A CO2-Responsive Imidazole-Functionalized Fluorescent Material Mediates Cancer Chemotherapy

Author:

Ngan Vo Thuy Thien1,Chiou Po-Yen1,Ilhami Fasih Bintang1ORCID,Bayle Enyew Alemayehu1ORCID,Shieh Yeong-Tarng2,Chuang Wei-Tsung3ORCID,Chen Jem-Kun4ORCID,Lai Juin-Yih1567,Cheng Chih-Chia15ORCID

Affiliation:

1. Graduate Institute of Applied Science and Technology, National Taiwan University of Science and Technology, Taipei 10607, Taiwan

2. Department of Chemical and Materials Engineering, National University of Kaohsiung, Kaohsiung 81148, Taiwan

3. National Synchrotron Radiation Research Center, Hsinchu 30076, Taiwan

4. Department of Materials Science and Engineering, National Taiwan University of Science and Technology, Taipei 10607, Taiwan

5. Advanced Membrane Materials Research Center, National Taiwan University of Science and Technology, Taipei 10607, Taiwan

6. R & D Center for Membrane Technology, Chung Yuan Christian University, Chungli, Taoyuan 32023, Taiwan

7. Department of Chemical Engineering and Materials Science, Yuan Ze University, Chungli, Taoyuan 32003, Taiwan

Abstract

We present a breakthrough in the synthesis and development of functional gas-responsive materials as highly potent anticancer agents suitable for applications in cancer treatment. Herein, we successfully synthesised a stimuli-responsive multifunctional material (I-R6G) consisting of a carbon dioxide (CO2)-sensitive imidazole moiety and spirolactam-containing conjugated rhodamine 6G (R6G) molecule. The resulting I-R6G is highly hydrophobic and non- or weakly fluorescent. Simple CO2 bubbling treatment induces hydrophobic I-R6G to completely dissolve in water and subsequently form self-assembled nanoparticles, which exhibit unique optical absorption and fluorescence behaviours in water and extremely low haemolytic ability against sheep red blood cells. Reversibility testing indicated that I-R6G undergoes reversible CO2/nitrogen (N2)-dependent stimulation in water, as its structural and physical properties can be reversibly and stably switched by alternating cycles of CO2 and N2 bubbling. Importantly, in vitro cellular assays clearly demonstrated that the CO2-protonated imidazole moiety promotes rapid internalisation of CO2-treated I-R6G into cancer cells, which subsequently induces massive levels of necrotic cell death. In contrast, CO2-treated I-R6G was not internalised and did not affect the viability of normal cells. Therefore, this newly created system may provide an innovative and efficient route to remarkably improve the selectivity, safety and efficacy of cancer treatment.

Funder

Ministry of Science and Technology, Taiwan

Publisher

MDPI AG

Subject

Pharmaceutical Science

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