2013
DOI: 10.1016/j.reactfunctpolym.2013.06.012
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Controlled release of doxorubicin from amphiphilic depsipeptide–PDO–PEG-based copolymer nanosized microspheres

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Cited by 15 publications
(11 citation statements)
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“…We selected hydrophobic copolymers from a depsipeptide and dilactide to covalently link low molecular weight PEIs as depsipeptide based copolymers are biodegradable with benefi cial biocompatibility during degradation. [48][49][50][51][52] Our strategy consists of the synthesis of biodegradable block copolymers based on PEI (1 800 g mol −1 ) and poly[(L-lactide)-co -(3( S )-methyl-2,5-morpholinedione)] (P(LA-co -MMD)) blocks, and the formation of nanoparticles thereof by self-assembly. [53][54][55] In our previous study, we have prepared microparticles from mPEG-b-P(MMD-co-GA)-g-PEI.…”
Section: Introductionmentioning
confidence: 99%
“…We selected hydrophobic copolymers from a depsipeptide and dilactide to covalently link low molecular weight PEIs as depsipeptide based copolymers are biodegradable with benefi cial biocompatibility during degradation. [48][49][50][51][52] Our strategy consists of the synthesis of biodegradable block copolymers based on PEI (1 800 g mol −1 ) and poly[(L-lactide)-co -(3( S )-methyl-2,5-morpholinedione)] (P(LA-co -MMD)) blocks, and the formation of nanoparticles thereof by self-assembly. [53][54][55] In our previous study, we have prepared microparticles from mPEG-b-P(MMD-co-GA)-g-PEI.…”
Section: Introductionmentioning
confidence: 99%
“…The modified electrospray method employed here allows for comparable or increased encapsulation of PDO (>70%) and PLGA (>80%), respectively, where traditional emulsion methods exhibit encapsulation efficiencies of 60–80% for PLGA . With respect to PDO, due to the material's relative insolubility, alternative methods for the fabrication of sustained delivery devices have been employed to include melt extrusion and thin film fabrication along with traditional emulsion techniques exhibiting encapsulation efficiencies of 26–62% for pure and copolymeric systems . In addition, release profiles of synthesized PDO/PLGA nanospheres (Figure ) revealed a minimized burst release within the first 8 h of incubation for both nanospheres and steady release to 18 days (PDO) and 6 days (PLGA), respectively.…”
Section: Resultsmentioning
confidence: 99%
“…Meanwhile, the copolymers synthesized from MMD shows different crystallization degrees owing to the optical activity of the monomer [35,40,41]. Moreover, the degradation products of MMD including L-amino acids can stimulate the proliferation of endothelial cells via a signal pathway and be properly metabolized by living tissues [42][43][44][45].…”
Section: Introductionmentioning
confidence: 99%
“…Currently, polydepsipeptides have been widely accepted as a valuable class of synthetic biodegradable polymers because the strong intermolecular hydrogen-bond interaction between the amide groups can achieve a higher reactivity in ring-opening polymerization (ROP), and the presence of easily hydrolysable ester linkages and amide-bonds can ensure high degradability [ 32 , 33 , 34 , 35 ]. In 1985, Helder et al synthesized polydepsipeptides by ROP of morpholine-2,5-dione derivatives for the first time [ 36 ].…”
Section: Introductionmentioning
confidence: 99%
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