Evidence map›Paper›PMID 37862704›Full record

ArticleACS applied materials & interfaces2023

Selective Endocytic Uptake of Targeted Liposomes Occurs within a Narrow Range of Liposome Diameters.

Grant Ashby, Kayla E Keng, Carl C Hayden, Sadhana Gollapudi, Justin R Houser, Sabah Jamal, Jeanne C Stachowiak

Open access · greenAbstract read
In one paragraph

Article in ACS applied materials & interfaces, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

12 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Liposomal Delivery of Cell Impermeable Phototoxic Ru(II) Complexes.Chembiochem : a European journal of chemical biology · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
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  12. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Grant AshbyDepartment of Biomedical Engineering, The University of Texas at Austin, Austin, Texas 78712, United States.
Kayla E KengDepartment of Biomedical Engineering, The University of Texas at Austin, Austin, Texas 78712, United States.
Carl C HaydenDepartment of Biomedical Engineering, The University of Texas at Austin, Austin, Texas 78712, United States.
Sadhana GollapudiDepartment of Biomedical Engineering, The University of Texas at Austin, Austin, Texas 78712, United States.
Justin R HouserDepartment of Biomedical Engineering, The University of Texas at Austin, Austin, Texas 78712, United States.
Sabah JamalDepartment of Biomedical Engineering, The University of Texas at Austin, Austin, Texas 78712, United States.
Jeanne C StachowiakDepartment of Biomedical Engineering, The University of Texas at Austin, Austin, Texas 78712, United States.ORCID 0000-0003-2501-142X
The University of Texas at Austin · US

Funding

Protein Networks as Synergistic Drivers of Membrane RemodelingR35GM139531 · NIGMS · UNIVERSITY OF TEXAS AT AUSTIN · PI Jeanne Casstevens Stachowiak · 2021 to 2026
$4.0M
NIGMS NIH HHS R35 GM139531
6 · The paper itself

Abstract

Cell surface receptors facilitate signaling and nutrient uptake. These processes are dynamic, requiring receptors to be actively recycled by endocytosis. Due to their differential expression in disease states, receptors are often the target of drug-carrier particles, which are adorned with ligands that bind specifically to receptors. These targeted particles are taken into the cell by multiple routes of internalization, where the best-characterized pathway is clathrin-mediated endocytosis. Most studies of particle uptake have utilized bulk assays rather than observing individual endocytic events. As a result, the detailed mechanisms of particle uptake remain obscure. To address this gap, we employed a live-cell imaging approach to study the uptake of individual liposomes as they interact with clathrin-coated structures. By tracking individual internalization events, we find that the size of liposomes rather than the density of the ligands on their surfaces primarily determines their probability of uptake. Interestingly, targeting has the greatest impact on endocytosis of liposomes of intermediate diameters, with the smallest and largest liposomes being internalized or excluded, respectively, regardless of whether they are targeted. These findings, which highlight a previously unexplored limitation of targeted delivery, can be used to design more effective drug carriers.

Indexed as

EndocytosisLiposomesBiological TransportClathrinDrug CarriersClathrinDrug CarriersLiposomesclathrin-mediated endocytosisdrug-carrierinternalizationliposometargeted deliveryTIRF microscopy

Identifiers

PMID37862704
PMCPMC11165932
OpenAlexW4387803859

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.