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
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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