Micellar Nanocontainers Distribute to Defined Cytoplasmic Organelles
By R. Savić, Laibin Luo, A. Eisenberg, D. Maysinger. Science, 2003
1,008 citations recorded by the source corpus.
Subfields: Biomaterials, Materials Chemistry, Organic Chemistry
View Paper: https://www.semanticscholar.org/paper/26896d269a4dda86bcfb93301bba424ed75974a8
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In Biomaterials
- Kazunori Kataoka
- Atsushi Harada
- Kostas Kostarelos
- C. Partidos
- A. Bianco
- M. Prato
- A. Kabanov
- A. C. Hunter
In Materials Chemistry
- Kostas Kostarelos
- M. Prato
- A. Bianco
- C. Partidos
- Kazunori Kataoka
- Atsushi Harada
- Vinayak Sant
- Y. Geng
In Organic Chemistry
- Kazunori Kataoka
- Kostas Kostarelos
- Atsushi Harada
- A. Bianco
- M. Prato
- Dennis E. Discher
- F. Ahmed
- Richard Hoogenboom
Citations in the corpus
- Pluronic block copolymers: evolution of drug delivery concept from inert nanocarriers to biological response modifiers. (2008, background): “Specific arrangements of polymeric molecules at the nanoscale achieved within such materials represent unique opportunities for safe and efficient delivery of drugs, genes, and imaging molecules [1-13].”
- Nanomedicine: current status and future prospects (2005, background): “Some polymeric micelles depending on the nature of their monomer constituents, can induce cell death via apoptosis or necrosis, or both (141, 142).”
- Block copolymer micelles: preparation, characterization and application in drug delivery. (2005, background): “Elsewhere, triple-labeling confocal microscopy in live cells indicated that the micelles were predominantly localized in the cytoplasm and distributed within several cytoplasmic organelles, but not in the nucleus [82].”
- Shape effects of filaments versus spherical particles in flow and drug delivery. (2007, background): “, as are a broad array of drug-laden, polymer-based spherical micelle”
- Supramolecular assemblies of block copolymers in aqueous media as nanocontainers relevant to biological applications (2006, methodology): “also reported the properties of PEG–poly(e-caprolactone) (PEG–PCL) micelles as drug carriers, cellular internalization in particular, obtained using a fluorescence technique [80,81].”
- Self-porating polymersomes of PEG-PLA and PEG-PCL: hydrolysis-triggered controlled release vesicles. (2004, background): “PEG–PLA or PEG–PCL block copolymers have both been described before [21–26], and very recent illustrations of PEG–PLA vesicles [27–29] highlight the need for detailed characterization of release and degradability.”