ReviewNanomedicine (London, England)2025
Emerging vesicular nanosystems capable of effectively targeting hepatocytes.
Review in Nanomedicine (London, England), 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
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.
- Hepatotropic Nanomedicine and Targeted Nanocarriers for Liver Diseases and Hepatocellular Carcinoma.International journal of nanomedicine · 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
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Liver indications are increasing in prevalence globally, with nanomedicines emerging as a potential treatment strategy. Hepatocytes play an important role in most liver diseases, making the ability to target these cells an important consideration in the development of therapeutics. Although nanomedicines administered intravenously do tend to accumulate in the liver thanks to its high blood flow, specifically targeting hepatocytes remains non-trivial due to several aspects of liver physiology. For example, hepatocytes are challenging to reach within the liver tissue due to limited fenestrae size in the liver vessels. Disease and age further reduce fenestration, meaning that optimal therapeutic effect is difficult to achieve. To overcome these obstacles, different nanomedicines have been rationally designed to possess optimized size and surface properties, along with hepatocyte-specific targeting ligands. This review discusses developments in vesicular nanotechnologies published in English since 2022, within the context of the unique challenges presented by hepatocyte delivery. The lipid nanoparticles, liposomes, niosomes, and lipid calcium phosphate nanoparticles discussed, from pre-clinical research to clinically approved treatments, represent significant advancements toward this goal. However, further challenges remain, and we expect to continue to see advancements in model development and novel nanosystems tailored for effectiveness in diseased states.
Indexed as
Identifiers
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.