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1.
Pakistan Journal of Pharmaceutical Sciences. 2013; 26 (4): 665-672
in English | IMEMR | ID: emr-126956

ABSTRACT

Many locally occurring species of Asteraceae are used as medicinal plants by various tribal and ethnic communities in Pakistan. Carthamus oxycantha is often occurs as weed in cultivated fields. Folk medicines indicated its use as an anti inflammatory and wound healing plant. It is used for wound healing by the local population in the form of powder paste. No scientific report, about the behavior of this plant has so far been published. The counter irritant studies of locally occurring Carthamus oxycantha was carried out. The main objectives of the project were to evaluate its wound healing effects on animal skin and the identity and characterization of chromatographically isolated fractions. For this purpose, different solvents with a broad range of polarity were successively used to extract non-polar compounds [petroleum ether extract], constituents intermediate polarities [chloroform extract] and polar constituents [methanol extract] from the whole herb of Carthamus oxycantha. The counter irritant activity of the crude extracts and isolated fractions was evaluated on rabbit's skin. Five fractions Co-1 to Co-5 were isolated from the active chloroform extract by column and thin layer chromatography. Co-1, Co-3 and Co-5 appeared to be the most potent counter irritant than others. A possible structure-activity relationship of these active compounds was investigated by using spectroscopy [UV and FTIR analysis]


Subject(s)
Animals, Laboratory , Irritants , Wound Healing , Rabbits , Chromatography , Spectrum Analysis
2.
Pakistan Journal of Pharmaceutical Sciences. 2013; 26 (1): 31-37
in English | IMEMR | ID: emr-146745

ABSTRACT

Euphorbia pilulifera is commonly found weed along road sides and loamy soils. This weed is commonly used as treatment of female disorders and respiratory problems. The latex of this weed causes irritation on hand on contact. To evaluate its irritant potentials, the dermatological investigation of irritant principles from locally occurring Euphorbia pilulifera was carried out. For this purpose, after collection and drying, a series of solvents with increasing polarity were used for the successive extraction of non-polar compounds [petroleum ether extract], constituents of intermediate polarities [chloroform extract] and polar constituents [methanol extract] from the whole herb of Euphorbia pilulifera. The chloroform extract of this weed was found most irritant to rabbit's skin. Chloroform extract was further subjected to column chromatography; four fractions Ep 1 to Ep 4 were isolated from active chloroform extract by column and thin layer chromatography. The irritant potentials of these isolated fractions were evaluated on rabbit's skin. Two fractions out of the four, Ep 1 and Ep 3 appeared to be the most irritant than others. A possible structure activity relationship of these active compounds was discussed in order to establish their activity


Subject(s)
Animals, Laboratory , Plant Extracts , Plants, Medicinal , Plant Weeds , Rabbits
3.
Pakistan Journal of Pharmaceutical Sciences. 2012; 25 (3): 589-594
in English | IMEMR | ID: emr-144410

ABSTRACT

Plenty of medicinal plants are available in Pakistan and are in human use as herbal medicines from ancient time. Present work is based on the evaluation of the use of Malva parviflora in skin irritation problems. For this purpose, powdered plant material [The aerial part and roots separately] was extracted by using successive solvent extraction method using petroleum ether, chloroform and methanol. Resulting three crude fractions were subjected to counterirritant investigations on rabbit's ear. Petroleum ether fraction exhibited prominent counter- irritant potential. Five compounds named, as MP-1, MP-2, MP-3, MP-4 and MP-5 were isolated from petroleum ether extract by column and thin layer chromatography. These compounds were subjected to UV spectrophotometer for detection of absorption of light, then FTIR for specific functional group identification and counter-irritant potentials was evaluated on rabbit's ear skin. The MP-1 and MP-2 exhibited excellent counter-irritant activity in different dilutions than others. However, dilution 100microg/ml showed maximum activity


Subject(s)
Animals , Plant Extracts/pharmacology , Irritants/antagonists & inhibitors , Spectrophotometry, Ultraviolet , Chromatography, Thin Layer , Spectroscopy, Fourier Transform Infrared , Rabbits , World Health Organization
4.
Pakistan Journal of Pharmacology. 2006; 23 (1): 61-65
in English | IMEMR | ID: emr-167426

ABSTRACT

A simple and sensitive reversed phase high-performance liquid chromatographic method was developed for simultaneous quantification of diltiazem and its major metabolite N-demethyldiltiazem in human plasma. The method involves one-step solvent extraction of diltiazem, N-demethyldiltiazem and the internal standard, verapamil with n-hexane and diethyl ether [50:50 v/v]. The mobile phase comprised 0.1M ammonium dihydrogen phosphate-acetonitrile [62:38 v/v] and triethylamine [0.08%] was added before the pH was ajusted to 5.9 with 85% phosphoric acid. Analysis was run at a flow rate of 1.0 ml/mm at a detection wavelength of 238 nm. The completion time for assay was not more than 10 minutes and lower limit of quantification was 5 ng/ml. The calibration curve for diltiazem and its metabolite was linear over a concentration range of 5-200 ng/ml and average recovery was about 90%. The coefficient of variation and percent error values of the assay method within and between day were all less than 10%

5.
PAFMJ-Pakistan Armed Forces Medical Journal. 2005; 55 (3): 214-218
in English | IMEMR | ID: emr-74045

ABSTRACT

A simple high-performance liquid chromatographic method was developed for determination of diltiazem in human plasma. Diltiazem and the internal standard, verapamil, were extracted from plasma samples using mixture of n-hexane and diethyl ether. The mobile phase was 0.1M ammonium dihydrogen phosphate - acetonitrile [62:38 v/v]. Triethylamine [0.08% v/v in the mobile phase] was added before the pH was adjusted to 5.9 with 85% phosphoric acid. Analysis was run at a flow rate of 1.0 ml/min at a detection wavelength of 238 nm. The method was specific and sensitive with a detection limit of 2.5 ng/ml at a signal-to-noise ratio of 3:1. The limit of quantification was set at 5 ng/ml. The calibration curve was linear over a concentration range of 5-160 ng/ml. Mean recovery value of the extraction procedure was about 90%, while the within and between day coefficient of variation and percent error values of the assay method were less than 10%


Subject(s)
Humans , Diltiazem/analysis , Verapamil/analysis , Sensitivity and Specificity , Plasma , Angina Pectoris/therapy
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