Leiden University, Leiden, The Netherlands
               type:PostalAddress
            type:Organization
            name:Utrecht University
            address:
               name:Department of Pharmaceutics, Utrecht Institute for Pharmaceutical Sciences (UIPS), Utrecht University, Utrecht, The Netherlands
               type:PostalAddress
            type:Organization
      name:Andrea Hawe
      affiliation:
            name:Leiden University
            address:
               name:Division of Drug Delivery Technology, Leiden/Amsterdam Center for Drug Research, Leiden University, Leiden, The Netherlands
               type:PostalAddress
            type:Organization
      name:Wim Jiskoot
      affiliation:
            name:Leiden University
            address:
               name:Division of Drug Delivery Technology, Leiden/Amsterdam Center for Drug Research, Leiden University, Leiden, The Netherlands
               type:PostalAddress
            type:Organization
      email:[email protected]
PostalAddress:
      name:Division of Drug Delivery Technology, Leiden/Amsterdam Center for Drug Research, Leiden University, Leiden, The Netherlands
      name:Department of Pharmaceutics, Utrecht Institute for Pharmaceutical Sciences (UIPS), Utrecht University, Utrecht, The Netherlands
      name:Division of Drug Delivery Technology, Leiden/Amsterdam Center for Drug Research, Leiden University, Leiden, The Netherlands
      name:Division of Drug Delivery Technology, Leiden/Amsterdam Center for Drug Research, Leiden University, Leiden, The Netherlands

External Links {🔗}(85)

Analytics and Tracking {📊}

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Libraries {📚}

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