Elemental Composition and Degradation Rate Impact the Biocompatibility of Copper Chalcogenide Nanocrystals

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Authors: Xingjian Zhong, G. Perry Katsarakes, Savani Nagarkar, Allison M. Dennis
Cited by: 1
References: 49

Abstract

High Resolution Image Download MS PowerPoint Slide Copper chalcogenide nanocrystals (NCs) are promising candidates for biophotonic applications due to their tunable optical properties. Concrete methods to examine the relationship between their degradation and toxicity are necessary to enable the development of nanoconstructs with reduced toxicity. This study compares the degradation and acute cytotoxicity of three compositions of micelle-coated copper chalcogenide NCs: the fluorescent semiconductor copper indium sulfide (CuInS 2 ), and two plasmonic semiconductors, copper sulfide (Cu 2– x S) and chalcopyrite copper iron sulfide (CuFeS 2 ). We developed a quantitative degradation assay to assess ion release from these ultrasmall nanocrystals, revealing that while all three particles biodegrade, CuInS 2 and CuFeS 2 undergo rapid degradation in an artificial lysosomal fluid, leading to a burst release of indium and iron ions. In cellular toxicity assays, CuInS 2 exhibited a significantly higher acute cytotoxicity than Cu 2– x S and CuFeS 2, primarily due to indium-induced necrosis. To mitigate this toxicity, an alternative surface-binding polymer coating was introduced, effectively reducing both the degradation rate and the cytotoxicity of CuInS 2 . These findings highlight the influence of both nanocrystal composition and coating chemistry in moderating the acute cytotoxicity of degradable nanocrystals, demonstrating that tuning of composition and degradation rate can be used to moderate nanoparticle toxicity.

Fields of Study & Subjects

Advanced Nanomaterials in Catalysis Selenium in Biological Systems Pineapple and bromelain studies

Publication details

Journal / source
ACS Applied Materials & Interfaces
Publisher
American Chemical Society (ACS)
Volume
18
Issue
9
Pages
14169–14180
Publication date
24 February 2026
Language
EN