1983
DOI: 10.1016/0142-9612(83)90069-8
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Synthesis of N-(2-hydroxypr opyl) methacrylamide copolymers with antimicrobial activity

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Cited by 43 publications
(10 citation statements)
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“…Because the amount of available drug is limited and there is no release of drug from the device into the adjacent fluid or tissue, the antimicrobial properties of covalently attached agents are limited. Although the authors claimed antimicrobial efficacy by antiadhesive and antiproliferative action of these hybrids [36][37][38] , no in vivo studies have yet demonstrated an antibacterial effect.…”
Section: Covalent Bonding Of Anti-infective Substancesmentioning
confidence: 93%
“…Because the amount of available drug is limited and there is no release of drug from the device into the adjacent fluid or tissue, the antimicrobial properties of covalently attached agents are limited. Although the authors claimed antimicrobial efficacy by antiadhesive and antiproliferative action of these hybrids [36][37][38] , no in vivo studies have yet demonstrated an antibacterial effect.…”
Section: Covalent Bonding Of Anti-infective Substancesmentioning
confidence: 93%
“…The HPMA copolymer with GFLG side chains is made by polymerization of HPMA and methacryloyl-GFLG-nitrophenyl ester monomers, and the drug is conjugated by aminolysis [186,189,192]. Drugs studied have included doxorubicin [185], insulin [193], and ampicillin [190]. The peptide sequence was selected because it is cleavable by cathepsin B, releasing the drug payload into the lysosomal compartment of the target cell, but other peptides could of course be used to target various other enzymes and thus other cell types or compartments of the body using this same basic system.…”
Section: Chemically-responsive Hydrogelsmentioning
confidence: 99%
“…Copolymerization of HPMA with a polymerizable derivative of a drug, e.g., N -(4-aminobenzensulfonyl)- N ′-butylurea [27] is the example of the first route. Insulin [28], chymotrypsin [29,30] and ampicillin [31] (Fig. 2) were attached to HPMA copolymers by aminolysis [32,33] of reactive polymeric precursors.…”
Section: Originsmentioning
confidence: 99%