Evidence map›Paper›PMID 38778440›Full record

ArticleAnalytical chemistry2024

Tracking Drugs and Lipids: Quantitative Mass Spectrometry Imaging of Liposomal Doxorubicin Delivery and Bilayer Fate in Three-Dimensional Tumor Models.

Arbil Lopez, Joseph H Holbrook, Gabrielle E Kemper, Jessica K Lukowski, William T Andrews, Amanda B Hummon

Abstract read
In one paragraph

Article in Analytical chemistry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. MALDI spatial proteomics: a mini review of approaches and techniques.Analytical methods : advancing methods and applications · 2026
    Review
  8. Article
  9. Review
  10. 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

6 authors.

Arbil LopezDepartment of Chemistry and Biochemistry, The Ohio State University, Columbus, Ohio 43210, United States.
Joseph H HolbrookOhio State Biochemistry Program, The Ohio State University, Columbus, Ohio 43210, United States.
Gabrielle E KemperDepartment of Chemistry and Biochemistry, The Ohio State University, Columbus, Ohio 43210, United States.
Jessica K LukowskiDepartment of Chemistry and Biochemistry, The Ohio State University, Columbus, Ohio 43210, United States.ORCID 0000-0002-0506-552X
William T AndrewsDepartment of Chemistry and Biochemistry, The Ohio State University, Columbus, Ohio 43210, United States.
Amanda B HummonDepartment of Chemistry and Biochemistry, The Ohio State University, Columbus, Ohio 43210, United States.ORCID 0000-0002-1969-9013

Funding

Spatial SILAC: Examining the Proteome in 3D Cell CulturesR01GM110406 · NIGMS · UNIVERSITY OF NOTRE DAME · PI HUMMON, AMANDA B. · 2014 to 2022
$3.0M
Electroblotting through enzymatic membranes to enhance MALDI tissue imaging of proteinsR21AG062144 · NIA · OHIO STATE UNIVERSITY · PI HUMMON, AMANDA B. · 2019 to 2020
$424k
NIA NIH HHS R21 AG062144NIGMS NIH HHS R01 GM110406
6 · The paper itself

Abstract

Targeted therapy to the tumor would greatly advance precision medicine. Many drug delivery vehicles have emerged, but liposomes are cited as the most successful to date. Recent efforts to develop liposomal drug delivery systems focus on drug distribution in tissues and ignore liposomal fate. In this study, we developed a novel method to elucidate both drug and liposomal bilayer distribution in a three-dimensional cell culture model using quantitative matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI qMSI) alongside fluorescence microscopy. Imaging liposomal distribution in a cell culture model is challenging, as lipids forming the bilayer are endogenous to the model system. To resolve this issue, we functionalized the bilayer by chemically cross-linking a fluorescent tag to the alkyne-containing lipid hexynoyl phosphoethanolamine (HPE). We synthesized liposomes incorporating the tagged HPE lipid and encapsulated within them doxorubicin, yielding a theranostic liposome capable of both drug delivery and monitoring liposomal uptake. We employed an "in-tissue" MALDI qMSI approach to generate a calibration curve with

Indexed as

DoxorubicinSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationAntibiotics, AntineoplasticCell Line, TumorDrug Delivery SystemsHumansLipid BilayersLiposomesMicroscopy, FluorescencePolyethylene GlycolsAntibiotics, AntineoplasticDoxorubicinLipid Bilayersliposomal doxorubicinLiposomesPolyethylene Glycols

Identifiers

PMID38778440
PMCPMC11646454

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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.