Binary mineral nanoparticles enable intravascular delivery of metal ions to tumors for metalloimmunotherapy

Although disruptions in metal ion homeostasis leading to severe cellular damage and regulated cell death are a promising strategy for cancer immunotherapy, challenges in overloading these ions to tumor cells without premature release have limited their therapeutic applications. In this study, we develop binary mineral nanoparticles incorporating both Ca<sup>2+</sup> and Na<sup>+</sup> ions to enhance the cytotoxic effects of ion interference in cancer immunotherapy. Engineered using a microfluidic system for uniform size distribution and scalability, these nanoparticles exhibit pH-sensitive ion release. Systemically administered, they preferentially accumulate in tumors, elevating intracellular Ca<sup>2+</sup> and Na<sup>+</sup> levels and inducing immunogenic cell death without calcium channel activators or other small-molecule inducers. Our binary mineral nanoparticles significantly enhance antitumor immunity, especially when combined with an immune checkpoint inhibitor, leading to long-term immunity and inhibition of metastasis. This nanotechnology-enabled synergistic delivery of Ca²⁺ and Na⁺ ions represents a promising adjunct to existing metalloimmunotherapy strategies for cancer eradication.

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Journal
Nature Communications
Published
2026-01-12
DOI
https://doi.org/10.1038/s41467-025-68279-y
Primary Topic
Nanoplatforms for cancer theranostics
Type
article
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article

Binary mineral nanoparticles enable intravascular delivery of metal ions to tumors for metalloimmunotherapy

Basavaraj R. Patil, Jong Oh Kim, Ngoc Duy Le, Bảo Lộc Nguyễn et al.
Nature Communications
Nanoplatforms for cancer theranostics
article

Binary mineral nanoparticles enable intravascular delivery of metal ions to tumors for metalloimmunotherapy

Basavaraj R. Patil, Jong Oh Kim, Ngoc Duy Le, Bảo Lộc Nguyễn, Chang Jae-Hoon, Daehyeon Ahn, Jung Min Lee, Sae Kwang Ku, Thi Oanh Oanh Nguyen, Duc-Vinh Pham, Jeonghwan Kim, Cao Dai Phung, Beomsu Kim, Jiwoo Hong
article en

Abstract

Although disruptions in metal ion homeostasis leading to severe cellular damage and regulated cell death are a promising strategy for cancer immunotherapy, challenges in overloading these ions to tumor cells without premature release have limited their therapeutic applications. In this study, we develop binary mineral nanoparticles incorporating both Ca<sup>2+</sup> and Na<sup>+</sup> ions to enhance the cytotoxic effects of ion interference in cancer immunotherapy. Engineered using a microfluidic system for uniform size distribution and scalability, these nanoparticles exhibit pH-sensitive ion release. Systemically administered, they preferentially accumulate in tumors, elevating intracellular Ca<sup>2+</sup> and Na<sup>+</sup> levels and inducing immunogenic cell death without calcium channel activators or other small-molecule inducers. Our binary mineral nanoparticles significantly enhance antitumor immunity, especially when combined with an immune checkpoint inhibitor, leading to long-term immunity and inhibition of metastasis. This nanotechnology-enabled synergistic delivery of Ca²⁺ and Na⁺ ions represents a promising adjunct to existing metalloimmunotherapy strategies for cancer eradication.

Nature CommunicationsVol. 17(1)
Daegu Haany University (KR), Soongsil University (KR), Yeungnam University (KR)
Good health and well-being
Openalex Percentile: Top 91%
Nanoplatforms for cancer theranostics
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Binary mineral nanoparticles enable intravascular delivery of metal ions to tumors for metalloimmunotherapy — Basavaraj R. Patil, Jong Oh Kim, et al. · Nature Communications (2026) | TGRS Research Map | TGRS