Evidence map›Paper›PMID 40809455›Full record

ArticleResearch (Washington, D.C.)2025

Mechanical Agitation-Assisted Transmembrane Drug Delivery by Magnetically Powered Spiky Nanorobots.

Xiaojia Liu, Zihan Xu, Yanan Che, Zichang Guo, Dongdong Jin, Qianqian Wang, Ning Liu, Xing Ma, Zhilu Yang

Abstract read
In one paragraph

Article in Research (Washington, D.C.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
  2. Article
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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.

Xiaojia LiuDongguan Key Laboratory of Smart Biomaterials and Regenerative Medicine, The Tenth Affiliated Hospital, Southern Medical University, Dongguan, Guangdong 523059, China.
Zihan XuSauvage Laboratory for Smart Materials, School of Integrated Circuits, Harbin Institute of Technology (Shenzhen), Shenzhen 518055, China.
Yanan CheDepartment of Mechanical and Automation Engineering, The Chinese University of Hong Kong, Hong Kong, SAR 999077, China.
Zichang GuoSauvage Laboratory for Smart Materials, School of Integrated Circuits, Harbin Institute of Technology (Shenzhen), Shenzhen 518055, China.
Dongdong JinSauvage Laboratory for Smart Materials, School of Integrated Circuits, Harbin Institute of Technology (Shenzhen), Shenzhen 518055, China.
Qianqian WangJiangsu Key Laboratory for Design and Manufacturing of Precision Medicine Equipment, School of Mechanical Engineering, Southeast University, Nanjing 211189, China.
Ning LiuSchool of Aerospace Engineering and Applied Mechanics, Tongji University, Shanghai 200092, China.
Xing MaSauvage Laboratory for Smart Materials, School of Integrated Circuits, Harbin Institute of Technology (Shenzhen), Shenzhen 518055, China.
Zhilu YangDongguan Key Laboratory of Smart Biomaterials and Regenerative Medicine, The Tenth Affiliated Hospital, Southern Medical University, Dongguan, Guangdong 523059, China.ORCID https://orcid.org/0000-0001-9901-0927

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breaking through cell membrane barriers is a crucial step for intracellular drug delivery in antitumor chemotherapy. Hereby, a magnetic nanorobot, capable of exerting mechanical agitation on cellular membrane to promote intracellular drug delivery, was developed. The main body of the nanorobots was composed of nano-scaled gold nanospikes that were deposited with Ni and Ti nanolayers for magnetic activation and biocompatibility, responsively. The nanorobots can be precisely navigated to target cancer cells under external magnetic field control. By virtue of the sharp nanospike structures, the magnetically powered rotation behavior of the nanorobots can impose mechanical agitation on the living cell membrane and thus improve the membrane permeability, leading to promoted transmembrane cargo delivery. Coarse-grained molecular dynamics simulation revealed that the mechanism of mechanical intervention regulated permeability of the bilayer lipid membrane, allowing for enhanced transmembrane diffusion of small cargo molecules. An in vitro study demonstrated that these nanorobots can markedly enhance the efficiency of drug entry into tumor cells, thus improving the effectiveness of tumor therapy under magnetic activation in vivo. This work paves a new way for overcoming cell membrane barriers for intracellular drug delivery by using a magnetic nanorobotic system, which is expected to promote further application of magnetically controlled nanorobot technology in the field of precision medicine.

Identifiers

PMID40809455
PMCPMC12349924

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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.