Evidence map›Paper›PMID 41181144›Full record

ReviewFrontiers in immunology2025

Liposome-mediated macrophage reprogramming: emerging strategies for chronic disease therapy.

Hongnv Zhang, Nan Hu, Zhenghao Wang, Shaodong Zhai

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Hongnv ZhangThird Hospital of Shanxi Medical University, Shanxi Bethune Hospital, Shanxi Academy of Medical Sciences, Tongji Shanxi Hospital, Taiyuan, China.
Nan HuThird Hospital of Shanxi Medical University, Shanxi Bethune Hospital, Shanxi Academy of Medical Sciences, Tongji Shanxi Hospital, Taiyuan, China.
Zhenghao WangThird Hospital of Shanxi Medical University, Shanxi Bethune Hospital, Shanxi Academy of Medical Sciences, Tongji Shanxi Hospital, Taiyuan, China.
Shaodong ZhaiThird Hospital of Shanxi Medical University, Shanxi Bethune Hospital, Shanxi Academy of Medical Sciences, Tongji Shanxi Hospital, Taiyuan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

With the rapid advancement of nanotechnology, the application of nanomedicine has become increasingly widespread, demonstrating remarkable potential for highly precise targeting and efficacious drug delivery. Compared to conventional drug delivery approaches, nanomedicine effectively addresses issues such as nonspecific drug distribution and severe adverse effects, significantly enhancing therapeutic efficacy through its targeted delivery mechanisms. As an innovative drug delivery vehicle, liposomes exhibit tremendous application potential owing to their outstanding biocompatibility, extensive applicability, remarkable ability to improve drug stability and bioavailability, precise targeting capabilities, membrane structures that facilitate drug permeation, and high degree of tunability. In the field of chronic disease management, liposomes serve as sophisticated vehicles for targeted and controlled drug delivery, offering innovative therapeutic approaches for various chronic conditions. Macrophages, which play a pivotal role in modulating inflammatory responses and promoting tissue repair, have emerged as crucial targets for alleviating inflammatory symptoms. Nevertheless, achieving precise and efficient targeting of macrophages remains a significant challenge in current research. This article systematically reviews recent advances in liposome-based therapies for chronic diseases, including cardiovascular diseases, cancers, chronic respiratory diseases (e.g., chronic obstructive pulmonary disease, pulmonary fibrosis, and asthma), and metabolic disorders (e.g., diabetes), with particular emphasis on the therapeutic potential of liposomes in modulating macrophage activity. Furthermore, it summarizes and analyzes the major challenges and obstacles currently faced in liposome research, providing novel insights for future research directions and facilitating the translation of research findings into clinical applications.

Indexed as

LiposomesMacrophagesAnimalsChronic DiseaseDrug Delivery SystemsHumansNanomedicineLiposomeschronic diseasesinflammationliposomemacrophagenanomedicines

Identifiers

PMID41181144
PMCPMC12575207

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.