Vera, 2017 - Google Patents
Peptide-Based Strategies of Delivering Semiconductor Nanocrystals into Living CellsVera, 2017
View PDF- Document ID
- 11114139279910071004
- Author
- Vera C
- Publication year
External Links
Snippet
Semiconductor nanocrystals or quantum dots (QDs) possess exceptional optical and physicochemical properties, for instance, their brightness and long fluorescence lifetimes, which makes them valuable for live-cell imaging. Due to their large size, QDs do not cross …
- 239000004054 semiconductor nanocrystal 0 title abstract description 4
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by the preceding groups
- G01N33/48—Investigating or analysing materials by specific methods not covered by the preceding groups biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/58—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving labelled substances
- G01N33/582—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving labelled substances with fluorescent label
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K49/00—Preparations for testing in vivo
- A61K49/001—Preparation for luminescence or biological staining
- A61K49/0013—Luminescence
- A61K49/0017—Fluorescence in vivo
- A61K49/0019—Fluorescence in vivo characterised by the fluorescent group
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers, inert additives
- A61K47/48—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers, inert additives the non-active ingredient being chemically bound to the active ingredient, e.g. polymer drug conjugates
- A61K47/48238—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers, inert additives the non-active ingredient being chemically bound to the active ingredient, e.g. polymer drug conjugates the modifying agent being a protein, peptide, polyamino acid
- A61K47/48246—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers, inert additives the non-active ingredient being chemically bound to the active ingredient, e.g. polymer drug conjugates the modifying agent being a protein, peptide, polyamino acid drug-peptide, protein or polyamino acid conjugates, i.e. the modifying agent being a protein, peptide, polyamino acid which being linked/complexed to a molecule that being the pharmacologically or therapeutically active agent
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by the preceding groups
- G01N33/48—Investigating or analysing materials by specific methods not covered by the preceding groups biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers, inert additives
- A61K47/48—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers, inert additives the non-active ingredient being chemically bound to the active ingredient, e.g. polymer drug conjugates
- A61K47/48007—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers, inert additives the non-active ingredient being chemically bound to the active ingredient, e.g. polymer drug conjugates the pharmacologically- or therapeutically-active agent being covalently bound or complexed to a modifying agent
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers, inert additives
- A61K47/48—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers, inert additives the non-active ingredient being chemically bound to the active ingredient, e.g. polymer drug conjugates
- A61K47/48769—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers, inert additives the non-active ingredient being chemically bound to the active ingredient, e.g. polymer drug conjugates the conjugate being characterized by a special physical or galenical form
- A61K47/48792—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers, inert additives the non-active ingredient being chemically bound to the active ingredient, e.g. polymer drug conjugates the conjugate being characterized by a special physical or galenical form the form being a colloid, emulsion, i.e. having at least a dispersed/continuous oil phase and a dispersed/continuous aqueous phase, dispersion or suspension
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Zong et al. | Peptide-functionalized gold nanoparticles: versatile biomaterials for diagnostic and therapeutic applications | |
Field et al. | Peptides for specifically targeting nanoparticles to cellular organelles: quo vadis? | |
Medintz et al. | Intracellular delivery of quantum dot− protein cargos mediated by cell penetrating peptides | |
Wu et al. | Development of viral nanoparticles for efficient intracellular delivery | |
Chen et al. | Transmembrane delivery of the cell-penetrating peptide conjugated semiconductor quantum dots | |
Boeneman et al. | Selecting improved peptidyl motifs for cytosolic delivery of disparate protein and nanoparticle materials | |
Martín et al. | Design, synthesis and characterization of a new anionic cell‐penetrating peptide: SAP (E) | |
Wang et al. | Peptide‐engineered fluorescent nanomaterials: Structure design, function tailoring, and biomedical applications | |
US8859284B2 (en) | Delivery of nanoparticles to neurons | |
Delehanty et al. | Delivering quantum dot-peptide bioconjugates to the cellular cytosol: escaping from the endolysosomal system | |
Brunetti et al. | Near-infrared quantum dots labelled with a tumor selective tetrabranched peptide for in vivo imaging | |
Breger et al. | Nanoparticle cellular uptake by dendritic wedge peptides: achieving single peptide facilitated delivery | |
Zhang et al. | Enhanced cellular entry and efficacy of tat conjugates by rational design of the auxiliary segment | |
Park et al. | Cell-selective intracellular drug delivery using doxorubicin and α-helical peptides conjugated to gold nanoparticles | |
Tian et al. | Advances in cell penetrating peptides and their functionalization of polymeric nanoplatforms for drug delivery | |
So et al. | HaloTag protein-mediated specific labeling of living cells with quantum dots | |
Wang et al. | A quantitative study of the intracellular fate of pH-responsive doxorubicin-polypeptide nanoparticles | |
US20130158244A1 (en) | Modular Functional Peptides for the Intracellular Delivery of Nanoparticles | |
Bayles et al. | Rapid cytosolic delivery of luminescent nanocrystals in live cells with endosome-disrupting polymer colloids | |
Panigrahi et al. | Cyclic peptide-based nanostructures as efficient siRNA carriers | |
Allen et al. | Hydrophobicity is a key determinant in the activity of arginine-rich cell penetrating peptides | |
Falciani et al. | Nanoparticles exposing neurotensin tumor‐specific drivers | |
Burns et al. | Cellular delivery of doxorubicin mediated by disulfide reduction of a peptide-dendrimer bioconjugate | |
Dmitriev et al. | Metallochelate coupling of phosphorescent Pt-porphyrins to peptides, proteins, and self-assembling protein nanoparticles | |
Arafiles et al. | Cell-surface-retained peptide additives for the cytosolic delivery of functional proteins |