Photo-degradation of a biological sample

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In summary, the group thinks that irradiance integrated over time is more appropriate for studying photo-induced degradation of a biological sample.
  • #1
alemns
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What the group thoughts are in relation to an experiment in which 520 nm monochromatic light will strike a biological sample, which it is not flat (most like resembling an arc) and can photo-bleach over time. Would irradiance (mW/cm2) or dose (mJ/cm2) be more appropriate to carry on studies on photo-induced degradation of the sample over time?
 
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  • #2
We see 520 nm as green, (at the blue end), daylight, near the peak of our vision.

The geometry of the source of 520 nm radiation, and whether the “arc” is a concave or a convex surface, may make a difference.

Total dose would be more relevant, since the sample accumulates joules and damage over time.
One watt is one joule per second.
 
  • #3
thank you.

light source it is going to be incoherent, from LED(s). Target surface receiving illumination is approximately concave in shape.

any references by chance, discussing the physics (papers or textbook)...

irradiance integrated over time isn't dose?
 
  • #4
alemns said:
irradiance integrated over time isn't dose?
The damage will be proportional to the dose, which is the integral of the irradiance, over time.
Dose (mJ/cm2) = exposure_time (seconds) * irradiance (mW/cm2);
 
  • #5
alemns said:
Would irradiance (mW/cm2) or dose (mJ/cm2) be more appropriate to carry on studies on photo-induced degradation of the sample over time?
I guess there have been assumptions about the actual experimental conditions and the chemistry of the surface.

The information in the OP is a bit sparse. the thermal effect would depend on the Mean Power over a period that's dependent on the actual nature of the surface.

If the potential damage relates to peaks of temperature then you'd need to know what temperature the surface could reach. What is the thermal Conductivity of the material? If the 'material' is 'alive' then we can't make any reliable predictions. Some living cells are very dependent on peaks of incident energy. (Consider the damage from exposure to sunlight.) This may or may not be relevant, of course but it would affect which of the quantities should be measured.

If the whole exercise is about damage related to illumination in general then perhaps both total (or medium term mean) and peak (short term) Energy should be studied. The experiment would reveal which is the important one.
 

1. What is photo-degradation of a biological sample?

Photo-degradation is the process by which a biological sample breaks down or deteriorates due to exposure to light. This can be caused by natural sunlight or artificial light sources such as UV lamps.

2. How does photo-degradation occur?

Photo-degradation occurs when the light energy absorbed by the biological sample causes chemical reactions that break down the molecular structure of the sample. This can lead to changes in color, texture, and composition of the sample.

3. What factors can affect the rate of photo-degradation?

The rate of photo-degradation can be influenced by several factors including the intensity and wavelength of light, the type of biological sample, and the presence of other substances such as oxygen or pollutants.

4. How can photo-degradation be prevented?

To prevent photo-degradation of a biological sample, it is important to store the sample in a cool, dark place and limit its exposure to light. Additionally, using protective coatings or packaging materials can help to block out harmful light and slow down the degradation process.

5. What are the potential consequences of photo-degradation on a biological sample?

The consequences of photo-degradation on a biological sample can vary depending on the type of sample and the extent of degradation. In some cases, it may simply alter the appearance or properties of the sample, while in others it can render the sample unusable for scientific research or medical purposes.

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