2003
DOI: 10.1016/j.jconrel.2003.05.002
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Polyion complex micelles entrapping cationic dendrimer porphyrin: effective photosensitizer for photodynamic therapy of cancer

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Cited by 160 publications
(94 citation statements)
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“…PS can be modified by encapsulated them in delivery agents such as liposomes [54], micelles [55,56,57,58], ceramic based nanoparticles [59], gold nanoparticles [60,61], and polymer nanoparticles [62]. Liposomes, for example, are able to encapsulate hydrophobic as well as hydrophilic drugs.…”
Section: 'Nano' Strategies For Photosensitizermentioning
confidence: 99%
“…PS can be modified by encapsulated them in delivery agents such as liposomes [54], micelles [55,56,57,58], ceramic based nanoparticles [59], gold nanoparticles [60,61], and polymer nanoparticles [62]. Liposomes, for example, are able to encapsulate hydrophobic as well as hydrophilic drugs.…”
Section: 'Nano' Strategies For Photosensitizermentioning
confidence: 99%
“…In addition, large dendritic wedges effectively prevent aggregation. [31][32][33][34] The high solubility of DP and DPc permits their use in PDT, a promising technology for less invasive cancer treatments. PDT involves the systemic administration of photosensitizers (PS) followed by the irradiation of the target tissue with laser light.…”
Section: Structure and Characteristics Of Dendrimer Porphyrin And Phtmentioning
confidence: 99%
“…When DP was used as a PS, it exhibited 10-100 times higher photocytotoxicity than protoporphyrin IX, a conventional PS, for treating Lewis lung carcinoma (LLC). 33 Moreover, the ionic surfaces of DP and DPc have been used to form polyion complex (PIC) micelles through electrostatic interactions. In vitro and in vivo experiments have demonstrated that PIC micelles are successful formulations for use in PDT.…”
Section: Structure and Characteristics Of Dendrimer Porphyrin And Phtmentioning
confidence: 99%
“…They are formed as a result of the reaction of double hydrophilic block copolymers containing ionic and nonionic blocks with macromolecules of opposite charge including oligonucleotides, plasmid DNA and proteins (Kabanov et al 1995;Harada and Kataoka 1999a, b;Nguyen et al 2000;Zhang et al 2003;Jaturanpinyo et al 2004), or surfactants of opposite charge (Bronich et al 1997(Bronich et al , 1998(Bronich et al , 1999Solomatin et al 2003Solomatin et al , 2004. For example, block ionomer complexes were prepared by reacting trypsin or lysozyme (that are positively charged under physiological conditions) with an anionic block copolymer, PEG-poly(α,β-aspartic acid) (Harada and Kataoka 1999b;Jaturanpinyo et al 2004).…”
Section: Nanomaterials For Drug Delivery Across the Blood-brain Barriermentioning
confidence: 99%