Evidence map›Paper›PMID 30925694›Full record

ArticleMolecules (Basel, Switzerland)2019

In Vitro Toxicity Study of a Porous Iron(III) Metal‒Organic Framework.

Gongsen Chen, Xin Leng, Juyuan Luo, Longtai You, Changhai Qu, Xiaoxv Dong, Hongliang Huang, Xingbin Yin, Jian Ni

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing 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

26 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. BioMOF-Based Anti-Cancer Drug Delivery Systems.Nanomaterials (Basel, Switzerland) · 2023
    Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Metal Organic Frameworks as Biosensing Materials for COVID-19.Cellular and molecular bioengineering · 2021
    Review
  19. Enhancement of Thermostability ofNanomaterials (Basel, Switzerland) · 2021
    Article
  20. 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

9 authors.

Gongsen ChenSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing 102488, China. gongsenchen@163.com.ORCID 0000-0003-1054-2631
Xin LengSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing 102488, China. 20160931927@bucm.edu.cn.
Juyuan LuoSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing 102488, China. luojy0329@163.com.
Longtai YouSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing 102488, China. ylt_svip@163.com.ORCID 0000-0002-5600-353X
Changhai QuSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing 102488, China. quchanghai@bucm.edu.cn.
Xiaoxv DongSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing 102488, China. dxiaoxv@163.com.
Hongliang HuangState Key Laboratory of Separation Membranes and Membrane Processes, Tianjin Polytechnic University, Tianjin 300387, China. huanghl@mail.buct.edu.cn.
Xingbin YinSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing 102488, China. yxbtcm@163.com.
Jian NiSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing 102488, China. njtcm@263.net.

Funding

Beijing University of Chinese Medicine Scientific Research Project for Distinguished Young Scholar No. 2018-JYB-XJQ005National Natural Science Foundation of China No. 81703715 and 21606007Training Programme Foundation for the Beijing Municipal Excellent Talents No. 2017000020124G295
6 · The paper itself

Abstract

A MIL series metal‒organic framework (MOF), MIL-100(Fe), was successfully synthesized at the nanoscale and fully characterized by TEM, TGA, XRD, FTIR, DLS, and BET. A toxicological assessment was performed using two different cell lines: human normal liver cells (HL-7702) and hepatocellular carcinoma (HepG2). In vitro cytotoxicity of MIL-100(Fe) was evaluated by the MTT assay, LDH releasing rate assay, DAPI staining, and annexin V/PI double staining assay. The safe dose of MIL-100(Fe) was 80 μg/mL. It exhibited good biocompatibility, low cytotoxicity, and high cell survival rate (HL-7702 cells' viability >85.97%, HepG2 cells' viability >91.20%). Therefore, MIL-100(Fe) has a potential application as a drug carrier.

Indexed as

Toxicity TestsApoptosisCell LineCell MembraneCell ShapeCell SurvivalHumansIronMetal-Organic FrameworksModels, MolecularParticle SizePorosityIronMetal-Organic FrameworksHepG2 cellsHL-7702 cellsin vitro toxicityMIL-100(Fe)

Identifiers

PMID30925694
PMCPMC6480057

What OpenQuestion holds

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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.