Fast screening method for early diagnostic of gastric cancer based on utilization of a chitosan - S-doped graphene - based needle stochastic sensors.

Needle stochastic sensors were developed for the assay of carbohydrate antigen 19-9 (CA 19-9) and carcinoembryonic antigen (CEA) in different biological samples (e.g., whole blood, tissues, urine, and saliva). Sulfur doped graphene powders were modified with chitosan; paraffin oil was added to form a homogeneous paste that was used as active side of the stochastic sensors. High sensitivities and low limits of determination were achieved for the assay of CA19-9 and CEA in biological samples. The validation of the proposed screening method (which is utilizing the stochastic sensors as screening tools) was made by using real biological samples obtained from confirmed patients with gastric cancer; very good correlations for the concentrations of CEA and CA19-9 were obtained using the needle stochastic sensors.

Rhodamine B - as New Chromophore for the Determination of Melatonin in Biological, Food, and Pharmaceutical Samples.

AIM AND OBJECTIVE: Melatonin is an essential biomarker for sleep-related disorders. Reliable methods of analysis are needed for melatonin. Therefore, a new chromophore (Rhodamine B) was proposed for the assay of melatonin; this method succeeded to enlarge the working concentration range and to decrease the limit of determination comparing with the method that just used the native fluorescence of melatonin. MATERIALS AND METHODS: Rhodamine B was proposed as a new chromophore for the assay of melatonin in biological, food, and pharmaceutical samples. Fluorescence was used for the determination of melatonin. RESULTS: The results obtained using Rhodamine B were compared with those obtained by the native fluorescence of melatonin. Using the new chromophore, melatonin was determined in the concentration range between 0.01 and 50 pmol L-1, with the detection limit of 2.4 fmol L-1. The recovery of melatonin was higher than 98.00% with a relative standard deviation of less than 0.10%, when the method was applied for the assay of melatonin in samples such as breast milk, whole blood, milk powder, and pharmaceutical formulations. CONCLUSION: Utilization of Rhodamine B enlarged the linear concentration range for the assay of melatonin and decreased the detection limit, making possible the assay of melatonin in a variety of samples such as pharmaceuticals, food, and biological samples.