
Dushyant Patel Extractive Spectrophotometric Method
S.K.P.C.P.E.R., Kherva 71 M .Pharm. Thesis
buffer solution was added in the different separating funnels. BCG solution or BTB
solution was added in excess each. Shaken well and extracted with 10 ml of chloroform.
Later the extracts were taken into 10 ml volumetric flasks, treated with anhydrous sodium
sulphate and volume was made up with chloroform, and then absorbances were
measured at 416 nm and 421 nm for BCG and BTB, respectively. It was found that after
addition of 2 ml of buffer in BCG and 2.5 ml of buffer in BTB, absorbance became
constant. Hence 2 ml and 2.5 ml of buffer solution were optimized for BCG method and
BTB method, respectively (Figure 5.2 A and B).
0
0.1
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0.7
0.8
0.9
0246
pHofbuffer
Absorbance
0
0.1
0.2
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0.4
0.5
0.6
0.7
0246
pHofbuffer
Absorbance
(A) (B)
Figure 5.1 Optimization of pH of Buffer for (A) GBP-BCG (B) GBP-BTB complex
0
0.1
0.2
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0.8
0.9
01234
mlOfBuffer
Absorbance
0
0.1
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0.5
0.6
0.7
0.8
01234
mlOfBuffer
Absorbance
(A) (B)
Figure 5.2 Optimization of volume of Buffer for (A) GBP-BCG (B) GBP-BTB complex
d) Stability study of drug dye complexes:
¾ The stability of the drug dye complexes was determined individually for both the dyes
(BCG and BTB). Working standard solution (5 ml) was pipette out and added to a
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