Sil Thanh Nguyen, Ngan Hong Tran, Yen Phuong Ngo, Vi Lan Le Truong, Tuyet Anh Thi Phan, Hien Trung Do, Tho Vinh Minh Chau Do
{"title":"基于槲皮素和槲皮素3- o -葡糖苷的高效液相色谱/PDA方法在荷叶药材质量标准中的应用研究","authors":"Sil Thanh Nguyen, Ngan Hong Tran, Yen Phuong Ngo, Vi Lan Le Truong, Tuyet Anh Thi Phan, Hien Trung Do, Tho Vinh Minh Chau Do","doi":"10.1016/j.rechem.2025.102291","DOIUrl":null,"url":null,"abstract":"<div><div>This study enhances quality control standards for <em>Folium Nelumbinis</em>, a medicinal herb in the Vietnamese and Chinese Pharmacopeias. Current standards are insufficient for accurately quantifying key bioactive compounds, nuciferine and quercetin 3-<em>O</em>-glucuronide, which are vital for the plant's pharmacological effects. The quality control standards include sensory characteristics, microscopic features, powder examination, physicochemical properties, limits for heavy metals, and qualitative. Additionally, simultaneous quantification of nuciferine and quercetin 3-<em>O</em>-glucuronide was achieved using HPLC on a GL Inert Sustain C18 column (250 mm × 4.6 mm, 5 μm). The mobile phase, consisting of acetonitrile (A) and 0.1 % triethylamine in water at pH 6.5 adjusted with 30 % acetic acid (B), was used with a flow rate of 1 mL/min and a detection wavelength of 270 nm. A 200 mg <em>Folium nelumbinis</em> powder was extracted with 6.0 mL of methanol and 1 % hydrochloric acid (6:4, <em>v</em>/v) via ultrasonication at 40 kHz and 500 W for 7 min, followed by centrifugation at 6000 rpm for 7 min (repeated three times). Physico-chemical standards studied are moisture content (8.74 %, <em>w</em>/w), impurities (0.74 %, w/w), fragmentation ratio (1.07 %, w/w), and ash content (6.50 %, w/w). The linearity of the calibration curve ranged from 12 to 48 μg/mL for nuciferine and 4–16 μg/mL for quercetin 3-<em>O</em>-glucuronide, and the square of the regression coefficient (r<sup>2</sup>) was 0.9990 and 0.9954, respectively. The limit of detection and quantification values were determined as 0.45 μg/mL and 1.50 μg/mL for nuciferine and 0.15 μg/mL and 0.50 μg/mL for quercetin 3-<em>O</em>-glucuronide. This research successfully establishes high-quality control standards for Lotus leaves in accordance with WHO guidelines and the Vietnamese Pharmacopoeia V. The validated HPLC method ensures precise and reliable quality control, supporting research consistency and practical herbal medicine application.</div></div>","PeriodicalId":420,"journal":{"name":"Results in Chemistry","volume":"15 ","pages":"Article 102291"},"PeriodicalIF":2.5000,"publicationDate":"2025-04-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Research on the application of the HPLC/PDA method to enhance the quality standards of Folium nelumbinis based on the bioactive nuciferine and quercetin 3-O-glucuronide\",\"authors\":\"Sil Thanh Nguyen, Ngan Hong Tran, Yen Phuong Ngo, Vi Lan Le Truong, Tuyet Anh Thi Phan, Hien Trung Do, Tho Vinh Minh Chau Do\",\"doi\":\"10.1016/j.rechem.2025.102291\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>This study enhances quality control standards for <em>Folium Nelumbinis</em>, a medicinal herb in the Vietnamese and Chinese Pharmacopeias. Current standards are insufficient for accurately quantifying key bioactive compounds, nuciferine and quercetin 3-<em>O</em>-glucuronide, which are vital for the plant's pharmacological effects. The quality control standards include sensory characteristics, microscopic features, powder examination, physicochemical properties, limits for heavy metals, and qualitative. Additionally, simultaneous quantification of nuciferine and quercetin 3-<em>O</em>-glucuronide was achieved using HPLC on a GL Inert Sustain C18 column (250 mm × 4.6 mm, 5 μm). The mobile phase, consisting of acetonitrile (A) and 0.1 % triethylamine in water at pH 6.5 adjusted with 30 % acetic acid (B), was used with a flow