Evidence map›Paper›PMID 41152929›Full record

ReviewJournal of nanobiotechnology2025

Recent advances in theranostic nanomaterials for overcoming traumatic brain injury.

Nam Cheol Hwang, Dong Min Lim, Tae Sik Goh, Jung Mo Kang, Jaehoon Kim, Shin Kim, Yun Hak Kim, Dokyoung Kim

Abstract readReview
In one paragraph

Review in Journal of nanobiotechnology, 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. Nanozyme-based therapeutic strategies for traumatic brain injury.International journal of pharmaceutics: X · 2026
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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.

Nam Cheol Hwang *Department of Biomedical Science, Graduate School, Kyung Hee University, Seoul, 02447, Republic of Korea.
Dong Min Lim *Interdisciplinary Program of Genomic Data Science, Pusan National University, Yangsan, 50612, Republic of Korea.
Tae Sik GohBiomedical Research Institute, Pusan National University Hospital, Busan, 49241, Republic of Korea.
Jung Mo KangBiomedical Research Institute, Pusan National University Hospital, Busan, 49241, Republic of Korea.
Jaehoon KimCollege of Medicine, Kyung Hee University, Seoul, 02447, Republic of Korea.
Shin KimDepartment of Immunology, School of Medicine, Keimyung University, Dalseo-gu, Daegu, 42601, Republic of Korea. god98005@dsmc.or.kr.
Yun Hak Kim *Department of Anatomy, School of Medicine, Pusan National University, Yangsan, 50612, Republic of Korea. yunhak10510@pusan.ac.kr.
Dokyoung KimDepartment of Biomedical Science, Graduate School, Kyung Hee University, Seoul, 02447, Republic of Korea. dkim@khu.ac.kr.

Funding

Korea Institute of Science and Technology 2E32852National Research Foundation of Korea RS-2023-00223764National Research Foundation of Korea RS-2024-00406152National Research Foundation of Korea RS-2024-00439078
6 · The paper itself

Abstract

Traumatic brain injury (TBI) is a major global health challenge characterized by complex secondary injury mechanisms involving oxidative stress, inflammation, and blood-brain barrier (BBB) disruption. Traditional biosensing and therapy strategies often face limitations due to ineffective biomarker detection and poor drug targeting at the injury site. Recently, theranostic nanomaterials have emerged as a promising solution, integrating diagnostic and therapeutic functionalities within a single nanoscale platform. This review explores the latest advances in nanotherapeutics and nanosensors for TBI management. The first section summarizes various nanotherapeutic approaches, including PEGylated-polystyrene nanoparticles, porous silicon nanoparticles, carbon dot nanoparticles, dendrimer nanoparticles, lipid nanoparticles (LNPs), and siRNA-based nanoparticles, all of which have demonstrated enhanced neuroprotection and targeted drug delivery in TBIs. Notably, LNPs exhibit further optimized biocompatibility and therapeutic efficacy, while carbon dot nanoparticles function as nanozymes to combat oxidative stress, thereby mitigating neuronal damage. The second section focuses on nanosensors for TBIs, including peptide-based nanosensors, ECM-targeted nanosensors, and biomarker-responsive platforms capable of real-time diagnosis and monitoring of TBI progression. Additionally, the use of polymeric and fibrinogen-based nanosensors is discussed as advanced strategies to improve precision detection and therapeutic control. This review provides a comprehensive overview of theranostic nanomaterials for TBIs, highlighting their transformative potential in diagnosis and targeted treatment, while addressing key translational challenges to clinical application.

Indexed as

Brain Injuries, TraumaticNanostructuresTheranostic NanomedicineAnimalsBlood-Brain BarrierDrug Delivery SystemsHumansNanoparticlesOxidative StressBiomedical engineeringBrainDrug deliveryNanotherapeuticsTranslational research

Identifiers

PMID41152929
PMCPMC12570421

What OpenQuestion holds

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LicenceCC BY
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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.