TO QUANTIFY THE LUTEOLIN CONTENT FROM THE AERIAL PARTS OF HETEROPOGON CONTORTUS (L.) BEAUV. (SPEAR GRASS) THROUGH HIGH-PERFORMANCE THIN-LAYER CHROMATOGRAPHY

Authors

  • Navjot Kaur Department of Botany, Punjabi University, Patiala - 147 002, Punjab, India.
  • Raghbir Chand Gupta Department of Botany, Punjabi University, Patiala - 147 002, Punjab, India.

DOI:

https://doi.org/10.22159/ajpcr.2018.v11i1.22116

Keywords:

Heteropogon contortus, Flavonoid, Luteolin, Different plant samples

Abstract

 

 Objective: The objective of this study was to quantify the luteolin content present in the extracts from different aerial plants (leaves, stem, and inflorescence) of Heteropogon contortus through high-performance thin-layer chromatography.

Methods: The chromatographic fingerprint analysis of the different plant extracts has been developed using optimized mobile phase toluene: ethyl acetate: formic acid (5:5:0.7 v/v) and the developed plate is derivatized with freshly prepared anisaldehyde-sulfuric acid. Then, the plate is heated at 110–120°C. The plate is scanned for densitometry measurements and to record the overlay spectra at 366 nm absorbance/reflectance wavelength. Quantification of luteolin marker compound in different extracts of H. contortus is estimated using 2–12 ng/spot.

Results: The yellow colored bands appearing on the chromatogram confirm the presence of luteolin marker compound in the different plant samples of H. contortus. Further, the presence of the luteolin marker is confirmed by comparing the Rf values (0.21) of the standard and the samples and from densitometry measurements by scanning the plate at 366 nm absorbance/reflectance. Line-to-line overlay spectra are obtained.

Conclusion: From this, it is concluded that leaf sample of H. contortus contains maximum amount of luteolin, i.e., 37.13 ± 0.11 mg/g of dry wt. than inflorescence (1.60 ± 0.013 mg/g of dry wt.) and stem (0.53 ± 0.014 mg/g of dry wt.). The leaves are good source of luteolin and can be used as an alternate natural source to synthesize herbal drugs to cure cancer, hypertension, and inflammatory diseases.

 

Downloads

Download data is not yet available.

Author Biographies

Navjot Kaur, Department of Botany, Punjabi University, Patiala - 147 002, Punjab, India.

Department of Botany

Research scholar

Raghbir Chand Gupta, Department of Botany, Punjabi University, Patiala - 147 002, Punjab, India.

Professor

References

Aiyelaagbe OO, Osamudiamen PM. Phytochemical screening for active compounds in Mangifera indica leaves from Ibadan, Oyo state. Plant Sci Res 2009;2:11-13.

Joshi C, Savai J, Varghese A, Pandita N. Validated HPTLC fingerprint analysis for simultaneous estimation of Quercetin, Kaempferol and Asiatic acid in leaves of two different chemotypes of Centella asiatica. Int Pharma Biol Res 2012;3:202-12.

Neuhouser ML. Dietary flavonoids and cancer risk: Evidence from human population studies. Nutr Cancer 2004;50:1-7.

Miean KH, Mohamed S. Flavonoid (myricetin, quercetin, kaempferol, luteolin, and apigenin) content of edible tropical plants. J Agric Food Chem 2001;49:3106-12. 5. Mencherini T, Picerno P, Scesa C, Aquino R. Triterpene, antioxidant, and antimicrobial compounds from Melissa officinalis. J Nat Prod 2007;70:1889-94.

Harborne JB, Williams CA. Advances in flavonoid research since 1992. Phytochemistry 2000;55:481-504.

Blake JD, Richards GN. Polysaccharides of tropical pasture herbage –I, studies on the distribution of the major polysaccharide components of spear grass (Heteropogon contortus) during growth. Aust J Chem 1970;23:2353-60.

Beveridce RJ, Dekker RF, Richards GN, Tows M. Identification of myo-isositol, galactikol, and rbffixose in spear grass (Heteropogon contortus). Aust J Chem 1972;25:677-8.

Chopra RN, Nayar SL, Chopra IC. Glossary of Indian Medicinal Plants. New Delhi, India: Council of Scientific and Industrial Research; 1956. p. 259-61.

Kirtikar KR, Basu BD. Indian Medicinal Plants. Vol II. Deharadun, India: International Book Distributors; 1935. p. 1074-6.

Ghante MH, Bhusari KP, Duragkar NJ. Evaluation of Heteropogon contortus (L.) Beauv. methanolic extract for mast cell, cell membrane and free radical stabilization. Indo Am J Pharma Res 2012;2:1015-26.

Ghante MH, Bhusari KP, Duragkar NJ. Bronchorelaxent and anti-inflammatory effect of Heteropogon contortus (L.) Beauv. Methanolic extract. Int J Pharm Tech Res 2013;5:99-104.

Shambhu N, Dighe V. Development, validation of HPTLC method for simultaneous quantitation of luteolin, apigenin from Cardiospermum halicacabum Linn. and Hydnocarpus pentandra (Buch-Ham.) Oken. Int J Pharm Pharm Sci 2014;6:408-12.

Kaur N, Gupta RC. Determination of sugar biomarkers in different plant parts of Lasiurus scindicus henrard (Poaceae) through high performance thin layer chromatography. Int J Sci Eng Res 2017;8:1237-49.

ICH Q2A. Text on Validation of Analytical Procedures. In: Proceedings of the International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use, Geneva; 1994.

Singh P, Singh D, Goel RK. Phytoflavonoids: Antiepileptics for the future. Int J Pharm Pharm Sci 2014;6:51-66.

Published

01-01-2018

How to Cite

Kaur, N., and R. C. Gupta. “TO QUANTIFY THE LUTEOLIN CONTENT FROM THE AERIAL PARTS OF HETEROPOGON CONTORTUS (L.) BEAUV. (SPEAR GRASS) THROUGH HIGH-PERFORMANCE THIN-LAYER CHROMATOGRAPHY”. Asian Journal of Pharmaceutical and Clinical Research, vol. 11, no. 1, Jan. 2018, pp. 191-4, doi:10.22159/ajpcr.2018.v11i1.22116.

Issue

Section

Original Article(s)