Why do we use Mint in toothpaste?

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Experiment To If Garlic or Mint is More Antibacterial.

Aim: 
To see what substance would be most ideal in toothpaste, by seeing what is the most antibacterial, out of garlic and mint.


Hypothesis:
I would expect mint to have some antibacterial properties, as it is used in nearly all toothpaste and is quite a strong tasting and smelling substance. However, garlic is very strong and when I eat a clove of garlic I got a far more strong, intense, hot feeling in my mouth, more so than mint. So I would expect garlic to be more antibacterial than garlic, but mint to be used in toothpaste for it’s taste.

Apparatus:

Agar Plate.

Bacteria Culture.

Garlic and Mint Extracts (liquid form).

Industrial Methylated Spirits.

Beakers.

Pipette.

Bunsen Burner.

Glass Spreader.

Small Paper Discs.

Petri Dish.

Forceps.

Sellotape.

Incubator.


Method:

First of all, I disinfected my work space, by rubbing methylated sprits over it. It then opened my culture, and using a new, sterilised pipette, I placed 1ml on the agar, and with the sterilised spreader (sterilised by running it over a Bunsen flame) I spreaded the culture evenly over agar plate and placed the Petri dish cover on top. I sterilised my glass spreader by dipping it in the beaker of methylated spirits, took it out, and flamed the spreader. I then used my sterilised forceps (via the flame again) and picked up a paper disk and placed it in the small beaker of mint extract, to let it soak into the paper. I then opened the Petri dish I had prepared earlier and placed the paper disk half way between the middle and the edge of the Petri disk, and then disinfect my forceps so that I can use them again. I do this three more times, so that I have a ‘square’ with four mint disks on each corner. I then put the lid on, and using tape up the dish, around the top vertically once, and around the top horizontally once aswell, not too much tape as I do not want to make anaerobic conditions inside the dish, then I label the dish, so in future I will know that it is mint extract used. I then prepare another Petri dish, the same way as I have done with the mint one, but instead of using mint extract, using garlic extract. I label this new dish differently, e.g. ‘Garlic’, to the mint dish, and then place then in an incubator at 25°C for a few days.

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I take them out of the incubator, and measure the diameter where microbes have not grown on the mint dish with a ruler, and compare this with the diameter of the garlic. Where the microbes have not grown, this is where the substance has killed them.

Results:

I got these results by averaging out the fifteen results I have a hold of. Although it appears that there are some anomalies in the original results, the averages look more realistic.

Safety:

The bacteria culture used here was certified safe from a company, and ...

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