2000
DOI: 10.1016/s0142-9612(00)00073-9
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Synthesis and degradation characteristics of salicylic acid-derived poly(anhydride-esters)

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Cited by 180 publications
(187 citation statements)
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“…Erdmann et al [49] have reported salicylic acid -based polymers in year 2000 and these have then been investigated extensively in the last few years. These salicylatebased polyanhydride -esters were collectively referred to as PolyAspirin because they hydrolytically degrade into salicylic acid, a nonsteroidal anti -infl ammatory drug.…”
Section: Salicylate -Based Polyanhydridesmentioning
confidence: 99%
“…Erdmann et al [49] have reported salicylic acid -based polymers in year 2000 and these have then been investigated extensively in the last few years. These salicylatebased polyanhydride -esters were collectively referred to as PolyAspirin because they hydrolytically degrade into salicylic acid, a nonsteroidal anti -infl ammatory drug.…”
Section: Salicylate -Based Polyanhydridesmentioning
confidence: 99%
“…M W of the copolyanhydrides decreases with an increase in dMOCPS fraction, which is similar to other copolyanhydrides containing SA residues. 3,4,25 Thermal properties of the copolyanhydrides were evaluated with DSC (Table I). It can be seen that glass-transition temperatures (T g ) of P(dMOCPS:SA) decreases from 52 to 9°C as dMOCPS content in- creases to 50%, then increases to 116°C in the case of P(dMOCPS) homopolymer, revealing a negative linearity of T g as a function of monomer fraction.…”
Section: Synthesis and Characterization Of The Copolyanhydridesmentioning
confidence: 99%
“…[14][15][16] Polymer 1 is unique in that the drug 2 is chemically incorporated into the polymer backbone, not attached as a side group nor physically admixed within the polyanhydride matrix by melting or dissolving the polymer. Thus, drug release is directly dependent on the hydrolytic cleavage of the anhydride and ester bonds.…”
Section: Introductionmentioning
confidence: 99%