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In the context of forming a Drug-DNA complex, if 500 µL of a 20 µM DNA solution is mixed with 500 µL of a 20 µM drug solution, but the absorbance spectra show a minimal peak for the drug, what might be a plausible explanation for the low observed peak?

A) The drug-DNA complex might have a different absorbance profile than the individual drug or DNA.
B) The concentration of the drug or DNA solutions might not be accurately calculated or measured.
C) The wavelength used for UV-VIS spectroscopy might not be appropriate for detecting the drug-DNA complex.
D) The mixing ratio of drug to DNA might not be optimal for complex formation.

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Final answer:

A minimal peak for the drug in the Drug-DNA complex absorbance spectra could be due to a different absorbance profile of the complex, inaccurate concentrations, use of an inappropriate wavelength, or a non-optimal mixing ratio for complex formation.

Step-by-step explanation:

In the context of forming a Drug-DNA complex, if you observe a minimal peak for the drug in the absorbance spectra, several explanations are possible.

  • A) The drug-DNA complex might have a different absorbance profile than the individual drug or DNA. This means the complex formed between the drug and DNA may absorb light at a different wavelength than either substance alone, which might cause a minimal peak at the expected wavelength.
  • B) The concentration of the drug or DNA solutions might not be accurately calculated or measured, leading to incorrect assumptions about expected absorbance peaks.
  • C) The wavelength used for UV-VIS spectroscopy might not be the right one to detect the new absorbance peak of the drug-DNA complex, as complexes often have different optical properties.
  • D) The mixing ratio of drug to DNA might not be optimal for complex formation. An incorrect ratio can affect the structure and stability of the complex, possibly affecting its absorbance characteristics.

To determine the concentration of the original sample in the provided exercise, one would use the Beer-Lambert law, which correlates absorbance with concentration through the formula Absorbance (at 260 nm) = ε•c•l, where ε is the absorption coefficient, l is the path length, and c is the concentration. In the given UV spectroscopy example of DNA concentration, we'd calculate the concentration of the DNA sample before dilution based on its absorbance post-dilution.

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