Evidence map›Paper›PMID 32104390›Full record

ArticleAsian journal of pharmaceutical sciences2018

Preparation and toxicity evaluation of a novel nattokinase-tauroursodeoxycholate complex.

Rui Feng, Jing Li, Jiepeng Chen, Lili Duan, XinRong Liu, Donghua Di, Yihui Deng, Yanzhi Song

Open access · diamondAbstract read
In one paragraph

Article in Asian journal of pharmaceutical sciences, 2018. 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 22% 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, 15 citations in OpenAlex.

  1. Article
  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

8 authors at 1 institution in 1 country.

Rui FengCollege of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China.
Jing LiCollege of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China.
Jiepeng ChenSungen Biotech Co., Ltd., Shantou 515000, China.
Lili DuanSungen Biotech Co., Ltd., Shantou 515000, China.
XinRong LiuCollege of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China.
Donghua DiCollege of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China.
Yihui DengCollege of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China.
Yanzhi SongCollege of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China.
Shenyang Pharmaceutical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nattokinase (NK), which has been identified as a potent fibrinolytic protease, has remarkable potential in treatment of thrombolysis, and even has the ability to ameliorate chronic vein thrombosis. To reduce the hemorrhagic risk from an intravenous injection of NK, nattokinase-tauroursodeoxycholate (NK-TUDCA) complex was prepared at different pH values and with different ratios of NK and TUDCA. When assessing survival time, survival state, tail injury, and the body weight of mice, it was found that the NK-TUDCA complex (NK: 10 kIU/ml; TUDCA: 10 mg/ml; pH 5.0) had a lower toxicity when administered at an NK dosage of 130 kIU/kg in the acute toxicity test and 13 kIU/kg in the repeated low-dose challenge. From the results of the

Indexed as

ComplexIn vitro thrombolytic testNattokinaseTauroursodeoxycholateToxicity test

Identifiers

PMID32104390
PMCPMC7032186
OpenAlexW2767645773

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.