Determination of ASC-J9 in Rat Blood by HPLC-MS/MS
WANG Feng-fei1, ZHANG Xiao-qian2, CAO Cong3, SHENTU Jian-zhong4*,TANG Lan1*
1.Zhejiang University of Technology�� Hangzhou 310014��China; 2. Wenzhou Medical University��Wenzhou 325035��China; 3.Zhejiang University�� Hangzhou 310023��China; 4. The First Affiliated Hospital of Zhejiang University�� Hangzhou 310001��China
Abstract��OBJECTIVE To establish an HPLC-MS/MS method for determination of ASC-J9 in rat blood. METHODS After liquid-liquid extraction, ASC-J9 was separated on a Symmetry C18colume, with mobile phase of acetonitrile-water containing 0.1% formic acid and 10 mmol��L-1 ammonium formate.The flow rate was 1.0 mL��min-1, mass shunt was 0.4 mL��min-1, and column temperature was main tained at 35 ��. Quantification was performed in positive ion multiple-reaction-monitoring(MRM) mode. RESULTS The calibration curve of ASC-J9 had good linearity in the concentration range of 3.54-1 180 ng��mL-1. The extraction recovery rate was within 83.19% to 87.27%,and the intra-day and inter-day RSDs were both less than 8.89%. CONCLUSION This method is specific, sensitive and suitable for determination of ASC-J9 in rat blood.
�����,������,�ܴ�,��������,���. ��ЧҺ��ɫ��-�������òⶨ����ȫѪ�ж��������ص�Ũ��[J]. �й�ҩѧ��־, 2015, 50(22): 1996-1999.
WANG Feng-fei, ZHANG Xiao-qian, CAO Cong, SHENTU Jian-zhong,TANG Lan. Determination of ASC-J9 in Rat Blood by HPLC-MS/MS. Chinese Pharmaceutical Journal, 2015, 50(22): 1996-1999.
WANG B H,ZHANG H W,ZHANG X F,et al. Research progress on pharmacology and dosage form of curcumin[J]. Chin Arch Trade Chin Med(��ҽҩѧ��),2013,31(5):1102-1105.
[2]
WEI X,DU Z Y,ZHENG X,et al. Synthesis and evaluation of curcumin-related compounds for anticancer activity[J]. Eur J Med Chem,2012,53(19):235-245.
[3]
XU Q.Overview of medication for prostate cancer[J]. Drug Evaluation(ҩƷ����),2014(11),(2):22-24.
[4]
SOH S F,HUANG C K,LEE S O, et al.Androgen receptor degradation enhancer ASC-J9 in mouse sera and organs with liquid chromatography tandem mass spectrometry[J]. J Pharm Biom Anal,2014,88:117-122.
[5]
HUANG X W,YANG L,DENG Y P,et al. Plasma protein blinding rates of curcumin by ultrafitration coupled with LC-MS[J]. Strait Pharm J(��Ͽҩѧ),2013,25(11):43-46.
[6]
YAMASHITA S,LAI K P,CHUANG K L,et al. ASC-J9 Suppresses castration resistant prostate cancer growth through degradation of full-length and splice variant androgen receptors[J]. Neoplasia,2012,14(1):74-83.
[7]
MIYAMOTO H,YANG Z M,CHEN Y T,et al. Promotion of bladder cancer development and progression by androgen receptor signals[J]. J Natl Cancer Inst,2007,99(7):558-568.
[8]
SHI Q, SHIH C C, LEE K H. Novel anti-prostate cancer curcumin analogues that enhance androgen receptor degradation activity[J]. Anticancer Agents Med Chem,2009,9(18):904-912.
[9]
WU M H, MA W L,HSU C L. Androgen receptor promotes hepatitis B virus-induced hepatocarcinogenesis through modulation of hepatitis B virus RNA transcription[J]. Sci Transl Med,2010,2(32):32-35.
[10]
FANG L Y,IZUMI K, LIANG L,et al. Infiltrating macrophages promote prostate tumorigenesis via modulating androgen receptor-mediated CCL4-STAT3 signaling[J]. Cancer Res,2014,73(18):5633-5646.
[11]
LIN T H, LEE S O,NIU Y J,et al. Differential androgen deprivation therapies with anti-androgens casodex/bicalutamide or MDV3100/enzalutamide versus anti-androgen receptorASC-J9 lead to promotion versus suppression of prostate cancer metastasis[J]. J Biol Chem,2013,288(27):19359-19369.