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eclipse 3 af4 separation system controller  (Waters Corporation)


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    Waters Corporation eclipse 3 af4 separation system controller
    Eclipse 3 Af4 Separation System Controller, supplied by Waters Corporation, used in various techniques. Bioz Stars score: 96/100, based on 820 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/eclipse 3 af4 separation system controller/product/Waters Corporation
    Average 96 stars, based on 820 article reviews
    eclipse 3 af4 separation system controller - by Bioz Stars, 2026-05
    96/100 stars

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    Selected fractograms at the incubation time points 0 min (maroon), 360 min (orange), and 2880 min (lime green) plotted during <t>AF4-MALLS</t> <t>separation</t> of donor liposomes ( A —F4M1, B —F4M2, C —F5M2) and acceptor liposomes, following incubation at 37 °C and with crossflow gradient of AF4 separation Method 3 ( A ) and Method 4 ( B , C ).
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    Selected fractograms at the incubation time points 0 min (maroon), 360 min (orange), and 2880 min (lime green) plotted during AF4-MALLS separation of donor liposomes ( A —F4M1, B —F4M2, C —F5M2) and acceptor liposomes, following incubation at 37 °C and with crossflow gradient of AF4 separation Method 3 ( A ) and Method 4 ( B , C ).

    Journal: International Journal of Molecular Sciences

    Article Title: Application of Asymmetrical Flow Field-Flow Fractionation for Characterizing the Size and Drug Release Kinetics of Theranostic Lipid Nanovesicles

    doi: 10.3390/ijms221910456

    Figure Lengend Snippet: Selected fractograms at the incubation time points 0 min (maroon), 360 min (orange), and 2880 min (lime green) plotted during AF4-MALLS separation of donor liposomes ( A —F4M1, B —F4M2, C —F5M2) and acceptor liposomes, following incubation at 37 °C and with crossflow gradient of AF4 separation Method 3 ( A ) and Method 4 ( B , C ).

    Article Snippet: An Eclipse separation system (Eclipse 3+ AF4, Wyatt Technology Europe GmbH, Dernbach, Germany) was connected to a degasser, isocratic pump, and an autosampler with temperature control (Agilent 1200 series; Agilent Technology, Böblingen, Germany).

    Techniques: Incubation, Liposomes

    AF4-MALLS methods used for liposome sizing and transfer study with applied crossflow profile, injection volume, and laser power.

    Journal: International Journal of Molecular Sciences

    Article Title: Application of Asymmetrical Flow Field-Flow Fractionation for Characterizing the Size and Drug Release Kinetics of Theranostic Lipid Nanovesicles

    doi: 10.3390/ijms221910456

    Figure Lengend Snippet: AF4-MALLS methods used for liposome sizing and transfer study with applied crossflow profile, injection volume, and laser power.

    Article Snippet: An Eclipse separation system (Eclipse 3+ AF4, Wyatt Technology Europe GmbH, Dernbach, Germany) was connected to a degasser, isocratic pump, and an autosampler with temperature control (Agilent 1200 series; Agilent Technology, Böblingen, Germany).

    Techniques: Injection, Liposomes

    ZnPc transfer from donor liposomes ( A )—F4M1, ( B )—F4M2, ( C )—F5M2 to acceptor liposomes during incubation for 48 h at 37 °C. Graphs present the amount of ZnPc relative to the initial content in incubation mixtures determined in the donor fraction (maroon), acceptor fraction (orange), and the total determined content (lime green) plotted over the incubation time. Donor and acceptor liposomes were separated by AF4-MALLS, fractions were collected and up-concentrated, and ZnPc content was determined spectrophotometrically.

    Journal: International Journal of Molecular Sciences

    Article Title: Application of Asymmetrical Flow Field-Flow Fractionation for Characterizing the Size and Drug Release Kinetics of Theranostic Lipid Nanovesicles

    doi: 10.3390/ijms221910456

    Figure Lengend Snippet: ZnPc transfer from donor liposomes ( A )—F4M1, ( B )—F4M2, ( C )—F5M2 to acceptor liposomes during incubation for 48 h at 37 °C. Graphs present the amount of ZnPc relative to the initial content in incubation mixtures determined in the donor fraction (maroon), acceptor fraction (orange), and the total determined content (lime green) plotted over the incubation time. Donor and acceptor liposomes were separated by AF4-MALLS, fractions were collected and up-concentrated, and ZnPc content was determined spectrophotometrically.

    Article Snippet: An Eclipse separation system (Eclipse 3+ AF4, Wyatt Technology Europe GmbH, Dernbach, Germany) was connected to a degasser, isocratic pump, and an autosampler with temperature control (Agilent 1200 series; Agilent Technology, Böblingen, Germany).

    Techniques: Liposomes, Incubation