Evidence map›Paper›PMID 32232589›Full record

ArticleNanoscale research letters2020

Designing Aptamer-Gold Nanoparticle-Loaded pH-Sensitive Liposomes Encapsulate Morin for Treating Cancer.

Xiaoyuan Ding, Chenyang Yin, Weiwei Zhang, Yu Sun, Zhenzhen Zhang, Endong Yang, Dongdong Sun, Weiyun Wang

Open access · goldAbstract read
In one paragraph

Article in Nanoscale research letters, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

24 citing papers in PubMed, 71 citations in OpenAlex.

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  14. Encapsulation of morin in lipid core/PLGA shell nanoparticles significantly enhances its anti-inflammatory activity and oral bioavailability.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2023
    Article
  15. Review
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  17. Nanotechnology in drug and gene delivery.Naunyn-Schmiedeberg's archives of pharmacology · 2022
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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 at 2 institutions in 1 country.

Xiaoyuan DingSchool of Life Sciences, Anhui Agricultural University, Hefei, 230036, China.
Chenyang YinSchool of Life Sciences, Anhui Agricultural University, Hefei, 230036, China.
Weiwei ZhangSchool of Biochemical Engineering, Anhui Polytechnic University, 8 Zheshan Road, Wuhu, 241000, Anhui, China.
Yu SunSchool of Life Sciences, Anhui Agricultural University, Hefei, 230036, China.
Zhenzhen ZhangSchool of Life Sciences, Anhui Agricultural University, Hefei, 230036, China.
Endong YangSchool of Life Sciences, Anhui Agricultural University, Hefei, 230036, China.
Dongdong SunSchool of Life Sciences, Anhui Agricultural University, Hefei, 230036, China. sunddwj@126.com.
Weiyun WangSchool of Life Sciences, Anhui Agricultural University, Hefei, 230036, China. weiywswzy@163.com.
Anhui Agricultural University · CNAnhui Polytechnic University · CN

Funding

National Major Science and Technology Projects of China 17030701023National Natural Science Foundation of China 21401002Natural Science Foundation of Anhui Province 1508085QB37Youth Science Fund Key Project of Anhui Agricultural University 2013ZR011
6 · The paper itself

Abstract

This study proposes the synthesis of a type of anticancer nanoparticle, aptamers and Au nanoparticle (Apt-Au)-modified Morin pH-sensitive liposome (MSL), which exhibits targeting properties. Tumors are difficult to cure because their microenvironment varies from that of normal tissue; its pH is lower than that of normal tissue, which generally impedes the effectiveness of drugs. Thus, pH-responsive drugs have attracted extensive attention. Gold nanoparticles (AuNPs) show potential as drug carriers because of their small size, good biocompatibility, easy surface modification, and strong cell penetration. Apt-Au@MSL exhibits excellent monodispersity and tumor-targeting properties and can be released in partly acidic environment via dialysis. We screened our model cancer cell by MTT assay and found that SGC-7901 cells can effectively suppress proliferation. In vivo results demonstrate that the administration of Apt-Au@MSL could inhibit tumor growth in xenograft mouse models. H&E staining and TUNEL assay further confirmed that Apt-Au@MSL can promote tumor apoptosis. Apt-Au@MSL may induce apoptosis by triggering overproduction of reactive oxygen species (ROS) and regulating multiple signal crosstalk. Both blood biochemistry tests and H&E staining suggested that these materials exhibit negligible acute toxicity and good biocompatibility in vivo. With its powerful function, Apt-Au@MSL can be used as a target-based anticancer material for future clinical cancer treatment.

Indexed as

AnticancerAptamerGold nanoparticleMorinpH-sensitive liposome

Identifiers

PMID32232589
PMCPMC7105578
OpenAlexW3013988308

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.