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Schematic representation of the relationship between C-laurdan emission and monolayer fluidity (A); Plot of GP distributions (B) and GP values versus mean diameter (C) in MBs prepared by tissue <t>homogeniser</t> Capmix and sonication. GP distributions refer to MBs in the clinical range (1–5 μm), shown in grey. Different point shapes (circle, square and diamond) and line styles (solid, dashed, dotted) represent different batches.
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Schematic representation of the relationship between C-laurdan emission and monolayer fluidity (A); Plot of GP distributions (B) and GP values versus mean diameter (C) in MBs prepared by tissue <t>homogeniser</t> Capmix and sonication. GP distributions refer to MBs in the clinical range (1–5 μm), shown in grey. Different point shapes (circle, square and diamond) and line styles (solid, dashed, dotted) represent different batches.
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Schematic representation of the relationship between C-laurdan emission and monolayer fluidity (A); Plot of GP distributions (B) and GP values versus mean diameter (C) in MBs prepared by tissue <t>homogeniser</t> Capmix and sonication. GP distributions refer to MBs in the clinical range (1–5 μm), shown in grey. Different point shapes (circle, square and diamond) and line styles (solid, dashed, dotted) represent different batches.
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Schematic representation of the relationship between C-laurdan emission and monolayer fluidity (A); Plot of GP distributions (B) and GP values versus mean diameter (C) in MBs prepared by tissue <t>homogeniser</t> Capmix and sonication. GP distributions refer to MBs in the clinical range (1–5 μm), shown in grey. Different point shapes (circle, square and diamond) and line styles (solid, dashed, dotted) represent different batches.
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Schematic representation of the relationship between C-laurdan emission and monolayer fluidity (A); Plot of GP distributions (B) and GP values versus mean diameter (C) in MBs prepared by tissue homogeniser Capmix and sonication. GP distributions refer to MBs in the clinical range (1–5 μm), shown in grey. Different point shapes (circle, square and diamond) and line styles (solid, dashed, dotted) represent different batches.

Journal: Ultrasonics Sonochemistry

Article Title: Comparison of ultrasound contrast agent production by sonication and mechanical agitation

doi: 10.1016/j.ultsonch.2026.107875

Figure Lengend Snippet: Schematic representation of the relationship between C-laurdan emission and monolayer fluidity (A); Plot of GP distributions (B) and GP values versus mean diameter (C) in MBs prepared by tissue homogeniser Capmix and sonication. GP distributions refer to MBs in the clinical range (1–5 μm), shown in grey. Different point shapes (circle, square and diamond) and line styles (solid, dashed, dotted) represent different batches.

Article Snippet: Then, vial was inserted into a custom made insert ( ) which was placed in a Precellys Evolution tissue homogeniser (Bertin technologies, Maryland, USA).

Techniques: Sonication

Effect of agitation frequency (A–C) and agitation time (B–D) on concentration (A–B) and mean size (C–D) of MBs produced with the tissue homogeniser.

Journal: Ultrasonics Sonochemistry

Article Title: Comparison of ultrasound contrast agent production by sonication and mechanical agitation

doi: 10.1016/j.ultsonch.2026.107875

Figure Lengend Snippet: Effect of agitation frequency (A–C) and agitation time (B–D) on concentration (A–B) and mean size (C–D) of MBs produced with the tissue homogeniser.

Article Snippet: Then, vial was inserted into a custom made insert ( ) which was placed in a Precellys Evolution tissue homogeniser (Bertin technologies, Maryland, USA).

Techniques: Concentration Assay, Produced