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Gold-centered self-assemblies provide unique pharmacokinetic properties. Therefore, researchers widely explore them for applications in catalysis and biomedicine. Most existing materials utilize gold nanoparticles or nanoclusters. However, this study investigates Gold(III) complexes as building blocks for tailored architectures. Specifically, researchers developed a self-assembly strategy using a gold-nicotinamide complex. Consequently, this formed uniform nanospheres. Notably, these stimuli-responsive gold nanomaterials undergo reversible disassembly and reassembly into cubic structures upon pH changes.
Metal coordination between gold and nicotinamide formed the primary building blocks. These blocks then self-organized into spherical nanoparticles via noncovalent interactions. Specifically, π-π stacking and hydrogen bonding between amide groups stabilize the structure. Experimental data and theoretical calculations identified these driving forces. Furthermore, pH-mediated changes alter the balance of these noncovalent hierarchies. As a result, the particles switch their morphology reversibly between spheres and cubes.
This research highlights the critical role of ligand architecture in controlling assembly. For instance, the use of nicotinamide as a ligand enables precise morphological programming. In addition, the ability to switch shapes based on environmental stimuli is vital for drug delivery. Specifically, the acidic microenvironment of tumors could trigger shape changes in these nanocarriers. Therefore, this work establishes valuable principles for creating organometallic nanomaterials for precision medicine.
Stimuli-responsive systems offer superior control over drug release profiles. Moreover, reversible assembly ensures that nanoparticles can be "programmed" for specific physiological conditions. This level of control might reduce off-target toxicity in oncology treatments. Consequently, future developments may focus on integrating these Au(III) assemblies into diagnostic and therapeutic devices. This study provides a robust foundation for next-generation smart materials.
Changes in pH alter the balance of noncovalent interactions, such as hydrogen bonding and π-π stacking. This chemical shift forces the nanospheres to disassemble and reassemble into cubic nanoparticles.
While gold nanoparticles are common, Au(III) complexes offer unique square-planar geometries. This coordination allows for functionally tailored self-assembly that remains underexplored in traditional gold nanomedicine.
These materials are ideal for targeted drug delivery, optical sensing, and oncology, where external or internal triggers like pH are used to control material behavior.
Disclaimer: This content is for informational and educational purposes only. It does not constitute medical advice or a professional recommendation. The information provided is based on early-stage research and may not yet be applicable to clinical practice. Refer to the latest local and national guidelines for clinical practice.
References
1. Xiao Y et al. Morphological Programming in Gold(III) Coordination Assemblies via pH-Modulated Noncovalent Hierarchy. ACS Appl Mater Interfaces. 2026 May 07. doi: 10.1021/acsami.6c01466. PMID: 42095289.
2. Movia D et al. Latest advances in combining gold nanomaterials with physical stimuli towards new responsive therapeutic and diagnostic strategies. Precision Nanomedicine. 2024.
3. Cai KSY et al. Controlled Supramolecular Assemblies of Luminescent Tridentate Cyclometalated Alkynyl Gold (III) Amphiphiles in Aqueous Media. Beilstein Archives. 2026.
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