Photodynamic Antibacterial Nanofibers with Tunable Pro- and Antioxidant Activity via N,S-Doped Carbon Quantum Dots for Corneal Tissue Engineering

材料科学 纳米纤维 X射线光电子能谱 静电纺丝 纳米技术 生物相容性 聚己内酯 光化学 聚乙烯吡咯烷酮 共轭体系 化学工程 光敏剂 傅里叶变换红外光谱 活性氧 氧化还原 聚乙烯醇 纳米颗粒 量子产额 量子点 光谱学 光热治疗 阿普辛尼 表面改性 生物物理学 抗氧化剂 粘附 纳米医学 荧光 接触角 药物输送 组织工程 组合化学 核化学 荧光光谱法
作者
Roksana Kurpanik,Anna Ścisłowska‐Czarnecka,Zofia Kucia,Agnieszka Lechowska-Liszka,Nikola Lenar,Agnieszka Różycka,Marcin Sarewicz,Grzegorz M. Szewczyk,Ewa Stodolak‐Zych
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:17 (51): 68955-68972 被引量:4
标识
DOI:10.1021/acsami.5c16701
摘要

High Resolution Image Download MS PowerPoint Slide Antibiotic resistance poses a critical challenge in ocular medicine, where treatments must combine antibacterial potency with tissue compatibility. Electrospun core–shell nanofibers offer an attractive solution for ocular applications as they provide a biomimetic extracellular matrix structure with controlled drug release and surface functionality. In this work, polycaprolactone (PCL) was used as the mechanically robust, biodegradable core, while polyvinylpyrrolidone (PVP) formed a hydrophilic shell to enhance wettability and ocular compatibility. The nanofibers were further functionalized with N,S-doped carbon quantum dots, exhibiting light-switchable redox behavior. Compositional and spectroscopic analyses revealed that N,S-doped CQDs possessed a significantly narrowed bandgap (3.14 eV) relative to cysteine- and tryptophan-derived CQDs, attributable to heteroatom-induced defect states and the formation of π–π conjugated domains, confirmed by X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared spectroscopy (FT-IR). XPS measurements showed valence band energies suitable for superoxide generation under illumination, consistent with the reported redox potentials. As a result, illuminated nanofibers produced reactive oxygen species (ROS), reducing Escherichia coli and Staphylococcus aureus populations by 90% and 80%, respectively. In the dark, the same CQDs exhibited up to 90% radical-scavenging activity, increasing BJ human fibroblast viability by 35%. Additional mechanistic evidence indicated that light enhances the adhesion of CQDs to bacterial membranes, further promoting ROS-mediated inactivation. With a high quantum yield of 50% and strong blue fluorescence (λ em = 445 nm, λ ex = 380 nm), the CQDs also offer imaging and diagnostic potential. Together, these findings position N,S-doped CQDs-modified core–shell nanofibers as a biologically adaptive platform capable of photodynamic antibacterial action while supporting cytoprotection and tissue regeneration─an innovative approach for combating antibiotic-resistant ocular infections.
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