Anti-tumor effect of intraperitoneal administration of cisplatin-loaded microspheres to human tumor xenografted nude mice

被引:28
作者
Tamura, T
Fujita, F
Tanimoto, M
Koike, M
Suzuki, A
Fujita, M
Horikiri, Y
Sakamoto, Y
Suzuki, T
Yoshino, H
机构
[1] Tanabe Seiyaku Co Ltd, Discovery Res Lab, DDS Res Dept, Yodogawa Ku, Osaka 5328505, Japan
[2] Expt Canc Chemotherapy Res Lab Co Ltd, Osaka 5620012, Japan
[3] Assoc Anticanc Drug Search, Osaka 5620012, Japan
[4] Osaka Univ, Dept Surg, Microbial Dis Res Inst, Suita, Osaka 5650871, Japan
关键词
cisplatin; microspheres; peritoneal carcinomatosis; human tumor; intraperitoneal administration;
D O I
10.1016/S0168-3659(02)00003-2
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This study evaluates the anti-tumor effect of cisplatin-loaded microspheres (CDDP-MS) against peritoneal carcinomatosis using human tumor xenografts. The incorporated CDDP was released from CDDP-MS for 3 weeks in vivo as well as in vitro. CDDP-MS at a dose of 35 mg/kg (at maximal tolerable dose (MTD)) showed effective anti-tumor activity (tumor growth inhibition rate (IR)=70.3%) against Li-7 (human liver cancer) xenografts transplanted into the peritoneal cavity. This procedure also resulted in increased life span (ILS (%)=47.2%). whereas CDDP dissolved in saline solution (CDDP-SOL) at a dose of 8 mg/kg (at MTD) was ineffective (IR=15.7%, ILS=2.6%). Likewise, CDDP-MS (35 mg/kg) significantly prolonged the mean survival time (ILS=50.8%) compared with a CDDP-SOL group (8 mg/kg) (ILS=13.1%) in the mice with Li-7 xenografts transplanted into the spleen. Furthermore, CDDP-MS showed markedly effective anti-tumor activity (IR=82.2%) against H-154 (human stomach cancer) xenografts, in which CDDP-SOL was effective (IR=69.5%) at the MTDs. The suppressive effect of CDDP-MS on accumulation of malignant ascites was intimately related to unchanged CDDP concentration in ascites. These results demonstrated that the administration of CDDP-MS resulted in an unchanged CDDP concentration in ascites, and induced a sustained tumor growth inhibition along with a prolonged survival time. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:295 / 307
页数:13
相关论文
共 30 条
[1]   Intraperitoneal cisplatin plus intravenous cyclophosphamide versus intravenous cisplatin plus intravenous cyclophosphamide for stage III ovarian cancer [J].
Alberts, DS ;
Liu, PY ;
Hannigan, EV ;
OToole, R ;
Williams, SD ;
Young, JA ;
Franklin, EW ;
ClarkePearson, DL ;
Malviya, VK ;
DuBeshter, B ;
Adelson, MD ;
Hoskins, WJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 335 (26) :1950-1955
[2]  
BOVEN E, 1992, CANCER RES, V52, P5940
[3]   TECHNICAL ASPECTS OF INTRAPERITONEAL CHEMOTHERAPY IN ABDOMINAL CARCINOMATOSIS [J].
BRALY, P ;
DOROSHOW, J ;
HOFF, S .
GYNECOLOGIC ONCOLOGY, 1986, 25 (03) :319-333
[4]  
CASPER ES, 1983, CANCER TREAT REP, V67, P235
[5]  
Crookes P, 1997, CANCER, V79, P1767, DOI 10.1002/(SICI)1097-0142(19970501)79:9<1767::AID-CNCR19>3.0.CO
[6]  
2-W
[7]   INTRAPERITONEAL CHEMOTHERAPY - ANALYSIS OF COMPLICATIONS WITH AN IMPLANTED SUBCUTANEOUS PORT AND CATHETER SYSTEM [J].
DAVIDSON, SA ;
RUBIN, SC ;
MARKMAN, M ;
JONES, WB ;
HAKES, TB ;
REICHMAN, B ;
ALMADRONES, L ;
CHAPMAN, D ;
LEWIS, JL ;
HOSKINS, WJ .
GYNECOLOGIC ONCOLOGY, 1991, 41 (02) :101-106
[8]   MULTIFACTORIAL ANALYSIS OF PARAMETERS INFLUENCING CHEMOSENSITIVITY OF HUMAN CANCER XENOGRAFTS IN NUDE-MICE [J].
FUJITA, F ;
FUJITA, M ;
TAGUCHI, T ;
SHIMOZUMA, K ;
SAKAMOTO, Y ;
KIMOTO, Y ;
HIRAI, T .
INTERNATIONAL JOURNAL OF CANCER, 1989, 43 (04) :637-644
[9]  
FUJITA M, 1994, AM ASS CANC RES, V35, P372
[10]  
FUJITA M, 1993, AM ASS CANC RES, V34, P370