Evidence map›Paper›PMID 39207095›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2024

Polymeric Microbubble Shell Engineering: Microporosity as a Key Factor to Enhance Ultrasound Imaging and Drug Delivery Performance.

Mirjavad Moosavifar, Roman A Barmin, Elena Rama, Anne Rix, Rustam A Gumerov, Thomas Lisson, Céline Bastard, Stephan Rütten, Noah Avraham-Radermacher, Jens Koehler and 13 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Harnessing Ultrasonic Technologies to TreatMolecules (Basel, Switzerland) · 2025
    Review
  8. 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

23 authors.

Mirjavad MoosavifarInstitute for Experimental Molecular Imaging, RWTH Aachen University Hospital, 52074, Aachen, Germany.
Roman A BarminInstitute for Experimental Molecular Imaging, RWTH Aachen University Hospital, 52074, Aachen, Germany.
Elena RamaInstitute for Experimental Molecular Imaging, RWTH Aachen University Hospital, 52074, Aachen, Germany.
Anne RixInstitute for Experimental Molecular Imaging, RWTH Aachen University Hospital, 52074, Aachen, Germany.
Rustam A GumerovDWI - Leibniz Institute for Interactive Materials, RWTH Aachen University, 52074, Aachen, Germany.
Thomas LissonChair for Medical Engineering, Ruhr University Bochum, 44780, Bochum, Germany.
Céline BastardDWI - Leibniz Institute for Interactive Materials, RWTH Aachen University, 52074, Aachen, Germany.
Stephan RüttenElectron Microscope Facility, RWTH Aachen University Hospital, 52074, Aachen, Germany.
Noah Avraham-RadermacherInstitute of Technical and Macromolecular Chemistry, RWTH Aachen University Hospital, 52074, Aachen, Germany.
Jens KoehlerDWI - Leibniz Institute for Interactive Materials, RWTH Aachen University, 52074, Aachen, Germany.
Michael PohlDWI - Leibniz Institute for Interactive Materials, RWTH Aachen University, 52074, Aachen, Germany.
Vedangi KulkarniInstitute for Experimental Molecular Imaging, RWTH Aachen University Hospital, 52074, Aachen, Germany.
Jasmin BaierInstitute for Experimental Molecular Imaging, RWTH Aachen University Hospital, 52074, Aachen, Germany.
Susanne KoletnikInstitute for Experimental Molecular Imaging, RWTH Aachen University Hospital, 52074, Aachen, Germany.
Rui ZhangInstitute for Experimental Molecular Imaging, RWTH Aachen University Hospital, 52074, Aachen, Germany.
Anshuman DasguptaInstitute for Experimental Molecular Imaging, RWTH Aachen University Hospital, 52074, Aachen, Germany.
Alessandro MottaInstitute for Experimental Molecular Imaging, RWTH Aachen University Hospital, 52074, Aachen, Germany.
Marek WeilerInstitute for Experimental Molecular Imaging, RWTH Aachen University Hospital, 52074, Aachen, Germany.
Igor I PotemkinDWI - Leibniz Institute for Interactive Materials, RWTH Aachen University, 52074, Aachen, Germany.
Georg SchmitzChair for Medical Engineering, Ruhr University Bochum, 44780, Bochum, Germany.
Fabian KiesslingInstitute for Experimental Molecular Imaging, RWTH Aachen University Hospital, 52074, Aachen, Germany.
Twan LammersInstitute for Experimental Molecular Imaging, RWTH Aachen University Hospital, 52074, Aachen, Germany.ORCID 0000-0002-1090-6805
Roger M PallaresInstitute for Experimental Molecular Imaging, RWTH Aachen University Hospital, 52074, Aachen, Germany.

Funding

European Research Council ERC CoG 864121Federal Ministry of Education and ResearchGerman Research Foundation 331065168German Research Foundation DFG: GRK 2375German Research Foundation LA2937/4-1German Research Foundation SFB 1066German Research Foundation SFB 985HORIZON EUROPE European Research Council NSC4DIPGLänder through the RWTH Junior Principal InvestigatorMinistry of Culture and Science of the German State of North Rhine-Westphalia
6 · The paper itself

Abstract

Microbubbles (MB) are widely used as contrast agents for ultrasound (US) imaging and US-enhanced drug delivery. Polymeric MB are highly suitable for these applications because of their acoustic responsiveness, high drug loading capability, and ease of surface functionalization. While many studies have focused on using polymeric MB for diagnostic and therapeutic purposes, relatively little attention has thus far been paid to improving their inherent imaging and drug delivery features. This study here shows that manipulating the polymer chemistry of poly(butyl cyanoacrylate) (PBCA) MB via temporarily mixing the monomer with the monomer-mimetic butyl cyanoacetate (BCC) during the polymerization process improves the drug loading capacity of PBCA MB by more than twofold, and the in vitro and in vivo acoustic responses of PBCA MB by more than tenfold. Computer simulations and physisorption experiments show that BCC manipulates the growth of PBCA polymer chains and creates nanocavities in the MB shell, endowing PBCA MB with greater drug entrapment capability and stronger acoustic properties. Notably, because BCC can be readily and completely removed during MB purification, the resulting formulation does not include any residual reagent beyond the ones already present in current PBCA-based MB products, facilitating the potential translation of next-generation PBCA MB.

Indexed as

Drug Delivery SystemsMicrobubblesPolymersUltrasonographyAnimalsContrast MediaMicePorosityContrast MediaPolymersdrug deliverydrug loadingmicrobubblesPBCAultrasound

Identifiers

PMID39207095
PMCPMC11516050

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.