Cytotoxicity, hemolysis, and acute in vivo toxicity of dendrimers based on melamine, candidate vehicles for drug delivery

Hui Ting Chen, Michael F. Neerman, Alan R. Parrish*, Eric E. Simanek

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

404 Scopus citations

Abstract

A small library of dendrimers was prepared from a common precursor that is available in 5 g scale in five linear steps at 56% overall yield. The precursor is a generation three dendrimer that displays 48 peripheral sites by incorporating AB4 surface groups. Manipulation of these sites provided six dendrimers that vary in the chemistry of the surface group (amine, guanidine, carboxylate, sulfonate, phosphonate, and PEGylated) that were evaluated for hemolytic potential and cytotoxicity. Cationic dendrimers were found to be more cytotoxic and hemolytic than anionic or PEGylated dendrimers. The PEGylated dendrimer was evaluated for acute toxicity in vivo. No toxicity-neither mortality nor abnormal blood chemistry based on blood urea nitrogen levels or alanine transaminase activity-was observed in doses up to 2.56 g/kg ip and 1.28 g/kg iv.

Original languageEnglish
Pages (from-to)10044-10048
Number of pages5
JournalJournal of the American Chemical Society
Volume126
Issue number32
DOIs
StatePublished - 18 Aug 2004

Fingerprint

Dive into the research topics of 'Cytotoxicity, hemolysis, and acute in vivo toxicity of dendrimers based on melamine, candidate vehicles for drug delivery'. Together they form a unique fingerprint.

Cite this