Evidence map›Paper›PMID 36717899›Full record

ArticleJournal of nanobiotechnology2023

Ultrasound targeted microbubble destruction-triggered nitric oxide release via nanoscale ultrasound contrast agent for sensitizing chemoimmunotherapy.

Yading Zhao, Dandan Shi, Lu Guo, Mengmeng Shang, Xiao Sun, Dong Meng, Shan Xiao, Xiaoxuan Wang, Jie Li

Open access · goldAbstract read
In one paragraph

Article in Journal of nanobiotechnology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
5.7field-weighted citation impact, top 3% 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

22 citing papers in PubMed, 52 citations in OpenAlex.

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  19. NO- and HNitric oxide : biology and chemistry · 2024
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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

9 authors at 1 institution in 1 country.

Yading ZhaoDepartment of Ultrasound, Qilu Hospital of Shandong University, Jinan, 250012, Shandong, China.
Dandan ShiDepartment of Ultrasound, Qilu Hospital of Shandong University, Jinan, 250012, Shandong, China.
Lu GuoDepartment of Ultrasound, Qilu Hospital of Shandong University, Jinan, 250012, Shandong, China.
Mengmeng ShangDepartment of Ultrasound, Qilu Hospital of Shandong University, Jinan, 250012, Shandong, China.
Xiao SunDepartment of Ultrasound, Qilu Hospital of Shandong University, Jinan, 250012, Shandong, China.
Dong MengDepartment of Ultrasound, Qilu Hospital of Shandong University, Jinan, 250012, Shandong, China.
Shan XiaoDepartment of Ultrasound, Qilu Hospital of Shandong University, Jinan, 250012, Shandong, China.
Xiaoxuan WangDepartment of Ultrasound, Qilu Hospital of Shandong University, Jinan, 250012, Shandong, China.
Jie LiDepartment of Ultrasound, Qilu Hospital of Shandong University, Jinan, 250012, Shandong, China. jieli@email.sdu.edu.cn.
Qilu Hospital of Shandong University · CN

Funding

National Natural Science Foundation of China No. 82071937
6 · The paper itself

Abstract

Immunotherapy had demonstrated inspiring effects in tumor treatment, but only a minority of people could benefit owing to the hypoxic and immune-suppressed tumor microenvironment (TME). Therefore, there was an urgent need for a strategy that could relieve hypoxia and increase infiltration of tumor lymphocytes simultaneously. In this study, a novel acidity-responsive nanoscale ultrasound contrast agent (L-Arg@PTX nanodroplets) was constructed to co-deliver paclitaxel (PTX) and L-arginine (L-Arg) using the homogenization/emulsification method. The L-Arg@PTX nanodroplets with uniform size of about 300 nm and high drug loading efficiency displayed good ultrasound diagnostic imaging capability, improved tumor aggregation and achieved ultrasound-triggered drug release, which could prevent the premature leakage of drugs and thus improve biosafety. More critically, L-Arg@PTX nanodroplets in combination with ultrasound targeted microbubble destruction (UTMD) could increase cellular reactive oxygen species (ROS), which exerted an oxidizing effect that converted L-Arg into nitric oxide (NO), thus alleviating hypoxia, sensitizing chemotherapy and increasing the CD8 + cytotoxic T lymphocytes (CTLs) infiltration. Combined with the chemotherapeutic drug PTX-induced immunogenic cell death (ICD), this promising strategy could enhance immunotherapy synergistically and realize powerful tumor treatment effect. Taken together, L-Arg@PTX nanodroplets was a very hopeful vehicle that integrated drug delivery, diagnostic imaging, and chemoimmunotherapy.

Indexed as

Contrast MediaNanoparticlesCell Line, TumorHumansHypoxiaImmunotherapyMicrobubblesNitric OxidePaclitaxelContrast MediaNitric OxidePaclitaxelChemoimmunotherapyHypoxiaNitric oxideReactive oxygen speciesUltrasound contrast agent

Identifiers

PMID36717899
PMCPMC9885630
OpenAlexW4318479552

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.