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REVIEW article

Front. Pharmacol.

Sec. Ethnopharmacology

From Bench to Bedside, Boswellic Acids in Anti-inflammatory Therapy — Mechanistic Insights, Bioavailability Challenges, and Optimization Approaches

Provisionally accepted
Chuhang  PengChuhang Peng1,2Yujia  YangYujia Yang1,2Yuzhi  WangYuzhi Wang1,2Bao  GongBao Gong2Xiuting  SunXiuting Sun1,2Xinquan  YangXinquan Yang2*
  • 1Chinese Academy of Medical Sciences & Peking Union Medical College Institute of Medicinal Plant Development, Beijing, China
  • 2Chinese Academy of Medical Sciences & Peking Union Medical College Institute of Medicinal Plant Development Hainan Branch, Haikou, China

The final, formatted version of the article will be published soon.

Boswellic acids (BAs), a group of pentacyclic triterpenoids derived from the gum resin of Boswellia species, exhibit promising anti-inflammatory potential through diverse mechanisms. This review provides a comprehensive and structured summary of BAs' anti-inflammatory actions, spanning key signaling pathways including NF-κB, MAPK, 5-LOX, COX-2, and NLRP3 inflammasome, as well as their modulation of cytokines, immune cell activity, and oxidative stress. We further highlight recent progress in molecular docking and dynamic simulations that elucidate BA–protein interactions at the structural level. The review integrates evidence from preclinical and clinical studies, with detailed pharmacological parameters such as model types, dose ranges, and control settings. Challenges related to BAs' poor solubility and limited bioavailability are critically addressed. Recent advances in delivery systems, including nanoparticles, micelles, phytosomes, and ligand-targeted carriers—are summarized with mechanistic insight. Safety, toxicity, and formulation limitations are also discussed to provide a balanced perspective on their clinical translation. Overall, this review aims to clarify how BAs exert multi-target immunomodulatory effects and proposes directions for future research and therapeutic development.

Keywords: Boswellic acids1, Anti-inflammatory mechanisms2, Bioavailability3, pharmacokinetics4, Clinical Trials5

Received: 26 Aug 2025; Accepted: 28 Oct 2025.

Copyright: © 2025 Peng, Yang, Wang, Gong, Sun and Yang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Xinquan Yang, xqyang@implad.ac.cn

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.