Skip to main content
Article

Isolation, Cytotoxicity Evaluation and HPLC-Quantification of the Chemical Constituents from Prangos pabularia

Saleem FarooqBio-organic Chemistry Section, CSIR-Indian Institute of Integrative Medicine, Jammu, IndiaShakeel-u-RehmanDepartment of Chemistry, University of Kashmir, Srinagar, IndiaNisar A. DangrooBio-organic Chemistry Section, CSIR-Indian Institute of Integrative Medicine, Jammu, IndiaDev PriyaCancer Pharmacology Division, CSIR-Indian Institute of Integrative Medicine, Jammu, IndiaJavid A. BandayDepartment of Chemistry, University of Kashmir, Srinagar, IndiaPyare Lal SangwanBio-organic Chemistry Section, CSIR-Indian Institute of Integrative Medicine, Jammu, IndiaMushtaq A. QurishiDepartment of Chemistry, University of Kashmir, Srinagar, IndiaSurrinder KoulBio-organic Chemistry Section, CSIR-Indian Institute of Integrative Medicine, Jammu, IndiaAjit Kumar SaxenaCancer Pharmacology Division, CSIR-Indian Institute of Integrative Medicine, Jammu, India
2014en
ABI

Abstract

Phytochemical analysis of the dichloromethane:methanol (1:1) extract of root parts of Prangos pabularia led to the isolation of twelve cytotoxic constituents, viz., 6-hydroxycoumarin (1), 7-hydroxycoumarin (2), heraclenol-glycoside (3), xanthotoxol (4), heraclenol (5), oxypeucedanin hydrate (6), 8-((3,3-dimethyloxiran-2-yl)methyl)-7-methoxy-2H-chromen-2-one (7), oxypeucedanin hydrate monoacetate (8), xanthotoxin (9), 4-((2-hydroxy-3-methylbut-3-en-1-yl)oxy)-7H-furo[3,2-g]chromen-7-one (10), imperatorin (11) and osthol (12). The isolates were identified using spectral techniques in the light of literature. 3-(4,5-dimethyl thiazol-2yl)-2,5-diphenyltetrazolium bromide (MTT) cytotoxicity screening of the isolated constituents was carried out against six human cancer cell lines including lung (A549 and NCI-H322), epidermoid carcinoma (A431), melanoma (A375), prostate (PC-3) and Colon (HCT-116) cell lines. Osthol (12) exhibited the highest cytotoxicity with IC50 values of 3.2, 6.2, 10.9, 14.5, 24.8, and 30.2 µM against epidermoid carcinoma (A431), melanoma (A375), lung (NCI-H322), lung (A549), prostate (PC-3) and colon (HCT-116) cell lines respectively. Epidermoid carcinoma cell line A431 was sensitive to most of the compounds followed by lung (A549) cancer cell line. Finally a simple and reliable HPLC method was developed (RP-HPLC-DAD) and validated for the simultaneous quantification of these cytotoxic constituents in Prangos pabularia. The extract was analyzed using a reversed-phase Agilent ZORBAX eclipse plus column C18 (4.6×250 mm, 5 µm) at 250 nm wavelength using a gradient water-methanol solvent system at a flow rate of 0.8 ml/min. The RP-HPLC method is validated in terms of recovery, linearity, accuracy and precision (intra and inter-day validation). This method, because of shorter analysis time, makes it valuable for the commercial quality control of Prangos pabularia extracts and its future pharmaceutical preparations.

Identifiers

Citations and references

Cited by 20 references