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|style="background-color: #EEE"|[[Image:BDLlogo_notext_lr.png|128px]]<span style="font-size:22px;"> Biomaterials Design Lab</span>
|style="background-color: #EEE"|[[Image:BDLlogo_notext_lr.png|128px]]<span style="font-size:22px;"> Biomaterials Design Lab</span>
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==Objective==
==Objective==
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Preparation of Stock Solutions
 
Stock solutions of a protein (lysozyme), and HAuCl4 were prepared. The stock solutions were used to make six solutions of varying concentrations containing HAuCl4, lysozyme, and H20.


==Description==
==Description==
# Add experimental record here. Include what, how, and why...
# Solutions of Colloidal Gold and Lysosyme were produced at different ratios to observe the formation of fibers
## Solutions were heated in a hot water bath and run through the Uv-vis to observe any color changes.
## Solutions were also cooked within the oven for an extended period of time to assist fiber formation.
# Kinetics of AuNP Formation
## Enough Lysozyme was added to three test tubes each containing 0.5 mL HAuCl<sub>4</sub> to make [Au]:[Lysozyme]=30 (see chart below for prescription to make such a solution). 
## The test tubes were covered with foil and placed in an 80°C hot water bath.
## Every 30 minutes half of the solution in one of the test tubes was poured into a plastic cuvette and placed in the UV-Vis Spectrometer.
## The UV-Vis from 800 nm to 360 nm was recorded and the above procedure was performed every 30 minutes until no more solution remained.


==Data==
==Data==
* Add data and results here...
Stock Solutions
* HAuCl4 → 0.04621g / 50ml DI Water
* Lysozyme → 0.0895g / 50ml DI Water
 
[[Image:Gold_-_DI_concentration_Table.jpg]]


==Notes==
==Notes==
This area is for any observations or conclusions that you would like to note.


Using a teflon coated spatula is recommended so the HAuCl4 does not bind to the metal on the spatula.


Use categories like tags. Change the "Course" category to the one corresponding to your course. The "Miscellaneous" tag can be used for particular experiments, as instructed by your professor. Please be sure to change or delete this tag as required so that the categories remain well organized.
During the heating process, the temperature fluctuated between 70-85°C


[[Category:Course]]
[[Category:Course]]

Latest revision as of 00:13, 27 September 2017

Biomaterials Design Lab Main project page
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Objective

Preparation of Stock Solutions

Stock solutions of a protein (lysozyme), and HAuCl4 were prepared. The stock solutions were used to make six solutions of varying concentrations containing HAuCl4, lysozyme, and H20.

Description

  1. Solutions of Colloidal Gold and Lysosyme were produced at different ratios to observe the formation of fibers
    1. Solutions were heated in a hot water bath and run through the Uv-vis to observe any color changes.
    2. Solutions were also cooked within the oven for an extended period of time to assist fiber formation.
  2. Kinetics of AuNP Formation
    1. Enough Lysozyme was added to three test tubes each containing 0.5 mL HAuCl4 to make [Au]:[Lysozyme]=30 (see chart below for prescription to make such a solution).
    2. The test tubes were covered with foil and placed in an 80°C hot water bath.
    3. Every 30 minutes half of the solution in one of the test tubes was poured into a plastic cuvette and placed in the UV-Vis Spectrometer.
    4. The UV-Vis from 800 nm to 360 nm was recorded and the above procedure was performed every 30 minutes until no more solution remained.

Data

Stock Solutions

  • HAuCl4 → 0.04621g / 50ml DI Water
  • Lysozyme → 0.0895g / 50ml DI Water

Notes

Using a teflon coated spatula is recommended so the HAuCl4 does not bind to the metal on the spatula.

During the heating process, the temperature fluctuated between 70-85°C