2017
DOI: 10.2147/ijn.s118197
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Effects of copolymer component on the properties of phosphorylcholine micelles

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Cited by 13 publications
(8 citation statements)
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“…When the amount of PLA is over 50%, the dissociated PLA from the micelles emerges in micellar preparation solution and the size of DPN almost maintains around 200 nm. The critical micelle concentration (CMC) value of DPN appears low, about 10 −3 mg mL −1 (Figure S1b, Supporting Information), which is similar to the value of the normal micelles of PCL‐ss‐PMPC . It also can be found that DPN can stably exist at 37.5 °C in 24 h with very few size change (Figure S1c, Supporting Information) but obvious size change under reduction condition (Figure S1d, Supporting Information), since the outer layer of DPN is a reduction‐sensitive amphiphilic polymer.…”
Section: Resultsmentioning
confidence: 54%
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“…When the amount of PLA is over 50%, the dissociated PLA from the micelles emerges in micellar preparation solution and the size of DPN almost maintains around 200 nm. The critical micelle concentration (CMC) value of DPN appears low, about 10 −3 mg mL −1 (Figure S1b, Supporting Information), which is similar to the value of the normal micelles of PCL‐ss‐PMPC . It also can be found that DPN can stably exist at 37.5 °C in 24 h with very few size change (Figure S1c, Supporting Information) but obvious size change under reduction condition (Figure S1d, Supporting Information), since the outer layer of DPN is a reduction‐sensitive amphiphilic polymer.…”
Section: Resultsmentioning
confidence: 54%
“…DPN and drug‐loaded DPN all appear negative zeta‐potential. Drug loading content (DLC) and drug loading efficiency (DLE) of DPN are higher than ordinary micelles . The DLC of DPN‐DI (DOX entrapped in inner layer together with PLA) is about 18.11%, which is higher than that of DPN‐DA (DOX in both PLA and PCL‐ss‐PMPC, 10.09%) and DPN‐DO (DOX in PCL‐ss‐PMPC, 7.76%).…”
Section: Resultsmentioning
confidence: 98%
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“…[55][56][57][58] As mentioned, Dox as the model drug can be loaded in the hydrophobic region of PLGAbased nanoparticles through interactions, ie, physical encapsulation and electrostatic attraction. Dox LE/EE in PLGA and PLGA-PEG-FA were determined to be 8.2%/89.3% and 7.9%/85.8%, respectively (Table S2).…”
Section: In Vitro Drug Release and Cellular Uptakementioning
confidence: 99%