Seo · Pharmacognosy magazine 2016 · in vitro cell culture and chromatographic analysis · n=?

Quantitative Analysis and In vitro Anti-inflammatory Effects of Gallic Acid, Ellagic Acid, and Quercetin from Radix Sanguisorbae.

Cited 58 times in the scientific literature.

Level 5 - mechanism / opinion, no new human data

In vitro cell line study and analytical chemistry quantification.

PubMed 27076745 · doi:10.4103/0973-1296.177908 · record verified 2026-08-28

What was done

Researchers developed a reversed-phase high-performance liquid chromatography coupled with photodiode array detection (HPLC-PDA) method to quantify gallic acid, ellagic acid, and quercetin in an extract of Radix Sanguisorbae. They then evaluated the anti-inflammatory properties and cytotoxicity of these three isolated marker compounds in lipopolysaccharide (LPS)-stimulated murine macrophage cells (RAW 264.7), measuring prostaglandin E2 (PGE2), tumor necrosis factor alpha (TNF-alpha), and interleukin-6 (IL-6).

What was found

Ellagic acid was the predominant marker component among those measured, quantified at 7.65 mg/g in the Radix Sanguisorbae extract. All three phytochemicals inhibited PGE2 production in LPS-stimulated RAW 264.7 macrophages without exhibiting cytotoxicity. Ellagic acid also significantly reduced the secretion of the proinflammatory cytokines TNF-alpha and IL-6, though exact numerical inhibition levels and concentrations for gallic acid and quercetin were not reported in the abstract.

Why it matters

This study provides an analytical method for quality control of Radix Sanguisorbae and identifies ellagic acid as a primary bioactive constituent contributing to its reported anti-inflammatory properties in vitro.

Limits

The study is restricted to in vitro testing in a murine cell line (RAW 264.7), lacking in vivo pharmacokinetic, bioavailability, or efficacy verification in animal models or humans. Specific concentrations, IC50 values, and numerical effect sizes for cytokine and PGE2 inhibition were omitted from the abstract.

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