Pharmacokinetics of Compound D, the Major Bioactive Component of Zingiber cassumunar, in Rats
© Georg Thieme Verlag KG Stuttgart New York. Rhizomes of Zingiber cassumunar have been used for many years in traditional Thai medicine as an anti-inflammatory agent. The major bioactive component of this plant is Compound D [E-4-(3′, 4′-dimethoxyphenyl)but-3-en-1-ol], which is a strong smooth muscl...
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th-mahidol.429392019-03-14T15:03:59Z Pharmacokinetics of Compound D, the Major Bioactive Component of Zingiber cassumunar, in Rats Phisit Khemawoot Natthaphon Hunsakunachai Tosapol Anukunwithaya Kunan Bangphumi Boonsri Ongpipattanakul Weena Jiratchariyakul Ruedee Soawakontha Thanakorn Inthachart Thaweephol Dechatiwongse Na Ayudhya Sittichai Koontongkaew Orapan Poachanukoon Chulalongkorn University Mahidol University Huachiew Chalermprakiet University Thammasat University Faculty of Medicine, Thammasat University Biochemistry, Genetics and Molecular Biology Chemistry Medicine © Georg Thieme Verlag KG Stuttgart New York. Rhizomes of Zingiber cassumunar have been used for many years in traditional Thai medicine as an anti-inflammatory agent. The major bioactive component of this plant is Compound D [E-4-(3′, 4′-dimethoxyphenyl)but-3-en-1-ol], which is a strong smooth muscle relaxant, and has antihistamine and anti-inflammatory actions. There is, however, incomplete information available for the pharmacokinetics of Compound D in mammals. In this study, we examined the pharmacokinetic profiles of Compound D in male Wistar rats. A standardized extract of Z. cassumunar containing 4% w/w Compound D was administered intravenously at 25 mg/kg or by oral gavage at 25, 75, or 250 mg/kg to Wistar rats. Blood, tissues, urine, and feces were collected from 0 to 48 h after dosing and the level of Compound D was determined by liquid chromatography-tandem mass spectrometry. The concentration of Compound D ranged from 10-100 μg/L, reached a maximum approximately 0.15 h after oral dosing. Compound D exhibited an excellent tissue to plasma ratio, ranging from 1- to 1000 in several organs at 1-4 h after oral dosing. Less than 1% of unchanged Compound D was excreted in the urine and feces. Further studies on tissue uptake and metabolite identification are required to obtain complete pharmacokinetic information and to develop appropriate dosing strategies of Compound D and the standardized extract of Z. cassumunar. 2018-12-11T02:11:21Z 2019-03-14T08:03:59Z 2018-12-11T02:11:21Z 2019-03-14T08:03:59Z 2016-08-01 Article Planta Medica. Vol.82, No.13 (2016), 1186-1191 10.1055/s-0042-104658 14390221 00320943 2-s2.0-84992303032 https://repository.li.mahidol.ac.th/handle/123456789/42939 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84992303032&origin=inward |
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Biochemistry, Genetics and Molecular Biology Chemistry Medicine Phisit Khemawoot Natthaphon Hunsakunachai Tosapol Anukunwithaya Kunan Bangphumi Boonsri Ongpipattanakul Weena Jiratchariyakul Ruedee Soawakontha Thanakorn Inthachart Thaweephol Dechatiwongse Na Ayudhya Sittichai Koontongkaew Orapan Poachanukoon Pharmacokinetics of Compound D, the Major Bioactive Component of Zingiber cassumunar, in Rats |
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© Georg Thieme Verlag KG Stuttgart New York. Rhizomes of Zingiber cassumunar have been used for many years in traditional Thai medicine as an anti-inflammatory agent. The major bioactive component of this plant is Compound D [E-4-(3′, 4′-dimethoxyphenyl)but-3-en-1-ol], which is a strong smooth muscle relaxant, and has antihistamine and anti-inflammatory actions. There is, however, incomplete information available for the pharmacokinetics of Compound D in mammals. In this study, we examined the pharmacokinetic profiles of Compound D in male Wistar rats. A standardized extract of Z. cassumunar containing 4% w/w Compound D was administered intravenously at 25 mg/kg or by oral gavage at 25, 75, or 250 mg/kg to Wistar rats. Blood, tissues, urine, and feces were collected from 0 to 48 h after dosing and the level of Compound D was determined by liquid chromatography-tandem mass spectrometry. The concentration of Compound D ranged from 10-100 μg/L, reached a maximum approximately 0.15 h after oral dosing. Compound D exhibited an excellent tissue to plasma ratio, ranging from 1- to 1000 in several organs at 1-4 h after oral dosing. Less than 1% of unchanged Compound D was excreted in the urine and feces. Further studies on tissue uptake and metabolite identification are required to obtain complete pharmacokinetic information and to develop appropriate dosing strategies of Compound D and the standardized extract of Z. cassumunar. |
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Chulalongkorn University |
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Chulalongkorn University Phisit Khemawoot Natthaphon Hunsakunachai Tosapol Anukunwithaya Kunan Bangphumi Boonsri Ongpipattanakul Weena Jiratchariyakul Ruedee Soawakontha Thanakorn Inthachart Thaweephol Dechatiwongse Na Ayudhya Sittichai Koontongkaew Orapan Poachanukoon |
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Article |
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Phisit Khemawoot Natthaphon Hunsakunachai Tosapol Anukunwithaya Kunan Bangphumi Boonsri Ongpipattanakul Weena Jiratchariyakul Ruedee Soawakontha Thanakorn Inthachart Thaweephol Dechatiwongse Na Ayudhya Sittichai Koontongkaew Orapan Poachanukoon |
author_sort |
Phisit Khemawoot |
title |
Pharmacokinetics of Compound D, the Major Bioactive Component of Zingiber cassumunar, in Rats |
title_short |
Pharmacokinetics of Compound D, the Major Bioactive Component of Zingiber cassumunar, in Rats |
title_full |
Pharmacokinetics of Compound D, the Major Bioactive Component of Zingiber cassumunar, in Rats |
title_fullStr |
Pharmacokinetics of Compound D, the Major Bioactive Component of Zingiber cassumunar, in Rats |
title_full_unstemmed |
Pharmacokinetics of Compound D, the Major Bioactive Component of Zingiber cassumunar, in Rats |
title_sort |
pharmacokinetics of compound d, the major bioactive component of zingiber cassumunar, in rats |
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2018 |
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https://repository.li.mahidol.ac.th/handle/123456789/42939 |
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1763497917647159296 |