Introduction: Nanoscale perfluorocarbon (PFC) droplets have been used to create imaging agents and drug delivery vehicles. However, development and characterization of new formulations of PFC droplets are hindered because of the lack of simple methods for quantitative and sensitive assessment of whole body tissue distribution and pharmacokinetics of the droplets. To address this issue, a general-purpose method for radiolabeling the inner core of nanoscale perfluorocarbon droplets with a hydrophobic and lipophobic fluorine-18 compound was developed, so that positron emission tomography (PET) and quantitative biodistribution studies can be employed to evaluate PFC nanodroplets in vivo.
Methods: A robust method to produce [F]CF(CF)(CH)F from a tosylate precursor using [F]F was developed. The product's effectiveness as a general label for different PFCs and its ability to distinguish the in vivo behavior of different PFC droplet formulations was evaluated using two types of PFC nanodroplets: fluorosurfactant-stabilized perfluorohexane (PFH) nanodroplets and lipid-stabilized perfluorooctylbromide (PFOB) nanodroplets. In vivo assessment of the F-labeled PFH and PFOB nanodroplets were conducted in normal mice following intravenous injection using small animal PET imaging and gamma counting of tissues and fluids.
Results: [F]CF(CF)(CH)F was produced in modest yield and was stable with respect to loss of fluoride in vitro. The labeled fluorocarbon was successfully integrated into PFH nanodroplets (~175 nm) and PFOB nanodroplets (~260 nm) without altering their mean sizes, size distributions, or surface charges compared to their non-radioactive analogues. No leakage of the radiolabel from the nanodroplets was detected after droplet formation in vitro. PET imaging and biodistribution data for the two droplet types tested showed significantly different tissue uptake and clearance patterns.
Conclusion: A convenient method for producing F-labeled PFC droplets was developed. The results highlight the potential utility of the strategy for pre-clinical evaluation of different PFC droplet formulations through direct PFC core labeling using a fluorinated radiolabel.
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http://dx.doi.org/10.1016/j.nucmedbio.2017.07.001 | DOI Listing |
Ultrasound Med Biol
February 2025
Department of Internal Medicine, University of Cincinnati, Cincinnati, OH, USA; Medical Sciences Program, University of Cincinnati, Cincinnati, OH, USA; Department of Biomedical Engineering, University of Cincinnati, Cincinnati, OH, USA; Department of Pediatrics Heart Institute, University of Cincinnati, Cincinnati, OH, USA. Electronic address:
Objective: Acoustic droplet vaporization (ADV) is the liquid-to-gas phase transition of perfluorocarbon (PFC) droplets to microbubbles upon ultrasound insonation. After ADV, gases dissolved in the surrounding fluid diffuse into microbubbles, enabling oxygen scavenging. Characterization of oxygen scavenging and transition efficiency (TE) in whole blood has so far been limited.
View Article and Find Full Text PDFSci Rep
November 2024
ABNOBA GmbH, 75223, Niefern-Öschelbronn, Germany.
Since flow characteristics are still largely unexplored for high-pressure homogenization, we investigated particle break-up at different Reynolds numbers and transition ranges in two channels (Y- and Z-channel). While the channel geometries are often treated as "black boxes", opening the channels and measuring their geometries allowed a detailed analysis of flow conditions. Transitions from laminar to turbulent flow for pressures of 250-2,000 bar have measurable effects on the sizes of perfluorocarbon (PFC)-nanoemulsion droplets emulsified by phospholipids processed simultaneously in liposomal conformation.
View Article and Find Full Text PDFJ Mech Behav Biomed Mater
December 2024
Department of Mechanical Engineering, University of Michigan, Ann Arbor, MI, USA. Electronic address:
Perfluorocarbon (PFC) droplets represent a novel class of phase-shift contrast agent with promise in applications in biomedical and bioengineering fields. PFC droplets undergo a fast liquid-gas transition upon exposure to acoustic or optical triggering, offering a potential adaptable and versatile tool as contrast agent in diagnostic imaging and localized drug delivery vehicles in therapeutics systems. In this paper, we utilize advanced imaging techniques to investigate ultra-high-speed inertial dynamics and rectified quasi-static (low-speed) diffusion evolution of optically induced PFC droplet vaporization within three different hydrogels, each of different concentrations, examining effects such as droplet size and PFC core on bubble dynamics and material viscoelastic properties.
View Article and Find Full Text PDFSoft Matter
October 2024
ABNOBA GmbH, Allmendstr. 55, Niefern-Öschelbronn 75223, Germany.
Phospholipids are the most ubiquitous emulsifiers in foods, beverages, pharmaceuticals, and human physiology, but their emulsifying properties are extremely complex. Differential analyses of mechanisms contributing to their functionality are presented in a modular approach. Addition of cholesterol to a natural phospholipid blend disturbs emulsification beyond specific thresholds for size, polydispersity and formation of emulsifying monolayers.
View Article and Find Full Text PDFNPJ Microgravity
May 2024
DESTEC, University of Pisa, Largo Lazzarino 1, Pisa, 56122, Italy.
Sessile water droplet evaporation in varied gravity and electric fields has been experimentally studied. Specifically, the influences of gravity and electric fields are investigated in the context of the heat flux distribution beneath the droplets, as well as the droplet mechanics and resulting shapes. Experimental testing was carried out during a European Space Agency (ESA) Parabolic Flight Campaign (PFC 66).
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