Source:http://linkedlifedata.com/resource/pubmed/id/19026950
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
8
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pubmed:dateCreated |
2008-11-25
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pubmed:abstractText |
The pharmacokinetics and internal radionuclide therapy of intraperitoneally administrated (188)Re-N,N-bis(2-mercaptoethyl)-N',N'-diethylethylenediamine (BMEDA)-labeled pegylated liposomal doxorubicin ((188)Re-DXR-liposome) were investigated in the C26 murine colon carcinoma ascites mouse model. After intraperitoneal administration of the nanotargeted bimodality (188)Re-DXR-liposome, the ascites and tumor accumulation of the radioactivity were observed, the levels of radioactivity within the ascites were maintained at relatively higher levels before 48 h and the levels of radioactivity in the tumor were maintained at steady levels after 4 h. The AUC((o-->infinity)) of (188)Re-DXR-liposome in blood, ascites and tumor was 9.3-, 4.2- and 4.7-fold larger than that of (188)Re-BMEDA, respectively. The maximum tolerated dose of intraperitoneally administrated (188)Re-DXR-liposome was determined in normal BALB/c mice. The survival, tumor and ascites inhibition of mice after (188)Re-DXR-liposome (22.2 MBq of (188)Re, 5 mg/kg of DXR) treatment were evaluated. Consequently, radiochemotherapeutics of (188)Re-DXR-liposome attained better survival time, tumor and ascites inhibition (decreased by 49% and 91% at 4 days after treatment; P<.05) in mice than radiotherapeutics of (188)Re-liposome or chemotherapeutics of Lipo-Dox did. Therefore, intraperitoneal administration of novel (188)Re-DXR-liposome could provide a benefit and promising strategy for delivery of passive nanotargeted bimodality radiochemotherapeutics in oncology applications.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Doxorubicin,
http://linkedlifedata.com/resource/pubmed/chemical/Polyethylene Glycols,
http://linkedlifedata.com/resource/pubmed/chemical/Radioisotopes,
http://linkedlifedata.com/resource/pubmed/chemical/Rhenium,
http://linkedlifedata.com/resource/pubmed/chemical/pegylated liposomal doxorubicin
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0969-8051
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
35
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
883-93
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pubmed:meshHeading |
pubmed-meshheading:19026950-Animals,
pubmed-meshheading:19026950-Ascites,
pubmed-meshheading:19026950-Autoradiography,
pubmed-meshheading:19026950-Colonic Neoplasms,
pubmed-meshheading:19026950-Doxorubicin,
pubmed-meshheading:19026950-Drug Stability,
pubmed-meshheading:19026950-Isotope Labeling,
pubmed-meshheading:19026950-Male,
pubmed-meshheading:19026950-Maximum Tolerated Dose,
pubmed-meshheading:19026950-Mice,
pubmed-meshheading:19026950-Mice, Inbred BALB C,
pubmed-meshheading:19026950-Nanotechnology,
pubmed-meshheading:19026950-Polyethylene Glycols,
pubmed-meshheading:19026950-Radioisotopes,
pubmed-meshheading:19026950-Rhenium,
pubmed-meshheading:19026950-Tomography, Emission-Computed, Single-Photon,
pubmed-meshheading:19026950-Tomography, X-Ray Computed
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pubmed:year |
2008
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pubmed:articleTitle |
Pharmacokinetics, micro-SPECT/CT imaging and therapeutic efficacy of (188)Re-DXR-liposome in C26 colon carcinoma ascites mice model.
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pubmed:affiliation |
Institute of Nuclear Energy Research, Taoyuan, Taiwan.
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pubmed:publicationType |
Journal Article
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