Evidence map›Paper›PMID 32756863›Full record

ArticleBioscience reports2020

Reparative and toxicity-reducing effects of liposome-encapsulated saikosaponin in mice with liver fibrosis.

Li-Yen Shiu, Han Hsiang Huang, Chun Yin Chen, Hsia-Ying Cheng, Chih I Chen, Shyh Ming Kuo

Open access · goldAbstract readComparative Study
In one paragraph

Article in Bioscience reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

11 citing papers in PubMed, 22 citations in OpenAlex.

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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 3 institutions in 1 country.

Li-Yen ShiuDepartment of Medical Research, E-Da Hospital, Kaohsiung City, Taiwan.
Han Hsiang HuangDepartment of Veterinary Medicine, National Chiayi University, Chiayi City, Taiwan.
Chun Yin ChenDepartment of Biomedical Engineering, I-Shou University, Kaohsiung City, Taiwan.
Hsia-Ying ChengCentral for General Education, I-Shou University, Kaohsiung City, Taiwan.
Chih I ChenDivision of Colon and Rectal Surgery, Department of Surgery, E-Da Hospital, Kaohsiung City, Taiwan.
Shyh Ming KuoDepartment of Biomedical Engineering, I-Shou University, Kaohsiung City, Taiwan.
E-Da Hospital · TWI-Shou University · TWNational Chiayi University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Saikosaponin d (SSd), a primary active component of the Chinese herb Bupleurum falcatum, has antitumor and antiliver fibrosis effects. However, the toxicity of SSd at high doses can induce conditions such as metabolic disorders and hemolysis in vivo, thus hampering its clinical use. The present study investigated the toxicity-reducing effects of liposome encapsulation of pure SSd and the therapeutic action of SSd-loaded liposomes (Lipo-SSd) in liver fibrosis in vitro and in vivo. Lipo-SSd (diameter, 31.7 ± 7.8 nm) was prepared at an entrapment efficiency of 94.1%. After 10-day incubation, a slow release profile of 56% SSd from Lipo-SSd was observed. The IC50 of SSd on hepatic stellate cells was approximately 2.9 μM. Lipo-SSd exhibited much lower cytotoxicity than did pure SSd. In the in vivo toxicity assay, Lipo-SSd significantly increased mice survival rate and duration compared with pure SSd at the same dose. These in vitro and in vivo data indicate that liposomal encapsulation can reduce the cytotoxicity of SSd. The histopathological analysis results demonstrated that in mice with thioacetamide-induced liver fibrosis, Lipo-SSd exerted more obvious fibrosis- and inflammation-alleviating and liver tissue-reparative effects than did pure SSd; these effects are potentially attributable to the sustained release of SSd. In conclusion, Lipo-SSd fabricated here have antiliver fibrosis effects and lower toxicity compared with that of pure SSd.

Indexed as

AnimalsApoptosisCell LineCell SurvivalChemical and Drug Induced Liver InjuryDelayed-Action PreparationsDose-Response Relationship, DrugDrug CompoundingDrug LiberationHepatic Stellate CellsHumansInhibitory Concentration 50LiposomesLiverLiver Cirrhosis, ExperimentalMaleDelayed-Action PreparationsLiposomesOleanolic AcidProtective Agentssaikosaponin DSaponinsThioacetamidecytotoxicityliposomeliver fibrosisSaikosaponin

Identifiers

PMID32756863
PMCPMC7426636
OpenAlexW3047553875

What OpenQuestion holds

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Read underepoch 390

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.