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Sunday, 24 May 2015

Prospects of Boswellic Acids as Potential Pharmaceutics

Planta Med 2015; 81(04): 259-271
DOI: 10.1055/s-0034-1396313
Reviews

Georg Thieme Verlag KG Stuttgart · New York

Prospects of Boswellic Acids as Potential Pharmaceutics


Zhiyong Du1, *, Zhenli Liu1, *, Zhangchi Ning2, Yuanyan Liu2, Zhiqian Song1, Chun Wang1, Aiping Lu3, 4
  • 1Institution of Basic Theory, China Academy of Chinese Medical Sciences, Beijing, China
  • 2School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing Municipal Key Laboratory for Basic Research of Chinese Medicine, Beijing, China
  • 3Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences, Beijing, China
  • 4School of Chinese Medicine, Hong Kong Baptist University, Kowloon Tong, Hong Kong SAR, China
Further Information

Abstract

Boswellic acids have long been considered the main bioactive components of frankincense, and many studies in vitro and in animals as well as several clinical studies have confirmed their various bioactivities. In particular, a large number of mechanistic studies have confirmed their anti-inflammatory and antitumor activities. However, not every boswellic acid exhibits a satisfactory pharmacological performance, which depends on the chemical structure and functional groups of the acid. To enhance the pharmacological values of boswellic acids, derivatization has been specifically applied with the aim of discovering more active derivatives of BAs. In addition, the preliminary pharmacokinetic studies of these compounds using various standard methods show their poor bioavailability in humans and rodents, which has led to questions of their pharmacological relevance and potentially limits their use in clinical practice and pharmaceutical development. To improve these effects, some approaches have shown some improvements in effectiveness, and the new formula compatibility approach is considered a very reasonable method for improving the bioavailability of boswellic acids.
* These authors contributed equally to this work.