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Eur J Med Chem ; 42(1): 20-9, 2007 Jan.
Article in English | MEDLINE | ID: mdl-17010482

ABSTRACT

This paper reports the synthesis and antiproliferative effects of new thiomer-diclofenac and fenoprofen conjugates, hydrophilic, bioadhesive, polymeric prodrugs, as well as antiproliferative effects of diclofenac, fenoprofen and a series of previously described polymer-fenoprofen conjugates on five tumor cell lines. Thiolated and nonthiolated polyaspartamides were the chosen polymeric components. Drug-loading ranged from 5.6 to 22.4%, and the amount of SH groups ranged from 6.9 to 45.6micromol g(-1). Tensile studies demonstrated a clear correlation between the amount of thiol and the mucoadhesive properties of the conjugates. The growth-inhibitory activity of the tested polymer-drug conjugates demonstrates that polyaspartamide-type polymers, especially thiolated polymers, enable inhibition of tumor cell growth with significantly lower doses of the active substance.


Subject(s)
Antineoplastic Agents/chemical synthesis , Diclofenac/analogs & derivatives , Diclofenac/chemical synthesis , Fenoprofen/analogs & derivatives , Fenoprofen/chemical synthesis , Nylons/chemistry , Prodrugs/chemical synthesis , Sulfhydryl Compounds/chemistry , Antineoplastic Agents/pharmacology , Aspartic Acid/analogs & derivatives , Aspartic Acid/chemistry , Cell Line, Tumor , Diclofenac/pharmacology , Drug Carriers , Drug Screening Assays, Antitumor , Fenoprofen/pharmacology , Humans , Prodrugs/pharmacology , Structure-Activity Relationship
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