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
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1Institution of Basic Theory, China Academy of Chinese Medical Sciences, Beijing, China
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2School of Chinese
Materia Medica, Beijing University of Chinese Medicine, Beijing
Municipal Key Laboratory for Basic Research of Chinese Medicine,
Beijing, China
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3Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences, Beijing, China
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4School of Chinese Medicine, Hong Kong Baptist University, Kowloon Tong, Hong Kong SAR, China
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.
Key words
Boswellia serrata
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Burseraceae -
boswellic acids -
derivatization -
pharmacokinetics -
analysis methods -
new formula
* These authors contributed equally to this work.