Quantitative Analysis, Extraction Optimization, and Biological Evaluation of Cudrania tricuspidata Leaf and Fruit Extracts

Cudrania tricuspidata Bureau (Moraceae) shows numerous pharmacological effects and has been used in traditional herbal remedies for inflammation, gastritis, tumors, and liver diseases. However, no validated analytical method for the standardization and optimization of the biological properties of C....

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Main Authors: Seung-Hui Song, Sung Hwan Ki, Dae-Hun Park, Hong-Seop Moon, Chang-Dai Lee, In-Soo Yoon, Seung-Sik Cho
Format: Article
Language:English
Published: MDPI AG 2017-09-01
Series:Molecules
Subjects:
Online Access:https://www.mdpi.com/1420-3049/22/9/1489
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author Seung-Hui Song
Sung Hwan Ki
Dae-Hun Park
Hong-Seop Moon
Chang-Dai Lee
In-Soo Yoon
Seung-Sik Cho
author_facet Seung-Hui Song
Sung Hwan Ki
Dae-Hun Park
Hong-Seop Moon
Chang-Dai Lee
In-Soo Yoon
Seung-Sik Cho
author_sort Seung-Hui Song
collection DOAJ
description Cudrania tricuspidata Bureau (Moraceae) shows numerous pharmacological effects and has been used in traditional herbal remedies for inflammation, gastritis, tumors, and liver diseases. However, no validated analytical method for the standardization and optimization of the biological properties of C. tricuspidata preparations has been reported. We developed and validated a reverse-phase high-performance liquid chromatography (HPLC) method for the separation and quantification of active markers. Ethanolic extracts of C. tricuspidata leaves were prepared and evaluated for chemical profiles and biological activities. The 80% ethanolic extract demonstrated the greatest antioxidant activity and phenolic content, while the 100% ethanolic extract had the greatest total flavonoid content and xanthine oxidase (XO) inhibitory activity. The validated HPLC method confirmed that chlorogenic acid, rutin, and kaempferol were present in C. tricuspidata leaf extracts. We postulated that the antioxidant and anti-hyperuricemic/gout effects of C. tricuspidata extract could be attributed to these marker compounds. Our results suggested that the flavonoid-rich fraction of the leaf extract may be utilized for the treatment and prevention of hyperuricemia-related diseases, and the validated method and marker compounds could be applied for the quality control of C. tricuspidata preparations.
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spelling doaj.art-a1604b9429264c91b546190ff5c349b32022-12-21T21:11:21ZengMDPI AGMolecules1420-30492017-09-01229148910.3390/molecules22091489molecules22091489Quantitative Analysis, Extraction Optimization, and Biological Evaluation of Cudrania tricuspidata Leaf and Fruit ExtractsSeung-Hui Song0Sung Hwan Ki1Dae-Hun Park2Hong-Seop Moon3Chang-Dai Lee4In-Soo Yoon5Seung-Sik Cho6Department of Pharmacy, College of Pharmacy, Mokpo National University, Muan-gun, Jeonnam 58554, KoreaLaboratory of Toxicology, College of Pharmacy, Chosun University, Dong-gu, Gwangju 61452, KoreaDepartment of Nursing, Dongshin University, Naju-si, Jeonnam 58245, KoreaDepartment of Pharmacy, College of Pharmacy, Mokpo National University, Muan-gun, Jeonnam 58554, KoreaDepartment of Business Administration, Mokpo National University, Muan-gun, Jeonnam 58554, KoreaDepartment of Manufacturing Pharmacy, College of Pharmacy, Pusan National University, Geumjeong-gu, Busan 46241, KoreaDepartment of Pharmacy, College of Pharmacy, Mokpo National University, Muan-gun, Jeonnam 58554, KoreaCudrania tricuspidata Bureau (Moraceae) shows numerous pharmacological effects and has been used in traditional herbal remedies for inflammation, gastritis, tumors, and liver diseases. However, no validated analytical method for the standardization and optimization of the biological properties of C. tricuspidata preparations has been reported. We developed and validated a reverse-phase high-performance liquid chromatography (HPLC) method for the separation and quantification of active markers. Ethanolic extracts of C. tricuspidata leaves were prepared and evaluated for chemical profiles and biological activities. The 80% ethanolic extract demonstrated the greatest antioxidant activity and phenolic content, while the 100% ethanolic extract had the greatest total flavonoid content and xanthine oxidase (XO) inhibitory activity. The validated HPLC method confirmed that chlorogenic acid, rutin, and kaempferol were present in C. tricuspidata leaf extracts. We postulated that the antioxidant and anti-hyperuricemic/gout effects of C. tricuspidata extract could be attributed to these marker compounds. Our results suggested that the flavonoid-rich fraction of the leaf extract may be utilized for the treatment and prevention of hyperuricemia-related diseases, and the validated method and marker compounds could be applied for the quality control of C. tricuspidata preparations.https://www.mdpi.com/1420-3049/22/9/1489C. tricuspidata Bureausimultaneous analysisHPLCxanthine oxidasehyperuricemia
spellingShingle Seung-Hui Song
Sung Hwan Ki
Dae-Hun Park
Hong-Seop Moon
Chang-Dai Lee
In-Soo Yoon
Seung-Sik Cho
Quantitative Analysis, Extraction Optimization, and Biological Evaluation of Cudrania tricuspidata Leaf and Fruit Extracts
Molecules
C. tricuspidata Bureau
simultaneous analysis
HPLC
xanthine oxidase
hyperuricemia
title Quantitative Analysis, Extraction Optimization, and Biological Evaluation of Cudrania tricuspidata Leaf and Fruit Extracts
title_full Quantitative Analysis, Extraction Optimization, and Biological Evaluation of Cudrania tricuspidata Leaf and Fruit Extracts
title_fullStr Quantitative Analysis, Extraction Optimization, and Biological Evaluation of Cudrania tricuspidata Leaf and Fruit Extracts
title_full_unstemmed Quantitative Analysis, Extraction Optimization, and Biological Evaluation of Cudrania tricuspidata Leaf and Fruit Extracts
title_short Quantitative Analysis, Extraction Optimization, and Biological Evaluation of Cudrania tricuspidata Leaf and Fruit Extracts
title_sort quantitative analysis extraction optimization and biological evaluation of cudrania tricuspidata leaf and fruit extracts
topic C. tricuspidata Bureau
simultaneous analysis
HPLC
xanthine oxidase
hyperuricemia
url https://www.mdpi.com/1420-3049/22/9/1489
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