Evidence map›Paper›PMID 38522178›Full record

ArticleJournal of colloid and interface science2024

Controlling spatial distribution of functional lipids in a supported lipid bilayer prepared from vesicles.

Hyun-Su Lee, Ye Chan Kim, Zhicheng Wang, Jacob S Brenner, Vladimir R Muzykantov, Jacob W Myerson, Russell J Composto

Open access · greenAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Journal of colloid and interface science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 46% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

7 authors at 2 institutions in 1 country.

Hyun-Su LeeDepartment of Materials Science and Engineering, University of Pennsylvania, Philadelphia, PA 19104, United States. Electronic address: leeh1@seas.upenn.edu.
Ye Chan KimDepartment of Materials Science and Engineering, University of Pennsylvania, Philadelphia, PA 19104, United States.
Zhicheng WangDivision of Pulmonary and Critical Care Medicine, University of Pennsylvania, Philadelphia, PA 19104, United States.
Jacob S BrennerDivision of Pulmonary and Critical Care Medicine, University of Pennsylvania, Philadelphia, PA 19104, United States.
Vladimir R MuzykantovDepartment of Systems Pharmacology and Translational Therapeutics, University of Pennsylvania, Philadelphia, PA 19104, United States.
Jacob W MyersonDepartment of Systems Pharmacology and Translational Therapeutics, University of Pennsylvania, Philadelphia, PA 19104, United States. Electronic address: myerson@pennmedicine.upenn.edu.
Russell J CompostoDepartment of Materials Science and Engineering, University of Pennsylvania, Philadelphia, PA 19104, United States; Department of Chemical and Biomolecular Engineering, University of Pennsylvania, Philadelphia, PA 19104, United States; Laboratory for Research on the Structure of Matter, University of Pennsylvania, Philadelphia, PA 19104, United States. Electronic address: composto@seas.upenn.edu.
University of Pennsylvania · USTranslational Therapeutics (United States) · US

Funding

Phenotypic Diversity in COVID-19UL1TR001878 · NCATS · UNIVERSITY OF PENNSYLVANIA · PI FITZGERALD, GARRET A · 2016 to 2025
$102.4M
Dual drug delivery to lung/blood interface in respiratory infections.R01HL157189 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI MUZYKANTOV, VLADIMIR R · 2021 to 2024
$2.9M
NCATS NIH HHS UL1 TR001878NHLBI NIH HHS R01 HL157189
6 · The paper itself

Abstract

Conjugating biomolecules, such as antibodies, to bioconjugate moieties on lipid surfaces is a powerful tool for engineering the surface of diverse biomaterials, including cells and nanoparticles. We developed supported lipid bilayers (SLBs) presenting well-defined spatial distributions of functional moieties as models for precisely engineered functional biomolecular-lipid surfaces. We used quartz crystal microbalance with dissipation (QCM-D) and atomic force microscopy (AFM) to determine how vesicles containing a mixture of 1,2-dipalmitoyl-sn-glycero-3-phosphatidylcholine (DPPC) and 1,2-distearoyl-sn-glycero-3-phosphoethanolamine-N-[azido(polyethylene glycol)-2000] (DSPE-PEG-N

Indexed as

Lipid BilayersSilicon DioxideImmunoglobulin GPolyethylene GlycolsImmunoglobulin GLipid Bilayerspolyethylene glycol 2000Polyethylene GlycolsSilicon DioxideAtomic force spectroscopyQuartz crystal microbalanceSupported lipid bilayer

Identifiers

PMID38522178
PMCPMC11100466
OpenAlexW4392673855

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.