Evidence map›Paper›PMID 29529359›Full record

ArticleBiochemistry2018

Tissue-like Neural Probes for Understanding and Modulating the Brain.

Guosong Hong, Robert D Viveros, Theodore J Zwang, Xiao Yang, Charles M Lieber

Abstract read
In one paragraph

Article in Biochemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. Review
  2. NongeneticACS nano · 2026
    Article
  3. Article
  4. Article
  5. Stitching Flexible Electronics into the Brain.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    Article
  6. Article
  7. Article
  8. The Future of Neuroscience: Flexible and Wireless Implantable Neural Electronics.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2021
    Review
  9. Review
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. The business of brain-computer interfaces.Nature biotechnology · 2019
    Article
  16. Review
  17. Article
  18. Article
  19. Novel electrode technologies for neural recordings.Nature reviews. Neuroscience · 2019
    Review
  20. Article
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

5 authors.

Guosong HongDepartment of Chemistry and Chemical Biology , Harvard University , Cambridge , Massachusetts 02138 , United States.
Robert D ViverosJohn A. Paulson School of Engineering and Applied Sciences , Harvard University , Cambridge , Massachusetts 02138 , United States.
Theodore J ZwangDepartment of Chemistry and Chemical Biology , Harvard University , Cambridge , Massachusetts 02138 , United States.
Xiao YangDepartment of Chemistry and Chemical Biology , Harvard University , Cambridge , Massachusetts 02138 , United States.
Charles M LieberDepartment of Chemistry and Chemical Biology , Harvard University , Cambridge , Massachusetts 02138 , United States.ORCID 0000-0002-6660-2456

Funding

Syringe-Injectable Mesh Electronics for Seamless Integration with the Central Nervous SystemDP1EB025835 · NIBIB · HARVARD UNIVERSITY · PI LIEBER, CHARLES M · 2017 to 2019
$3.5M
Syringe Injectable Electronics Platform for Chronic Mapping and Modulation of Neural Circuits in AddictionR21DA043985 · NIDA · HARVARD UNIVERSITY · PI LIEBER, CHARLES M · 2017 to 2018
$436k
Brain Aging Studies with Single-Neuron Resolution Using Syringe-Injectable ElectronicsK99AG056636 · NIA · HARVARD UNIVERSITY · PI HONG, GUOSONG · 2017 to 2018
$255k
NIA NIH HHS K99 AG056636NIBIB NIH HHS DP1 EB025835NIDA NIH HHS R21 DA043985
6 · The paper itself

Abstract

Electrophysiology tools have contributed substantially to understanding brain function, yet the capabilities of conventional electrophysiology probes have remained limited in key ways because of large structural and mechanical mismatches with respect to neural tissue. In this Perspective, we discuss how the general goal of probe design in biochemistry, that the probe or label have a minimal impact on the properties and function of the system being studied, can be realized by minimizing structural, mechanical, and topological differences between neural probes and brain tissue, thus leading to a new paradigm of tissue-like mesh electronics. The unique properties and capabilities of the tissue-like mesh electronics as well as future opportunities are summarized. First, we discuss the design of an ultraflexible and open mesh structure of electronics that is tissue-like and can be delivered in the brain via minimally invasive syringe injection like molecular and macromolecular pharmaceuticals. Second, we describe the unprecedented tissue healing without chronic immune response that leads to seamless three-dimensional integration with a natural distribution of neurons and other key cells through these tissue-like probes. These unique characteristics lead to unmatched stable long-term, multiplexed mapping and modulation of neural circuits at the single-neuron level on a year time scale. Last, we offer insights on several exciting future directions for the tissue-like electronics paradigm that capitalize on their unique properties to explore biochemical interactions and signaling in a "natural" brain environment.

Indexed as

Action PotentialsAnimalsBiomimetic MaterialsBrainElectrodes, ImplantedElectronicsElectrophysiological PhenomenaEquipment DesignHumansNerve NetNeuronsPliabilitySingle-Cell Analysis

Identifiers

PMID29529359
PMCPMC6039269

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Registered trials

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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.