ReviewMaterials today. Bio2026
Aptamer-liposome targeted nanotherapeutics for cancer therapy: Bibliometric analysis, recent developments and future perspectives.
Review in Materials today. Bio, 2026. 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 Scaffold-Based 3D Models for Decoding Cancer Biology and Advancing Therapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026Review
- Aptamers in cancer therapy: Why has clinical translation lagged behind preclinical promise?Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · 2026Review
- Advances in porphyrin-based photosensitizers for photodynamic therapy of A549 lung cancer.Frontiers in pharmacology · 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
9 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
As one of the leading causes of death worldwide, cancer has driven the advancement of targeted therapy toward greater precision and reduced off-target effects. Liposomes, with their biocompatibility, tunable properties, and clinical success, are among the most promising nanocarriers, yet their tumor-targeting specificity remains limited. Aptamer-functionalized liposomes provide a synergistic solution by combining selective aptamer-receptor recognition with efficient drug encapsulation, achieving enhanced tumor targeting and controlled release. Recent advances have expanded this platform toward multi-targeting, stimuli-responsive systems, and theranostic applications, thereby extending the potential of conventional liposomes. This review offers an integrated perspective on the structural design, internalization pathways, and therapeutic applications of aptamer-liposome systems across various cancers. Key barriers, including aptamer instability, scalable conjugation, and limited clinical translation, are critically discussed, alongside emerging strategies to address them. The convergence of aptamer targeting and liposomal delivery represents a transformative step toward next-generation nanotherapeutics, offering a paradigm shift in precision oncology by enabling personalized, selective, and multifunctional cancer therapy.
Indexed as
Identifiers
What Socratic 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 Socratic graph.