Evidence map›Paper›PMID 26984128›Full record

ArticlePharmaceutical research2016

A Multi-Functional Tumor Theranostic Nanoplatform for MRI Guided Photothermal-Chemotherapy.

Jinjin Shi, Binghua Wang, Zhaoyang Chen, Wei Liu, Jingjing Pan, Lin Hou, Zhenzhong Zhang

Erratum issuedAbstract read
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In one paragraph

Article in Pharmaceutical research, 2016. 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 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 12% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

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  15. Folate-mediated chemotherapy and diagnostics: An updated review and outlook.Journal of controlled release : official journal of the Controlled Release Society · 2017
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Jinjin ShiSchool of Pharmaceutical Sciences, Zhengzhou University, 100 Science Road, Zhengzhou, 450001, China.
Binghua WangSchool of Pharmaceutical Sciences, Zhengzhou University, 100 Science Road, Zhengzhou, 450001, China.
Zhaoyang ChenSchool of Pharmaceutical Sciences, Zhengzhou University, 100 Science Road, Zhengzhou, 450001, China.
Wei LiuSchool of Pharmaceutical Sciences, Zhengzhou University, 100 Science Road, Zhengzhou, 450001, China.
Jingjing PanSchool of Pharmaceutical Sciences, Zhengzhou University, 100 Science Road, Zhengzhou, 450001, China.
Lin HouSchool of Pharmaceutical Sciences, Zhengzhou University, 100 Science Road, Zhengzhou, 450001, China. houlin_pharm@163.com.
Zhenzhong ZhangSchool of Pharmaceutical Sciences, Zhengzhou University, 100 Science Road, Zhengzhou, 450001, China. shijin1026@163.com.
Zhengzhou University · CNSouth China Institute of Collaborative Innovation · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo develop a multi-functional theranostic nanoplatform with increased tumor retention, improving antitumor efficacy and decreased side effects of chemotherapy drugs.

methodsGO@Gd nanocomposites was synthesized via decorating gadolinium (Gd) nanoparticles (GdNP) onto graphene oxide (GO), and then functionalized by polyethylene glycol (PEG2000), folic acid (FA), a widely used tumor targeting molecule, was linked to GO@Gd-PEG, finally, doxorubicin (DOX) was loaded onto GO@Gd-PEG-FA and obtained a tumor-targeting drug delivery system (GO@Gd-PEG-FA/DOX). GO@Gd-PEG-FA/DOX was characterized and explored its theranostic applications both in a cultured MCF-7 cells and tumor-bearing mice.

resultsGO@Gd-PEG-FA/DOX could efficiently cross the cell membranes, lead to more apoptosis and afford higher antitumor efficacy without obvious toxic effects to normal organs owing to its prolonged blood circulation and 7.6-fold higher DOX uptake of tumor than DOX. Besides, GO@Gd-PEG-FA/DOX also served as a powerful photothermal therapy (PTT) agent for thermal ablation of tumor and a strong T1-weighted contrast agent for tumor MRI diagnosis. The multi-functional nanoplatform also could selectively kill cancer cells in highly localized regions via the excellent tumor-targeting and MRI guided PTT abilities.

conclusionsGO@Gd-PEG-FA/DOX exhibited excellent photothermal-chemotherapeutic efficacy, tumor-targeting property and tumor diagnostic ability.

Indexed as

Drug CarriersMagnetic Resonance ImagingNanoparticlesAnimalsAntibiotics, AntineoplasticApoptosisBiological TransportBreast NeoplasmsContrast MediaDose-Response Relationship, DrugDoxorubicinFemaleFolic AcidGadoliniumGraphiteHumansAntibiotics, AntineoplasticContrast MediaDoxorubicinDrug CarriersFolic AcidGadoliniumGraphiteOxidespolyethylene glycol 2000Polyethylene GlycolsbioimagingGO@Gdhybrid nanosystemtheranostictumor-targeting

Identifiers

PMID26984128
OpenAlexW2299385957

What OpenQuestion holds

Textmetadata
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.