Evidence map›Paper›PMID 39378358›Full record

ArticleACS applied materials & interfaces2024

Metal Complexation for the Rational Design of Gemcitabine Formulations in Cancer Therapy.

Federica Carnamucio, Claudia Foti, Massimiliano Cordaro, Franz Saija, Giuseppe Cassone, Sandro R P da Rocha, Ottavia Giuffrè

Abstract read
In one paragraph

Article in ACS applied materials & interfaces, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Comprehensive Speciation and Computational Study of CuMolecules (Basel, Switzerland) · 2025
    Article
  2. 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

7 authors.

Federica CarnamucioDepartment of Pharmaceutics and Center for Pharmaceutical Engineering and Sciences - School of Pharmacy, Virginia Commonwealth University, Richmond, Virginia 23284, United States.ORCID 0000-0003-2218-953X
Claudia FotiDipartimento di Scienze Chimiche, Biologiche, Farmaceutiche ed Ambientali, Università di Messina, Viale F. Stagno d'Alcontres 31, 98166 Messina, Italy.ORCID 0000-0003-2649-7660
Massimiliano CordaroDipartimento di Scienze Chimiche, Biologiche, Farmaceutiche ed Ambientali, Università di Messina, Viale F. Stagno d'Alcontres 31, 98166 Messina, Italy.
Franz SaijaInstitute for Chemical-Physical Processes National Research Council of Italy, Viale Ferdinando Stagno d'Alcontres, 37, 98158 Messina, Italy.ORCID 0000-0002-5970-9001
Giuseppe CassoneInstitute for Chemical-Physical Processes National Research Council of Italy, Viale Ferdinando Stagno d'Alcontres, 37, 98158 Messina, Italy.ORCID 0000-0003-1895-2950
Sandro R P da RochaDepartment of Pharmaceutics and Center for Pharmaceutical Engineering and Sciences - School of Pharmacy, Virginia Commonwealth University, Richmond, Virginia 23284, United States.
Ottavia GiuffrèDipartimento di Scienze Chimiche, Biologiche, Farmaceutiche ed Ambientali, Università di Messina, Viale F. Stagno d'Alcontres 31, 98166 Messina, Italy.ORCID 0000-0002-8486-8733

Funding

Shifting the immune infiltrates in osteosarcoma lung metastases with locally targeted CSF-1Ris for combination therapiesR21CA259969 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI DA ROCHA, SANDRO R. P. · 2021 to 2021
$399k
NCI NIH HHS R21 CA259969
6 · The paper itself

Abstract

Nanoformulation of chemotherapies represents a promising strategy to enhance outcomes in cancer therapy. Gemcitabine is a chemotherapeutic agent approved by the Food and Drug Administration for the treatment of various solid tumors. Nevertheless, its therapeutic effectiveness is constrained by its poor metabolic stability and pharmacokinetic profile. Nanoformulations of gemcitabine in lipid and polymer nanocarriers usually lead to poor loading capability and an inability to effectively control its release profile due to the physicochemical characteristics of the drug and matrices. Here, we propose metal-gemcitabine complexation with biorelevant metal cations as a strategy to alter the properties of gemcitabine in a noncovalent manner, paving the way for the development of novel nanoformulations. A speciation study on gemcitabine and Mn

Indexed as

DeoxycytidineGemcitabineAntineoplastic AgentsDrug CarriersDrug CompoundingHumansMolecular Dynamics SimulationNanoparticlesNeoplasmsAntineoplastic AgentsDeoxycytidineDrug CarriersGemcitabineCa2+cancer therapyDFT calculation, ab initiogemcitabinemetal complexationMn2+, Zn2+

Identifiers

PMID39378358
PMCPMC11503523

What OpenQuestion holds

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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.