Evidence map›Paper›PMID 37631321›Full record

ArticlePharmaceutics2023

Cardiomyocyte-Targeting Peptide to Deliver Amiodarone.

Maliha Zahid, Beth Weber, Ray Yurko, Kazi Islam, Vaishavi Agrawal, Jack Lopuszynski, Hisato Yagi, Guy Salama

Open access · goldAbstract read
In one paragraph

Article in Pharmaceutics, 2023. 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
1.5field-weighted citation impact, top 15% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

Maliha ZahidDepartment of Cardiovascular Diseases, Mayo Clinic, Rochester, MN 55905, USA.
Beth WeberPittsburgh Heart, Lung, Blood, and Vascular Medicine Institute, Division of Cardiology, Department of Medicine, University of Pittsburgh School of Medicine, University of Pittsburgh Medical Center, Pittsburgh, PA 15213, USA.
Ray YurkoPeptide Synthesis Facility, University of Pittsburgh, Pittsburgh, PA 15219, USA.
Kazi IslamPeptide Synthesis Facility, University of Pittsburgh, Pittsburgh, PA 15219, USA.
Vaishavi AgrawalDietrich School of Arts and Sciences, University of Pittsburgh, Pittsburgh, PA 15260, USA.
Jack LopuszynskiDepartment of Cardiovascular Diseases, Mayo Clinic, Rochester, MN 55905, USA.
Hisato YagiDepartment of Developmental Biology, University of Pittsburgh, Pittsburgh, PA 15201, USA.
Guy SalamaPittsburgh Heart, Lung, Blood, and Vascular Medicine Institute, Division of Cardiology, Department of Medicine, University of Pittsburgh School of Medicine, University of Pittsburgh Medical Center, Pittsburgh, PA 15213, USA.ORCID 0000-0002-5306-8178
University of Pittsburgh · USMayo Clinic · USUniversity of Pittsburgh Medical Center · US

Funding

Targeting Underlying Pathophysiological Mechanisms to Develop Novel Therapies for Chronic Obstructive Lung DiseaseR01HL153407 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI ZAHID, MALIHA · 2020 to 2024
$3.0M
Targeted delivery of amiodarone to the heart for atrial fibrillation utilizing novel cardiac targeting peptidesR41HL150908 · NHLBI · VIVASC THERAPEUTICS INC. · PI ZAHID, MALIHA · 2020 to 2020
$327k
NHLBI NIH HHS R01 HL153407NHLBI NIH HHS R41 HL150908
6 · The paper itself

Abstract

backgroundAmiodarone is underutilized due to significant off-target toxicities. We hypothesized that targeted delivery to the heart would lead to the lowering of the dose by utilizing a cardiomyocyte-targeting peptide (CTP), a cell-penetrating peptide identified by our prior phage display work.

methodsCTP was synthesized thiolated at the N-terminus, conjugated to amiodarone via Schiff base chemistry, HPLC purified, and confirmed with MALDI/TOF. The stability of the conjugate was assessed using serial HPLCs. Guinea pigs (GP) were injected intraperitoneally daily with vehicle (7 days), amiodarone (7 days; 80 mg/kg), CTP-amiodarone (5 days; 26.3 mg/kg), or CTP (5 days; 17.8 mg/kg), after which the GPs were euthanized, and the hearts were excised and perfused on a Langendorff apparatus with Tyrode's solution and blebbistatin (5 µM) to minimize the contractions. Voltage (RH237) and Ca

resultsThe CTP-amiodarone remained stable for up to 21 days at 37 °C. At ~1/15th of the dose of amiodarone, the CTP-amiodarone decreased the CV in hearts significantly compared to the control GPs (0.92 ± 0.05 vs. 1.00 ± 0.03 ms,

conclusionsOur data suggest that CTP can deliver amiodarone to cardiomyocytes at ~1/15th the total molar dose of the amiodarone needed to produce a comparable slowing of CVs. The ability of CTP to decrease the AP durations and CaTD

Indexed as

amiodaroneatrial fibrillationcardiac targeting peptidecell penetrating peptides

Identifiers

PMID37631321
PMCPMC10459552
OpenAlexW4385704477

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.