Evidence map›Paper›PMID 42619255›Full record

ReviewAdvanced healthcare materials2026

Mitochondria-Targeted Nanotherapies in Aging Neurodegenerative Disorders: Emerging Prospects and Clinical Potential.

Dnyandev G Gadhave, Ashish B Jadhav, Nitin B Waghamode, Shubham Khot, Rajiya Khan, Ravi Hole, Shankar M Dhobale, Manoj Aswar, Keshav Raj Paudel

Abstract readReview
In one paragraph

Review in Advanced healthcare materials, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Dnyandev G GadhaveDepartment of Pharmaceutics, Dattakala Shikshan Sanstha's, Dattakala College of Pharmacy (Affiliated to Savitribai Phule Pune University), Pune, Maharashtra, India.ORCID https://orcid.org/0000-0003-2557-3115
Ashish B JadhavDepartment of Quality Assurance, Dattakala Shikshan Sanstha's, Dattakala College of Pharmacy (Affiliated to Savitribai Phule Pune University), Pune, Maharashtra, India.ORCID https://orcid.org/0009-0006-3139-7487
Nitin B WaghamodeDepartment of Pharmacognosy, Dattakala Shikshan Sanstha's, Dattakala College of Pharmacy (Affiliated to Savitribai Phule Pune University), Pune, Maharashtra, India.
Shubham KhotDepartment of Pharmaceutics, Marathwada Mitra Mandal's College of Pharmacy, Pune, Maharashtra, India.ORCID https://orcid.org/0000-0002-5599-6648
Rajiya KhanDepartment of Pharmaceutics, HSBPVT'S, Group of Institutions, College of Pharmacy (Affiliated to Savitribai Phule Pune University), Ahmednagar, Maharashtra, India.
Ravi HoleDepartment of Pharmaceutics, Dattakala Shikshan Sanstha's, Dattakala Institute of Pharmaceutical Science and Research (Affiliated to Dr. Babasaheb Ambedkar Technological University, Lonere), Pune, Maharashtra, India.
Shankar M DhobaleDepartment of Pharmaceutics, SCSSS's Sitabai Thite College of Pharmacy, Pune, Maharashtra, India.ORCID https://orcid.org/0000-0002-0557-7242
Manoj AswarDepartment of Pharmacology, Marathwada Mitra Mandal's College of Pharmacy, Pune, Maharashtra, India.ORCID https://orcid.org/0000-0001-7159-4326
Keshav Raj PaudelNICM Health Research Institute and School of Science, Western Sydney University, Westmead, New South Wales, Australia.ORCID https://orcid.org/0000-0002-3591-2080

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aging is a significant risk factor of neurodegenerative disorders (NDs) such as Huntington's, Alzheimer's, Parkinson's, amyotrophic lateral sclerosis (ALS), and multiple sclerosis (MS). Although several clinical, neuroimaging, and biomarker-based diagnostic approaches are available for NDs, their limited sensitivity for early-stage detection, disease specificity, and prediction of disease progression continue to present significant clinical challenges, often resulting in delayed diagnosis and therapeutic intervention. According to previously published works, the preliminary pathological feature of such disorders is mitochondrial dysfunction. This may lead to elevated oxidative stress, impaired mitophagy, unbalanced mitochondrial function, and bioenergetic failure. This review examines how mitochondria-targeted nanotherapeutic approaches can overcome these pathological barriers and improve therapeutic outcomes in aging-associated neurodegeneration. Targeted delivery of drug-loaded nanocarriers, such as gene-delivery, lipid-based, metallic, and polymeric nanoparticles, has emerged as a potential platform to deliver medication directly to defective mitochondria. It may increase mitochondrial biogenesis, maintain redox balance, and protect against neuronal degeneration. This work incorporates disease-specific mitochondrial pathology with current progress in targeted nanotherapeutics, age-associated delivery barriers, clinical revolution, and emerging artificial intelligence (AI)-enabled precision therapeutic approaches. Mitochondria-targeted nanotherapeutics depict a potential disease-modifying strategy for aging-related NDs. However, further advancements in targeting efficacy, scalable production, long-term safety, and clinical validation can facilitate a successful clinical revolution.

Indexed as

AgingMitochondriaNanomedicineNanoparticlesNeurodegenerative DiseasesAnimalsDrug Delivery SystemsHumansblood–brain barrierclinical insightsmechanistic insightsmitochondrial dysfunctionnanotechnologyneurodegenerative disorders

Identifiers

PMID42619255
PMCPMC13612936

What OpenQuestion holds

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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.