Evidence map›Paper›PMID 37452514›Full record

ArticleSmall (Weinheim an der Bergstrasse, Germany)2023

Real-Time, In Situ Imaging of Macrophages via Phase-Change Peptide Nanoemulsions.

Inhye Kim, Jacob C Elliott, Atip Lawanprasert, Grace M Wood, Julianna C Simon, Scott H Medina

Open access · hybridAbstract read
In one paragraph

Article in Small (Weinheim an der Bergstrasse, Germany), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.3field-weighted citation impact, top 22% of its field
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

6 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Life at the interface: Engineering bio-nanomaterials through interfacial molecular self-assembly.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology
    Review
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

6 authors at 1 institution in 1 country.

Inhye KimDepartment of Biomedical Engineering, Pennsylvania State University, University Park, PA, 16802-4400, USA.
Jacob C ElliottGraduate Program in Acoustics, Pennsylvania State University, University Park, PA, 16802-4400, USA.
Atip LawanprasertDepartment of Biomedical Engineering, Pennsylvania State University, University Park, PA, 16802-4400, USA.
Grace M WoodGraduate Program in Acoustics, Pennsylvania State University, University Park, PA, 16802-4400, USA.
Julianna C SimonDepartment of Biomedical Engineering, Pennsylvania State University, University Park, PA, 16802-4400, USA.
Scott H MedinaDepartment of Biomedical Engineering, Pennsylvania State University, University Park, PA, 16802-4400, USA.ORCID 0000-0001-5441-2164
Pennsylvania State University · US

Funding

Understanding and controlling the cellular fate of fluorine-modified biologicsR35GM142902 · NIGMS · PENNSYLVANIA STATE UNIVERSITY, THE · PI Scott Hammond Medina · 2021 to 2026
$2.2M
Ultrasound-programmable gene editing in kidneysR21DK128638 · NIDDK · PENNSYLVANIA STATE UNIVERSITY, THE · PI MEDINA, SCOTT HAMMOND · 2021 to 2022
$379k
NIDDK NIH HHS R21 DK128638NIGMS NIH HHS R35 GM142902
6 · The paper itself

Abstract

Macrophages are specialized phagocytes that play central roles in immunity and tissue repair. Their diverse functionalities have led to an evolution of new allogenic and autologous macrophage products. However, realizing the full therapeutic potential of these cell-based therapies requires development of imaging technologies that can track immune cell migration within tissues in real-time. Such innovations will not only inform treatment regimens and empower interpretation of therapeutic outcomes but also enable prediction and early intervention during adverse events. Here, phase-changing nanoemulsion contrast agents are reported that permit real-time, continuous, and high-fidelity ultrasound imaging of macrophages in situ. Using a de novo designed peptide emulsifier, liquid perfluorocarbon nanoemulsions are prepared and show that rational control over interfacial peptide assembly affords formulations with tunable acoustic sensitivity, macrophage internalization, and in cellulo stability. Imaging experiments demonstrate that emulsion-loaded macrophages can be readily visualized using standard diagnostic B-mode and Doppler ultrasound modalities. This allows on-demand and long-term tracking of macrophages within porcine coronary arteries, as an exemplary model. The results demonstrate that this platform is poised to open new opportunities for non-invasive, contrast-enhanced imaging of cell-based immunotherapies in tissues, while leveraging the low-cost, portable, and safe nature of diagnostic ultrasound.

Indexed as

MacrophagesPhagocytesAnimalsPeptidesSwineUltrasonographyPeptidesfluorinemacrophagepeptideself-assemblyultrasound

Identifiers

PMID37452514
PMCPMC10787802
OpenAlexW4384401351

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.