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initial characterization of crude extracts from phyllanthus amarus

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values (0.13; 0.80; 0.88) as fractions 2, 7, and 8 (0.14; 0.83; 0.91) <strong>from</strong> detection method<br />

I (Appendix D, Tables D.1 and D.2). Therefore these fractions/compounds are most<br />

probably the same and detection method II can be eliminated for the determination <strong>of</strong><br />

samples <strong>from</strong> location PD.<br />

Table 4.2 Presence/absence <strong>of</strong> fractions in <strong>crude</strong> P. <strong>amarus</strong> <strong>extracts</strong> detected by<br />

UV-365 nm and Dragendorff (DRG) reagent (detection method II).<br />

Cross-reference with Figure C.5 and Table D.2<br />

Fraction<br />

Extraction\<br />

Location<br />

A1<br />

B1<br />

C1<br />

A2<br />

B2<br />

C2<br />

A3<br />

B3<br />

C3<br />

1 2 3 Total<br />

-<br />

-<br />

+<br />

-<br />

+<br />

+<br />

-<br />

-<br />

-<br />

Extraction: A=50% MeOH in H2O; B= 99% methanol; C= 50% MeOH in CHCl3<br />

Location: 1= PD; 2= PN; 3= PZ<br />

The use <strong>of</strong> mobile phase chlor<strong>of</strong>orm/methanol= 9:1 resulted in some compounds<br />

that were partially separated. The two last compounds were still blended (Figure C.4).<br />

The mobile phase chlor<strong>of</strong>orm/methanol= 98:2 (Figure C.6) gave basically the same<br />

results as mobile phase 95:5 (Figure C.5).<br />

-<br />

+<br />

+<br />

-<br />

+<br />

+<br />

-<br />

+<br />

+<br />

-<br />

+<br />

+<br />

-<br />

+<br />

+<br />

-<br />

+<br />

+<br />

0<br />

2<br />

3<br />

0<br />

3<br />

3<br />

0<br />

2<br />

2<br />

From extract A <strong>of</strong> location PD and PN (Table 4.3 and Figure C.8), only one<br />

fraction (number 7) became visible. Fraction 3 was detected only in extract C. This is an<br />

32

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