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Self microemulsifying formulation of Lagerstroemia speciosa against chemically induced hepatotoxicity

Self microemulsifying formulation is an approach used for enhancing the bioavailability of poorly soluble molecules due to their lipidic nature and small particle size. The objective of the present study was to evaluate the hepatoprotective activity of poorly soluble hydroxy- and polyhydroxy-organic...

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Autores principales: Amresh, Gupta, Agarwal, Vipin Kumar, Rao, Chandana Venkateswara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5755996/
https://www.ncbi.nlm.nih.gov/pubmed/29322005
http://dx.doi.org/10.1016/j.jtcme.2017.05.005
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author Amresh, Gupta
Agarwal, Vipin Kumar
Rao, Chandana Venkateswara
author_facet Amresh, Gupta
Agarwal, Vipin Kumar
Rao, Chandana Venkateswara
author_sort Amresh, Gupta
collection PubMed
description Self microemulsifying formulation is an approach used for enhancing the bioavailability of poorly soluble molecules due to their lipidic nature and small particle size. The objective of the present study was to evaluate the hepatoprotective activity of poorly soluble hydroxy- and polyhydroxy-organic phytomolecules rich Lagerstroemia speciosa leaves extract in modern formulation i.e. “Self microemulsifying System”. Different doses of SME (Self microemulsifying) formulation of L. speciosa leaves extract were evaluated for the hepatoprotective activity against carbon tetrachloride induced liver toxicity in rats. The parameters evaluated were (a) biochemical parameters like serum enzymes: aspartate aminotransferase (AST), serum glutamate pyruvate transaminase (ALT), serum alkaline phosphatase (ALP) and total bilirubin (b) liver antioxidant parameters as estimation of Lipid peroxidation (LPO), catalase (CAT), Superoxide dismutase (SOD) activity and concentration of reduced glutathione (GSH). Oral administration of SME formulation provided the significant protection in marker enzyme of treated group at 100 mg/kg, p.o. as AST (P < 0.001), ALT (P < 0.001), ALP (P < 0.001) and total bilirubin (P < 0.001) comparable to the group treated with silymarin. Treatment with SME formulation at the doses of 100 mg/kg, p.o. significantly prevented the rise in levels of LPO significantly (P < 0.001). The GSH, SOD and CAT contents had significantly (P < 0.001) increased in SME formulation treated groups whereas carbon tetrachloride intoxicated group had shown significant decrease in these parameters compared to control group. Formulation at the dose 100 mg/kg, p.o. has shown maximum protection which was almost comparable to those of the normal control and standard. The histological observations further uphold the results for hepatoprotective activity.
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spelling pubmed-57559962018-01-10 Self microemulsifying formulation of Lagerstroemia speciosa against chemically induced hepatotoxicity Amresh, Gupta Agarwal, Vipin Kumar Rao, Chandana Venkateswara J Tradit Complement Med Original Article Self microemulsifying formulation is an approach used for enhancing the bioavailability of poorly soluble molecules due to their lipidic nature and small particle size. The objective of the present study was to evaluate the hepatoprotective activity of poorly soluble hydroxy- and polyhydroxy-organic phytomolecules rich Lagerstroemia speciosa leaves extract in modern formulation i.e. “Self microemulsifying System”. Different doses of SME (Self microemulsifying) formulation of L. speciosa leaves extract were evaluated for the hepatoprotective activity against carbon tetrachloride induced liver toxicity in rats. The parameters evaluated were (a) biochemical parameters like serum enzymes: aspartate aminotransferase (AST), serum glutamate pyruvate transaminase (ALT), serum alkaline phosphatase (ALP) and total bilirubin (b) liver antioxidant parameters as estimation of Lipid peroxidation (LPO), catalase (CAT), Superoxide dismutase (SOD) activity and concentration of reduced glutathione (GSH). Oral administration of SME formulation provided the significant protection in marker enzyme of treated group at 100 mg/kg, p.o. as AST (P < 0.001), ALT (P < 0.001), ALP (P < 0.001) and total bilirubin (P < 0.001) comparable to the group treated with silymarin. Treatment with SME formulation at the doses of 100 mg/kg, p.o. significantly prevented the rise in levels of LPO significantly (P < 0.001). The GSH, SOD and CAT contents had significantly (P < 0.001) increased in SME formulation treated groups whereas carbon tetrachloride intoxicated group had shown significant decrease in these parameters compared to control group. Formulation at the dose 100 mg/kg, p.o. has shown maximum protection which was almost comparable to those of the normal control and standard. The histological observations further uphold the results for hepatoprotective activity. Elsevier 2017-06-03 /pmc/articles/PMC5755996/ /pubmed/29322005 http://dx.doi.org/10.1016/j.jtcme.2017.05.005 Text en © 2018 Center for Food and Biomolecules, National Taiwan University. Production and hosting by Elsevier Taiwan LLC. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Amresh, Gupta
Agarwal, Vipin Kumar
Rao, Chandana Venkateswara
Self microemulsifying formulation of Lagerstroemia speciosa against chemically induced hepatotoxicity
title Self microemulsifying formulation of Lagerstroemia speciosa against chemically induced hepatotoxicity
title_full Self microemulsifying formulation of Lagerstroemia speciosa against chemically induced hepatotoxicity
title_fullStr Self microemulsifying formulation of Lagerstroemia speciosa against chemically induced hepatotoxicity
title_full_unstemmed Self microemulsifying formulation of Lagerstroemia speciosa against chemically induced hepatotoxicity
title_short Self microemulsifying formulation of Lagerstroemia speciosa against chemically induced hepatotoxicity
title_sort self microemulsifying formulation of lagerstroemia speciosa against chemically induced hepatotoxicity
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5755996/
https://www.ncbi.nlm.nih.gov/pubmed/29322005
http://dx.doi.org/10.1016/j.jtcme.2017.05.005
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