Evidence map›Paper›PMID 40334292›Full record

ArticleUltrasonics sonochemistry2025

Optimising the manufacture of perfluorocarbon nanodroplets through varying sonication parameters.

Christopher K Campbell, Kirsten O'Brien, Dariusz Kosk, Robin M H Rumney, Peter Glynne-Jones, Peter R Birkin, Gareth LuTheryn, Jeremy S Webb, Eleanor Stride, Dario Carugo and 1 more

Abstract read
In one paragraph

Article in Ultrasonics sonochemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Christopher K CampbellNuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences (NDORMS), University of Oxford, Oxford, UK.
Kirsten O'BrienBone and Joint Research Group, Faculty of Medicine, University of Southampton, Southampton, UK; School of Engineering, University of Southampton, Southampton, UK.
Dariusz KoskBone and Joint Research Group, Faculty of Medicine, University of Southampton, Southampton, UK; School of Engineering, University of Southampton, Southampton, UK.
Robin M H RumneySchool of Pharmacy & Biomedical Sciences, University of Portsmouth, Portsmouth, UK.
Peter Glynne-JonesSchool of Engineering, University of Southampton, Southampton, UK.
Peter R BirkinDepartment of Chemistry, University of Southampton, Southampton, UK.
Gareth LuTherynNuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences (NDORMS), University of Oxford, Oxford, UK.
Jeremy S WebbNational Biofilms Innovation Centre (NBIC), School of Biological Sciences, University of Southampton, Southampton, UK.
Eleanor StrideInstitute of Biomedical Engineering, University of Oxford, UK.
Dario CarugoNuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences (NDORMS), University of Oxford, Oxford, UK.
Nicholas D EvansBone and Joint Research Group, Faculty of Medicine, University of Southampton, Southampton, UK; School of Engineering, University of Southampton, Southampton, UK. Electronic address: n.d.evans@soton.ac.uk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Perfluorocarbon nanodroplets (PFC-NDs) are promising ultrasound-responsive theranostic agents with applications in both diagnostic imaging and drug delivery. The acoustic vaporisation threshold, extravasation potential, and stability of PFC-NDs are all affected by their size. However, methods to ensure reproducible size and concentration during production by sonication are lacking. To address this need, we examined the effect of temperature, sonication time, sonication intensity, PFC concentration and sonicator tip height on ND characteristics. PFC-NDs with a perfluoro-n-pentane (PFP) core and a phospholipid shell were manufactured by probe-sonication. Pulsed sonication was used to maintain the sample temperature below the boiling point of PFP. Median particle diameter was measured using nanoparticle tracking analysis. PFC-ND diameter increased with increasing PFP concentration, with a stronger relationship as sonicator tip height increased. Above 5% v/v PFP, there was a qualitative increase in the number of particles visible by light microscopy. Increasing the sonication duration did not yield a significant change in ND size. A minimum amplitude of 60% was required for mixing to occur, with amplitudes of 80% and 100% resulting in foam production. Sonicator power output was linear with respect to time but differed depending on sample volume, composition, and vessel geometry. This study indicates that controlling the processing parameters can facilitate reproducible manufacturing of PFC-NDs.

Indexed as

FluorocarbonsNanoparticlesSonicationParticle SizeTemperatureFluorocarbonsParticle manufacturePerfluorocarbon nanodropletUltrasound

Identifiers

PMID40334292
PMCPMC12147839

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.