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pubmed-article:9169989pubmed:dateCreated1997-7-10lld:pubmed
pubmed-article:9169989pubmed:abstractTextA co-polymer of O-methyl polyethylene(glycol)-O'-succinate (MPEGs, m.w. 5100) and poly-l-lysine (PL, median m.w. 32700, degree of polymerization 256) has been synthesized by covalent grafting. The resultant MPEGs-PL (30% modification degree of epsilon-amino groups) had a hydrodynamic diameter corresponding to a 690 kD protein. Free amino groups (180/mol of the co-polymer) were used for conjugation of diethylene pentaacetic or succinic acid residues to MPEGs-PL. The potential of the resultant compound as a carrier of therapeutic and diagnostic drugs was studied using a rodent carcinoma models. The co-polymer had a blood pool half-life of 36h in adenocarcinoma-bearing rats. Radioactively labeled preparations were resistant to trans-chelation with apotransferrin and stable in blood for 24 h. The co-polymer accumulated in solid tumors at the level of 1.5-2% injected dose/g of tumor in 24 h. At that time, 34-40% of the accumulated polymer was associated with tumor cell fraction. The co-polymer non-covalently associated with cis-diamminedichloroplatinum(II), showed a cytostatic effect against mouse F9 carcinoma, and induced a reversal in tumor growth after intravenous administration.lld:pubmed
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pubmed-article:9169989pubmed:pagination321-30lld:pubmed
pubmed-article:9169989pubmed:dateRevised2003-11-14lld:pubmed
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pubmed-article:9169989pubmed:year1997lld:pubmed
pubmed-article:9169989pubmed:articleTitleA long-circulating co-polymer in "passive targeting" to solid tumors.lld:pubmed
pubmed-article:9169989pubmed:affiliationDepartment of Radiology, Massachusetts General Hospital, Boston 02129, USA. abogdanov@helix.mgh.harvard.edulld:pubmed
pubmed-article:9169989pubmed:publicationTypeJournal Articlelld:pubmed
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