Advances Research on Nanomedicine

A special issue of Biomedicines (ISSN 2227-9059). This special issue belongs to the section "Biomedical Engineering and Materials".

Deadline for manuscript submissions: 31 May 2026 | Viewed by 1638

Special Issue Editor


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Guest Editor
State Key Laboratory of Molecular Developmental Biology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China
Interests: nanocluster; photo dynamic therapy (PDT); radio-dynamic therapy (RDT); bionanotechnology; bioimaging

Special Issue Information

Dear Colleagues,

This Special Issue, entitled “Advances Research on Nanomedicine”, aims to highlight the latest advancements in nanomedicine research and examine its broad application in health.

The scope of this Special Issue includes, but is not limited to, the following topics:

  1. Artificial Intelligence-Assisted Nanomedicine Synthesis
    • Exploring the integration of artificial intelligence in the design and production of nanomedicines to enhance efficiency and precision.
  2. Nanomedicine in Oncology Therapies
    • Investigating the application of nanomedicines in cancer treatments, focusing on reactive oxygen species (ROS)-based therapies such as photodynamic therapy (PDT), radiodynamic therapy (RDT), radiodynamic therapy (RDT), and chemodynamic therapy (CDT).
  3. Novel Nanomedicine Delivery Strategies
    • Exploring innovative methods for delivering nanomedicines to target tissues, including transdermal, intranasal, and interstitium routes.
  4. Nanomedicine and Tumor Immunotherapy
    • Examining how nanomedicines can enhance the effectiveness of tumor immunotherapies, potentially improving immune system responses against cancer.

We invite researchers, clinicians, and experts to submit original research articles, reviews, and commentaries that will contribute to the advancement of scientific knowledge and technological progress in the field of nanomedicine.

Dr. Rongcheng Han
Guest Editor

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Keywords

  • multifunctional nanomaterials
  • nanomedicine
  • tumor
  • theranostics
  • artificial intelligence (AI)
  • immunotherapy

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Published Papers (1 paper)

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Review

32 pages, 2350 KB  
Review
STING-Activating Nanoparticles Combined with PD-1/PD-L1 Blockade: A Synergistic Approach in Cancer Immunotherapy
by Dorota Bartusik-Aebisher, Kacper Rogóż and David Aebisher
Biomedicines 2025, 13(9), 2160; https://doi.org/10.3390/biomedicines13092160 - 4 Sep 2025
Viewed by 1351
Abstract
Objectives: Immunotherapy combining agonists of the cyclic GMP-AMP synthase–stimulator of interferon genes (cGAS-STING) pathway with PD-1/PD-L1 blockade shows promising preclinical results, although in clinical practice, it faces pharmacokinetic barriers, systemic toxicity, and an immunosuppressive tumor microenvironment (TME). Recent advances in and expansion [...] Read more.
Objectives: Immunotherapy combining agonists of the cyclic GMP-AMP synthase–stimulator of interferon genes (cGAS-STING) pathway with PD-1/PD-L1 blockade shows promising preclinical results, although in clinical practice, it faces pharmacokinetic barriers, systemic toxicity, and an immunosuppressive tumor microenvironment (TME). Recent advances in and expansion of the cGAS-STING pathway as a therapeutic target have further highlighted its central role in innate and adaptive immune activation. The aim of this paper is to review combination strategies of STING and PD-1/PD-L1 checkpoint blockade therapies, triple-therapy strategies using a third component such as chemotherapy, radiotherapy, photodynamic therapy (PDT), and others, and the use of nanoparticles as carriers for these drugs. Methods: Reports in the literature on the mechanisms of STING + PD-1/PD-L1 synergy, as well as with the use of a third component and delivery systems, were analyzed. Current challenges and limitations, as well as prospects for the development of these therapies, are noted. Results: Activation of the cGAS-STING synergizes with blocking the PD-1/PD-L1 axis. The addition of a third component further enhances the anti-tumor effect through a stronger induction of immunogenic cell death (ICD), increased production of interferons and pro-inflammatory cytokines, repolarization of macrophages, and enhanced infiltration of T lymphocytes. Conclusions: Therapy with STING agonists and PD-1/PD-L1 checkpoint inhibitors, supported by nanotechnology vehicles and using a third therapeutic component, overcomes key pharmacological and immunological limitations. This multimodal immunotherapeutic strategy holds high translational promise, offering more effective and safer solutions in cancer immunotherapy. Full article
(This article belongs to the Special Issue Advances Research on Nanomedicine)
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