1996
DOI: 10.1016/0168-3659(96)01322-3
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Crosslinked α,β-polyasparthydrazide hydrogels: effect of crosslinking degree and loading method on cytarabine release rate

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Cited by 24 publications
(7 citation statements)
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“…2 Recently, hydrogels have been extensively studied as drug carriers, especially for proteins. Hydrogels have been made from different polymers such as dextran, 3 gelatin, 4-6 amylose, 7-9 cellulose, 10 chitosan, 11 fibrin, 12 collagen, 13,14 alginate, 15,16 poly(vinyl alcohol), 17 poly(hydroxyethyl methacrylate), 18,19 poly(hydroxyethyl acrylate), 20 poly(acrylic acid) (Carbopol), 21 polyasparthydrazide, 22 and poly(ethylene glycol) (PEG). 23,24 Most hydrogel-based drug delivery systems are designed as implants that release drug locally at a predetermined rate.…”
Section: Introductionmentioning
confidence: 99%
“…2 Recently, hydrogels have been extensively studied as drug carriers, especially for proteins. Hydrogels have been made from different polymers such as dextran, 3 gelatin, 4-6 amylose, 7-9 cellulose, 10 chitosan, 11 fibrin, 12 collagen, 13,14 alginate, 15,16 poly(vinyl alcohol), 17 poly(hydroxyethyl methacrylate), 18,19 poly(hydroxyethyl acrylate), 20 poly(acrylic acid) (Carbopol), 21 polyasparthydrazide, 22 and poly(ethylene glycol) (PEG). 23,24 Most hydrogel-based drug delivery systems are designed as implants that release drug locally at a predetermined rate.…”
Section: Introductionmentioning
confidence: 99%
“…The drug release rate is strongly dependent on the characteristics of the gel structure, which, in some cases, can be easily modified [1][2][3]. Under this respect matrices based on κ-carrageenan deserve great interest.…”
Section: Introductionmentioning
confidence: 99%
“…The literatures on preparation and uses of water-insoluble polyaspartyl polymers have been reported, but they were mostly centered on waterabsorbing materials or drug-loading carriers. [4][5][6][7][8] Moreover, organic solvents, such as DMF, DMSO, and so on, were used in the preparation processes. Such a process is harmful to human being and expensive in cost, and the recovery of these solvents releases many wastewater, which brings up grave environmental concerns.…”
Section: Introductionmentioning
confidence: 99%
“…But it is still necessary to extend their applications, especially as water‐insoluble polyaspartyl polymers. The literatures on preparation and uses of water‐insoluble polyaspartyl polymers have been reported, but they were mostly centered on water‐absorbing materials or drug‐loading carriers 4–8. Moreover, organic solvents, such as DMF, DMSO, and so on, were used in the preparation processes.…”
Section: Introductionmentioning
confidence: 99%