A chemiluminescence method for the determination of verapamil hydrochloride in pharmaceutical and environmental samples based on an Fe3O4 nanoparticles enhanced NaHCO3–H2O2 system

2017 ◽  
Vol 9 (47) ◽  
pp. 6705-6712 ◽  
Author(s):  
Mortaza Iranifam ◽  
Nasim Rahmati Hendekhale

In this work, an Fe3O4 nanoparticles (NPs)-enhanced chemiluminescence (CL) method was developed for the determination of verapamil hydrochloride (VRP).

2018 ◽  
Vol 10 (5) ◽  
pp. 541-547 ◽  
Author(s):  
Junmei Zhang ◽  
Xiaoxia Chen ◽  
Yue Li ◽  
Suqin Han ◽  
Yao Du ◽  
...  

Nitrogen doped carbon quantum dots (NCQDs) were synthesized via an ultrasonic method with ascorbic acid as the carbon source and ammonia as the nitrogen source.


2017 ◽  
Vol 41 (19) ◽  
pp. 10659-10667 ◽  
Author(s):  
Javad Hassanzadeh ◽  
Alireza Khataee ◽  
Yones Mosaei Oskoei ◽  
Hassan Fattahi ◽  
Nafiseh Bagheri

A novel molecularly imprinted polymer (MIP) based chemiluminescence (CL) assay is described for the determination of TNT in environmental samples.


2016 ◽  
Vol 78 (2) ◽  
pp. 446-456 ◽  
Author(s):  
Sara Karimi Behzad ◽  
Mostafa M. Amini ◽  
Ali Balati ◽  
Mohammad Ghanbari ◽  
Omid Sadeghi

RSC Advances ◽  
2018 ◽  
Vol 8 (42) ◽  
pp. 23720-23726 ◽  
Author(s):  
Huihui Xu ◽  
Qiyong Cai ◽  
Qiuyu Nie ◽  
Zhun Qiao ◽  
Song Liu ◽  
...  

An ultrasensitive CL system for the determination of ascorbic acid in medicinal tablets was developed based on the enhancement effect of cobalt oxyhydroxide nanosheets on the luminol–H2O2 system.


2007 ◽  
Vol 61 (7) ◽  
pp. 706-710 ◽  
Author(s):  
Xiaofeng Xie ◽  
Xili He ◽  
Zhenghua Song

A novel chemiluminescence method combined with the flow injection technique for the determination of carbon monoxide is presented in this paper. The chemiluminescence signal based on the reaction between myoglobin and luminol in an alkaline medium was remarkably enhanced by carbon monoxide. The enhanced chemiluminescence intensity was linear with carbon monoxide concentration in the range from 0.01 to 10.0 pmol·L−1, and the detection limit was 3 × 10−3 pmol·L−1 (3σ). The whole process, including sampling and washing, could be completed in 0.5 min with a relative standard deviation of less than 4.0%. The proposed method was applied successfully in the assay of carbon monoxide in human serum and artificial water samples without any pretreatment procedure.


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