rate of 1 mL/min and a detection wavelength of 270 nm. A 200 mg <em>Folium nelumbinis</em> powder was extracted with 6.0 mL of methanol and 1 % hydrochloric acid (6:4, <em>v</em>/v) via ultrasonication at 40 kHz and 500 W for 7 min, followed by centrifugation at 6000 rpm for 7 min (repeated three times). Physico-chemical standards studied are moisture content (8.74 %, <em>w</em>/w), impurities (0.74 %, w/w), fragmentation ratio (1.07 %, w/w), and ash content (6.50 %, w/w). The linearity of the calibration curve ranged from 12 to 48 μg/mL for nuciferine and 4–16 μg/mL for quercetin 3-<em>O</em>-glucuronide, and the square of the regression coefficient (r<sup>2</sup>) was 0.9990 and 0.9954, respectively. The limit of detection and quantification values were determined as 0.45 μg/mL and 1.50 μg/mL for nuciferine and 0.15 μg/mL and 0.50 μg/mL for quercetin 3-<em>O</em>-glucuronide. This research successfully establishes high-quality control standards for Lotus leaves in accordance with WHO guidelines and the Vietnamese Pharmacopoeia V. 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引用次数: 0
摘要
本研究旨在提高越中药典药材荷叶的质量控制标准。目前的标准不足以准确定量对植物药理作用至关重要的关键生物活性化合物,如nuciferine和槲皮素3-O-glucuronide。质量控制标准包括感官特征、显微特征、粉末检验、理化性质、重金属限量和定性。此外,在GL Inert Sustain C18色谱柱(250 mm × 4.6 mm, 5 μm)上,采用高效液相色谱法同时定量了荷叶碱和槲皮素3- o -葡糖苷。流动相为乙腈(A)和0.1%三乙胺,pH为6.5,用30%醋酸(B)调节,流速为1 mL/min,检测波长为270 nm。取200mg荷叶粉,用6.0 mL甲醇和1%盐酸(6:4,v/v),在40 kHz和500 W下超声提取7 min, 6000 rpm离心7 min(重复3次)。理化指标为水分含量(8.74%,w/w)、杂质含量(0.74%,w/w)、破碎率(1.07%,w/w)和灰分含量(6.50%,w/w)。槲皮素3- o -葡萄糖苷的线性范围为12 ~ 48 μg/mL,槲皮素3- o -葡萄糖苷的线性范围为4 ~ 16 μg/mL,回归系数(r2)的平方分别为0.9990和0.9954。检测限和定量值分别为:荷叶碱0.45 μg/mL和1.50 μg/mL,槲皮素3- o -葡糖苷0.15 μg/mL和0.50 μg/mL。本研究根据世界卫生组织指南和越南药典第五版建立了荷叶的高质量控制标准,有效的高效液相色谱法保证了质量控制的准确性和可靠性,支持了研究的一致性和草药的实际应用。
Research on the application of the HPLC/PDA method to enhance the quality standards of Folium nelumbinis based on the bioactive nuciferine and quercetin 3-O-glucuronide
This study enhances quality control standards for Folium Nelumbinis, a medicinal herb in the Vietnamese and Chinese Pharmacopeias. Current standards are insufficient for accurately quantifying key bioactive compounds, nuciferine and quercetin 3-O-glucuronide, which are vital for the plant's pharmacological effects. The quality control standards include sensory characteristics, microscopic features, powder examination, physicochemical properties, limits for heavy metals, and qualitative. Additionally, simultaneous quantification of nuciferine and quercetin 3-O-glucuronide was achieved using HPLC on a GL Inert Sustain C18 column (250 mm × 4.6 mm, 5 μm). The mobile phase, consisting of acetonitrile (A) and 0.1 % triethylamine in water at pH 6.5 adjusted with 30 % acetic acid (B), was used with a flow rate of 1 mL/min and a detection wavelength of 270 nm. A 200 mg Folium nelumbinis powder was extracted with 6.0 mL of methanol and 1 % hydrochloric acid (6:4, v/v) via ultrasonication at 40 kHz and 500 W for 7 min, followed by centrifugation at 6000 rpm for 7 min (repeated three times). Physico-chemical standards studied are moisture content (8.74 %, w/w), impurities (0.74 %, w/w), fragmentation ratio (1.07 %, w/w), and ash content (6.50 %, w/w). The linearity of the calibration curve ranged from 12 to 48 μg/mL for nuciferine and 4–16 μg/mL for quercetin 3-O-glucuronide, and the square of the regression coefficient (r2) was 0.9990 and 0.9954, respectively. The limit of detection and quantification values were determined as 0.45 μg/mL and 1.50 μg/mL for nuciferine and 0.15 μg/mL and 0.50 μg/mL for quercetin 3-O-glucuronide. This research successfully establishes high-quality control standards for Lotus leaves in accordance with WHO guidelines and the Vietnamese Pharmacopoeia V. The validated HPLC method ensures precise and reliable quality control, supporting research consistency and practical herbal medicine application.