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Etude de différentes méthodes de biofonctionnalisation pour la ...

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III. <strong>Etu<strong>de</strong></strong>s du film Lan gmuir-Blodgett enzymatique<br />

All of the measurements were carried out in individual mo<strong>de</strong>. A saturated calomel electro<strong>de</strong> was<br />

used as reference electro<strong>de</strong>. The drain current and tension were fixed at loo pA and 0.5 V<br />

respectively.<br />

The steady state was obtained within 30s.<br />

In our work, we <strong>de</strong>termined the inhibition <strong>de</strong>gree of enzyme by comparing the activity of ENFETs<br />

before and after the inhibition.<br />

Vg<br />

SCE<br />

ODA<br />

enzyme<br />

Iso<strong>la</strong>te (Si02 +Sj<br />

Metal<br />

Electrolyte<br />

LB enzymatic<br />

me m b ra n e<br />

I(ÛTIIÌTÍIAÏ<br />

OTS<br />

Canal "<br />

Source<br />

Substrate Silicium<br />

////7///<br />

VD<br />

Figure 1. Schematic illustration of the BuChE-FET coated with an<br />

enzymatic LB fl/rn.<br />

3. Results and discussion<br />

3. 1. Surface pressure-area (r -A) isotherm characteristics of the Lan gmuir mono/ayers<br />

-A isotherms for the steary<strong>la</strong>mine mono<strong>la</strong>yer and mixed BuChE/steary<strong>la</strong>mine mono<strong>la</strong>yer are<br />

shown in Fig 2. Since the enzyme BuChE is generally negatively charged and amine is positively<br />

charged at the subphase pH =5.5.[20][21], BuChE molecules are adsorbed and permeated into the<br />

steary<strong>la</strong>mine mono<strong>la</strong>yer through this electrostatic force. After 3 hours of equilibration, the surface<br />

pressure kept constant and equal to 26 mN m1, then the mono<strong>la</strong>yer compression was carried out.<br />

Ill

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