Evidence map›Paper›PMID 32666304›Full record

ArticlePharmaceutical research2020

Construction of Nucleolin-Targeted Lipid Nanobubbles and Contrast-Enhanced Ultrasound Molecular Imaging in Triple-Negative Breast Cancer.

Kejing Fang, Luofu Wang, Haiyun Huang, Minmin Lan, Daijia Shen, Shiwu Dong, Yanli Guo

Abstract read
PubMed Publisher
In one paragraph

Article in Pharmaceutical research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

13 citing papers in PubMed, 29 citations in OpenAlex.

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  12. Nanosized Contrast Agents in Ultrasound Molecular Imaging.Frontiers in bioengineering and biotechnology · 2021
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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

7 authors at 1 institution in 1 country.

Kejing FangDepartment of Ultrasound, Southwest Hospital, Army Medical University, Chongqing, 400038, China.
Luofu WangDepartment of Urology, Army Characteristic Medical Center, Chongqing, 400042, China.
Haiyun HuangDepartment of Ultrasound, Southwest Hospital, Army Medical University, Chongqing, 400038, China.
Minmin LanDepartment of Ultrasound, Southwest Hospital, Army Medical University, Chongqing, 400038, China.
Daijia ShenDepartment of Ultrasound, Southwest Hospital, Army Medical University, Chongqing, 400038, China.
Shiwu DongDepartment of Biomedical Materials Science, Army Medical University, Chongqing, 400038, China. dongshiwu@tmmu.edu.cn.
Yanli GuoDepartment of Ultrasound, Southwest Hospital, Army Medical University, Chongqing, 400038, China. guoyanli71@aliyun.com.ORCID http://orcid.org/0000-0003-1685-4441
Army Medical University · CN

Funding

International Science & Technology Cooperation Program of China 2015DFA30920National Natural Science Foundation of China 81771856Science & Technology (International Science & Technology Cooperation) Research Base Construction Program of Chongqing cstc2014gjhz110004
6 · The paper itself

Abstract

purposeTo construct aptamer AS1411-functionalized targeted lipid nanobubbles that could simultaneously target abnormally highly expressed nucleolin (NCL) on tumor tissue and neovasculature. Additionally, the study of their contrast-enhanced ultrasound molecular imaging capabilities in vitro and in vivo to explore new methods and approaches for the early and accurate diagnosis of triple-negative breast cancer (TNBC).

methodsFirst, the targeted lipid-nucleic acid molecules were constructed by an amide reaction. Then, the targeted lipid nanobubbles (AS1411-NBs) and nontargeted lipid nanobubbles (NBs) were prepared by membrane hydration, mechanical vibration and centrifugal floatation. The physicochemical characteristics and contrast-enhanced ultrasound imaging capabilities of AS1411-NBs and NBs were compared and analyzed in vitro and in vivo.

resultsThere were no significant differences between the AS1411-NBs and NBs in their concentration, average particle size or ultrasound imaging capabilities in vitro (P > 0.05). However, AS1411-NBs could simultaneously target NCL in tumor tissue and neovasculature to effectively prolong the duration of contrast-enhanced ultrasound imaging compared to NBs in vivo. The area under the time-intensity curve was significantly different between AS1411-NBs and NBs (P < 0.001), and the drug loading capacity of the AS1411-NBs was also significantly higher than that of the NBs (P < 0.05).

conclusionsAptamer AS1411-functionalized targeted lipid nanobubbles could significantly prolong the duration of contrast-enhanced ultrasound imaging to achieve dual-targeted ultrasound molecular imaging of tumor tissue and neovasculature. AS1411-NBs also have higher drug loading and targeted drug delivery capabilities compared with NBs, which can provide new methods and approaches for the early accurate diagnosis and effective treatment of TNBC.

Indexed as

MicrobubblesAnimalsBreast NeoplasmsCell Line, TumorContrast MediaDrug Delivery SystemsFemaleHumansLipidsMiceMice, Inbred BALB CMolecular ImagingNeovascularization, PathologicNucleolinParticle SizePhosphoproteinsContrast MediaLipidsNucleolinPhosphoproteinsRNA-Binding Proteinsaptamer AS1411nucleolintargeted lipid nanobubblestriple-negative breast cancerultrasound molecular imaging

Identifiers

PMID32666304
OpenAlexW3043448688

What OpenQuestion holds

Textmetadata
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.