Subscribe to RSS
DOI: 10.1055/s-0031-1280384
© Georg Thieme Verlag KG Stuttgart · New York
Quantitative Determination of Decursin, Decursinol Angelate, and Decursinol in Mouse Plasma and Tumor Tissue Using Liquid-Liquid Extraction and HPLC
Publication History
received June 22, 2011
revised Nov. 1, 2011
accepted Nov. 6, 2011
Publication Date:
24 November 2011 (online)

Abstract
The pyranocoumarin compound decursin and its isomer decursinol angelate (DA) are the major hydrophobic phytochemicals in the root of Angelica gigas Nakai (AGN, Korean Angelica), a major traditional medicinal herb. The ethanol extract of AGN and especially the purified decursin and DA have been shown to exhibit antitumor activities by our collaborative team and others. Although decursinol has been identified as a major hydrolysis metabolite of decursin and DA in vivo in previous pharmacokinetic studies with mouse and rat, other recently published results sharply disputed this conclusion. In this study, we set up a practical method for the concurrent analysis of decursin, DA, and decursinol in mouse plasma and tumor tissues by liquid–liquid extraction and HPLC-UV and applied the method to several animal experiments. Plasma or tumor homogenate was extracted directly with ethyl acetate. The extraction efficiency for decursin/DA (quantitated together) and decursinol was between 82–95 % in both mouse plasma and tumor homogenate. The lower limit of quantitation (LLOQ) was approximately 0.25 µg/mL for decursin/DA and 0.2 µg/mL for decursinol in mouse plasma. In a pilot pharmacokinetic study, male C57BL/6 mice were given a single dose of 4.8 mg decursin/DA mixture (∼ 240 mg/kg) per mouse either by oral gavage or intraperitoneal injection. Maximum plasma concentrations for decursin/DA and decursinol were 11.2 and 79.7 µg/mL, respectively, when decursin/DA was administered via intraperitoneal injection, and 0.54 and 14.9 µg/mL via oral gavage. Decursin/DA and decursinol contents in the tumor tissues from nude mouse xenografts correlated very well with those in plasma. Overall, our results confirm the conclusion that the majority of decursin/DA hydrolyze to decursinol in rodent models with a tiny fraction remaining as the intact compounds administered.
Key words
decursin/decursinol angelate - decursinol - HPLC - mouse plasma - tumor tissue - Angelica gigas - Apiaceae
References
- 1
Sarker S D, Nahar L.
Natural medicine: the genus Angelica.
Curr Med Chem.
2004;
11
1479-1500
Reference Ris Wihthout Link
- 2
Ahn M J, Lee M K, Kim Y C, Sung S H.
The simultaneous determination of coumarins in Angelica gigas root by high performance liquid chromatography-diode array detector coupled with
electrospray ionization/mass spectrometry.
J Pharm Biomed Anal.
2008;
46
258-266
Reference Ris Wihthout Link
- 3
Jiang C, Lee H J, Li G X, Guo J M, Malewicz B, Zhao Y, Lee E O, Lee J H, Kim M S, Kim S H, Lu J X.
Potent antiandrogen and androgen receptor activities of an Angelica gigas-containing herbal formulation: identification of decursin as a novel and active compound
with implications for prevention and treatment of prostate cancer.
Cancer Res.
2006;
66
453-463
Reference Ris Wihthout Link
- 4
Yim D, Singh R P, Agarwal C, Lee S, Chi H, Agarwal R.
A novel anticancer agent, decursin, induces G(1) arrest and apoptosis in human prostate
carcinoma cells.
Cancer Res.
2005;
65
1035-1044
Reference Ris Wihthout Link
- 5
Song G Y, Lee J H, Cho M, Park B S, Kim D E, Oh S.
Decursin suppresses human androgen-independent PC3 prostate cancer cell proliferation
by promoting the degradation of beta-catenin.
Mol Pharmacol.
2007;
72
1599-1606
Reference Ris Wihthout Link
- 6
Lee H J, Lee E O, Lee J H, Lee K S, Kim K H, Kim S H, Lu J.
In vivo anti-cancer activity of Korean Angelica gigas and its major pyranocoumarin decursin.
Am J Chin Med.
2009;
37
127-142
Reference Ris Wihthout Link
- 7
Jiang C, Guo J, Wang Z, Xiao B, Lee H J, Lee E O, Kim S H, Lu J.
Decursin and decursinol angelate inhibit estrogen-stimulated and estrogen-independent
growth and survival of breast cancer cells.
Breast Cancer Res.
2007;
9
R77
Reference Ris Wihthout Link
- 8
Kim W J, Lee M Y, Kim J H, Suk K, Lee W H.
Decursinol angelate blocks transmigration and inflammatory activation of cancer cells
through inhibition of PI3K, ERK and NF-kappaB activation.
Cancer Lett.
2010;
296
35-42
Reference Ris Wihthout Link
- 9
Kim W J, Lee S J, Choi Y D, Moon S K.
Decursin inhibits growth of human bladder and colon cancer cells via apoptosis, G1-phase
cell cycle arrest and extracellular signal-regulated kinase activation.
Int J Mol Med.
2010;
25
635-641
Reference Ris Wihthout Link
- 10
Son S H, Park K K, Park S K, Kim Y C, Kim Y S, Lee S K, Chung W Y.
Decursin and decursinol from Angelica gigas inhibit the lung metastasis of murine colon carcinoma.
Phytother Res.
advance online publication
2010;
DOI: 10.1002/ptr.3372
Reference Ris Wihthout Link
- 11
Lee S, Lee Y S, Jung S H, Shin K H, Kim B K, Kang S S.
