Evidence map›Paper›PMID 24591828›Full record

ArticleInternational journal of nanomedicine2014

In vivo enhancement of anticancer therapy using bare or chemotherapeutic drug-bearing nanodiamond particles.

Yingqi Li, Yaoli Tong, Ruixia Cao, Zhimei Tian, Binsheng Yang, Pin Yang

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

13 citing papers in PubMed, 61 citations in OpenAlex.

  1. Review
  2. Application of Carbon Nanoparticles in Oncology and Regenerative Medicine.International journal of molecular sciences · 2021
    Review
  3. Article
  4. Article
  5. Targeting Nanodiamonds to the Nucleus in Yeast Cells.Nanomaterials (Basel, Switzerland) · 2020
    Article
  6. Review
  7. Nanoparticle-Mediated Combination Therapy: Two-in-One Approach for Cancer.International journal of molecular sciences · 2018
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. 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

6 authors at 1 institution in 1 country.

Yingqi LiDepartment of Chemistry, College of Chemistry and Chemical Engineering, Taiyuan, People's Republic of China ; Key Laboratory of Chemical Biology and Molecular Engineering of Ministry of Education, Institute of Molecular Science, Shanxi University, Taiyuan, People's Republic of China.
Yaoli TongDepartment of Chemistry, College of Chemistry and Chemical Engineering, Taiyuan, People's Republic of China.
Ruixia CaoDepartment of Chemistry, College of Chemistry and Chemical Engineering, Taiyuan, People's Republic of China.
Zhimei TianKey Laboratory of Chemical Biology and Molecular Engineering of Ministry of Education, Institute of Molecular Science, Shanxi University, Taiyuan, People's Republic of China.
Binsheng YangKey Laboratory of Chemical Biology and Molecular Engineering of Ministry of Education, Institute of Molecular Science, Shanxi University, Taiyuan, People's Republic of China.
Pin YangKey Laboratory of Chemical Biology and Molecular Engineering of Ministry of Education, Institute of Molecular Science, Shanxi University, Taiyuan, People's Republic of China.
Shanxi University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThis study investigated the use of nanodiamond particles (NDs) as a promising material for drug delivery in vivo and in vitro.

methodsHepG2 cells (a human hepatic carcinoma cell line) were used to determine the characteristics of a nanodiamond-doxorubicin complex (ND-DOX) when taken up by cells in vitro using laser scanning confocal microscopy and dialysis experiments. We also compared the survival rate and histopathology of tumor-bearing mice after treatment with NDs or ND-DOX in vivo.

resultsIn vitro investigation showed that ND-DOX has slow and sustained drug release characteristics compared with free doxorubicin. In vivo, the survival rate of tumor-bearing mice treated with ND-DOX was four times greater than that of mice treated with free doxorubicin. Interestingly, the survival rate in mice treated with NDs alone was close to that of mice treated with free doxorubicin. This indicates that treatment with ND-DOX can prolong the lifespan of tumor-bearing mice significantly compared with conventional doxorubicin and that NDs can have this effect as well. Histopathological analysis showed that neither the NDs nor ND-DOX were toxic to the kidney, liver, or spleen in contrast with the well-known toxic effects of free doxorubicin on the kidney and liver. Further, both the bare NDs and ND-DOX could suppress tumor growth effectively.

conclusionNDs can potentially prolong survival, and ND-DOX may act as a nanodrug with promising chemotherapeutic efficacy and safety.

Indexed as

Drug Delivery SystemsAnimalsAntineoplastic AgentsDelayed-Action PreparationsDoxorubicinDrug CarriersHep G2 CellsHumansHydrogen-Ion ConcentrationLiver Neoplasms, ExperimentalMiceNanodiamondsNanomedicineXenograft Model Antitumor AssaysAntineoplastic AgentsDelayed-Action PreparationsDoxorubicinDrug CarriersNanodiamondscancerdrug deliverynanodiamondsurvival ratesustained releasetreatment

Identifiers

PMID24591828
PMCPMC3937184
OpenAlexW2138966657

What OpenQuestion holds

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LicenceCC BY-NC
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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.