Evidence map›Paper›PMID 28774010›Full record

ArticleMaterials (Basel, Switzerland)2016

A Natural Bacterium-Produced Membrane-Bound Nanocarrier for Drug Combination Therapy.

Ruimin Long, Yuangang Liu, Qinglei Dai, Shibin Wang, Qiongjia Deng, Xia Zhou

Abstract read
In one paragraph

Article in Materials (Basel, Switzerland), 2016. 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
–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

13 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Bacteria-Based Nanoprobes for Cancer Therapy.International journal of nanomedicine · 2024
    Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Biology · 2020
    Review
  11. Review
  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.

Ruimin LongCollege of Chemical Engineering, Huaqiao University, Xiamen 361021, China. simplever@126.com.
Yuangang LiuCollege of Chemical Engineering, Huaqiao University, Xiamen 361021, China. ygliu@hqu.edu.cn.
Qinglei DaiCollege of Chemical Engineering, Huaqiao University, Xiamen 361021, China. m18968015279@163.com.
Shibin WangCollege of Chemical Engineering, Huaqiao University, Xiamen 361021, China. sbwang@hqu.edu.cn.
Qiongjia DengCollege of Chemical Engineering, Huaqiao University, Xiamen 361021, China. dengqiongjia@126.com.
Xia ZhouCollege of Chemical Engineering, Huaqiao University, Xiamen 361021, China. josiechou1993@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To minimize the non-specific toxicity of drug combination during cancer therapy, we prepared a new system synthesized from bacteria to deliver the anticancer drugs cytosine arabinoside (Ara-C) and daunorubicin (DNR). In this study, we selected genipin (GP) and poly-l-glutamic acid (PLGA) as dual crosslinkers. Herewith, we demonstrated the preparation, characterization and in vitro antitumor effects of Ara-C and DNR loaded GP-PLGA-modified bacterial magnetosomes (BMs) (ADBMs-P). The results show that this new system is stable and exhibits optimal drug-loading properties. The average diameters of BMs and ADBMs-P were 42.0 ± 8.6 nm and 65.5 ± 8.9 nm, respectively, and the zeta potential of ADBMs-P (-42.0 ± 6.4 mV) was significantly less than that of BMs (-28.6 ± 7.6 mV). The optimal encapsulation efficiency and drug loading of Ara-C were 68.4% ± 9.4% and 32.4% ± 2.9%, respectively, and those of DNR were 36.1% ± 2.5% and 17.9% ± 1.6%. Interestingly, this system also exhibits long-term release behaviour sequentially, without an initial burst release. The Ara-C drug continued to release about 85% within 40 days, while DNR release lasted only for 13 days. Moreover, similar to free drugs, ADBMs-Ps are strongly cytotoxic to cancer cells in vitro (HL-60 cells), with the inhibition rate approximately 96%. This study reveals that this new system has a potential for drug delivery application in the future, especially for combination therapy.

Indexed as

drug combination therapydual crosslinkersmagnetosomesnatural carrier

Identifiers

PMID28774010
PMCPMC5457273

What OpenQuestion holds

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Registered trials

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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.