ReviewInternational journal of nanomedicine2026
Targeted Nanoboron Delivery Platform for Boron Neutron Capture Therapy in Refractory Solid Tumors.
Review in International journal of nanomedicine, 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.
- Nanocarrier Strategies for Boron Drug Delivery in BNCT.Micromachines · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Boron neutron capture therapy (BNCT) represents a promising binary radiotherapy for refractory solid tumors. However, its clinical translation has been historically constrained by the suboptimal pharmacokinetics of conventional boron agents (eg, BPA and BSH), characterized by low tumor selectivity and rapid clearance. This review provides a comprehensive analysis of how nanoengineered delivery platforms-including lipid-based, polymeric, inorganic, and biomimetic nanocarriers-are revolutionizing BNCT. We focus on their advanced targeting mechanisms (passive EPR effect, active ligand/receptor engagement, and nuclear localization), which collectively enable significantly enhanced tumor boron accumulation (T/N ratios of 6-17) and prolonged intratumoral retention. Furthermore, we critically examine the integration of multimodal imaging techniques (PET, MRI) for real-time dosimetry and treatment planning, which is essential for precision-guided BNCT. Despite remarkable preclinical progress, key translational challenges persist, including the standardization of neutron sources, long-term biocompatibility of nanocarriers, and scalable GMP-compliant manufacturing. In conclusion, the convergence of targeted nanomedicine, precision imaging, and immunomodulation is forging a robust platform. This positions BNCT as an emerging, clinically viable modality within the precision oncology arsenal for refractory malignancies.
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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.