Triticum aestivum (leaf)

From AHPA Botanical Identity References Compendium
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             | reference= Method Developed by Alkemists Laboratories
 
             | reference= Method Developed by Alkemists Laboratories
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            | }}
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{{HPTLC | source=HPTLC Association
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            | companyimage=HPTLC-assoc-Logo-farbig-Text-schwarz-300x47.png
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            | companyURL=http://www.hptlc-association.org/
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            | mainimage=Curcuma longa w nim-UV 254 nm-hptlc-association.png
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            | caption1=Turmeric adulteration with nimesulide (rhizome) HPTLC ID - UV 254 nm
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            | description=Turmeric adulteration with nimesulide (rhizome) (''Curcuma longa'')
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            | image2=Curcuma longa w nim-2,5-Dichloro-1,4-benzoquinone reagent, UV 366 nm-hptlc-association.png
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            | caption2=Turmeric adulteration with nimesulide (rhizome) HPTLC ID - 2,5-Dichloro-1,4-benzoquinone reagent, UV 366 nm
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            | image3=Curcuma longa w nim-2,5-Dichloro-1,4-benzoquinone reagent, white RT-hptlc-association.png
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            | caption3=Turmeric adulteration with nimesulide (rhizome) HPTLC ID - 2,5-Dichloro-1,4-benzoquinone reagent, white RT
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            |
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            | stationaryphase=Stationary phase, i.e. Silica gel 60, F254
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            | mobilephase=Toluene, acetic acid (4:1) (v/v)
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            | prep=Sample: Mix 0.2 g of powdered sample with 3 mL of methanol, sonicate for 10 minutes, then centrifuge or filter the solution and use the supernatant/filtrate as test solution.
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Derivatization reagent: 2,5-Dichloro-1,4-benzoquinone reagent, Preparation: 0.50 g of 2,5-Dichloro-1,4-benzoquinone is dissolved in 80 mL of dimethyl sulfoxide and then diluted with 160 mL of tetrahydrofuran, Use: Dip (time 0, speed 5), dry in a stream of cold air for 3 min.
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            | detection=Saturated chamber; developing distance 70 mm from lower edge; relative humidity 33%
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            | referencesamples=Reference: Dissolve 1.0 mg of nimesulide in 10 mL of methanol.
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            | lanes=Lanes, from left to right (Track, Volume, Sample):
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# 2 µL Turmeric 1 (not spiked)
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# 2 µL Turmeric 1 (spiked w/ 1% nimesulide)
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# 2 µL Turmeric 1 (w/ 2% nimesulide)
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# 2 µL Turmeric 1 (w/ 5% nimesulide)
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# 2 µL Turmeric 1 (w/ 10% nimesulide)
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# 2 µL Turmeric 2 (not spiked)
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# 2 µL Turmeric 2 (w/ 1% nimesulide)
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# 2 µL Turmeric 2 (w/ 2% nimesulide)
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# 2 µL Turmeric 2 (w/ 5% nimesulide)
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# 2 µL Turmeric 2 (w/ 10% nimesulide)
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# 2 µL Turmeric 3 (not spiked)
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# 2 µL Turmeric 3 (w/ 1% nimesulide)
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# 2 µL Turmeric 3 (w/ 2% nimesulide)
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# 2 µL Turmeric 3 (w/ 5% nimesulide)
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# 2 µL Turmeric 3 ( w/ 10% nimesulide)
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            | notes=''Images presented in this entry are examples and are not intended to be used as basis for setting specifications for quality control purposes.''
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System suitability test: Nimesulide: Rf ~  0.51
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Test for adulteration: Compare result with reference images. The fingerprint of the test solution is similar to that of the corresponding botanical reference sample. Additional weak zones may be present. The chromatogram of the test solution shows no zone at Rf ~ 0.51 corresponding in color and position to that of the nimesulide reference standard.
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             | }}
 
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Revision as of 23:45, 24 June 2013

Contents

Introduction

Macroscopic Entries

Microscopic Entries

Unicellular thick walled tapering trichome observed at 400x with Acidified Chloral Hydrate Glycerol Solution.

