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  • For the nanoparticles sample it is necessary to make sure the final concentration of the nanoparticles will not exceed 1 mM.
  • For the buffer solution, it is enough to dissolve 8 g of NaCl in DI water.
  • For the SDS solution, 2 g of SDS should be dissolved very slowly in approximate 200 mL of DI water, then 100 mL aliquots of DI water is added until the volume is 1 L. This is in order to avoid the formation of bubbles and foam in the solution.

Instrument preparation

Due to the sensitivity of the equipment, it is important to rinse and clean the tubing before loading any sample or performing any experiments. To rinse the tubing and the chambers, use a solution of 2% of SDS. For this purpose, a cycle in the autosampler equipment is program with the steps shown in [link] .

Summary of cleaning processes.
Step Duration (min) Speed (μL/min) Volume (mL)
DI water (1:2) 10 100 1
SDS (1:1) 20 300 6
DI water (1:2) 10 100 1

Once the equipment is cleaned, it is ready to perform an experiment, a second program in the autosampler is loaded with the parameters shown in [link] .

Experimental set-up.
Step Duration (min) Speed (μL/min) Volume (mL)
Buffer (1:3) 7 100 0.7
Nanoparticles (1:4) 30 100 3.0

The purpose of flowing the buffer in the beginning is to provide a background signal to take into account when running the samples. Usually a small quantity of the sample is loaded into the sensor at a very slow flow rate in order to let the deposition take place.

Data acquisition

Example data obtained with the above parameters is shown in [link] . The blue squares depict the change in the frequency. As the experiment continues, the frequency decreases as more mass is deposited. On the other hand, shown as the red squares, the dissipation increases, describing the increase of both the height and certain loss of the rigidity in the layer from the top of the sensor. To illustrate the different steps of the experiment, each section has been color coded. The blue part of the data obtained corresponds to the flow of the buffer, while the yellow part corresponds to the deposition equilibrium of the nanoparticles onto the gold surface. After certain length of time equilibrium is reached and there is no further change. Once equilibrium indicates no change for about five minutes, it is safe to say the deposition will not change.

Data of deposition of nMag in a gold surface.

Instrument clean-up

As a measure preventive care for the equipment, the same cleaning procedure should be followed as what was done before loading the sample. Use of a 2% solution of SDS helps to ensure the equipment remains as clean as possible.

Data modeling

Once the data has been obtained, QTools (software that is available in the software suit of the equipment) can be used to convert the change in the frequency to areal mass, via the Sauerbrey equation, [link] . The correspondent graph of areal mass is shown in [link] . From this graph we can observe how the mass is increasing as the nMag is deposited in the surface of the sensor. The blue section again illustrates the part of the experiment where only buffer was been flown to the chamber. The yellow part illustrates the deposition, while the green part shows no change in the mass after a period of time, which indicates the deposition is finished. The conversion from areal mass to mass is a simple process, as gold sensors come with a definite area of 1 cm 2 , but a more accurate measure should be taken when using functionalized sensors.

Areal mass of deposition of nMag into gold surface.

It is important to take into account the limitations of the Saubery equation, because the equation accounts for a uniform layer on top of the surface of the sensor. Deviations due to clusters of material deposited in one place or the formation of partial multilayers in the sensor cannot be calculated through this model. Further characterization of the surface should be done to have a more accurate model of the phenomena.

Bibliography

  • Biolin Scientific, Cleaning and Immobilization Protocols (2004).
  • F. Hook, Development of a Novel QCM Technique for Protein Adsorption Studies , Chalmers University (1997).
  • C. Ziez, Theoretical and Experimental Analysis on Nanoparticle-Nanoparticle and Nanoparticle-Surface Interactions and their Role in Defining their Stability and Mobility , Rice University (2013).

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Assimilatory nitrate reduction is a process that occurs in some microorganisms, such as bacteria and archaea, in which nitrate (NO3-) is reduced to nitrite (NO2-), and then further reduced to ammonia (NH3).
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Prevent foreign microbes to the host
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They are friends to host only when Host immune system is strong and become enemies when the host immune system is weakened . very bad relationship!
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cell is the smallest unit of life
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cell is the structural and functional unit of life
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Binomial nomenclature
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Source:  OpenStax, Nanomaterials and nanotechnology. OpenStax CNX. May 07, 2014 Download for free at http://legacy.cnx.org/content/col10700/1.13
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