Cells involved in the capture of nanoparticles in hematopoietic organs

被引:52
作者
Gibaud, S
Demoy, M
Andreux, JP
Weingarten, C
Gouritin, B
Couvreur, P
机构
[1] UNIV PARIS 11,FAC PHARM,LAB PHYSICOCHIM PHARMACOTECH & BIOPHARM,CNRS,URA 1218,F-92296 CHATENAY MALABRY,FRANCE
[2] UNIV PARIS 11,FAC PHARM,HEMATOL LAB,F-92296 CHATENAY MALABRY,FRANCE
关键词
D O I
10.1021/js960032d
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The affinity of nanoparticles for hematopoietic organs could be valuable for the targeting of certain stimulating factors to those tissues, but this affinity should also be taken into account in the toxicological evaluation of those carriers, especially when they are loaded with antimitotic compounds such as doxorubicin. However, the cells responsible for the capture of the nanoparticles and their localization in these organs is an important point to know before trying to modulate the nanoparticle's tissue distribution. Thus, we have studied, in this paper, the capture, the localization, and the retention in the bone marrow and in the spleen of biodegradable poly(isohexyl cyanoacrylate) nanoparticles as well as of nonbiodegradable polystyrene nanoparticles. The histological localization of these nanoparticles has been completed by cytological localization with a method used in cytochemistry for the evaluation of intracellular accumulation of various substances, such as iron deposits in bone marrow sideroblasts. These data indicate that, in the bone marrow, after a quick passage through the endothelium, nanoparticles were dispersed throughout in the tissue and captured by all types of phagocytizing cells. In the spleen, nanoparticles were mainly localized in large angular capturing cells in the marginal zone of the lymphoid follicles.
引用
收藏
页码:944 / 950
页数:7
相关论文
共 14 条
[1]   HEPATIC TISSUE DISTRIBUTION OF DOXORUBICIN-LOADED NANOPARTICLES AFTER IV ADMINISTRATION IN RETICULOSARCOMA M-5076 METASTASIS-BEARING MICE [J].
CHIANNILKULACHAI, N ;
AMMOURY, N ;
CAILLOU, B ;
DEVISSAGUET, JP ;
COUVREUR, P .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1990, 26 (02) :122-126
[2]   DOXORUBICIN-LOADED NANOPARTICLES - INCREASED EFFICIENCY IN MURINE HEPATIC METASTASES [J].
CHIANNILKULCHAI, N ;
DRIOUICH, Z ;
BENOIT, JP ;
PARODI, AL ;
COUVREUR, P .
SELECTIVE CANCER THERAPEUTICS, 1989, 5 (01) :1-11
[3]   TOXICITY OF POLYALKYLCYANOACRYLATE NANOPARTICLES .2. DOXORUBICIN-LOADED NANOPARTICLES [J].
COUVREUR, P ;
KANTE, B ;
GRISLAIN, L ;
ROLAND, M ;
SPEISER, P .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1982, 71 (07) :790-792
[4]  
CROCKER PR, 1990, BLOOD, V76, P1131
[5]   ISOLATION AND CHARACTERIZATION OF RESIDENT STROMAL MACROPHAGES AND HEMATOPOIETIC-CELL CLUSTERS FROM MOUSE BONE-MARROW [J].
CROCKER, PR ;
GORDON, S .
JOURNAL OF EXPERIMENTAL MEDICINE, 1985, 162 (03) :993-1014
[6]  
DACIE JV, 1966, ACTA MED SCAND, VS179, P237
[7]  
DIJKSTRA CD, 1985, IMMUNOLOGY, V55, P23
[8]   ENDOCYTOSIS BY ENDOTHELIAL PHAGOCYTES - UPTAKE OF BOVINE SERUM-ALBUMIN GOLD CONJUGATES IN BONE-MARROW [J].
GEOFFROY, JS ;
BECKER, RP .
JOURNAL OF ULTRASTRUCTURE RESEARCH, 1984, 89 (03) :223-239
[9]   INCREASED BONE-MARROW TOXICITY OF DOXORUBICIN BOUND TO NANOPARTICLES [J].
GIBAUD, S ;
ANDREUX, JP ;
WEINGARTEN, C ;
RENARD, M ;
COUVREUR, P .
EUROPEAN JOURNAL OF CANCER, 1994, 30A (06) :820-826
[10]  
Graddock CG, 1972, HEMATOLOGY, P607