Hach-Lange LUMISTOX 300 LPV321 User Manual User Manual

Page 16

Advertising
background image

LUMIStox 300 Operating Manual

Dr. Bruno Lange GmbH

______________________________________________________________________________

______________________________________________________________________________

Page: 16

2.6 Determining the EC value

The EC value is the concentration of a sample that causes 20% (EC20) or 50% (EC50)

inhibition in the luminescent bacteria test (EC = effective concentration). A dilution

series of no less than 3 and no more than 9 dilution levels, for double determinations, is

used to determine these values. The LUMIStox 300 can only calculate an EC value if

the value lies within the concentrations for which 10 to 90% inhibition are measured in

the test. A single luminescent bacteria test can be used to determine EC values for up

to three incubation periods, e.g. for 5, 15 and 30 minutes. The control solution and 9

samples (dilutions) can be measured with one LUMIStherm.

Incorrect individual measurements of initial or final luminescence can be annulled

immediately with <C> and carried out again.

Work steps

1.

Prepare and dilute the sample(s).

2.

Pipette 1.5 ml sample (dilution) into measuring cuvettes and bring to the correct

temperature in row A of the LUMIStherm. The highest sample concentration

should be positioned on the extreme right.

3.

Bring 1.5 ml control solution (2% NaCl solution) to the correct temperature in

position A1 of the LUMIStherm.

4.

Reactivate the preserved bacteria as described in the package circular.

5.

Pipette 0.5 ml bacteria suspension into measuring cuvettes (2 per sample

dilution) and leave to stand for 15 minutes in rows B and C of the LUMIStherm to

acquire the correct temperature.

6.

Select evaluation mode <EC> and the required luminescent bacteria test, e.g.

<480> for LCK480, on the LUMIStox 300.

7.

Enter the initial settings for the test into the LUMIStox 300.

8.

Measure the initial luminescence of the bacteria at the specified time intervals.

9.

Immediately after each measurement, pipette 0.5 ml control solution or sample

dilution from the corresponding position in row A into the bacteria suspension in

row B or C. Wait for the residual incubation time to elapse.

10.

Measure the final luminescence of the control and test solutions for each of the

specified time intervals.

11.

Record or print the results.

Advertising