ArticleMaterials today. Bio2025
Bone marrow-targeted thrombopoietin delivery via engineered platelet-derived vesicle-loaded dissolving microneedles for treating ionizing radiation-induced injury.
Article in Materials today. Bio, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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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.
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.
Who cites it
1 citing paper in PubMed.
- Dissolving microneedle patches loaded with resveratrol albumin nanoclusters for corneal anti-angiogenic therapy.International journal of pharmaceutics: X · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
13 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Exposure to a nuclear accident or a radiological attack may cause serious death events due to hematopoietic acute radiation syndrome (H-ARS). While thrombopoietin (TPO) shows promise in mitigating myelosuppression, its clinical use is restricted due to high doses, strict schedules, and systemic toxicity from conventional administration. This study developed a dissolving microneedle patch loaded with engineered activated platelet-derived vesicles encapsulating TPO (TLEVs@MN) for targeted treatment of H-ARS. Activated platelet-derived vesicles were isolated via ultracentrifugation and then modified with glutathione. Glutathione-based anti-ROS modification effectively protected vesicles from radiation-induced oxidative damage, enhancing their stability and targeting efficiency. Using mild sonication, TPO was efficiently encapsulated into engineered vesicles without compromising membrane protein integrity. Further loading into dissolving MNs facilitated minimally invasive transdermal delivery while ensuring long-term vesicle stability during storage. TLEVs@MNs effectively activated the JAK2/STAT3 pathway, restoring mitochondrial function in hematopoietic stem cells. Pharmacokinetic and biodistribution analyses demonstrated that administration of TPO using TLEVs@MNs achieved the precise TPO delivery to bone marrow hematopoietic stem and progenitor cells, significantly improving survival rates and hematopoietic recovery in irradiated animal models. These findings highlighted TLEVs@MN patch as a promosing and robust TPO delivery platform for managing IR-induced hematopoietic injury.
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Registered trials
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.