ArticleScientific reports2026
Explainable AI for gastrointestinal lesion surveillance and precision targeted drug delivery.
Article in Scientific reports, 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.
- Transforming Nanomaterials Development with Artificial Intelligence Techniques.Nanotechnology, science and applications · 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
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The Internet of Bio-NanoThings (IoBNT) promises revolutionary healthcare applications, particularly in targeted drug delivery. However, major challenges remain including safe nanodevice design, monitoring their behavior in biological environments and enabling reliable communication with external control systems. This work proposes an AI-assisted IoBNT architecture that combines gastrointestinal (GI) imaging with intelligent therapeutic supervision. A wireless ingestible imaging device (WIID) captures GI images, while an Artificial Intelligence Ciphered Link (AICL) analyzes them using convolutional neural networks (CNNs) trained with supervised contrastive learning and cost-sensitive fine-tuning. Unlike prior studies focused solely on tumors, our system is evaluated on the HyperKvasir dataset covering 25 GI disease classes, including neoplastic and inflammatory conditions. Explainable AI methods (GradCAM family) are employed with quantitative validation to improve model transparency. Drug transport and release are modeled using a multi-compartment pharmacokinetic framework with uncertainty analysis. Security protections using Quadratic Map Privacy Algorithm (QMPA), threat modeling and failsafe dosing limits are incorporated to enhance clinical safety. The system achieves 91.4% classification accuracy (weighted F1 = 0.91) on HyperKvasir, with stronger performance in neoplastic classes and lower accuracy in rare categories, emphasizing the importance of class-balanced evaluation. These results demonstrate the feasibility of integrating AI-based disease detection with controlled drug delivery, representing a step toward closed-loop, adaptive IoBNT therapeutics.
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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.