Evidence map›Paper›PMID 41445542›Full record

ReviewInternational journal of nanomedicine2025

Self-Assembled Nanoparticles: Overcoming Limitations of Conventional Nanomedicines for Enhanced Tumor Therapy.

Xinlei Tang, Rujia Xie, Bozhi Zeng, Chengcheng Yi, Hui Su, Congcong Chen, Lili Zhou, Xinhua Xia, Jianguo Zeng, Jing Yang

Abstract readReview
In one paragraph

Review in International journal of nanomedicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

10 authors.

Xinlei TangSchool of Pharmacy, Hunan University of Chinese Medicine, Changsha, 410208, People's Republic of China.
Rujia XieSchool of Pharmacy, Hunan University of Chinese Medicine, Changsha, 410208, People's Republic of China.
Bozhi ZengSchool of Pharmacy, Hunan University of Chinese Medicine, Changsha, 410208, People's Republic of China.
Chengcheng YiSchool of Pharmacy, Hunan University of Chinese Medicine, Changsha, 410208, People's Republic of China.
Hui SuSchool of Pharmacy, Hunan University of Chinese Medicine, Changsha, 410208, People's Republic of China.
Congcong ChenSchool of Pharmacy, Hunan University of Chinese Medicine, Changsha, 410208, People's Republic of China.
Lili ZhouSchool of Pharmacy, Hunan University of Chinese Medicine, Changsha, 410208, People's Republic of China.
Xinhua XiaSchool of Pharmacy, Hunan University of Chinese Medicine, Changsha, 410208, People's Republic of China.
Jianguo ZengHunan Key Laboratory of Traditional Chinese Veterinary Medicine, Hunan Agricultural University, Changsha, Hunan, 410128, People's Republic of China.
Jing YangSchool of Pharmacy, Hunan University of Chinese Medicine, Changsha, 410208, People's Republic of China.ORCID 0009-0005-2971-5725

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The high mortality rate associated with cancer presents a significant clinical challenge, necessitating breakthroughs to overcome the limitations of traditional therapies, which often entail substantial side effects, as well as the complexities associated with existing nanodelivery systems (NDDS) that lack adequate targeting capabilities. Self-assembled nanoparticles (SANs) form spontaneously through weak interactions between drugs and functional molecules, such as hydrogen bonds and hydrophobic interactions. They exhibit revolutionary advantages, including ultra-high drug loading capacity, stimulus responsiveness, precise drug release, self-driven targeting capabilities, and a straightforward preparation process that does not require complex carrier synthesis. This review systematically summarizes the latest advancements in SANs for tumor therapy, emphasizing their molecular design principles and mainstream preparation strategies, while detailing their efficacy in multi-modal synergistic therapies, including chemotherapy, photodynamic/photothermal therapy, immunotherapy, and gene therapy. The technology of SANs establishes a robust foundation for the development of highly efficient and low-toxicity anti-cancer strategies, demonstrating significant potential to offer a transformative new paradigm for clinical precision therapy. We believe that the continued evolution of SANs holds great promise for clinical translation, potentially offering transformative solutions for personalized oncology in the near future.

Indexed as

Antineoplastic AgentsNanomedicineNanoparticle Drug Delivery SystemNanoparticlesNeoplasmsAnimalsCombined Modality TherapyDrug CompoundingDrug LiberationGenetic TherapyHumansImmunotherapyPhotochemotherapyPhotothermal TherapyTheranostic NanomedicineAntineoplastic AgentsNanoparticle Drug Delivery Systemmolecular designnanodrug delivery systemnon-covalent interactionsself-assembled nanoparticlestumor therapy

Identifiers

PMID41445542
PMCPMC12722421

What Socratic holds

Textmetadata
LicenceCC BY-NC
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.