2009
DOI: 10.1021/la803769q
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Membrane Stabilization of Biodegradable Polymersomes

Abstract: Biodegradable polymersomes are promising vehicles for a range of applications. Their stabilization would improve many properties, including the retention and controlled release of polymersome contents, yet this has not been previously accomplished. Here, we present the first example of stabilizing fully biodegradable polymersomes through acrylation of the hydrophobic terminal end of polymersome-forming poly(caprolactone-b-ethylene glycol). Exposure of the resulting polymersomes loaded with a hydrophobic photoi… Show more

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Cited by 33 publications
(28 citation statements)
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References 31 publications
(53 reference statements)
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“…Vesicles made from biodegradable and bioresorbable polymers have wide appeal for in vivo use as they can facilitate both sustained release of therapeutic drugs and imaging (19,20). Polymersomes made through self assembly of the diblock copolymer polyethyleneoxide (PEO)-b-polycaprolactone (PCL) hydrolytically degrade at the PCL block ester linkage (21).…”
Section: Resultsmentioning
confidence: 99%
“…Vesicles made from biodegradable and bioresorbable polymers have wide appeal for in vivo use as they can facilitate both sustained release of therapeutic drugs and imaging (19,20). Polymersomes made through self assembly of the diblock copolymer polyethyleneoxide (PEO)-b-polycaprolactone (PCL) hydrolytically degrade at the PCL block ester linkage (21).…”
Section: Resultsmentioning
confidence: 99%
“…This cross-linking method is used extensively in the formation of hydrogels 37 but has been sparingly used to modify polymer vesicles. 38 By optimizing this method, we ensured minimal damage to proteins or functional groups attached to the polymer from free-radicals in solution.…”
Section: Resultsmentioning
confidence: 99%
“…At different time intervals, 0.1 mL aliquots of the mixture were withdrawn, diluted with 1.0 mL of Tris buffer, and then the fluorescence (F i ) was measured (excitation maximum, 490 nm; emission maximum, 520 nm). To obtain the maximal fluorescence (F T ), 0.05 mL of a freshly eluted fraction was disrupted with 3% (w/v) Triton X-100, 30,43 the final concentration of which was 0.1% (w/v), followed by diluting to 3.575 mL with Tris buffer before recording the fluorescence. The extent of release (%) over time was calculated from (F i /F T )×100.…”
Section: 폴리머 제37권 제3호 2013년mentioning
confidence: 99%