Alex Senchak Grade 9 Central Catholic High School 1 Colloidal Silver Antibacterial Assessment.

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Alex Senchak Grade 9 Central Catholic High School 1 Colloidal Silver Antibacterial Assessment

Transcript of Alex Senchak Grade 9 Central Catholic High School 1 Colloidal Silver Antibacterial Assessment.

Page 1: Alex Senchak Grade 9 Central Catholic High School 1 Colloidal Silver Antibacterial Assessment.

Alex SenchakGrade 9

Central Catholic High School

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Colloidal Silver Antibacterial Assessment

Page 2: Alex Senchak Grade 9 Central Catholic High School 1 Colloidal Silver Antibacterial Assessment.

Bacteria that cause infections are becoming increasingly resistant to antibiotics and other antimicrobial agents.

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Problem

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Gram Bacteria Stain Categories

Gram Positive (Staph) Gram Negative (E. Coli)

Cell wall is thin extra layer of lipopolysaccharide which adds extra level of protection.

If the toxin enters the circulatory system it causes a toxic reaction.

This outer membrane protects the bacteria from several antibiotics.

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Most pathogenic bacteria in humans are gram-positive organisms.

Simple cell wall.Antibiotics such as

penicillin work against the formation of the cell wall.

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Disables enzymes that power bacteria.

Colloidal Silver as an antibiotic.Argyria: Caused by overuse of Colloidal Silver.

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Colloidal Silver

Paul Karason “Blue Man”

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To determine if Colloidal Silver will affect the survivorship of E. Coli and Staphylococcus Epidermidis.

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Purpose

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Colloidal Silver exposure will not significantly reduce the survivorship of E. Coli or Staphylococcus Epidermidis.

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Null Hypothesis

HypothesisColloidal Silver exposure will significantly

reduce the survivorship of E. Coli and Staphylococcus Epidermidis.

Page 9: Alex Senchak Grade 9 Central Catholic High School 1 Colloidal Silver Antibacterial Assessment.

Large glass jar Beaker Micro and macro pipettes

+ tips Spreader bars 76 LB agar plates (1%

Tryptone, 0.5% Yeast Extract, 1% NaCl)

Escherichia Coli bacteria Staphylococcus

Epidermidis bacteria Colloidal Silver making

kit:GeneratorSilver ElectrodesBuffer

TDS meter Burner Turn-table Tube racks Vortex Incubator Gloves\goggles Klett

Spectrophotometer SDF (sterile dilution

fluid). 20 sterile test tubes Ethanol

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Materials

Page 10: Alex Senchak Grade 9 Central Catholic High School 1 Colloidal Silver Antibacterial Assessment.

1. Sterile glass container, beaker and measuring cup were used to transfer liquid.

2. Used measuring cup to pour approximately 470 ml of distilled water into the glass container.

3. Attached silver electrodes to generator.4. Electrodes were suspended in the solution and powered for

75 minutes.5. This process was performed in the dark for efficiency. 6. The deposition of dark particles on the electrodes provided

evidence of colloidal silver. 7. After 75 minutes a TDS meter was used to determine the

concentration of silver in the solution.8. The silver solution was stored in the dark until use.

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Procedure : Making Colloidal Silver

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Picture of Colloidal Silver

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1. Bacteria (E. coli and Staph) was grown overnight in sterile LB media.

2. A sample of the overnight culture was added to fresh media in a sterile sidearm flask.

3. The culture was placed in an incubator (37°C) until a density of 50 Klett spectrophotometer units was reached. This represents a cell density of approximately 108 cells/mL.

4. The culture was diluted in sterile dilution fluid to a concentration of approximately 105 cells/mL.

5. A colloidal silver suspension was mixed with the appropriate amount of SDF to create colloidal silver concentrations of 13%, 6.5%, 1.3%, and 0.13%.

Procedure for Testing Silver on Bacteria

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Page 13: Alex Senchak Grade 9 Central Catholic High School 1 Colloidal Silver Antibacterial Assessment.

