ReviewFrontiers in bioengineering and biotechnology2025
Biomimetic erythrocyte-based drug delivery systems for organ-targeted therapy.
Review in Frontiers in bioengineering and biotechnology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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
3 citing papers in PubMed.
- Biomimetic Targeted Drug Delivery for Liver Failure in Abdominal Sepsis: Focus on Autologous Erythrocyte Ghosts.International journal of molecular sciences · 2026Review
- Beyond autologousMolecular therapy. Oncology · 2026Review
- Blood Cell-Based Drug Delivery Systems: From Biological and Mechanical Design to Clinical Applications.Bioengineering (Basel, Switzerland) · 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
Enhancing drug accumulation in target organs while minimizing adverse effects is critical for pharmacological therapies. Therefore, the development of advanced drug-targeting platforms is essential for clinical application. These systems must not only enable precise organ-specific targeting but also improve drug bioavailability and extend systemic circulation. In recent years, significant progress has been made in blood cell-inspired drug delivery strategies, with red blood cells-based (RBCs-based) platforms showing particular promise due to their inherent physiological advantages. Nevertheless, the development of organ-specific RBCs-mediated delivery systems remains challenging. We categorize and summarize various drug loading methods for existing RBCs, along with their advantages, disadvantages, and treated disease types. We then focus on describing various design strategies of RBCs-based delivery systems targeting specific organs and review their current applications. Additionally, we discuss current challenges and future perspectives regarding RBCs-based targeted delivery platforms.
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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 Socratic graph.