Title of article :
Molecular recognition of pyrimidine and xanthine bases by lipophilic calixarenes derived from resorcinol. Part II
Author/Authors :
Pietraszkiewicz، نويسنده , , O and Brzَzka، نويسنده , , Z and Pietraszkiewicz، نويسنده , , M، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2001
Pages :
4
From page :
117
To page :
120
Abstract :
Ion-selective field effect transistors (ISFETs) were tested for their suitability for clinical work. They were intended for use in the analysis of blood and serum, where the concentration of specific ions, e.g. sodium and potassium, is of critical importance. The optical sensitivity of ISFETs and a new membrane composition for use in the clinical chemistry were evaluated. ISFETs with a polyimide/valinomycin membrane were shown to operate satisfactorily in the presence of proteins, encouraging the further development of these ISFETs as clinical sensors. ETH 2041 (tetra-n-undecyl 3,3′, 4,4′–benzophenone tetracarboxylate) and DGD (diethylene dibenzoate) were the plasticizers used and their performances were compared. Valinomycin was used as ionophore. The membranes were calibrated using the dip (solutions in the 10−1–10−5 mol dm−3 KCl range) and the constant volume dilution methods. Both membrane compositions gave good Nernstian responses. The ETH 2041 plasticizer was found to yield devices more selective to potassium ion than the more easily usable DGD.
Keywords :
Molecular recognition , Lipophilic calixarenes , Resorcinol
Journal title :
Materials Science and Engineering C
Serial Year :
2001
Journal title :
Materials Science and Engineering C
Record number :
2097586
Link To Document :
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