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Water and Solute Permeability of Plant Cuticles: Measurement and ...

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6.4 Simulation <strong>of</strong> Foliar Penetration 191<br />

-ln (1-M t /M 0)<br />

2.5 95<br />

2.0<br />

1.5<br />

1.0<br />

0.5<br />

0.026<br />

0.021<br />

8 x 10<br />

0.0<br />

0<br />

0 10 20 30 40 50 60<br />

-4<br />

0.071<br />

Time (h)<br />

tebuconazole<br />

2,4-D<br />

urea<br />

0.17<br />

0.047<br />

Fig. 6.23 Simulation <strong>of</strong> foliar penetration at 25 ◦ C using astomatous isolated Stephanotis CM.<br />

Small aqueous droplets (2µl) were pipetted on the centre <strong>of</strong> the outer surface <strong>of</strong> the CM, <strong>and</strong><br />

during the first 48 h evaporation was prevented by 100% humidity over the donor droplets. At 48 h,<br />

humidity was lowered to allow evaporation <strong>of</strong> solvent water, <strong>and</strong> desorption from the inner surface<br />

was continued. Means <strong>of</strong> 15–20 CM are shown. Numbers on regression lines are rate constants in<br />

s −1 . (Redrawn from Schönherr <strong>and</strong> Baur 1994)<br />

film (Tesafilm). A phospholipid suspension (PLS) served as receiver solution, <strong>and</strong><br />

0.5 ml were pipetted into the receiver compartment <strong>of</strong> the apparatus. The chambers<br />

were placed into the wells <strong>of</strong> the aluminium plate maintained at 25 ◦ C. The<br />

receiver solutions were withdrawn <strong>and</strong> replaced by fresh ones at 12 h intervals, <strong>and</strong><br />

radioactivity was determined by scintillation counting. After 48 h the Tesafilm was<br />

removed; the water <strong>of</strong> the droplets evaporated quickly, <strong>and</strong> desorption was resumed.<br />

At the end <strong>of</strong> the experiment the CM was cut out with a scalpel, the radioactive<br />

residues were dissolved in scintillation cocktail <strong>and</strong> counted. Data analysis was the<br />

same as in UDOS. The natural logarithms <strong>of</strong> (1 − Mt/M0) was plotted against time.<br />

The slopes <strong>of</strong> the lines are the rate constants <strong>of</strong> desorption (k), but their physical<br />

meaning differs from UDOS rate constant (k ∗ ) because in SOFP solutes are not<br />

dissolved in cutin. In the experiment depicted in Fig. 6.23, solutes were initially<br />

dissolved in water or in lactic acid buffer. Their state after droplet drying is uncertain.<br />

2,4-D was probably dissolved in concentrated lactic acid, <strong>and</strong> most <strong>of</strong> the very<br />

lipophilic tebuconazole was probably dissolved in epicuticular wax. Urea is hygroscopic,<br />

<strong>and</strong> all or part <strong>of</strong> it may have formed a concentrated urea solution. Due to<br />

these uncertainties, SOFP rate constants are more difficult to analyse.<br />

Desorption plots were linear both before <strong>and</strong> after droplet drying. Slopes measured<br />

with aqueous solutions are the rate constants, <strong>and</strong> they were constant both<br />

prior to <strong>and</strong> after droplet drying. Hence, solute concentrations in droplets decreased<br />

92<br />

86<br />

78<br />

63<br />

Percentage penetrated

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