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SPECTROSCOPIC ANALYSIS OF CHOLESTEROL ENZYME CHOX IN PVA ON THE INDICATOR ELECTRODE MEMBRANE OF CHOLESTEROL ANALYTE WITH THE POTENTIOMETRIC BIOSENSOR METHOD
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The spectrum pattern analysis of the urease enzyme immobilization technique in PVA, a PVA polymer that is soluble in warm water, has been carried out. There are differences in the spectrum patterns of PVA, PVA-KTpClPB and PVAEnzyme-KTpClPB solutions, respectively UVA, UVB and UVC. The purpose of this study was to create a cholesterol sensor whose analyte cholesterol on the indicator electrode was coated with a PVA-Enzyme cholesterol (ChOx)/GA 2.9%/PANI-p-toluenesulfonic acid/PVC-KTpClPB-o-NPOE 61% membrane. The method used is the potentiometric biosensor method of ChOx enzyme immobilization technique in PVA, which is symbolized by (PVA-E ChOx). This study was conducted by comparing the indicator electrode membrane coated with PVA- variation of Enzyme cholesterol (ChOx)/GA 2.9%/PANI-benzenesulfonic acid/PVC-KTpClPB-o-NPOE 61%. ChOx enzyme was varied at 1:1 and 1:3. The results of the UV-Vis analysis of ChOx enzyme immobilization in PVA obtained a spectrum pattern that was the same as the ChOx spectrum pattern on the ChOx enzyme 1:1. After obtaining the best results from the PVA-E ChOx membrane at 1:1. Continued coating of the first indicator electrode GA 2.9% / PANI-ptoluenesulfonic acid / PVC-KTpClPB-o-NPOE 61%. The second electrode GA 2.9% / PANI-benzenesulfonic acid / PVC-KTpClPB-o-NPOE 61%. Both membranes were analyzed by EDX, XRD, and FTIR, each placed on a tungsten wire and glass preparation, to determine the best membrane. The best membrane is PVA-E1 ChOx / GA 2.9% / PANIp-toluenesulfonic acid / PVC-KTpClPB-o-NPOE 61%.
Rasayan Journal of Chemistry
Title: SPECTROSCOPIC ANALYSIS OF CHOLESTEROL ENZYME CHOX IN PVA ON THE INDICATOR ELECTRODE MEMBRANE OF CHOLESTEROL ANALYTE WITH THE POTENTIOMETRIC BIOSENSOR METHOD
Description:
The spectrum pattern analysis of the urease enzyme immobilization technique in PVA, a PVA polymer that is soluble in warm water, has been carried out.
There are differences in the spectrum patterns of PVA, PVA-KTpClPB and PVAEnzyme-KTpClPB solutions, respectively UVA, UVB and UVC.
The purpose of this study was to create a cholesterol sensor whose analyte cholesterol on the indicator electrode was coated with a PVA-Enzyme cholesterol (ChOx)/GA 2.
9%/PANI-p-toluenesulfonic acid/PVC-KTpClPB-o-NPOE 61% membrane.
The method used is the potentiometric biosensor method of ChOx enzyme immobilization technique in PVA, which is symbolized by (PVA-E ChOx).
This study was conducted by comparing the indicator electrode membrane coated with PVA- variation of Enzyme cholesterol (ChOx)/GA 2.
9%/PANI-benzenesulfonic acid/PVC-KTpClPB-o-NPOE 61%.
ChOx enzyme was varied at 1:1 and 1:3.
The results of the UV-Vis analysis of ChOx enzyme immobilization in PVA obtained a spectrum pattern that was the same as the ChOx spectrum pattern on the ChOx enzyme 1:1.
After obtaining the best results from the PVA-E ChOx membrane at 1:1.
Continued coating of the first indicator electrode GA 2.
9% / PANI-ptoluenesulfonic acid / PVC-KTpClPB-o-NPOE 61%.
The second electrode GA 2.
9% / PANI-benzenesulfonic acid / PVC-KTpClPB-o-NPOE 61%.
Both membranes were analyzed by EDX, XRD, and FTIR, each placed on a tungsten wire and glass preparation, to determine the best membrane.
The best membrane is PVA-E1 ChOx / GA 2.
9% / PANIp-toluenesulfonic acid / PVC-KTpClPB-o-NPOE 61%.
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