2010
DOI: 10.1016/j.biomaterials.2010.02.001
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Structure-biocompatibility relationship of dendritic polyglycerol derivatives

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Cited by 118 publications
(110 citation statements)
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“…18) in an attempt to explore the effects of post-modification of hyperbranched polyglycerol with primary amines in the favorable 1,2-orientation [144]. In a previous study, the polyglycerolamine architecture, which consists of primary amine groups spread all around the polyglycerol structure, has showed promising properties as a prospective system for gene delivery, namely high charge with a relative low cytotoxicity, and an optimal charge/pH behavior so far as the buffering capacity is concerned [139]. Of all the polyglycerol systems analyzed for gene transfection, the hyperbranched polyglycerolamine showed the highest affinity towards DNA fragments, according to the ethidium bromide displacement assay.…”
Section: Hyperbranched Polyglycerolmentioning
confidence: 98%
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“…18) in an attempt to explore the effects of post-modification of hyperbranched polyglycerol with primary amines in the favorable 1,2-orientation [144]. In a previous study, the polyglycerolamine architecture, which consists of primary amine groups spread all around the polyglycerol structure, has showed promising properties as a prospective system for gene delivery, namely high charge with a relative low cytotoxicity, and an optimal charge/pH behavior so far as the buffering capacity is concerned [139]. Of all the polyglycerol systems analyzed for gene transfection, the hyperbranched polyglycerolamine showed the highest affinity towards DNA fragments, according to the ethidium bromide displacement assay.…”
Section: Hyperbranched Polyglycerolmentioning
confidence: 98%
“…This could substantially increase the internalization of active components, specifically into targeted cells, enhancing the therapeutic benefits and decreasing the adverse side effects [136][137][138]. Recently we demonstrated that post-modified hyperbranched polyglycerol presents sufficiently low zeta potentials, lower interactions with serum albumin, enhanced cellular uptake, and higher cellular viability on human hematopoietic cell line U-937, to be considered a promising candidate for a systematic delivery of therapeutic agents [139].…”
Section: Hyperbranched Polyglycerolmentioning
confidence: 98%
“…The cell compatibility results show that the hbPGs are as safe as linear PEG polymers or dextran, which indicates the suitability of hbPG derivatives in delivering therapeutic agents systemically. 122 In an interesting work, Haag and coworkers have recently observed a molecular mass and size-dependent cellular uptake of hbPG, indicating a molecular weight/size optimum around 200 kDa/12 nm. 123 Their data suggest that the HIGHLIGHT higher molecular weight hbPGs (40-870 kDa) predominantly accumulate in the cytoplasm and that endocytotic uptake can be suppressed for lower molecular weights (2-20 kDa).…”
Section: Biocompatibilitymentioning
confidence: 99%
“…Type and proportion of surface functional groups have a profound impact on the surface charge of the polymers. [25] In the repeating unit of PSA, the number of primary, secondary, tertiary amino groups and sulfone groups is 0.12, 0.65, 2.25 and 1.05, Scheme 1. Synthesis route of PSA.…”
Section: Zeta-potential Measurementsmentioning
confidence: 99%