User:Samiye Yaman/Notebook/Lab 581/2013/03/27: Difference between revisions

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==Objective==


==Description==
==Description==
'''Part 1: Freeze-thaw vortex cycle of liposomes'''
*The course is designed by American University to experiment different aspects of PVOH films.
 
*5 freeze-thaw vortex cycle for liposome coated hydrogel. (vortex for 30sec, freeze (completely) by using liquid nitrogen then thaw (completely)in a water bath. Repeat the cycle 5 times.
 
*Centrifuge the solution(4000rpm for 5 min) then remove the 25mM Tris solution from the epi-test tube.
 
*Add 1.5 mL of 25mM Tris buffer back to the epi test tube with hydrogels.
 
 
'''Part 2: Prepare a concentration range for R6G'''
 
*Add 2mg of PVOH to 6 different epi test tubes.
 
*Add 1.5 ml of phosphate buffer.
 
*Add different volume of 1mM R6G to each epi test tube. (10μL, 15μL, 20μL, 25μL, 30μL, 35μL)
 
 
'''Part 3: Preparing hydrogels for pH analysis'''
 
* Centrifuge hydrogel solutions with containing methyl red and bromophenol blue prepared on 3/22
 
* After the centrifuge, collect supernatant and place it in to a sepetrate epi-tube.
 
*Add 1mL phosphate buffer to hyrdogels.(repeat the process 3 times.
 
*Uv-Vis of measurement of each supernantant was done.Additionally stock solution of the dyes were also measured with UV-vis.


*During the course PVOH films with different molecular weight will be produced. Effects of cross-linking, addition of different molecules such as gluteraldehyde, different acids, porphrin will be also tested.
==Data==


*UV-Vis spectrum, Atomic Absorption spectrum, X-Ray, FTIR, DMA, ISE and many other instruments will be used to analyze the results.
==Notes==

Revision as of 06:06, 3 April 2013

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Objective

Description

Part 1: Freeze-thaw vortex cycle of liposomes

  • 5 freeze-thaw vortex cycle for liposome coated hydrogel. (vortex for 30sec, freeze (completely) by using liquid nitrogen then thaw (completely)in a water bath. Repeat the cycle 5 times.
  • Centrifuge the solution(4000rpm for 5 min) then remove the 25mM Tris solution from the epi-test tube.
  • Add 1.5 mL of 25mM Tris buffer back to the epi test tube with hydrogels.


Part 2: Prepare a concentration range for R6G

  • Add 2mg of PVOH to 6 different epi test tubes.
  • Add 1.5 ml of phosphate buffer.
  • Add different volume of 1mM R6G to each epi test tube. (10μL, 15μL, 20μL, 25μL, 30μL, 35μL)


Part 3: Preparing hydrogels for pH analysis

  • Centrifuge hydrogel solutions with containing methyl red and bromophenol blue prepared on 3/22
  • After the centrifuge, collect supernatant and place it in to a sepetrate epi-tube.
  • Add 1mL phosphate buffer to hyrdogels.(repeat the process 3 times.
  • Uv-Vis of measurement of each supernantant was done.Additionally stock solution of the dyes were also measured with UV-vis.

Data

Notes
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