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1.
Anal Chim Acta ; 1070: 104-111, 2019 Sep 06.
Article in English | MEDLINE | ID: mdl-31103163

ABSTRACT

Herein, we introduce a nanopaper-based analytical device (NAD) or "lab-on-nanopaper" device for visual sensing of human serum albumin (HSA) in human blood serums, which relies on embedding of curcumin within transparent bacterial cellulose (BC) nanopaper. BC nanopaper is an appropriate candidate to be an excellent platform for the development of optical (bio)sensors due to having exceptional properties such as optical transparency, high flexibility, porosity, biodegradability, and printability. The hydrophilic test zones were created on the fabricated bioplatform through creating the hydrophobic walls via laser printing technology. The color changes of curcumin embedded in BC nanopaper (CEBC) due to the inhibitory effect of HSA on the curcumin degradation in alkaline solutions, which can be monitored visually (naked eye/Smartphone camera) or spectroscopically using a spectrophotometer, were linearly proportional to the HSA concentration in the range of 10-300 µM and 25-400 µM, respectively. The developed NAD/CEBC as a novel albumin assay kit was successfully utilized to the determination of HSA in human blood serum samples with satisfactory results. Building upon the fascinating features of BC nanopaper as a very promising bioplatform in optical (bio)sensing applications we are confident "lab-on-nanopaper" devices/NADs, which take the advantages of the nanopaper and also meet the ASSURED criteria, could be considered as a new generation of optical (bio)sensing platforms that are currently based on paper, glass or plastic substrates.


Subject(s)
Bacteria/chemistry , Cellulose/chemistry , Curcumin/chemistry , Nanostructures/chemistry , Paper , Serum Albumin, Human/analysis , Humans
2.
Talanta ; 77(3): 1032-6, 2009 Jan 15.
Article in English | MEDLINE | ID: mdl-19064087

ABSTRACT

A novel optical sensor based on a redox reaction for the determination of iodide has been developed. The optode membrane is constructed by immobilization of methyltrioctylammonium chloride on triacetylcellulose polymer. The exchange of chloride as counter ion with iodate in the membrane changes the color to yellow, when it is placed in acidic solution of iodide. The sensor can readily be regenerated by 0.1 mol L(-1) NaOH in less than 15s. The optode has a linear range of 3.94 x 10(-6) to 5.51 x 10(-5)mol L(-1) of iodide ions with a limit of detection 7.44 x 10(-7)mol L(-1). The relative standard deviation for eight replicate measurements of 3.94 x 10(-6) and 1.57 x 10(-5)mol L(-1) of iodide was 2.83 and 1.38%, respectively. The sensor was successfully applied to the determination of iodide in tablet, powdered milk and urine samples.


Subject(s)
Iodides/analysis , Iodides/chemistry , Spectrophotometry/methods , Animals , Ions/chemistry , Milk/chemistry , Oxidation-Reduction , Reproducibility of Results , Sulfuric Acids/chemistry , Urine/chemistry
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