Evidence map›Paper›PMID 28895767›Full record

ArticleDrug delivery2017

Promising galactose-decorated biodegradable poloxamer 188-PLGA diblock copolymer nanoparticles of resibufogenin for enhancing liver cancer therapy.

Hao Dong, Li Tian, Meng Gao, Hong Xu, Chenghong Zhang, Li Lv, Jianbin Zhang, Changyuan Wang, Yan Tian, Xiaochi Ma

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Drug delivery, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 31% 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

9 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Drug delivery · 2021
    Article
  6. Drug delivery · 2021
    Article
  7. Review
  8. Article
  9. Resibufogenin inhibits ovarian clear cell carcinoma (OCCC) growthAmerican journal of translational research · 2019
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Hao Donga College of Pharmacy , Dalian Medical University , Dalian , China.
Li Tianb Department of Pharmaceutics , The First Affiliated Hospital of Dalian Medical University , Dalian , China.
Meng Gaoa College of Pharmacy , Dalian Medical University , Dalian , China.
Hong Xuc College of Basic Medical Sciences , Dalian Medical University , Dalian , China.
Chenghong Zhangc College of Basic Medical Sciences , Dalian Medical University , Dalian , China.
Li Lva College of Pharmacy , Dalian Medical University , Dalian , China.
Jianbin Zhanga College of Pharmacy , Dalian Medical University , Dalian , China.
Changyuan Wanga College of Pharmacy , Dalian Medical University , Dalian , China.
Yan Tiana College of Pharmacy , Dalian Medical University , Dalian , China.
Xiaochi Maa College of Pharmacy , Dalian Medical University , Dalian , China.
Dalian Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Liver cancer is one of the major diseases affecting human health. Modified drug delivery systems through the asialoglycoprotein receptor, which is highly expressed on the surface of hepatocytes, have become a research focus for the treatment of liver cancer. Resibufogenin (RBG) is a popular traditional Chinese medicine and natural anti-cancer drug that was isolated from Chansu, but its cardiotoxicity and hydrophobicity have limited its clinical applications. Galactosyl-succinyl-poloxamer 188 and galactosyl-succinyl-poloxamer 188-polylactide-co-glycolide (Gal-SP188-PLGA) were synthesized using galactose, P188, and PLGA to achieve active liver-targeting properties. RBG-loaded Gal-SP188-PLGA nanoparticles (RGPPNs) and coumarin-6-loaded Gal-SP188-PLGA nanoparticles (CGPPNs) were prepared. The in vitro cellular uptake, cytotoxicity, and apoptosis of nanoparticles in HepG2 cells were analyzed. The in vivo therapeutic effects of nanoparticles were assessed in a hepatocarcinogenic mouse model. The results showed that Gal-SP188-PLGA was successfully synthesized. The cellular uptake assay demonstrated that CGPPNs had superior active liver-targeting properties. The ratio of apoptotic cells was increased in the RGPPN group. In comparison to the other groups, RGPPNs showed superior in vivo therapeutic effects and anticancer efficacy. Thus, the active liver-targeting RGPPNs, which can enhance the pharmacological effects and decrease the toxicity of RBG, are expected to become a promising and effective treatment for liver cancer.

Indexed as

NanoparticlesAnimalsBufanolidesGalactoseHumansLactic AcidLiver NeoplasmsMicePoloxamerPolyglycolic AcidPolylactic Acid-Polyglycolic Acid CopolymerBufanolidesbufogeninGalactoseLactic AcidPoloxamerPolyglycolic AcidPolylactic Acid-Polyglycolic Acid Copolymeractive liver-targeting nanoparticlesasialoglycoprotein receptorGal-SP188–PLGALiver cancerresibufogenin

Identifiers

PMID28895767
PMCPMC8240972
OpenAlexW2755566083

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.