Team:Aachen/Safety

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(Biosafety)
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= Biosafety =
= Biosafety =
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Our iGEM team is committed to consider all aspects of the entire project, including biosafety. For this project, two biosafety aspects have to be consider. On the one hand, we are using ''E.coli'' as genetically modified organism, and on the other hand, we are detecting ''Pseudomonas aeruginosa'', a human pathogen. While using ''P. aeruginoas'', we should prevent proliferation. For ''E.coli'', we have to look after the non-release of genetically modified organisms. In general, we developed and designed the measurement device as closed system for a better safety handling. This way, neither the sampled pathogens nor the genetically modified sensor cells can escape our biosensor unit. Moreover, the electronic components are in a separate compartment and inaccessible for the user, preventing electric shock or other injuries. For the detection, we are using one-time usage sampling and sensor chips which can be disposed of after autoclaving or irradation with strong UV light.
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Our iGEM team is committed to consider all aspects of the entire project, including biosafety. For this project, two biosafety aspects have to be consider. On the one hand, we are using ''E.coli'' as ''''genetically modified organism'''', and on the other hand, we are detecting ''Pseudomonas aeruginosa'', a '''human pathogen'''. When sampling ''P. aeruginosa'', we should prevent proliferation and spread of the bacterium. For ''E.coli'', we have to look after the non-release of genetically modified organisms. In general, we developed and designed the measurement device as '''closed system''' for a better safety handling. This way, neither the sampled pathogens nor the genetically modified sensor cells can escape our biosensor unit. Moreover, the electronic components are in a separate compartment and inaccessible for the user, preventing electric shock or other injuries. For the detection, we are using one-time usage sampling and sensor chips which can be disposed of after '''autoclaving or irradation''' with strong UV light.
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To detect ''P. aeruginosa'' cells, an sampling agar chip is slightly pressed against the solid surface to be tested. Afterwards, the sampling chip is immediately introduced into our measurement device and will not be removed until the detection is finished and the chips have be doused with disinfectant. The sensor chips must be handled in S1 environments only since they contain genetically modified ''E. coli''. However, once introduced into the measurement device, the sensor chips, too, will not be removed before disinfection.  
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To detect ''P. aeruginosa'' cells, an sampling agar chip is slightly pressed against the solid surface to be tested. Afterwards, the sampling chip is immediately introduced into our measurement device and will not be removed until the detection is finished and the chips have be doused with disinfectant. The sensor chips must be handled in '''S1 environments only''' since they contain genetically modified ''E. coli''. However, once introduced into the measurement device, the sensor chips, too, will not be removed before disinfection.  
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The living cells inside the measurement device are effectively killed after a detection by using desinfectants such as Bacillol. For this procedure, the drawer of the measurement device is opened and Bacillol is poured over the sampling and sensor chips. Afterwards, both chips can be autoclaved and be disposed of. The whole lining of the measurement device is build from plastic so that it can be disinfected easily.
+
The living cells inside the measurement device are effectively killed after a detection by '''using desinfectants''' such as Bacillol. For this procedure, the drawer of the measurement device is opened and Bacillol is poured over the sampling and sensor chips. Afterwards, both chips can be autoclaved and be disposed of. The whole lining of the measurement device is build from plastic so that it can be disinfected easily.
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To simulate the worst case scenario, we did replica plating of some sensor chips. In three experiments, we got an arithmetic mean of five colonies which were picked up. We concluded that the risk of infection is still really low even if the measurement device and chips are not handled properly.
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To '''simulate the worst case scenario''', we did replica plating of some sensor chips. In three experiments, we got an arithmetic mean of five colonies which were picked up. We concluded that the '''risk of infection is really low''' even if the measurement device and chips are not handled properly.
{{Team:Aachen/Footer}}
{{Team:Aachen/Footer}}

Revision as of 16:11, 8 October 2014

Biosafety

Our iGEM team is committed to consider all aspects of the entire project, including biosafety. For this project, two biosafety aspects have to be consider. On the one hand, we are using E.coli as 'genetically modified organism', and on the other hand, we are detecting Pseudomonas aeruginosa, a human pathogen. When sampling P. aeruginosa, we should prevent proliferation and spread of the bacterium. For E.coli, we have to look after the non-release of genetically modified organisms. In general, we developed and designed the measurement device as closed system for a better safety handling. This way, neither the sampled pathogens nor the genetically modified sensor cells can escape our biosensor unit. Moreover, the electronic components are in a separate compartment and inaccessible for the user, preventing electric shock or other injuries. For the detection, we are using one-time usage sampling and sensor chips which can be disposed of after autoclaving or irradation with strong UV light.

To detect P. aeruginosa cells, an sampling agar chip is slightly pressed against the solid surface to be tested. Afterwards, the sampling chip is immediately introduced into our measurement device and will not be removed until the detection is finished and the chips have be doused with disinfectant. The sensor chips must be handled in S1 environments only since they contain genetically modified E. coli. However, once introduced into the measurement device, the sensor chips, too, will not be removed before disinfection.

The living cells inside the measurement device are effectively killed after a detection by using desinfectants such as Bacillol. For this procedure, the drawer of the measurement device is opened and Bacillol is poured over the sampling and sensor chips. Afterwards, both chips can be autoclaved and be disposed of. The whole lining of the measurement device is build from plastic so that it can be disinfected easily. To simulate the worst case scenario, we did replica plating of some sensor chips. In three experiments, we got an arithmetic mean of five colonies which were picked up. We concluded that the risk of infection is really low even if the measurement device and chips are not handled properly.