Colorimetric Sensors for Recognition of Chiral Drugs Using Gold Nanoparticles

IF 3 4区 化学 Q2 CHEMISTRY, ANALYTICAL
Chirality Pub Date : 2025-05-30 DOI:10.1002/chir.70039
Asma Obaid, Nujud Maslamani, Ameerah Teqah, Hind Siddiq, Reem Ghubayra, Ibtisam Mousa, Arniza Khairani Mohd Jamil, Sharifah Mohamad
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Abstract

Using L-cysteine capped gold nanoparticles (L-Cys-AuNPs) as a colorimetric sensor, an easy, low-cost, and highly efficient strategy for the optical chiral identification of ketoprofen enantiomers was developed. R-ketoprofen tends to rapidly adsorb onto L-Cys-AuNPs, resulting in a color change of the solution from red to purple; however, no significant change was observed upon the addition of S-ketoprofen. The potential of L-cysteine capped with AuNPs (L-Cys-AuNPs) as chiral selectors for the recognition of ketoprofen enantiomers has been investigated using UV–Vis, FESEM, FT-IR, SERS, and zeta potential. The recognition process is easily identified by the naked eye or by using a UV–Vis spectrometer. Sensors L-Cys-AuNPs revealed a good linear response to ketoprofen enantiomers in the concentration range of 8.33–33.33 μM with a relative standard deviation of 3.08%. And detection limit of 2.35 μM. The proposed method was applied to determine the ketoprofen racemic mixture in water samples and commercial tablets. This method represents easy, inexpensive, simple, and very effective methods for the recognition of ketoprofen enantiomers.

Abstract Image

利用金纳米颗粒识别手性药物的比色传感器
利用l -半胱氨酸包盖金纳米粒子(L-Cys-AuNPs)作为比色传感器,建立了一种简单、低成本、高效的酮洛芬对映体光学手性鉴定方法。r -酮洛芬倾向于快速吸附在L-Cys-AuNPs上,导致溶液由红色变为紫色;然而,在添加s -酮洛芬后,没有观察到明显的变化。利用UV-Vis, FESEM, FT-IR, SERS和zeta电位研究了以AuNPs (L-Cys-AuNPs)封顶的l -半胱氨酸作为识别酮洛芬对映体的手性选择器的潜力。识别过程很容易通过肉眼或使用紫外-可见光谱仪识别。L-Cys-AuNPs对酮洛芬对映体在8.33 ~ 33.33 μM范围内具有良好的线性响应,相对标准偏差为3.08%。检测限为2.35 μM。该方法可用于水样和市售片剂中酮洛芬消旋混合物的测定。该方法是识别酮洛芬对映体的一种简便、廉价、简单、有效的方法。
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来源期刊
Chirality
Chirality 医学-分析化学
CiteScore
4.40
自引率
5.00%
发文量
124
审稿时长
1 months
期刊介绍: The main aim of the journal is to publish original contributions of scientific work on the role of chirality in chemistry and biochemistry in respect to biological, chemical, materials, pharmacological, spectroscopic and physical properties. Papers on the chemistry (physiochemical, preparative synthetic, and analytical), physics, pharmacology, clinical pharmacology, toxicology, and other biological aspects of chiral molecules will be published.
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