Evidence map›Paper›PMID 28467853›Full record

ArticleACS nano2017

Nanomotor-Enabled pH-Responsive Intracellular Delivery of Caspase-3: Toward Rapid Cell Apoptosis.

Berta Esteban-Fernández de Ávila, Doris E Ramírez-Herrera, Susana Campuzano, Pavimol Angsantikul, Liangfang Zhang, Joseph Wang

Open access · greenAbstract read
In one paragraph

Article in ACS nano, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
18.0field-weighted citation impact, top 1% 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

50 citing papers in PubMed, 199 citations in OpenAlex.

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  4. Micro/Nano-Motors for Enhanced Tumor Diagnosis and Therapy.International journal of molecular sciences · 2025
    Review
  5. Review
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  8. Review
  9. Biorobotic Drug Delivery for Biomedical Applications.Molecules (Basel, Switzerland) · 2024
    Review
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. Review
  18. Optical and Photoacoustic ImagingChemical & biomedical imaging · 2023
    Review
  19. Review
  20. 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

6 authors at 2 institutions in 2 countries.

Berta Esteban-Fernández de ÁvilaDepartment of Nanoengineering, University of California, San Diego , La Jolla, California 92093, United States.
Doris E Ramírez-HerreraDepartment of Nanoengineering, University of California, San Diego , La Jolla, California 92093, United States.
Susana CampuzanoDepartment of Analytical Chemistry, Complutense University of Madrid , E-28040 Madrid, Spain.
Pavimol AngsantikulDepartment of Nanoengineering, University of California, San Diego , La Jolla, California 92093, United States.
Liangfang ZhangDepartment of Nanoengineering, University of California, San Diego , La Jolla, California 92093, United States.ORCID 0000-0003-0637-0654
Joseph WangDepartment of Nanoengineering, University of California, San Diego , La Jolla, California 92093, United States.ORCID 0000-0002-4921-9674
University of California San Diego · USUniversidad Complutense de Madrid · ES

Funding

Tumor-Targeted Chemo-Immunotherapy for Osteosarcoma MetastasisR01CA200574 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI LI, SHULIN, ZHANG, LIANGFANG · 2016 to 2020
$1.8M
NCI NIH HHS R01 CA200574
6 · The paper itself

Abstract

Direct and efficient intracellular delivery of enzymes to cytosol holds tremendous therapeutic potential while remaining an unmet technical challenge. Herein, an ultrasound (US)-propelled nanomotor approach and a high-pH-responsive delivery strategy are reported to overcome this challenge using caspase-3 (CASP-3) as a model enzyme. Consisting of a gold nanowire (AuNW) motor with a pH-responsive polymer coating, in which the CASP-3 is loaded, the resulting nanomotor protects the enzyme from release and deactivation prior to reaching an intracellular environment. However, upon entering a cell and exposure to the higher intracellular pH, the polymer coating is dissolved, thereby directly releasing the active CASP-3 enzyme to the cytosol and causing rapid cell apoptosis. In vitro studies using gastric cancer cells as a model cell line demonstrate that such a motion-based active delivery approach leads to remarkably high apoptosis efficiency within a significantly shorter time and with a lower amount of CASP-3 compared to other control groups not involving US-propelled nanomotors. For instance, the reported nanomotor system can achieve 80% apoptosis of human gastric adenocarcinoma cells within only 5 min, which dramatically outperforms other CASP-3 delivery approaches. These results indicate that the US-propelled nanomotors may act as a powerful vehicle for cytosolic delivery of active therapeutic proteins, which would offer an attractive means to enhance the current landscape of intracellular protein delivery and therapy. While CASP-3 is selected as a model protein in this study, the same nanomotor approach can be readily applied to a variety of different therapeutic proteins.

Indexed as

ApoptosisCaspase 3Cell Line, TumorDelayed-Action PreparationsGoldHumansHydrogen-Ion ConcentrationNanowiresPolymersRecombinant ProteinsCASP3 protein, humanCaspase 3Delayed-Action PreparationsGoldPolymersRecombinant Proteinsapoptosiscaspase-3intracellular deliverynanomotorpH-responsive polymerultrasound

Identifiers

PMID28467853
PMCPMC5894870
OpenAlexW2611904495

What OpenQuestion holds

Textmetadata
LicenceTDM
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 OpenQuestion graph.