A validated UHPLC-MS/MS method for determination of TQ-B3203 in human plasma and its application to a pharmacokinetic study in Chinese patients with advanced solid tumor

被引:3
作者
Yang, Fen [1 ]
Zhou, Jun [2 ]
Bo, Yunhai [1 ]
Yin, Han [1 ]
Liu, Xiao Hong [1 ]
Li, Jian [2 ]
机构
[1] Peking Univ, Natl Drug Clin Trial Ctr, Key Lab Carcinogenesis & Translat Res, Canc Hosp & Inst,Minist Educ, Beijing, Peoples R China
[2] Peking Univ, Dept Gastrointestinal Oncol, Key Lab Carcinogenesis & Translat Res, Canc Hosp & Inst,Minist Educ Beijing, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
mass spectrometry; pharmacokinetics; solid tumor; TQ-B3203; TOPOISOMERASE-I; LIPOPHILICITY; CAMPTOTHECIN;
D O I
10.1002/jssc.202001023
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
TQ-B3203 is a new topoisomerase I inhibitor derived from camptothecin. In this paper, a simple and reliable ultra high-performance liquid chromatography-tandem mass spectrometric method was developed and validated for determination of TQ-B3203 in human plasma with TQ-B3203-d(8) used as the internal standard. Bis(p-nitrophenyl)phosphate (2 mol/L) was added to ensure the stability of TQ-B3203 in human plasma. Plasma samples were protein precipitated by methanol and processed samples were chromatographed on an AQUITY BEH C-8 column (50 x 2.1 mm, id 1.7 mu m) with acetonitrile and water (0.1% formic acid) as the mobile phase. The calibration curves showed good linearity (R >= 0.99) over the concentration range of 0.5-500 ng/mL. Within- and between-run precision were <= 5.8% and the accuracy was within the range of -8.3 to 14.0%. This method was further successfully applied to a pharmacokinetic study of TQ-B3203 in Chinese advanced solid cancer patients after administration of TQ-B3203 liposome injection.
引用
收藏
页码:945 / 953
页数:10
相关论文
共 16 条
[1]   Camptothecin analogs with enhanced activity against human breast cancer cells. I. Correlation of potency with lipophilicity and persistence in the cleavage complex [J].
Adams, DJ ;
da Silva, MW ;
Flowers, JL ;
Kohlhagen, G ;
Pommier, Y ;
Colvin, OM ;
Manikumar, G ;
Wani, MC .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2006, 57 (02) :135-144
[2]  
[Anonymous], 2011, GUIDELINE BIOANALYTI
[3]  
[Anonymous], 2018, Guidance for Industry: Bioanalytical Method Validation
[4]   The novel silatecan 7-tert-butyldimethylsilyl-10-hydroxycamptothecin displays high lipophilicity, improved human blood stability, and potent anticancer activity [J].
Bom, D ;
Curran, DP ;
Kruszewski, S ;
Zimmer, SG ;
Strode, JT ;
Kohlhagen, G ;
Du, W ;
Chavan, AJ ;
Fraley, KA ;
Bingcang, AL ;
Latus, LJ ;
Pommier, Y ;
Burke, TG .
JOURNAL OF MEDICINAL CHEMISTRY, 2000, 43 (21) :3970-3980
[5]   A PHASE-II STUDY OF CPT-11, A NEW DERIVATIVE OF CAMPTOTHECIN, FOR PREVIOUSLY UNTREATED NON-SMALL-CELL LUNG-CANCER [J].
FUKUOKA, M ;
NIITANI, H ;
SUZUKI, A ;
MOTOMIYA, M ;
HASEGAWA, K ;
NISHIWAKI, Y ;
KURIYAMA, T ;
ARIYOSHI, Y ;
NEGORO, S ;
MASUDA, N ;
NAKAJIMA, S ;
TAGUCHI, T ;
ASAKAWA, M ;
NAKABAYASI, T ;
NAKAI, T ;
KURITA, Y ;
KINAMERI, K ;
NOMURA, K ;
NAGAO, K ;
SAIJO, N ;
OHE, Y ;
SUGIURA, T ;
SHIMOKATA, K ;
SAKA, H ;
NEGORO, S ;
NAKAJIMA, S ;
TOHDA, Y ;
FUJII, M ;
OTA, M ;
HARA, N ;
HARA, Y ;
FUJISAWA, K ;
NAKANO, S ;
ARAKI, J ;
NIITANI, H ;
MIYATA, Y .
JOURNAL OF CLINICAL ONCOLOGY, 1992, 10 (01) :16-20
[6]   Pros and cons of the liposome platform in cancer drug targeting [J].
Gabizon, Alberto A. ;
Shmeeda, Hilary ;
Zalipsky, Samuel .
JOURNAL OF LIPOSOME RESEARCH, 2006, 16 (03) :175-183
[7]  
HSIANG YH, 1988, CANCER RES, V48, P1722
[8]   肝脏和肠道酯酶在药物代谢及新药研发中的作用 [J].
姜金方 ;
李秀立 ;
陈笑艳 ;
钟大放 .
药学学报 , 2018, (02) :177-185
[9]   Crystal structures of human topoisomerase I in covalent and noncovalent complexes with DNA [J].
Redinbo, MR ;
Stewart, L ;
Kuhn, P ;
Champoux, JJ ;
Hol, WGJ .
SCIENCE, 1998, 279 (5356) :1504-1513
[10]  
Schubert R., 2002, EUR J PHARM BIOPHARM, V54, P358