Source: Elan M. Sudberg, Alkemist Laboratories [1]

AP-LOGO-Laboratories Crop - Copy.jpg
Triticum aestivum - Alkemist Laboratories.jpg



HPTLC Entries

AP-LOGO-Laboratories Crop - Copy.jpg
(thumbnail)
Triticum aestivum HPTLC ID - Vanillin/H2SO4 Reagent -> 110° C 5 min -> UV 365 nm

Wheat grass (grass) (Triticum aestivum)

Lane Assignments Lanes, from left to right (Track, Volume, Sample):

  1. 3 μL Aescin~0.1% in CH3OH
  2. 2 μL Triticum aestivum-1 (grass)
  3. 4 μL Triticum aestivum-1 (grass)
  4. 3 μL Triticum aestivum-2 (grass)
  5. 3 μL Triticum aestivum-2 (grass)
  6. 3 μL Triticum aestivum-3 (grass)
  7. 3 μL Triticum aestivum-4 (grass)
  8. 3 μL Aescin~0.1% in CH3OH

Reference materials used here have been authenticated by macroscopic, microscopic &/or TLC studies according to the reference source cited below held at Alkemists Laboratories, Costa Mesa, CA. 

Stationary Phase Silica gel 60, F254, 10 x 10 cm HPTLC plates 

Mobile Phase chloroform: methanol: water [6.4/5/1] 

Sample Preparation Method 0.3 g + 3 ml CH3OH sonicated + heated @ 50° C ~ 1 hr 

Detection Method Vanillin/H2SO4 Reagent -> 110° C 5 min -> UV 365 nm 

Reference see Method Developed by Alkemists Laboratories


Source: Elan M. Sudberg, Alkemist Laboratories [2]

HPTLC-assoc-Logo-farbig-Text-schwarz-300x47.png
(thumbnail)
Turmeric adulteration with nimesulide (rhizome) HPTLC ID - UV 254 nm

Turmeric adulteration with nimesulide (rhizome) (Curcuma longa)

Lane Assignments Lanes, from left to right (Track, Volume, Sample):

  1. 2 µL Turmeric 1 (not spiked)
  2. 2 µL Turmeric 1 (spiked w/ 1% nimesulide)
  3. 2 µL Turmeric 1 (w/ 2% nimesulide)
  4. 2 µL Turmeric 1 (w/ 5% nimesulide)
  5. 2 µL Turmeric 1 (w/ 10% nimesulide)
  6. 2 µL Turmeric 2 (not spiked)
  7. 2 µL Turmeric 2 (w/ 1% nimesulide)
  8. 2 µL Turmeric 2 (w/ 2% nimesulide)
  9. 2 µL Turmeric 2 (w/ 5% nimesulide)
  10. 2 µL Turmeric 2 (w/ 10% nimesulide)
  11. 2 µL Turmeric 3 (not spiked)
  12. 2 µL Turmeric 3 (w/ 1% nimesulide)
  13. 2 µL Turmeric 3 (w/ 2% nimesulide)
  14. 2 µL Turmeric 3 (w/ 5% nimesulide)
  15. 2 µL Turmeric 3 ( w/ 10% nimesulide) 

Reference Sample(s) Reference: Dissolve 1.0 mg of nimesulide in 10 mL of methanol. 

Stationary Phase Stationary phase, i.e. Silica gel 60, F254 

Mobile Phase Toluene, acetic acid (4:1) (v/v) 

Sample Preparation Method Sample: Mix 0.2 g of powdered sample with 3 mL of methanol, sonicate for 10 minutes, then centrifuge or filter the solution and use the supernatant/filtrate as test solution.

Derivatization reagent: 2,5-Dichloro-1,4-benzoquinone reagent, Preparation: 0.50 g of 2,5-Dichloro-1,4-benzoquinone is dissolved in 80 mL of dimethyl sulfoxide and then diluted with 160 mL of tetrahydrofuran, Use: Dip (time 0, speed 5), dry in a stream of cold air for 3 min. 

Detection Method Saturated chamber; developing distance 70 mm from lower edge; relative humidity 33% 

Other Notes Images presented in this entry are examples and are not intended to be used as basis for setting specifications for quality control purposes.

System suitability test: Nimesulide: Rf ~ 0.51

Test for adulteration: Compare result with reference images. The fingerprint of the test solution is similar to that of the corresponding botanical reference sample. Additional weak zones may be present. The chromatogram of the test solution shows no zone at Rf ~ 0.51 corresponding in color and position to that of the nimesulide reference standard.

Source: HPTLC Association [3]


Other Points of Interest


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