A reductant colorimetric method for the rapid detection of certain cephalosporins via the production of gold and silver nanoparticles

被引:13
作者
Ali, Ramadan [1 ]
Ali, Hassan Refat H. [2 ]
Batakoushy, Hany A. [1 ]
Derayea, Sayed M. [3 ]
Elsutohy, Mohamed M. [1 ]
机构
[1] Al Azhar Univ, Fac Pharm, Dept Pharmaceut Analyt Chem, Assiut 71524, Egypt
[2] Assiut Univ, Fac Pharm, Dept Pharmaceut Analyt Chem, Assiut 71526, Egypt
[3] Menia Univ, Fac Pharm, Dept Analyt Chem, Al Minya 61519, Egypt
关键词
Cephalosporins analysis; Gold nanoparticles; Silver nanoparticles; Surface plasmon resonance; Clinical laboratories; PHARMACEUTICAL FORMULATIONS; SPECTROFLUOROMETRIC METHOD; CEFEPIME; SODIUM; SIZE; NEUROTOXICITY; ANTIBIOTICS; DEGRADATION; MECHANISMS; GREEN;
D O I
10.1016/j.microc.2019.02.023
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A simple colorimetric method for the quantitative detection of two cephalosporins, cefoperazone (CFZ) and cefepime (CPM), has been developed and validated for the application in clinical and quality control laboratories. The method was based on exploiting the reducing properties of cephalosporins due to the 7-aminoce-phalosporanic acid dihydrothiazine and a beta-lactam ring to produce gold (GNPs) or silver (AgNPs) nanoparticles from their corresponding metal solutions. The resulting nanoparticles exhibited surface plasmon resonance signals at 530-550 nm or 430 nm for GNPs or AgNPs, respectively, with an intensity dependent on drug concentration that permits the quantitative analysis. Furthermore, the resulting nanoparticles were characterised using a dynamic light scattering instrument and transmission electron microscopy. Factors influence the reaction, such as the reagents volume, pH, temperature and reaction time, have been studied and optimised. In addition, the study was validated according to the official guidelines and extended to evaluate the antimicrobial activity to assess potential drug degradation during the analysis. Overall, the method developed in this study can be used for the quantitative analysis of CFZ and CPM in pure forms and pharmaceutical preparations with relatively good sensitivity and selectivity as well as, acceptable accuracy and precision.
引用
收藏
页码:864 / 871
页数:8
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