Evidence map›Paper›PMID 39323205›Full record

ReviewNanoscale2024

Harnessing exosomes for advanced osteoarthritis therapy.

Andrew Selvadoss, Helna M Baby, Hengli Zhang, Ambika G Bajpayee

Abstract readReview
In one paragraph

Review in Nanoscale, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Review
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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

4 authors.

Andrew SelvadossDepartment of Chemical Engineering, Northeastern University, Boston, MA 02115, USA. a.bajpayee@northeastern.edu.ORCID http://orcid.org/0009-0002-4905-1004
Helna M BabyDepartment of Bioengineering, Northeastern University, Boston, MA 02115, USA.
Hengli ZhangDepartment of Bioengineering, Northeastern University, Boston, MA 02115, USA.
Ambika G BajpayeeDepartment of Chemical Engineering, Northeastern University, Boston, MA 02115, USA. a.bajpayee@northeastern.edu.ORCID http://orcid.org/0000-0002-8458-7464

Funding

Intra-cartilage depot delivery of electrically-charged IL-1RA for targeting osteoarthritis-associated inflammation and catabolism in multiple joint tissuesR01AR075121 · NIAMS · NORTHEASTERN UNIVERSITY · PI BAJPAYEE, AMBIKA GOEL · 2020 to 2025
$2.5M
Anti-catabolic drug anchored cationic exosomes for cartilage targeting and repairR21EB028385 · NIBIB · NORTHEASTERN UNIVERSITY · PI BAJPAYEE, AMBIKA GOEL · 2019 to 2021
$628k
NIAMS NIH HHS R01 AR075121NIBIB NIH HHS R21 EB028385
6 · The paper itself

Abstract

Exosomes are nanosized, lipid membrane vesicles secreted by cells, facilitating intercellular communication by transferring cargo from parent to recipient cells. This capability enables biological crosstalk across multiple tissues and cells. Extensive research has been conducted on their role in the pathogenesis of degenerative musculoskeletal diseases such as osteoarthritis (OA), a chronic and painful joint disease that particularly affects cartilage. Currently, no effective treatment exists for OA. Given that exosomes naturally modulate synovial joint inflammation and facilitate cartilage matrix synthesis, they are promising candidates as next generation nanocarriers for OA therapy. Recent advancements have focused on engineering exosomes through endogenous and exogenous approaches to enhance their joint retention, cartilage and chondrocyte targeting properties, and therapeutic content enrichment, further increasing their potential for OA drug delivery. Notably, charge-reversed exosomes that utilize electrostatic binding interactions with cartilage anionic aggrecan glycosaminoglycans have demonstrated the ability to penetrate the full thickness of early-stage arthritic cartilage tissue following intra-articular administration, maximizing their therapeutic potential. These exosomes offer a non-viral, naturally derived, cell-free carrier for OA drug and gene delivery applications. Efforts to standardize exosome harvest, engineering, and property characterization methods, along with scaling up production, will facilitate more efficient and rapid clinical translation. This article reviews the current state-of-the-art, explores opportunities for exosomes as OA therapeutics, and identifies potential challenges in their clinical translation.

Indexed as

ExosomesOsteoarthritisAnimalsCartilage, ArticularChondrocytesDrug CarriersDrug Delivery SystemsHumansDrug Carriers

Identifiers

PMID39323205
PMCPMC11799831

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.