Skip to main content

Week Four Progress

Our focus this week was finding the correct placebo for our design. Prior to this week, we had expected to use zinc oxide in our module but we realized it did not have a high enough molecular weight. Therefore, the zinc oxide would disperse from the hydrogel beads too rapidly. After some research and guidance from our professor, we decided to use Fluorescein Isothiocyanate-Bovine Serum Album (FITC-BSA), which is a hydrophilic protein with a molecular weight of 66 kg/mol [1]. FITC-BSA will also be our signal source for measuring the rate of dispersion from the beads. As seen in Figure 1, FITC-BSA is vivid in color and allows the protein's diffusion throughout the hydrogel to be observed easily. We've decided to initially use 0.25 mg/ml as the concentration of FITC-BSA within our design.

Image result for fitc bsa
Figure 1: FITC-BSA (green) seen in samples of HeLa cells [2]

References:
[1]  Bovine Serum Albumin Conjugates Product Information, 1st ed. Molecular Probes, 2005.
[2] S. Sarker, R. Hokama, S. Takeoka, Intracellular delivery of FITC − BSA (green) in HeLa cells. Intracellular Delivery of Universal Proteins Using a Lysine Headgroup Containing Cationic Liposomes: Deciphering the Uptake Mechanism, 2013.



Comments

Popular posts from this blog

Week Nine Progress

The progress underwent during week nine of the hydrogel restructuring module entailed rectifying the errors made during the first and second testing rounds conducted during week seven. The results of first and second testing trials revealed egregious errors upon obtaining the results of the spectrophotometry of week eight. The spectrophotometry results delineated a consistent decrease in fluorescent intensity over time. Nonetheless, an ideal graph would illustrate a sustained increase in fluorescent intensity, thereby paralleling an increase in the percentage of therapeutic that is released. The increase in fluorescent intensity which had resulted from the week seven testing may be attributed to the experimental errors which occurred during the construction of hydrogel samples, and are described in full detail in the Week Eight Progress Report.  During week nine, new hydrogel samples were generated in a comparable fashion to the construction of samples during the second phase of t...

Week One Progress

Figure 1: Diagram of preliminary design The culmination of the hydrogel modulation design will yield a hydrogel wound dressing utilized for the therapeutic treatment of first-degree and second-degree exterior burns. A physical prototype of the hydrogel wound dressing will be produced by precipitating food-grade sodium alginate in a calcium chloride solution. The reaction yields spheres of low-density gel surrounded by a thin gelatinous membrane. The construction of an alginate dressing necessitates ionic cross-linking of the alginate solution with calcium ions, as to form the gel component. Both the high-density and low- density hydrogel layers will be generated in unison, before undergoing the freeze-drying process as to produce porous sheets. The physical prototype will be accompanied by a computer generated model of the hydrogel wound dressing, as evidenced in figure 1. The required components to construct the hydrogel adhesive were determined and subsequently purchased. The r...

Week Two Progress

The objectives of the week two lab consisted of preparing for the construction of the therapeutic-infused hydrogel adhesive. As such, a bill of materials was devised to determine the requisite laboratory supplies. It was determined that chemical components and laboratory glassware would be required to conduct the precipitation reaction between calcium chloride and sodium alginate. As the therapeutic agent, to be injected into the hydrogel 'beads', has not yet been determined, a comparable placebo had not been established. Nonetheless, each team member is to conduct research to determine an appropriate therapeutic for the hydrogel adhesive before a comparable placebo may be determined. Research regarding a possible therapeutic agent is to be completed before the week three lab. Once a therapeutic agent is agreed upon, a placebo, of comparable physical properties, will be ordered. The week two activities were completed in preparation for the construction of a preliminary design ...