Evidence map›Paper›PMID 39309187›Full record

ArticleInternational journal of nanomedicine2024

EGFR-Targeted and NIR-Triggered Lipid-Polymer Hybrid Nanoparticles for Chemo-Photothermal Colorectal Tumor Therapy.

Fang Fang, Yun Yan Chen, Xin-Ming Zhang, Jin Tang, Yu-Hao Liu, Chen-Shuo Peng, Yu Sun

Abstract read
In one paragraph

Article in International journal of nanomedicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

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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.

Fang Fang *School of Pharmacy, Wannan Medical College, Wuhu, 241002, People's Republic of China.
Yun Yan Chen *School of Pharmacy, Wannan Medical College, Wuhu, 241002, People's Republic of China.
Xin-Ming ZhangSchool of Chemistry and Materials Science, Anhui Normal University, Wuhu, 241002, People's Republic of China.
Jin TangSchool of Pharmacy, Wannan Medical College, Wuhu, 241002, People's Republic of China.ORCID 0000-0002-6070-7302
Yu-Hao LiuSchool of Pharmacy, Wannan Medical College, Wuhu, 241002, People's Republic of China.
Chen-Shuo PengSchool of Pharmacy, Wannan Medical College, Wuhu, 241002, People's Republic of China.
Yu SunSchool of Pharmacy, Wannan Medical College, Wuhu, 241002, People's Republic of China.ORCID 0000-0002-0054-0563

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Epidermal growth factor receptor (EGFR) is a major target for the treatment of colorectal cancer. Thus, anti-EGFR antibody conjugated lipid-polymer hybrid nanoparticles can offer a potential means of enhancing the efficacy of chemotherapeutics in EGFR overexpressing cancers. In addition, the combination of chemotherapy and photothermal therapy is a promising strategy for cancer treatment. Hence, it is highly desirable to develop a safe and effective delivery system for colorectal tumor therapy. Methods: In this study, EGFR-targeted and NIR-triggered lipid-polymer hybrid nanoparticles (abbreviated as Cet-Iri-NPs) were prepared with copolymer PPG-PEG, lipids DSPE-PEG-Mal and lecithin as carriers, CPT-11 as an anticancer chemotherapeutic agent, indocyanine green (ICG) as a photothermal agent, and cetuximab as a surface-targeting ligand. Results: In vitro analyses revealed that Cet-Iri-NPs were spherical with size of 99.88 nm, charge of 29.17 mV, drug entrapment efficiency of 51.72%, and antibody conjugation efficiency of 41.70%. Meanwhile, Cet-Iri-NPs exhibited a remarkable photothermal effect, and pH/NIR-triggered faster release of CPT-11 with near infrared (NIR) laser irradiation, which induced enhanced cytotoxicity against SW480 cells. Furthermore, the promoted tumor-growth suppression effect of Cet-Iri-NPs on SW480 tumor xenograft nude mice was achieved under NIR laser irradiation. Conclusion: These results indicate that the well-defined Cet-Iri-NPs are a promising platform for targeted colorectal cancer treatment with chemo-photothermal therapy.

Indexed as

CetuximabColorectal NeoplasmsErbB ReceptorsIndocyanine GreenIrinotecanNanoparticlesPhotothermal TherapyAnimalsAntineoplastic AgentsCamptothecinCell Line, TumorDrug CarriersHumansInfrared RaysLecithinsLipidsAntineoplastic AgentsCamptothecinCetuximabDrug CarriersEGFR protein, humanErbB ReceptorsIndocyanine GreenIrinotecanLecithinsLipidsPolyethylene GlycolsPolymersCetuximabChemo-photothermal therapyIndocyanine greenNanoparticlesTargeted cancer therapy

Identifiers

PMID39309187
PMCPMC11416794

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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.