Evidence map›Paper›PMID 32801686›Full record

ArticleInternational journal of nanomedicine2020

Novel Albumin Nanoparticle Enhanced the Anti-Insulin-Resistant-Hepatoma Activity of Metformin.

Zhong Lu, Li Qi, Ya-Ru Lin, Lei Sun, Lin Zhang, Gui-Chun Wang, Jia-Qiu Li, Jin-Ming Yu

Abstract read
In one paragraph

Article in International journal of nanomedicine, 2020. 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
–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

3 citing papers in PubMed.

  1. Review
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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

8 authors.

Zhong LuDepartment of Oncology, Clinical College of Weifang Medical University, Weifang 261031, People's Republic of China.
Li QiDepartment of Oncology, Clinical College of Weifang Medical University, Weifang 261031, People's Republic of China.
Ya-Ru LinDepartment of Oncology, Clinical College of Weifang Medical University, Weifang 261031, People's Republic of China.
Lei SunDepartment of Oncology, Clinical College of Weifang Medical University, Weifang 261031, People's Republic of China.
Lin ZhangDepartment of Oncology, Clinical College of Weifang Medical University, Weifang 261031, People's Republic of China.
Gui-Chun WangDepartment of Oncology, Clinical College of Weifang Medical University, Weifang 261031, People's Republic of China.
Jia-Qiu LiDepartment of Oncology, Clinical College of Weifang Medical University, Weifang 261031, People's Republic of China.
Jin-Ming YuDepartment of Oncology, Clinical College of Weifang Medical University, Weifang 261031, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionMetformin is an ideal candidate to treat the liver tumor with insulin resistance because of its good performance in the treatment of type 2 diabetes and the advantage in cancer therapy. We aim to develop a delivery system with higher efficiency than free drug.

methodsMetformin-bovine serum albumin (met-BSA) nanoparticles (NPs) were prepared using the anti-solvent precipitation method with a stabilizer of BSA for particle growth. The therapeutic effect of the drug was tested by the insulin-resistant HepG2 cells and C57BL/6J mice at a glucose starvation condition. The interaction mechanism of the drug and the protein during the formation of the NPs was tested using a series of spectroscopy.

resultsMetformin and BSA formed nonporous and spherical particles of about 200 nm with proper lognormal distribution and thermostability. The cellular uptake, as well as the anti-liver cancer activities of met-BSA, was enhanced dramatically compared with the free drug. The thermodynamic studies suggested that the weak binding of metformin to BSA was governed by hydrogen bonds and van der Waals forces. Moreover, the results of synchronous, circular dichroism (CD) and three-dimensional fluorescence demonstrated that the BSA skeleton and chromophore microenvironments were changed in the presence of metformin.

conclusionTherefore, met-BSA has been proved as a simple yet effective therapeutic agent for cancer with insulin resistance, promising for future clinic translations in cancer treatment.

Indexed as

Insulin ResistanceAnimalsCarcinoma, HepatocellularCircular DichroismDiabetes Mellitus, Type 2Drug Delivery SystemsHep G2 CellsHumansHydrogen BondingLiver NeoplasmsMaleMetforminMice, Inbred C57BLNanoparticlesSerum Albumin, BovineThermodynamicsMetforminSerum Albumin, Bovinebovine serum albuminliver cancermetforminnanoparticlespectroscopy

Identifiers

PMID32801686
PMCPMC7387832

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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.