Evidence map›Paper›PMID 37056970›Full record

ArticleRSC advances2023

Aptamer modified Zr-based porphyrinic nanoscale metal-organic frameworks for active-targeted chemo-photodynamic therapy of tumors.

Haidi Feng, Lu Zhao, Zhiqiang Bai, Zhihui Xin, Chaoyu Wang, Lizhen Liu, Jinping Song, Haifei Zhang, Yunfeng Bai, Feng Feng

Open access · goldAbstract read
In one paragraph

Article in RSC advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

3 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
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

10 authors at 3 institutions in 2 countries.

Haidi FengSchool of Chemistry and Chemical Engineering, Shanxi Provincial Key Laboratory of Chemical Biosensing, Shanxi Datong University Datong 037009 P. R. China baiyunfeng1130@126.com feng-feng64@263.net.
Lu ZhaoSchool of Chemistry and Chemical Engineering, Shanxi Provincial Key Laboratory of Chemical Biosensing, Shanxi Datong University Datong 037009 P. R. China baiyunfeng1130@126.com feng-feng64@263.net.
Zhiqiang BaiSchool of Chemistry and Chemical Engineering, Shanxi Provincial Key Laboratory of Chemical Biosensing, Shanxi Datong University Datong 037009 P. R. China baiyunfeng1130@126.com feng-feng64@263.net.
Zhihui XinSchool of Chemistry and Chemical Engineering, Shanxi Provincial Key Laboratory of Chemical Biosensing, Shanxi Datong University Datong 037009 P. R. China baiyunfeng1130@126.com feng-feng64@263.net.
Chaoyu WangSchool of Chemistry and Chemical Engineering, Shanxi Provincial Key Laboratory of Chemical Biosensing, Shanxi Datong University Datong 037009 P. R. China baiyunfeng1130@126.com feng-feng64@263.net.
Lizhen LiuSchool of Chemistry and Chemical Engineering, Shanxi Provincial Key Laboratory of Chemical Biosensing, Shanxi Datong University Datong 037009 P. R. China baiyunfeng1130@126.com feng-feng64@263.net.
Jinping SongSchool of Chemistry and Chemical Engineering, Shanxi Provincial Key Laboratory of Chemical Biosensing, Shanxi Datong University Datong 037009 P. R. China baiyunfeng1130@126.com feng-feng64@263.net.
Haifei ZhangDepartment of Chemistry, University of Liverpool Crown Street Liverpool L69 7ZD UK.ORCID https://orcid.org/0000-0001-5142-5824
Yunfeng BaiSchool of Chemistry and Chemical Engineering, Shanxi Provincial Key Laboratory of Chemical Biosensing, Shanxi Datong University Datong 037009 P. R. China baiyunfeng1130@126.com feng-feng64@263.net.ORCID https://orcid.org/0000-0003-1675-0570
Feng FengSchool of Chemistry and Chemical Engineering, Shanxi Provincial Key Laboratory of Chemical Biosensing, Shanxi Datong University Datong 037009 P. R. China baiyunfeng1130@126.com feng-feng64@263.net.ORCID https://orcid.org/0000-0002-0063-2724
Shanxi Datong University · CNShanxi University · CNUniversity of Liverpool · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Active-targeted nanoplatforms could specifically target tumors compared to normal cells, making them a promising therapeutic agent. The aptamer is a kind of short DNA or RNA sequence that can specifically bind to target molecules, and could be widely used as the active targeting agents of nanoplatforms to achieve active-targeted therapy of tumors. Herein, an aptamer modified nanoplatform DOX@PCN@Apt-M was designed for active-targeted chemo-photodynamic therapy of tumors. Zr-based porphyrinic nanoscale metal organic framework PCN-224 was synthesized through a one-pot reaction, which could produce cytotoxic

Identifiers

PMID37056970
PMCPMC10087063
OpenAlexW4364861383

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.