Evidence map›Paper›PMID 36639133›Full record

ArticleBiomacromolecules2023

Targeted Drug Delivery Using a Plug-to-Direct Antibody-Nanogel Conjugate.

Uyen Huynh, Peidong Wu, Jingyi Qiu, Theeraphop Prachyathipsakul, Khushboo Singh, D Joseph Jerry, Jingjing Gao, S Thayumanavan

Open access · greenAbstract read
In one paragraph

Article in Biomacromolecules, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
5.5field-weighted citation impact, top 4% of its field
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

16 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Antibody-Nanoparticle Conjugates in Therapy: Combining the Best of Two Worlds.Small (Weinheim an der Bergstrasse, Germany) · 2025
    Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. 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

8 authors at 1 institution in 1 country.

Uyen HuynhDepartment of Chemistry, University of Massachusetts, Amherst, Massachusetts 01003, United States.
Peidong WuDepartment of Chemistry, University of Massachusetts, Amherst, Massachusetts 01003, United States.
Jingyi QiuDepartment of Biomedical Engineering, University of Massachusetts, Amherst, Massachusetts 01003, United States.
Theeraphop PrachyathipsakulDepartment of Chemistry, University of Massachusetts, Amherst, Massachusetts 01003, United States.
Khushboo SinghDepartment of Chemistry, University of Massachusetts, Amherst, Massachusetts 01003, United States.
D Joseph JerryCenter for Bioactive Delivery, Institute for Applied Life Sciences, University of Massachusetts, Amherst, Massachusetts 01003, United States.
Jingjing GaoDepartment of Chemistry, University of Massachusetts, Amherst, Massachusetts 01003, United States.
S ThayumanavanDepartment of Chemistry, University of Massachusetts, Amherst, Massachusetts 01003, United States.ORCID 0000-0002-6475-6726
University of Massachusetts Amherst · US

Funding

Biotechnology Training Program in Applied Life SciencesT32GM135096 · NIGMS · UNIVERSITY OF MASSACHUSETTS AMHERST · PI Jeanne Ann Hardy, Ashish A. Kulkarni · 2020 to 2026
$3.9M
Protein-Induced Self-Assembly and Disassembly of Nanostructures Based on OligoR35GM136395 · NIGMS · UNIVERSITY OF MASSACHUSETTS AMHERST · PI Sankaran Thayumanavan · 2020 to 2026
$3.5M
NIGMS NIH HHS R35 GM136395NIGMS NIH HHS T32 GM135096
6 · The paper itself

Abstract

Targeted drug delivery using antibody-drug conjugates has attracted great attention due to its enhanced therapeutic efficacy compared to traditional chemotherapy. However, the development has been limited due to a low drug-to-antibody ratio and laborious linker-payload optimization. Herein, we present a simple and efficient strategy to combine the favorable features of polymeric nanocarriers with antibodies to generate an antibody-nanogel conjugate (ANC) platform for targeted delivery of cytotoxic agents. Our nanogels stably encapsulate several chemotherapeutic agents with a wide range of mechanisms of action and solubility. We showcase the targetability of ANCs and their selective killing of cancer cells over-expressing disease-relevant antigens such as human epidermal growth factor receptor 2, epidermal growth factor receptor, and tumor-specific mucin 1, which cover a broad range of breast cancer cell types while maintaining low to no toxicity to non-targeted cells. Overall, our system represents a versatile approach that could impact next-generation nanomedicine in antibody-targeted therapeutics.

Indexed as

Antineoplastic AgentsImmunoconjugatesNeoplasmsCell Line, TumorDrug Delivery SystemsHumansNanogelsPolyethylene GlycolsPolyethyleneimineAntineoplastic AgentsImmunoconjugatesNanogelspolyethylene glycol polyethyleneimine nanogelPolyethylene GlycolsPolyethyleneimine

Identifiers

PMID36639133
PMCPMC9928872
OpenAlexW4316012196

What OpenQuestion holds

Textmetadata
LicenceTDM
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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 OpenQuestion graph.