Hey readers!
It's been a productive few days -- here's what I've been up to! This past week, I've been working on my Methods Assignment, where we were given the task of honing in on the methods of 4 (I did 5) sources, examining their methods, and applying their findings to my initial idea of my methods. Since I turned it in yesterday, here's what some exciting new information I found.
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Dab, Squidward...Dab! |
Although going into this project, I definitely knew I'd need a quantitative method to perform tests to optimize the HemaDrop preparation method to create uniform thin solid films of blood. I was like Squidward in this parade: I knew what I wanted to do (dab, aka develop a solid experimental design), but I need some instigation.
Nonetheless, studying the methods of others allowed me to determine specifically the type of experimental procedure I want to conduct. Additionally, sources, like Acharya et al and Dar et al, emphasized the importance of using controls in experimental studies. In this way, I can prove causation from the results from using hyper-hydrophilic films by manipulating variables in a controlled manner.
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Triggered... |
Additionally, the important aspect of all procedures was the emphasis on consistent, reproducible sample preparation. For this, I definitely need to establish a clear protocol for sample preparation. Another aspect I realized about my methods was that to check sample variability, more participants should be used than just me. In this way, I can greatly increase the validity of my study. To get these participants, I will need to adapt our current IRB approval and consent forms to apply directly to my project. I feel good about this, as I was part of the IRB approval process at ASU, so I have some level of experience. The laboratories we work at are already Biosafety Level 2, which is required for obtaining human blood samples. In this way, my research will also be ethical. I will most likely use fellow interns as participants (convenience sampling), as they will be willing to be pricked (even though it's painless) and at the lab anyways.
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That's me crossing over my methods section and nailing the 3-pointer. |
An unexpected part of my methods that I uncovered with the methods assignment was that I definitely want to incorporate qualitative observations into my methods. As seen in Acharya's thesis, specific criteria like phase separation, cracking, cratering, and lack of uniformity can be used to classify samples and explain quantitative results. This will really give my research a holistic perspective that would otherwise be lacking.

I also realized that our procedure for capillary sampling can be much more streamlined. Although we did use the correct grade lancet for pricking finger tips, specific procedures, like those outlined in Fan et al, which employ rubefacients (dilate the capillaries) and capillary tubes, increase the validity of the results, as those are the standard of care for obtaining microliters of blood from patients.
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Capillary sampling in action! |
By following a more standardized procedure, our results can be more standardized and replicable.
Now... what am I worried about??
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Rip... |
A major concern that I have with my research right now is making sure I have enough time to collect data and perform all my experiments within a few weeks. I'm trying to fix this by planning out a clear schedule with Dr. Herbots and getting ahead on testing by starting in January (probably). By next week, I should have a clear picture of my research plan and get a headstart on my proposal!
Well, in the meantime, let's keep loving blood and doing some fun research!
Yash, have you had the chance to sit down with Dr. Herbots to talk about a schedule? I thought you were meeting yesterday, so I'd love to hear about what you guys discussed in terms of your timeline.
ReplyDeleteI'm really happy that the methods assignment proved useful for you. Did you end up using the sources we found together? Or other sources?
I also like the idea of you using qualitative methods to deepen your quantitative results.
Hi Yash, Happy to hear that all is going well. I agree that you should incorporate qualitative analyses into your study, it should provide a greater insight to observations available in your study. It could also be useful for error analysis (not that you'll have any errors). The timeline should be very important to your study because its all about feasibility at this point. I'm sure PSF 3rd floor fam will help you out. Also I'm curious about the ethicality. Are there any ethical protocols that you need to follow other than obtaining consent? Like certain tests you can't use? Or would you just have to justify it?
ReplyDelete-
Ashwath V.
Hey Yash,
ReplyDeleteI think the emphasis on sample validity is something that I am glad you determined was really important to ensure your results are more accurate. Increasing sample size can only help, even though I know the patient consent can be tricky. Do you know what size you are planning to use? And how you can justify that number? Do you get the demographic information/health record of the patient blood samples? If so, do you think that could affect your results in anyway?
I also agree that if you plan out your schedule now, I am sure you can allocate enough time to each step, and be able to finish on time. It is good you are worrying about that now. A little bit of stress should help in you getting this done before you need to start rushing.
The qualitative aspect was really cool, because I never thought your project always seemed very experimental/cause and effect, but incorporating that qualitative part could really enhance the credibility of your procedure and make it understandable for a wider audience.
Good job and looking forward to seeing you conduct actual research!
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Sunskruthi