Evidence map›Paper›PMID 34429597›Full record

ArticleInternational journal of nanomedicine2021

Albumin-encapsulated Nanoparticles of Naproxen Platinum(IV) Complexes with Inflammation Inhibitory Competence Displaying Effective Antitumor Activities in vitro and in vivo.

Linming Li, Yan Chen, Qingpeng Wang, Zuojie Li, Zhifang Liu, Xuewen Hua, Jun Han, Chunxiao Chang, Zhengping Wang, Dacheng Li

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

6 citing papers in PubMed, 23 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Linming Li *Institute of Biopharmaceutical Research, Liaocheng University, Liaocheng, 252059, People's Republic of China.
Yan Chen *Institute of Biopharmaceutical Research, Liaocheng University, Liaocheng, 252059, People's Republic of China.
Qingpeng WangInstitute of Biopharmaceutical Research, Liaocheng University, Liaocheng, 252059, People's Republic of China.
Zuojie LiInstitute of Biopharmaceutical Research, Liaocheng University, Liaocheng, 252059, People's Republic of China.
Zhifang LiuInstitute of Biopharmaceutical Research, Liaocheng University, Liaocheng, 252059, People's Republic of China.
Xuewen HuaInstitute of Biopharmaceutical Research, Liaocheng University, Liaocheng, 252059, People's Republic of China.
Jun HanInstitute of Biopharmaceutical Research, Liaocheng University, Liaocheng, 252059, People's Republic of China.ORCID 0000-0001-9224-0033
Chunxiao ChangShandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, 250022, People's Republic of China.
Zhengping WangInstitute of Biopharmaceutical Research, Liaocheng University, Liaocheng, 252059, People's Republic of China.
Dacheng LiInstitute of Biopharmaceutical Research, Liaocheng University, Liaocheng, 252059, People's Republic of China.
Liaocheng University · CNShandong Tumor Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPlatinum(IV) complexes with inflammation inhibitory properties are much favored in improving antitumor activities. Nanodrug-delivery system as a preferable measure for antitumor therapy are widely explored in platinum(IV) drug delivery. PURPOSE: The aim for this study was to develop novel bovine serum albumin (BSA) nanoparticles (NPs) based on naproxen platinum(IV) complexes to display a synergistic antitumor mechanism targeting cyclooxygenase-2 (COX-2), metalloproteinase-9 (MMP-9) and inducible nitric oxide synthase (iNOS).

methodsHerein, we reported the preparation of two BSA NPs of naproxen platinum(IV) complexes, and their antitumor activities were investigated in vitro and in vivo.

resultsBoth NPs possessed relatively uniform size and good stability for 30 days in aqueous solution. They exhibited prominent antitumor activities in vitro, and showed great potential in reversing drug resistance. Furthermore, these two NPs played superior tumor growth suppression in vivo in contrast to the free compounds, which were comparable to that of cisplatin and oxaliplatin, but induced lower toxic influences than platinum(II) drugs especially to spleen and liver. Moreover, the naproxen platinum(IV) NPs could decrease tumor inflammation targeting COX-2, MMP-9 and iNOs, and decreasing NO production, which would be in favor of enhancing the antitumor competence, and reducing toxicity.

conclusionTaken together, BSA NPs of naproxen platinum(IV) complexes demonstrated a powerful antitumor efficacy in vitro and in vivo. The platinum(IV) NPs with inflammation inhibitory competence targeting multiple enzymes reported in this work afford a new strategy for the development of antitumor therapy to overcome drawbacks of clinical platinum(II) drugs.

Indexed as

Antineoplastic AgentsNanoparticlesAnimalsCell Line, TumorHumansInflammationMiceNaproxenPlatinumSerum Albumin, BovineAntineoplastic AgentsNaproxenPlatinumSerum Albumin, Bovinebovine serum albumin nanoparticlescyclooxygenase-2inducible nitric oxide synthasemetalloproteinases-9synergistic antitumor efficacy

Identifiers

PMID34429597
PMCPMC8375242
OpenAlexW3195292558

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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.