Evidence map›Paper›PMID 40180319›Full record

ArticleACS nano2025

Nanocarrier Drug Release and Blood-Brain Barrier Penetration at Post-Stroke Microthrombi Monitored by Real-Time Förster Resonance Energy Transfer.

Igor Khalin, Nagappanpillai Adarsh, Martina Schifferer, Antonia Wehn, Valeria J Boide-Trujillo, Uta Mamrak, Joshua Shrouder, Thomas Misgeld, Severin Filser, Andrey S Klymchenko and 1 more

Abstract read
In one paragraph

Article in ACS nano, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. 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

11 authors.

Igor KhalinInstitute for Stroke and Dementia Research (ISD), LMU University Hospital, LMU Munich, Munich 81377, Germany.ORCID 0000-0003-1041-5747
Nagappanpillai AdarshLaboratory de Biophotonique et Pharmacologie, University of Strasbourg, Strasbourg 60024, France.
Martina SchiffererGerman Center for Neurodegenerative Diseases (DZNE), Munich 81377, Germany.
Antonia WehnInstitute for Stroke and Dementia Research (ISD), LMU University Hospital, LMU Munich, Munich 81377, Germany.
Valeria J Boide-TrujilloLaboratory de Biophotonique et Pharmacologie, University of Strasbourg, Strasbourg 60024, France.
Uta MamrakInstitute for Stroke and Dementia Research (ISD), LMU University Hospital, LMU Munich, Munich 81377, Germany.
Joshua ShrouderInstitute for Stroke and Dementia Research (ISD), LMU University Hospital, LMU Munich, Munich 81377, Germany.
Thomas MisgeldGerman Center for Neurodegenerative Diseases (DZNE), Munich 81377, Germany.
Severin FilserInstitute for Stroke and Dementia Research (ISD), LMU University Hospital, LMU Munich, Munich 81377, Germany.
Andrey S KlymchenkoLaboratory de Biophotonique et Pharmacologie, University of Strasbourg, Strasbourg 60024, France.ORCID 0000-0002-2423-830X
Nikolaus PlesnilaInstitute for Stroke and Dementia Research (ISD), LMU University Hospital, LMU Munich, Munich 81377, Germany.

Funding

European Research Council 648528
6 · The paper itself

Abstract

Nanotechnology holds great promise for improving the delivery of therapeutics to the brain. However, current approaches often operate at the organ or tissue level and are limited by the lack of tools to dynamically monitor cargo delivery in vivo. We have developed highly fluorescent lipid nanodroplets (LNDs) that enable tracking of nanocarrier behavior at the subcellular level while also carrying a Förster resonance energy transfer (FRET)-based drug delivery detection system (FedEcs) capable of monitoring cargo release in vivo. Using two-photon microscopy, we demonstrate that circulating LNDs in naïve mouse brain vasculature exhibit 3D real-time FRET changes, showing size-dependent stability over 2 h in blood circulation. Further, in the Nanostroke model, dynamic intravital two-photon imaging revealed that LNDs accumulated within cerebral postischemic microthrombi, where they released their cargo significantly faster than in normal blood circulation. Furthermore, the blood-brain barrier (BBB) became permeable at the microclot sites thereby allowing accumulated FedEcs-LNDs to cross the BBB and deliver their cargo to the brain parenchyma. This microthrombi-associated translocation was confirmed at the ultrastructural level via volume-correlative light-electron microscopy. Consequently, FedEcs represents an advanced tool to quantitatively study the biodistribution and cargo release of nanocarriers at high resolution in real-time. By enabling us to resolve passive targeting mechanisms poststroke, specifically, accumulation, degradation, and extravasation via poststroke microthrombi, this system could significantly enhance the translational validation of nanocarriers for future treatments of brain diseases.

Indexed as

Blood-Brain BarrierDrug CarriersFluorescence Resonance Energy TransferNanoparticlesStrokeThrombosisAnimalsDrug LiberationLipidsMiceMice, Inbred C57BLDrug CarriersLipidsblood-brain barriercorrelative light-electron microscopymicrothrombosisnanocarriersstroke

Identifiers

PMID40180319
PMCPMC12020413

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.