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Targeted Cancer Therapies02:57

Targeted Cancer Therapies

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The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
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An Activatable Caged Palladium Nanocomposite for Targeted Cancer Therapy.

Jiadong Tang1, Chi Li1, Wenjie Ma1

  • 1School of Chemistry and Molecular Engineering, East China Normal University, Shanghai, 200241, China.

Angewandte Chemie (International Ed. in English)
|March 26, 2025
PubMed
Summary
This summary is machine-generated.

We developed a novel palladium nanocomposite that enhances intracellular catalysis for disease treatment. This targeted system offers improved efficiency and controllable activity in tumor environments, enabling selective drug synthesis and therapy.

Keywords:
AptamerCatalyzed deprotectionChemotherapyMetal nanoclusterProdrug

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Area of Science:

  • Biomedical Engineering
  • Nanotechnology
  • Catalysis

Background:

  • Palladium nanoparticles (Pd NPs) show promise for intracellular catalysis but suffer from low efficiency, poor solubility, and constant activity.
  • Limitations include limited active sites and uncontrolled catalytic behavior, hindering therapeutic applications.

Purpose of the Study:

  • To develop a high-performance palladium nanocomposite for enhanced intracellular catalysis and targeted disease treatment.
  • To overcome the limitations of traditional Pd NPs through a cage-confined strategy.

Main Methods:

  • Synthesized ultrafine Pd NPs confined within molecular cages.
  • Incorporated glucose oxidase (GOx) and AS1411 aptamer-modified hyaluronic acid (HA).
  • Evaluated targeting ability and activatable catalysis in response to tumor microenvironment factors (acidic pH, hyaluronidase).

Main Results:

  • The cage-confined strategy yielded ultrafine Pd NPs with increased accessible active sites, boosting catalytic efficiency.
  • The nanocomposite demonstrated targeted delivery and activatable catalysis, enabling selective drug synthesis in tumor environments.
  • Exhibited CAT-, OXD-, and GPx-like activities, promoting ROS generation and GSH depletion for enhanced oxidative stress and therapy.

Conclusions:

  • The developed nanocomposite offers a high-performance metal-based intracellular catalytic system.
  • Cage confinement enhances Pd NP performance for bioorthogonal catalysis and targeted disease theranostics.
  • This approach enables the synthesis of molecules for effective disease treatment and diagnosis.