生物膜
化学
纳米颗粒
抗生素
细胞外基质
金属
基质(化学分析)
胞外聚合物
细菌
细胞外
化学工程
纳米技术
材料科学
色谱法
生物化学
有机化学
生物
工程类
遗传学
作者
Wafaa Aljuhani,Matthew P. Wylie,Rudra N. Purusottam,Colin P. McCoy,Steven E. J. Bell
出处
期刊:Biomacromolecules
[American Chemical Society]
日期:2025-04-07
卷期号:26 (5): 2900-2908
被引量:5
标识
DOI:10.1021/acs.biomac.4c01707
摘要
Understanding the interplay between nanoparticles, biomaterials and drug molecules in biological environments is important but studying these interactions in complex systems such as biofilms is challenging. Here, surface-enhanced Raman spectroscopy (SERS) with gold nanostars (NS) was used to monitor how biofilm components influence the binding and SERS signals of two antibiotics, levofloxacin (Levo) and ampicillin (Amp). The SERS signals of both antibiotics were reduced by approximately 70% (Levo) and 90% (Amp) in biofilm environments. Investigations of mixtures of model biofilm components: adenine (nucleic acids), alginate (polysaccharides) and albumin (proteins), revealed that their interactions with NS are governed by coupled equilibria. This gave surprising results, for example, alginate reduced the interference from adenine and albumin, so adding alginate increased the intensity of the antibiotic signals 4x. These findings highlight the importance of matrix component interactions in modulating detection sensitivity and show that these effects are critical in allowing clinically relevant detection levels to be achieved.
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