0%Stock

0.13%Stock

1.3%Stock

6.5%Stock

12.87%Stock

Microbe 0.1 ml

0.1 ml 0.1 ml 0.1 ml 0.1 ml

SDF 9.9 ml

9.8 ml 8.9 ml 4.9 ml 0 ml

ColloidalSilver

0 ml 0.1 ml 1 ml 5 ml 9.9 ml

Total 10 ml 10 ml 10 ml 10 ml 10 ml13

Chart of Concentration

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6. 100 µL of cell culture was then added to the silver solutions, yielding a final volume of 10 mL and a cell density of approximately 103 cells/mL.

7. The solutions were vortexed and allowed to sit at room temperature for 15 minutes.

8. After vortexing to evenly suspend the cells, 100 µL aliquots were removed from the tubes and spread on LB agar plates.

9. The plates were incubated at 37°C for 24 hours.

10. The resulting colonies were counted visually. Each colony was assumed to have arisen from one cell.

Procedure Cont.

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% of Silver in Solution0.00

50.00

100.00

150.00

200.00

250.00 213.00

181.83

156.67139.50

15.17

00.131.36.512.87

0.13% 12.87%

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Effect of Silver on E. Coli

Colo

nie

s

P= 7.53E-24

0% 1.3% 6.5%

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Dunnett’s Test Analysis (E. coli)

T Critical = 3.26 (significant)

Alpha = .05

Silver Concentration

T Value Interpretation

0.13% 6.75 Significant

1.3% 12.92 Significant

6.5% 15.91 Significant

12.87% 42.82 Significant

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% of Silver in Solution0.00

50.00

100.00

150.00

200.00

250.00201.17

156.67

141.33128.67

110.67 00.131.36.512.87

0.13%1.3% 6.5% 12.87%

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Effect of Silver on Staph

Colo

nie

s

P= 3.75E-19

0%

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Dunnett’s Test Analysis (Staph)

T Critical = 3.26 (significant)

Alpha = .05

Silver Concentration

T Value Interpretation

0.13% 13.69 Significant

1.3% 18.41 Significant

6.5% 22.31 Significant

12.87% 27.85 Significant

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0.13% 1.30% 6.50% 12.87%0%

10%

20%

30%

40%

50%

60%

70%

80%

90%

E. coliStaph

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Survivorship Percentage Compared to ControlP

erc

en

tag

e o

f S

urv

ivin

g C

olo

nie

s

% of Silver in Solution

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There appeared to be a dosage effect of the silver on the bacteria. Increasing amounts of silver led to less bacteria surviving.

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Observation

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ConclusionNull Hypothesis

Colloidal Silver exposure will not significantly reduce the survivorship of E. Coli or Staphylococcus Epidermidis.REJECTED

HypothesisColloidal Silver exposure will significantly reduce the survivorship of E. Coli and Staphylococcus Epidermidis.ACCEPTED

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Test a higher concentration of colloidal silver on bacteria.

Test different types of bacteria.

Infuse the agar with silver to provide a prolonged surface exposure.

There was a lag time when plating the cells. Exposure times to the silver varied slightly.

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Limitations Extensions

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Bukhari, Mohammad. "Student Presentation on Staphylococcus Epidermis." Web. 2 Nov. 2009. <http://web.uconn.edu/mcbstaff/graf/Student%20presentations/S%20epidermidis/sepidermidis.html>.

"Colloidal Silver General Information." Web. 25 Oct. 2009. <http://www.lifedevice.com/General%20Info.htm>.

"Colloidal Silver Studies-Univiversity of North Texas and SilverKare." Web. 28 Oct. 2009. <http://www.silvermedicine.org/colloidalsilverstudytexas.html>.

"Colloidal Slilver kills over disease causing bacteria." Kombacha Power Products. Web. 28 Oct. 2009. <http://www.kombuchapower.com/colloidal_silver.htm>.

"E. coli." Kids Health from Nemours. Web. 28 Oct. 2009. <http://kidshealth.org/kid/stay_healthy/food/ecoli.html#>.

"Silver Poisoning & Argyria: FDA, EPA, WHO." Colloidal Silver Safety and Toxicity Center. Web. 3 Nov. 2009. <http://www.silvermedicine.org/safetyinformation.html>.

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Works Cited

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E. Coli Results

Staph Results

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102 cells103 cells/mL

105 cells/mL with silver

108 cells/mL (Bacteria)

100 uL100 uL

107 cells/mL (Bacteria)

200 uL400 uL

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