Chemo-embolization of experimental liver metastases.: Part I:: distribution of biodegradable microspheres of different sizes in an animal model for the locoregional therapy

被引:56
作者
Bastian, P
Bartkowski, R
Köhler, H
Kissel, T
机构
[1] Univ Marburg, Dept Pharmaceut & Biopharm, D-35037 Marburg, Germany
[2] Univ Gottingen, Dept Gen Surg, D-3400 Gottingen, Germany
关键词
microparticles; poly(D; L-lactide-co-glycolide); embolization; chemo-embolization; liver metastases; hepatoma;
D O I
10.1016/S0939-6411(98)00047-2
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
An experimental in vivo rat model was established to simulate the embolization therapy of non-resectable liver metastases with microparticulate systems. The effects of biodegradable microspheres on a transplanted liver-tumor cell Line in rat livers were investigated with respect to particle size. The distribution of fluorescence-labelled microspheres was investigated to characterize the effects of long-term embolization with biodegradable microspheres, and the suitability and relevance of this animal model. Novikoff hepatoma cells were implanted into the central liver lobe of Sprague-Dawley rats. After seven days, four batches of fluorescence-marked microspheres (17 mu m, 25 mu m, 30 mu m, and 40 mu m) were administered into the proper hepatic artery. Liver(including the tumor), lung and spleen were isolated and frozen sections and tissue cubes of liver-, border-, and tumor tissue were prepared. The sections were examined by fluorescence microscopy. The cubes were extracted and the fluorescence of the marker quantified. During operation, microspheres smaller than 40 pm did not cause complete embolization. The slides showed the spreading of the smaller particles to the spleen and lung. Only 40 mu m particles accumulated in the liver and were rarely detectable in other organs. The extraction showed a high concentration of the 40 mu m particles in the border tissue. Apparently they were trapped proximal to the tumor capillary system and therefore showed a high ratio of border/tumor concentration. Microparticles smaller than 40 mu m had a border/tumor concentration ratio of less than one and were distributed to the spleen and lung. In conclusion, a mean particle diameter of at least 40 mu m is required for embolization. Thus, the model shows similarity to clinical situations in the treatment of human liver tumor and metastases. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:243 / 254
页数:12
相关论文
共 40 条
  • [1] ACKERMAN NB, 1969, SURGERY, V66, P1067
  • [2] REGIONAL DELIVERY OF MICROSPHERES TO LIVER METASTASES - THE EFFECTS OF PARTICLE-SIZE AND CONCENTRATION ON INTRAHEPATIC DISTRIBUTION
    ANDERSON, JH
    ANGERSON, WJ
    WILLMOTT, N
    KERR, DJ
    MCARDLE, CS
    COOKE, TG
    [J]. BRITISH JOURNAL OF CANCER, 1991, 64 (06) : 1031 - 1034
  • [3] [Anonymous], 1992, REG CANC
  • [4] CONTROLLED BLOCKING OF HEPATIC-ARTERY FLOW WITH ENZYMATICALLY DEGRADABLE MICROSPHERES COMBINED WITH ONCOLYTIC DRUGS
    ARONSEN, KF
    HELLEKANT, C
    HOLMBERG, J
    ROTHMAN, U
    TEDER, H
    [J]. EUROPEAN SURGICAL RESEARCH, 1979, 11 (02) : 99 - 106
  • [5] EXPERIMENTS ON THE EFFICACY AND TOXICITY OF LOCOREGIONAL CHEMOTHERAPY OF LIVER-TUMORS WITH 5-FLUORO-2'-DEOXYURIDINE (FUDR) AND 5-FLUOROURACIL (5-FU) IN AN ANIMAL-MODEL
    BARTKOWSKI, R
    BERGER, MR
    AGUIAR, JLA
    HENNE, TH
    DORSAM, J
    GEELHAAR, GH
    SCHLAG, P
    HERFARTH, C
    [J]. JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 1986, 111 (01) : 42 - 46
  • [6] ESTIMATION OF LIVER-TUMOR VOLUME USING DIFFERENT FORMULAS - AN EXPERIMENTAL-STUDY IN RATS
    CARLSSON, G
    GULLBERG, B
    HAFSTROM, L
    [J]. JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 1983, 105 (01) : 20 - 23
  • [7] In vitro and in vivo evaluation of PLAGA (50/50) microspheres containing 5-fluorouracil prepared by a solvent evaporation method
    Ciftci, K
    Kas, HS
    Hincal, AA
    Ercan, TM
    Guven, O
    Ruacan, S
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1996, 131 (01) : 73 - 82
  • [8] MICROSPHERES OF 5-FLUOROURACIL USING POLY(DL-LACTIC ACID) - IN-VITRO RELEASE PROPERTIES AND DISTRIBUTION IN MICE AFTER IV ADMINISTRATION
    CIFTCI, K
    HINCAL, AA
    KAS, HS
    ERCAN, MT
    RUACAN, S
    [J]. EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 1994, 1 (05) : 249 - 258
  • [9] CIVALLERI D, 1991, CANCER, V68, P988, DOI 10.1002/1097-0142(19910901)68:5<988::AID-CNCR2820680513>3.0.CO
  • [10] 2-8