3.1 Introduction
Traditional medicines have been
used worldwide for centuries, and over 80% of the world population use
traditional medicines to maintain health and cure diseases [ 1 ]. A fundamental prerequisite for the proper delivery of
healthcare with traditional medicines is the use of authentic herbal materials.
When adulterants or erroneous substitutes are dispensed instead, they could
compromise treatments or even cause adverse reactions. In the early 1990s in
Belgium, rapidly progressive interstitial fibrosis and end-stage renal failure
were observed in some 80 women taking a slimming regimen of herbal medicinal
product made from various herbs including Fangji (Stephaniae Tetrandrae Radix)
and Houpo (Magnoliae officinalis Cortex)
[ 2 ] . It was later revealed that
the herb Fangji was adulterated by another herb Guangfangji derived from Aristolochia
fangchi which contains the carcinogenic aristolochic acids [ 3 ]. Many more cases of aristolochic acid nephropathy have
subsequently been reported in many Western and Asian countries [ 4– 8 ]. In addition, substitution of
the traditional medicinal herb Lingxiaohua (Campsis Flos) derived from Campsis
grandiflora by a toxic herb Yangjinhua (Daturae Flos) derived from Datura
metel caused four cases of herbal poisoning in Hong Kong [ 4 ]. In 1996, the herb Weilingxian (Clematidis Radix et
Rhizoma) derived from Clematis species was substituted by a herb derived
from Podophyllum hexandrum [ 9 ].
Subsequently, several poisoning cases were reported worldwide, drawing global
attention to the severe side effects and life-threatening consequences of
adulteration of medicinal materials and their products [ 10, 11 ]. Adulteration is due to: (1)
erroneous adulteration caused by sharing of similar features or absence of
distinguishable characters, (2) intentional substitution of high-value
materials by inexpensive substances, (3) misuse caused by sharing of similar
common names, and (4) historical use of local substitutes. In order to ensure
safety, efficacy and quality of traditional medicines and their products,
identification of medicinal materials is necessary.
There are a number of effective
identification methods which evolve with the improvement of technologies. In
the past, identification of medicinal materials is based on the description of
morphological features as stated in Shengnong Bencaojing (~200 ad
). In a later record, Bencao Gangmu (1,593 ad), morphological features
were graphically illustrated. Nowadays, morphological and microscopic features
provide first-line identification of medicinal materials. These methods
complemented with chemical profiles obtained from thin-layer chromatography (TLC),
high-pressure liquid chromatography (HPLC), or liquid chromatography/mass
spectrometry (LC/MS) are applied to increase the accuracy of identification.
In 1990s, the introduction of
molecular techniques was a major breakthrough in the history of identification
of traditional medicines. Recently, identification of living organisms,
including medicinal materials, by DNA barcodes has been proposed [ 12– 15 ]. The DNA barcode initiative
provides an international standard reference for organism identification. In
the Pharmacopoeia of the People’s Republic of China (2010 edition),
molecular techniques have been added as standard means of identification for
three medicinal materials including Beimu (Fritillariae Cirrhosae Bulbus),
Wushaoshe (Zaocys) and Qishe (Agkistrodon). It is foreseeable that molecular
protocols will be included for more medicinal materials in future editions.
This chapter reviews and comments
on the commonly used molecular authentication techniques. An account on the
strategies and examples for identifying plant and animal medicinal materials at
different taxonomic levels is also included.
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