2022
DOI: 10.1007/978-3-031-12658-1_14
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Polymersomes for Targeted Drug and Gene Delivery Systems

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Cited by 3 publications
(2 citation statements)
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“…The thicker membrane contributes to a less permeable structure with relatively low lateral mobility, enabling the polymersomes to encapsulate substantial amounts of drugs with minimal leakage. Additionally, polymersomes offer advantages such as biocompatibility, a low aggregation rate, longer blood circulation time, immune evasion, and improved uptake in targeted cells. In terms of drug release, polymersomes can release drugs in response to stimuli (e.g., pH, temperature, etc.) and control drug release by forming pores .…”
Section: Introductionmentioning
confidence: 99%
“…The thicker membrane contributes to a less permeable structure with relatively low lateral mobility, enabling the polymersomes to encapsulate substantial amounts of drugs with minimal leakage. Additionally, polymersomes offer advantages such as biocompatibility, a low aggregation rate, longer blood circulation time, immune evasion, and improved uptake in targeted cells. In terms of drug release, polymersomes can release drugs in response to stimuli (e.g., pH, temperature, etc.) and control drug release by forming pores .…”
Section: Introductionmentioning
confidence: 99%
“…[9][10][11] (3) More functional effects can be achieved by modifying the surface of polymersomes. 12,13 Biodegradable materials such as polylactide acid (PLA), poly ε-caprolactone (PCL), or non-biodegradable materials such as polybutadiene (PBD) can be used as the hydrophobic blocks. [14][15][16][17] The hydrophilic blocks mainly contain polyethylene glycol (PEG), polyacrylic acid (PAA), poly glycolic acid (PGA) and so on.…”
Section: Introductionmentioning
confidence: 99%