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  • Author or Editor: M. Iqbal x
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Summary

Andrographolide and betulinic acid are the terpenoids having potential anti-cancer activity. The cytotoxicity activity of both the drugs was carried out separately and in combination on liver cancer HepG2 cell lines. High-performance liquid chromatography (HPLC) and high-performance thin-layer chromatography (HPTLC) methods were developed and validated for simultaneous estimation of these two terpenoids as per the International Conference on Harmonization (ICH) guidelines, which was applied for quantification in nanoformulation. The retention time by HPLC and retardation factor by HPTLC for andrographolide and betulinic acid were found to be 2.2 and 6.6 min, and 0.24 ± 0.01 and 0.66 ± 0.01, respectively. Both the methods were validated for accuracy, precision, repeatability, robustness, limit of detection (LOD), and limit of quantitation (LOQ). The content of andrographolide and betulinic acid in nanoformulation was found to be 96.0% and 98.0% by HPLC and 96.59% and 98.33% by HPTLC, respectively, of labelled claim.

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Alkaline and acidic pH of soil limit crop yield. Products of phenylpropanoid pathway play a key part in plant abiotic stress tolerance. It was aimed to assess efficacy of tyrosinepriming for activation of enzyme involved in phenolic accumulation induction of pH tolerance in maize seedlings. Seeds of two maize cultivars, namely Sadaf (pH tolerant) and S-2002 (pH sensitive), were grown under three pH levels (3, 7 and 11). Eight and twelve days old seedlings were harvested and parted into roots and shoots for the assessment of growth, enzymatic and non-enzymatic antioxidants. PAL activity was directly correlated with total soluble phenolics, flavonoids, growth and seedling vigour. Lower accumulation of phenolics and PAL activity in the pH sensitive (S-2002) cultivar indicated greater oxidative damage caused by pH extremes. Priming improved antioxidative potential by enhancing PAL activity and phenolics accumulation and hence increased growth in maize seedlings.

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Summary

An accurate, sensitive, precise, rapid and isocratic reversed-phase HPLC (RPHPLC) method for analysis of buspirone in the bulk drug and in solid dosage formulations has been developed and validated. The best separation was achieved on a 250 mm × 4.6 mm i.d., 5-μm particle, RP C18 column with 70:30 (υ/υ) methanol-0.01 m sodium dihydrogen phosphate buffer (pH 3.5) as mobile phase at a flow rate of 0.8 mL min−1. UV detection was at 244 nm. Response was a linear function of concentration over the range 0.05–20 μg mL−1 (r = 0.9998) and the limits of detection and quantitation were 3.7 and 11.3 ng mL−1, respectively. The method was validated in accordance with ICH guidelines. The drug was subjected to oxidative, hydrolytic, photolytic, and thermal stress. Degradation products produced as a result of this stress did not interfere with detection of buspirone and the assay can thus be regarded as stability-indicating. The method was used for quantification of buspirone in commercial buspirone tablets and to check content uniformity. The excipients present in the formulation did not interfere with the assay. The method is suitable for application in quality-control laboratories, because it is simple and rapid with good accuracy and precision.

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