Evidence map›Paper›PMID 35440570›Full record

ArticleNature communications2022

Bioorthogonal in situ assembly of nanomedicines as drug depots for extracellular drug delivery.

Ziyang Cao, Dongdong Li, Liang Zhao, Mengting Liu, Pengyue Ma, Yingli Luo, Xianzhu Yang

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

18 citing papers in PubMed, 57 citations in OpenAlex.

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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 at 2 institutions in 1 country.

Ziyang CaoDepartment of General Surgery, Guangzhou First People's Hospital, South China University of Technology, 510006, Guangzhou, P. R. China.ORCID 0000-0003-0661-4022
Dongdong LiSchool of Biomedical Sciences and Engineering, South China University of Technology, Guangzhou International Campus, 511442, Guangzhou, P. R. China.
Liang ZhaoSchool of Biomedical Sciences and Engineering, South China University of Technology, Guangzhou International Campus, 511442, Guangzhou, P. R. China.
Mengting LiuSchool of Biomedical Sciences and Engineering, South China University of Technology, Guangzhou International Campus, 511442, Guangzhou, P. R. China.
Pengyue MaDepartment of General Surgery, Guangzhou First People's Hospital, South China University of Technology, 510006, Guangzhou, P. R. China.
Yingli LuoNational Engineering Research Center for Tissue Restoration and Reconstruction, and Key Laboratory of Biomedical Engineering of Guangdong Province, South China University of Technology, 510006, Guangzhou, P. R. China.
Xianzhu YangDepartment of General Surgery, Guangzhou First People's Hospital, South China University of Technology, 510006, Guangzhou, P. R. China. yangxz@scut.edu.cn.ORCID 0000-0002-1006-0950
South China University of Technology · CNGuangzhou First People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Developing precise nanomedicines to improve the transport of anticancer drugs into tumor tissue and to the final action site remains a critical challenge. Here, we present a bioorthogonal in situ assembly strategy for prolonged retention of nanomedicines within tumor areas to act as drug depots. After extravasating into the tumor site, the slightly acidic microenvironment induces the exposure of cysteine on the nanoparticle surface, which subsequently undergoes a bioorthogonal reaction with the 2-cyanobenzothiazole group of another neighboring nanoparticle, enabling the formation of micro-sized drug depots to enhance drug retention and enrichment. This in situ nanoparticle assembly strategy remarkably improves the antimetastatic efficacy of extracellular-targeted drug batimastat, and also leads to the simultaneous enhanced retention and sustained release of multiple agents for combined cocktail chemoimmunotherapy to finally elicit a potent antitumor immune response. Such in situ assembly of nanomedicines represents a generalizable strategy towards extracellular drug delivery and cocktail chemoimmunotherapy.

Indexed as

Antineoplastic AgentsNanoparticlesNeoplasmsDrug Delivery SystemsDrug LiberationHumansNanomedicinePharmaceutical PreparationsTumor MicroenvironmentAntineoplastic AgentsPharmaceutical Preparations

Identifiers

PMID35440570
PMCPMC9018704
OpenAlexW4224229957

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.