ReviewJournal of controlled release : official journal of the Controlled Release Society2026
Equip your vehicle for the right terrain: Using features of local pathology to guide engineering of targeted drug delivery systems.
Review in Journal of controlled release : official journal of the Controlled Release Society, 2026. 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
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.
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.
- Decoupling Physisorption from Chemisorption in Clickable Lipid Nanoparticles.ACS nanoscience Au · 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
5 authors.
Funding
Abstract
Drug delivery systems (DDS) have been engineered to target therapeutics to the primary site of disease for many varied pathologies. Lung disorders are especially advantaged, as the pulmonary endothelium's direct interface with the bloodstream makes it accessible and highly susceptible to injury. As such, the endothelium is damaged in many pathologies, characterized by dysregulation and structural and functional changes. Over the years, scientists have exploited these key features of endothelial dysfunction for targeted drug delivery. This review combines past and present research on DDS design directed toward the pathological pulmonary endothelium. Scientists have engineered DDS for endothelial delivery through the modification of nanocarrier size, shape, rigidity, and surface features, and the use of ligand-directed, biomimetic, stimuli-responsive, and physicochemical targeting strategies. While recent advances have brought these approaches closer to clinical relevance, challenges remain in their translation to therapeutic applications.
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What OpenQuestion holds
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.