A Novel and Highly Sensitive Resonance Scattering Spectral Assay for Horseradish Peroxidase Using Cationic Surfactant
A novel and ultrasensitive resonance scattering (RS) spectral assay was proposed for detection of horseradish peroxidase (HRP) activity. It was based on that the HRP strongly catalyze H 2 O 2 oxidation of excess I − to form , the resulting combined with four cationic surfactant (CS), including tetra...
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Veröffentlicht in: | Journal of fluorescence 2008-11, Vol.18 (6), p.1059-1064 |
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Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
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Zusammenfassung: | A novel and ultrasensitive resonance scattering (RS) spectral assay was proposed for detection of horseradish peroxidase (HRP) activity. It was based on that the HRP strongly catalyze H
2
O
2
oxidation of excess I
−
to form
, the resulting
combined with four cationic surfactant (CS), including tetradecyl pyridinium bromide (TPB), cetyltrimethyl ammonium bromide (CTMA), cetylpyridinium chloride (CPCM) and tetradecyl dimethylbenzyl ammonium chloride (TDMBA) to produce association particles (TPB-I
3
)
n
, (CTMA-I
3
)
m
, (CPCM-I
3
)
l
and (TDMBA-I
3
)
k
, which exhibit a strongest resonance scattering peak at 478, 423, 538 and 491 nm, respectively. For the four systems of TPB, CPCM, CTMBA and TDMBA, the HRP activity determined was in the linear range of 0.004–5.6, 0.04–3.2, 0.04–8.0, 0.08–8.0 ng/mL, with a detection limit of 0.0034, 0.040, 0.033, 0.016 ng/mL, respectively. The TPB resonance scattering spectral assay was best and has been applied to the analysis of HRP in real samples, with satisfactory results. |
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ISSN: | 1053-0509 1573-4994 |
DOI: | 10.1007/s10895-008-0350-1 |