Evidence map›Paper›PMID 40836187›Full record

ReviewDrug delivery and translational research2025

Antibody-conjugated polymer nanoparticles for brain cancer.

San San Amelia Tai, Hooi Leong Loo, Athirah Bakhtiar, Paul Chi-Lui Ho, Lay Hong Chuah

Abstract readReview
In one paragraph

Review in Drug delivery and translational research, 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. Article
  2. Review
  3. Antibody-Empowered Nanomedicine for Precise Biomedical Applications.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  4. Article
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

5 authors.

San San Amelia TaiDivision of Biosciences, University College London, Gower Street, WC1E 6BT, London, United Kingdom.
Hooi Leong LooSchool of Pharmacy, Monash University Malaysia, Bandar Sunway, Subang Jaya, 47500, Selangor, Malaysia.
Athirah BakhtiarSchool of Pharmacy, Monash University Malaysia, Bandar Sunway, Subang Jaya, 47500, Selangor, Malaysia.
Paul Chi-Lui HoSchool of Pharmacy, Monash University Malaysia, Bandar Sunway, Subang Jaya, 47500, Selangor, Malaysia.
Lay Hong ChuahSchool of Pharmacy, Monash University Malaysia, Bandar Sunway, Subang Jaya, 47500, Selangor, Malaysia. alice.chuah@monash.edu.ORCID http://orcid.org/0000-0001-8283-0849

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Brain cancer remains a significant global health challenge, affecting over a million individuals worldwide. It includes primary tumors such as gliomas, particularly glioblastoma multiforme (GBM) being one of the most aggressive forms, and secondary brain tumors resulting from metastases of breast or lung cancer. A major obstacle in treating these malignancies is the blood-brain barrier (BBB), which limits effective drug delivery to tumor sites. Nanoparticles have long been explored as versatile drug delivery vehicles due to their potential to improve tumor specificity, penetrate the BBB, and enhance drug bioavailability. To further refine these delivery systems, antibodies have been conjugated to nanoparticles to target specific tumor biomarkers, thereby enhancing therapeutic precision and efficacy. In preclinical studies, antibody-conjugated polymer nanoparticles have demonstrated promising capabilities in achieving both targeted delivery and BBB penetration. This review first outlines the pathophysiology and mechanisms underlying brain cancer. It then discusses how polymer nanoparticles address current therapeutic limitations, particularly in overcoming the BBB and improving pharmacokinetics. Various polymer nanoparticles are explored, including polymeric micelles, dendrimers, nanocapsules, nanospheres, nanogels, and polymersomes, each offering distinct therapeutic advantages. We further examine the impact of surface modification with antibodies to enhance tumor targeting, discussing their physiochemical properties, as well as in vitro and in vivo findings. Finally, the review critically evaluates the current challenges in the development of antibody-conjugated polymer nanoparticles, identifies research gaps, and future directions of this promising field.

Indexed as

Antineoplastic AgentsBrain NeoplasmsImmunoconjugatesNanoparticlesPolymersAnimalsBlood-Brain BarrierHumansAntineoplastic AgentsImmunoconjugatesPolymersAntibodyBrain cancerConjugationNanoformulationsTargeted therapyTargetingTumor

Identifiers

PMID40836187
PMCPMC12507923

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.