Please use this identifier to cite or link to this item: http://10.1.7.192:80/jspui/handle/123456789/8309
Title: Phytochemical Evaluation and In Vitro Antioxidant and Anti-Inflammatory Effects Of Clerodendrum Serratum Roots
Authors: Acharya, Niyati S.
Patel, Jagruti J.
Keywords: Clerodendrum serratum
Quality issues
Phytochemical analysis
Phenolics
antioxidant
Anti-inflammatory
Issue Date: 2016
Publisher: Innovare Academic Sciences Pvt Ltd
Series/Report no.: IPFP0317;
Abstract: with its phytochemical analysis. Methods: The crude 70% methanolic extract (MECSR) and ethyl acetate (EFCSR), n-butanol (BFCSR) and residual aqueous fractions (AQFCSR) of C. serratum roots were prepared and analyzed for qualitative and quantitative phytochemical study using reported methods. The in vitro anti-inflammatory effects were studied using protein denaturation and proteinase inhibitory assays whereas in vitro free radical scavenging effects were established using DPPH (1,1-diphenyl-2-picrylhydrazyl), modified 2,2’-azinobis (3-ethylbenzothiazoline)-6-sulfonic acid (ABTS) and trolox equivalent antioxidant capacity (TEAC) assays. Results: The qualitative and quantitative phytochemical studies of crude extract and fractions showed the presence of phenolics, flavonoids, saponins, and carbohydrates. All analyzed samples showed dose-dependent anti-inflammatory and free radical scavenging effects in the studied in vitro assays. The IC50 Conclusion: Among the analyzed samples, the EFCSR showed significantly higher free radical scavenging and anti-inflammatory effects in studied assays. The observed activities might be attributed to the higher content of polyphenols present in EFCSR fraction of roots. The present study will provide scientific data to reinforce the traditional claims of roots for treating inflammation, pain and other oxidative stress related diseases. values of MECSR, EFCSR, BFCSR and AQFCSR for scavenging the DPPH and ABTS radical ranged from 12.52±2.21 to 200.47±2.84 μg/ml and 18.12±1.76 to 216.08±1.90 μg/ml, respectively, while that of protein denaturation and proteinase inhibition assays were ranged from 70.76±1.40 to 110.13±1.63 μg/ml and 76.66±2.02 to 116.55±2.19 μg/ml.
Description: International Journal of Pharmacy and Pharmaceutical Sciences, Vol 8, Issue 8, 2016:158-163
URI: http://10.1.7.192:80/jspui/handle/123456789/8309
Appears in Collections:Faculty Papers

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