Activity-Guided Laboratory-Scale Process Development and Preliminary Quality Characterization of Synotis solidaginea Extract: Ethanol Extraction, Macroporous Resin Purification, Antioxidant Activity, and Safety Evaluation

This study developed an activity-guided laboratory-scale process for an extract of the aerial parts of Synotis solidaginea. Extraction conditions using 0–100% (v/v) ethanol–water solutions were screened using 2,2-diphenyl-1-picrylhydrazyl (DPPH) and 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) assays and HaCaT keratinocyte responses, followed by fractionation with AB-8 macroporous resin. The 20–50% ethanol range provided a favorable balance between antioxidant activity and cytocompatibility; 50% ethanol extraction followed by 40% ethanol elution was selected. The final dried purified S. solidaginea extract (SSE) maintained HaCaT viability above 90% at 0.01–0.2 mg/mL under the tested conditions. Under the experimental conditions evaluated, a pooled sample comprising equal masses of ten final SSE batches was classified as non-irritating in the acute eye and repeated skin irritation tests, and negative results were reported in the Ames assay and the Chinese hamster lung (CHL) cell chromosome-aberration assay. These findings are limited to the tested material and endpoints and do not establish comprehensive safety. Rutin identification was supported by liquid chromatography–tandem mass spectrometry (LC-MS/MS), and its content was determined using a preliminary high-performance liquid chromatography (HPLC) method. Reported rutin contents in ten independently prepared laboratory-scale process batches derived from a single homogenized raw-material batch ranged from 2.34% to 2.54%, with a relative standard deviation (RSD) of 2.43%. Microbiological results met the adopted limits at the time of testing. These findings support laboratory-scale process development and preliminary chemical and quality characterization of S. solidaginea extract. Further studies should evaluate independent raw-material lots, complete analytical method validation, and assess storage stability and application-specific safety.

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Journal
Processes
Published
2026-11-04
DOI
https://doi.org/10.3390/pr14213561
Primary Topic
Medicinal Plant Research
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article
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article

Activity-Guided Laboratory-Scale Process Development and Preliminary Quality Characterization of Synotis solidaginea Extract: Ethanol Extraction, Macroporous Resin Purification, Antioxidant Activity, and Safety Evaluation

尼珍, Zhuoga Basang, Jianglan Zhang, 崔浪军 et al.
Processes
Medicinal Plant Research
article

Activity-Guided Laboratory-Scale Process Development and Preliminary Quality Characterization of Synotis solidaginea Extract: Ethanol Extraction, Macroporous Resin Purification, Antioxidant Activity, and Safety Evaluation

尼珍, Zhuoga Basang, Jianglan Zhang, 崔浪军, Chen Liu, Ying Liao, Zhuoma Yongzong, Huan Yang, Qiwu Yang
article en

Abstract

This study developed an activity-guided laboratory-scale process for an extract of the aerial parts of Synotis solidaginea. Extraction conditions using 0–100% (v/v) ethanol–water solutions were screened using 2,2-diphenyl-1-picrylhydrazyl (DPPH) and 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) assays and HaCaT keratinocyte responses, followed by fractionation with AB-8 macroporous resin. The 20–50% ethanol range provided a favorable balance between antioxidant activity and cytocompatibility; 50% ethanol extraction followed by 40% ethanol elution was selected. The final dried purified S. solidaginea extract (SSE) maintained HaCaT viability above 90% at 0.01–0.2 mg/mL under the tested conditions. Under the experimental conditions evaluated, a pooled sample comprising equal masses of ten final SSE batches was classified as non-irritating in the acute eye and repeated skin irritation tests, and negative results were reported in the Ames assay and the Chinese hamster lung (CHL) cell chromosome-aberration assay. These findings are limited to the tested material and endpoints and do not establish comprehensive safety. Rutin identification was supported by liquid chromatography–tandem mass spectrometry (LC-MS/MS), and its content was determined using a preliminary high-performance liquid chromatography (HPLC) method. Reported rutin contents in ten independently prepared laboratory-scale process batches derived from a single homogenized raw-material batch ranged from 2.34% to 2.54%, with a relative standard deviation (RSD) of 2.43%. Microbiological results met the adopted limits at the time of testing. These findings support laboratory-scale process development and preliminary chemical and quality characterization of S. solidaginea extract. Further studies should evaluate independent raw-material lots, complete analytical method validation, and assess storage stability and application-specific safety.

ProcessesVol. 14(21)
Shaanxi Normal University (CN)
Openalex Percentile: Top 17%
Medicinal Plant Research
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