A Green and Simple Carbon-dot-based Fluorescent Probe for Selective and Sensitive Detection of Ranitidine Hydrochloride

被引:0
|
作者
Mohammadi, Nahideh [1 ]
Akhgari, Farhad [2 ]
Samadi, Naser [1 ]
机构
[1] Urmia Univ, Fac Chem, Dept Analyt Chem, Orumiyeh, Iran
[2] Malek Ashtar Univ Technol, Fac Pass Def, Tehran, Iran
来源
关键词
Carbon dots; Green synthesis; Urtica dioica; Ranitidine hydrochloride; Fluorescence quenching; ONE-STEP SYNTHESIS; QUANTUM DOTS; RECENT PROGRESS; NITROGEN; CARBONIZATION; NANOPARTICLES; NANOSENSOR; IONS; ACID;
D O I
暂无
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Herein, a novel fluorescent probe was designed and synthesized for the selective and sensitive detection of ranitidine hydrochloride based on the quenched fluorescence signal of carbon dots (CDs). The one-step hydrothermal treatment of Urtica dioica extract was used to prepare CDs. The as-synthesized CDs exhibited excellent water dispersibility and had a blue color under UV light irradiation (365 nm) with 12.49% of quantum yield (QY). The structural and optical properties of CDs were investigated using UV-Vis spectrophotometer, transmission electron microscopy (TEM), and Fourier transform infrared (FT-IR) spectroscopy. The as-synthesized CDs were used as a simple, sensitive, and inexpensive probe for the detection of ranitidine hydrochloride in pharmaceutical samples. The absorption spectrum of ranitidine overlapped with the excitation spectrum of CDs and the fluorescence intensity of CDs effectively decreased with the increase of ranitidine concentration due to the inner filter effect (IFE). A fluorometric assay was formed based on these findings that had a linear response in the ranitidine hydrochloride concentration range of 0.167-14.03 mu g ml(-1) with a detection limit as low as 0.081 mu g ml(-1). This new sensing assay was green and had beneficial features such as simplicity, rapidity, inexpensiveness, and ease of operation without the need for further modification. Using the suggested method, ranitidine hydrochloride was successfully measured in the pharmaceutical preparations.
引用
收藏
页码:525 / 536
页数:12
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