Anti-tumor activities of decursinol angelate and decursin from Angelica gigas.
Arch Pharm Res.
2003;
26
727-730
Reference Ris Wihthout Link
- 12
Xia Y, Min K H, Lee K.
Synthesis and biological evaluation of decursin, prantschimgin and their derivatives.
Bull Korean Chem Soc.
2009;
30
43-48
Reference Ris Wihthout Link
- 13
Kim H J, Kim S M, Park K R, Jang H J, Na Y S, Ahn K S, Kim S H.
Decursin chemosensitizes human multiple myeloma cells through inhibition of STAT3
signaling pathway.
Cancer Lett.
2011;
301
29-37
Reference Ris Wihthout Link
- 14
Kim H H, Bang S S, Choi J S, Han H, Kim I H.
Involvement of PKC and ROS in the cytotoxic of anti-leukemic decursin and its derivatives
mechanism and their structure-activity relationship in human K562 erythroleukemia
and U937 myeloleukemia cells.
Cancer Lett.
2005;
223
191-201
Reference Ris Wihthout Link
- 15
Ahn Q, Jeong S J, Lee H J, Kwon H Y, Han I, Kim H S, Lee E O, Ahn K S, Jung M H, Zhu S, Chen C Y, Kim S H.
Inhibition of cyclooxygenase-2-dependent survivin mediates decursin-induced apoptosis
in human KBM-5 myeloid leukemia cells.
Cancer Lett.
2010;
298
212-221
Reference Ris Wihthout Link
- 16
Guo J, Jiang C, Wang Z, Lee H J, Hu H, Malewicz B, Lee J H, Baek N I, Jeong J H, Kim D K, Kang K S, Kim S H, Lu J.
A novel class of pyranocoumarin anti-androgen receptor signaling compounds.
Mol Cancer Ther.
2007;
6
907-917
Reference Ris Wihthout Link
- 17
Jung M H, Lee S H, Ahn E M, Lee Y M.
Decursin and decursinol angelate inhibit VEGF-induced angiogenesis via suppression
of the VEGFR-2-signaling pathway.
Carcinogenesis.
2009;
30
655-661
Reference Ris Wihthout Link
- 18
Lee Y Y, Lee S, Jin J L, Yun-Choi H S.
Platelet anti-aggregatory effects of coumarins from the roots of Angelica genuflexa and A. gigas.
Arch Pharm Res.
2003;
26
723-726
Reference Ris Wihthout Link
- 19
Li L, Li W, Jung S W, Lee Y M, Kim Y H.
Protective effects of decursin and decursinol angelate against amyloid beta-protein-induced
oxidative stress in the PC12 cell line: the role of Nrf2 and antioxidant enzymes.
Biosci Biotechnol Biochem.
2011;
75
434-442
Reference Ris Wihthout Link
- 20
Yoo H H, Lee M W, Kim Y C, Yun C H, Kim D H.
Mechanism-based inactivation of cytochrome p 450 2A6 by decursinol angelate isolated
from Angelica gigas.
Drug Metab Dispos.
2007;
35
1759-1765
Reference Ris Wihthout Link
- 21
Park R J, Kim N J, Lee K T, Seo S H.
Comparative studies on concentration of decursinol in plasma after oral administration
of Angelicae Gigantis Radix extract and combined use of decursin and Cnidii Rhizoma
extract or Bupleuri Radix extract in rats.
Korean J Pharmacognosy.
2001;
32
72-78
Reference Ris Wihthout Link
- 22
Kim K M, Kim M J, Kang J S.
Absorption, distribution, metabolism, and excretion of decursin and decursinol angelate
from Angelica gigas Nakai.
J Microbiol Biotechnol.
2009;
19
1569-1572
Reference Ris Wihthout Link
- 23
Zhang Y, Shaik A A, Xing C, Chai Y, Li L, Zhang J, Zhang W, Kim S H, Lu J, Jiang C.
A synthetic decursin analog with increased in vivo stability suppresses androgen receptor signaling in vitro and in vivo.
Invest New Drugs.
advance online publication
2011;
DOI: 10.1007/s10637-011-9738-x
Reference Ris Wihthout Link
- 24
Li L, Shaik A A, Zhang J, Nhkata K, Wang L, Zhang Y, Xing C, Kim S H, Lu J.
Preparation of penta-O-galloyl-beta-D-glucose from tannic acid and plasma pharmacokinetic
analyses by liquid-liquid extraction and reverse-phase HPLC.
J Pharm Biomed Anal.
2011;
54
545-550
Reference Ris Wihthout Link
- 25
Weon J B, Yang H J, Ma J Y, Ma C J.
A HPLC-DAD method for the simultaneous determination of five marker components in
the traditional herbal medicine Bangpungtongsung-san.
Pharmacogn Mag.
2011;
7
60-64
Reference Ris Wihthout Link
- 26
Kim K Y, Lee S, Cha C J.
Biotransformation of plant secondary metabolite decursin by Mycobacterium sp. PYR1001.
J Agric Food Chem.
2010;
58
2931-2934
Reference Ris Wihthout Link
Dr. Junxuan Lü
Department of Biomedical Sciences
Texas Tech University Health Sciences Center, School of Pharmacy
1300 S. Coulter St
Amarillo, TX 79106
USA
Phone: +1 80 63 56 40 15 ext. 250
Fax: +1 80 63 56 46 43
Email: junxuan.lu@ttuhsc.edu