Evidence map›Paper›PMID 33898179›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2021

Biomimetic Liposomal Nanoplatinum for Targeted Cancer Chemophototherapy.

Xue-Liang Liu, Xiao Dong, Si-Cong Yang, Xing Lai, Hai-Jun Liu, Yuhao Gao, Hai-Yi Feng, Mao-Hua Zhu, Yihang Yuan, Qin Lu and 3 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 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 75 papers.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed
13.5field-weighted citation impact, top 1% 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

75 citing papers in PubMed, 216 citations in OpenAlex.

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15 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 3 institutions in 2 countries.

Xue-Liang LiuHongqiao International Institute of Medicine Tongren Hospital and State Key Laboratory of Oncogenes and Related Genes Department of Pharmacology and Chemical Biology Shanghai Jiao Tong University School of Medicine Shanghai 200025 China.
Xiao DongHongqiao International Institute of Medicine Tongren Hospital and State Key Laboratory of Oncogenes and Related Genes Department of Pharmacology and Chemical Biology Shanghai Jiao Tong University School of Medicine Shanghai 200025 China.
Si-Cong YangHongqiao International Institute of Medicine Tongren Hospital and State Key Laboratory of Oncogenes and Related Genes Department of Pharmacology and Chemical Biology Shanghai Jiao Tong University School of Medicine Shanghai 200025 China.
Xing LaiHongqiao International Institute of Medicine Tongren Hospital and State Key Laboratory of Oncogenes and Related Genes Department of Pharmacology and Chemical Biology Shanghai Jiao Tong University School of Medicine Shanghai 200025 China.
Hai-Jun LiuHongqiao International Institute of Medicine Tongren Hospital and State Key Laboratory of Oncogenes and Related Genes Department of Pharmacology and Chemical Biology Shanghai Jiao Tong University School of Medicine Shanghai 200025 China.
Yuhao GaoHongqiao International Institute of Medicine Tongren Hospital and State Key Laboratory of Oncogenes and Related Genes Department of Pharmacology and Chemical Biology Shanghai Jiao Tong University School of Medicine Shanghai 200025 China.
Hai-Yi FengHongqiao International Institute of Medicine Tongren Hospital and State Key Laboratory of Oncogenes and Related Genes Department of Pharmacology and Chemical Biology Shanghai Jiao Tong University School of Medicine Shanghai 200025 China.
Mao-Hua ZhuHongqiao International Institute of Medicine Tongren Hospital and State Key Laboratory of Oncogenes and Related Genes Department of Pharmacology and Chemical Biology Shanghai Jiao Tong University School of Medicine Shanghai 200025 China.
Yihang YuanHongqiao International Institute of Medicine Tongren Hospital and State Key Laboratory of Oncogenes and Related Genes Department of Pharmacology and Chemical Biology Shanghai Jiao Tong University School of Medicine Shanghai 200025 China.
Qin LuHongqiao International Institute of Medicine Tongren Hospital and State Key Laboratory of Oncogenes and Related Genes Department of Pharmacology and Chemical Biology Shanghai Jiao Tong University School of Medicine Shanghai 200025 China.
Jonathan F LovellDepartment of Biomedical Engineering University at Buffalo State University of New York Buffalo NY 14260 USA.
Hong-Zhuan ChenInstitute of Interdisciplinary Integrative Biomedical Research Shuguang Hospital Shanghai University of Traditional Chinese Medicine Shanghai 201203 China.
Chao FangHongqiao International Institute of Medicine Tongren Hospital and State Key Laboratory of Oncogenes and Related Genes Department of Pharmacology and Chemical Biology Shanghai Jiao Tong University School of Medicine Shanghai 200025 China.ORCID 0000-0002-9236-7752
Shanghai Jiao Tong University · CNShanghai University of Traditional Chinese Medicine · CNUniversity at Buffalo, State University of New York · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Photodynamic therapy (PDT) of cancer is limited by tumor hypoxia. Platinum nanoparticles (nano-Pt) as a catalase-like nanoenzyme can enhance PDT through catalytic oxygen supply. However, the cytotoxic activity of nano-Pt is not comprehensively considered in the existing methods to exert their multifunctional antitumor effects. Here, nano-Pt are loaded into liposomes via reverse phase evaporation. The clinical photosensitizer verteporfin (VP) is loaded in the lipid bilayer to confer PDT activity. Murine macrophage cell membranes are hybridized into the liposomal membrane to confer biomimetic and targeting features. The resulting liposomal system, termed "nano-Pt/VP@MLipo," is investigated for chemophototherapy in vitro and in vivo in mouse tumor models. At the tumor site, oxygen produced by nano-Pt catalyzation improves the VP-mediated PDT, which in turn triggers the release of nano-Pt via membrane permeabilization. The ultrasmall 3-5 nm nano-Pt enables better penetration in tumors, which is also facilitated by the generated oxygen gas, for enhanced chemotherapy. Chemophototherapy with a single injection of nano-Pt/VP@MLipo and light irradiation inhibits the growth of aggressive 4T1 tumors and their lung metastasis, and prolongs animal survival without overt toxicity.

Indexed as

AnimalsBiomimeticsBreast NeoplasmsFemaleLiposomesMetal NanoparticlesMiceMice, Inbred BALB CPhotochemotherapyPhotosensitizing AgentsPlatinumLiposomesPhotosensitizing AgentsPlatinumbiomimeticsliposomesphotodynamic therapyplatinum nanoparticlestumor penetration

Identifiers

PMID33898179
PMCPMC8061387
OpenAlexW3133511051

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.