Evidence map›Paper›PMID 37565561›Full record

ArticleCurrent drug delivery2024

A Novel Etanercept-loaded Nano-emulsion for Targeted Treatment of Inflammatory Arthritis

Chenglong Li, Guanting Lu, Yue Jiang, Huaiyu Su, Chen Li

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Article in Current drug delivery, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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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

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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

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4 · The record

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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.

Chenglong LiDepartment of Pharmacy, Deyang People's Hospital, Deyang 618000, China.ORCID 0000-0001-8171-6227
Guanting LuLaboratory of Translational Medicine Research, Department of Pathology, Deyang People's Hospital, Deyang 618000, China.
Yue JiangDepartment of Pharmacy, Deyang People's Hospital, Deyang 618000, China.
Huaiyu SuDepartment of Pharmacy, Deyang People's Hospital, Deyang 618000, China.
Chen LiCentre for Translational Research in Cancer, Sichuan Cancer Hospital & Institute, Chengdu 610000, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRheumatoid arthritis (RA) is a systemic autoimmune disease (AD), and the global incidence rate is 0.5 ~ 1%. Existing medications might reduce symptoms, however, there is no known cure for this illness. Etanercept (EN) can competitively inhibit TNF-α binding to the TNF receptor on the cell surface to treat RA. However, subcutaneous injection of free EN predisposes to systemic distribution and induces immune system hypofunction. Draining lymph nodes (LNs) play a significant role in the onset, maintenance, and progression of RA as they are the primary sites of aberrant immune response and inflammatory cytokine production.

aimThe purpose of this study was to successfully treat RA with etanercept by encapsulating it in nanoemulsions (NEs/EN) and then delivering it specifically to draining LNs. The EN-loaded NEs were prepared by high-pressure homogenization method and modified with DSPE-mPEG

methodsA novel nano-emulsion (NE) was constructed to deliver EN (NE/EN) to RA-draining LNs. To decrease aggregation and load EN, DSPE-mPEG

resultsCircular dichroism spectrum and L929 cell experiment confirmed that NEs encapsulation had no impact on the biological activity of EN.

conclusionNEs/EN effectively improve the effectiveness of EN in the treatment of RA. Our work provides an experimental foundation for expanding the clinical application of EN.

Indexed as

Arthritis, RheumatoidEmulsionsEtanerceptLymph NodesAnimalsAntirheumatic AgentsArthritis, ExperimentalMiceMice, Inbred DBANanoparticlesParticle SizeAntirheumatic AgentsEmulsionsEtanerceptdraining lymph nodesetanercept-loaded nano-emulsioninflammatory arthritisRheumatoid arthritistargeted treatment.TNF-α

Identifiers

PMID37565561

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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.