Giunchedi et al., 2001 - Google Patents
Emulsion spray-drying for the preparation of albumin-loaded PLGA microspheresGiunchedi et al., 2001
View PDF- Document ID
- 6976540092687163772
- Author
- Giunchedi P
- Conti B
- Genta I
- Conte U
- Puglisi G
- Publication year
- Publication venue
- Drug development and industrial pharmacy
External Links
Snippet
The purpose of this work was to study the encapsulation of bovine serum albumin (BSA) in polylactide-co-glycolide (PLGA) microspheres using an emulsion/spray-drying method. Albumin was dissolved in an aqueous phase (w) in the presence of surfactant and …
- 239000004005 microsphere 0 title abstract description 48
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1605—Excipients; Inactive ingredients
- A61K9/1629—Organic macromolecular compounds
- A61K9/1641—Organic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyethylene glycol, poloxamers
- A61K9/1647—Polyesters, e.g. poly(lactide-co-glycolide)
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1605—Excipients; Inactive ingredients
- A61K9/1629—Organic macromolecular compounds
- A61K9/1652—Polysaccharides, e.g. alginate, cellulose derivatives; Cyclodextrin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1682—Processes
- A61K9/1694—Processes resulting in granules or microspheres of the matrix type containing more than 5% of excipient
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/50—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
- A61K9/51—Nanocapsules; Nanoparticles
- A61K9/5107—Excipients; Inactive ingredients
- A61K9/513—Organic macromolecular compounds; Dendrimers
- A61K9/5146—Organic macromolecular compounds; Dendrimers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyethylene glycol, polyamines, polyanhydrides
- A61K9/5153—Polyesters, e.g. poly(lactide-co-glycolide)
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/50—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
- A61K9/5005—Wall or coating material
- A61K9/5021—Organic macromolecular compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/50—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
- A61K9/51—Nanocapsules; Nanoparticles
- A61K9/5192—Processes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/50—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
- A61K9/5089—Processes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/141—Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Giunchedi et al. | Emulsion spray-drying for the preparation of albumin-loaded PLGA microspheres | |
| Li et al. | Microencapsulation of nanoemulsions: novel Trojan particles for bioactive lipid molecule delivery | |
| Ravi et al. | Development and characterization of polymeric microspheres for controlled release protein loaded drug delivery system | |
| Deshmukh et al. | Solvent evaporation and spray drying technique for micro-and nanospheres/particles preparation: A review | |
| Budhian et al. | Production of haloperidol-loaded PLGA nanoparticles for extended controlled drug release of haloperidol | |
| Esposito et al. | Production of Eudragit microparticles by spray-drying technique: influence of experimental parameters on morphological and dimensional characteristics | |
| Müller et al. | Preparation and characterization of spray-dried polymeric nanocapsules | |
| Jiang et al. | Effect of osmotic pressure in the solvent extraction phase on BSA release profile from PLGA microspheres | |
| US6616869B2 (en) | Process for preparing microparticles through phase inversion phenomena | |
| Feczkó et al. | Comparison of the preparation of PLGA–BSA nano-and microparticles by PVA, poloxamer and PVP | |
| JP2582186B2 (en) | Encapsulation method and its products | |
| JPH02504025A (en) | Preparation of multiwalled polymeric microcapsules | |
| Hong et al. | Novel preparation method for sustained-release PLGA microspheres using water-in-oil-in-hydrophilic-oil-in-water emulsion | |
| Jaraswekin et al. | Effect of poly (lactide-co-glycolide) molecular weight on the release of dexamethasone sodium phosphate from microparticles | |
| JPH0753725A (en) | Pseudolatex and method for producing microparticles or nanoparticles, and pharmaceutical preparation containing them | |
| Jiao et al. | Preparation and characterization of heparin-loaded polymeric microparticles | |
| Rassu et al. | Ketoprofen spray-dried microspheres based on Eudragit® RS and RL: study of the manufacturing parameters | |
| Muhaimin et al. | Impact of dispersion time interval and particle size on release profiles of propranolol HCl and carbamazepines from microparticle blends system | |
| Zheng et al. | A one-step modified method to reduce the burst initial release from PLGA microspheres | |
| Thakare et al. | Nonionic surfactant structure on the drug release, formulation and physical properties of ethylcellulose microspheres | |
| Erden et al. | Factors influencing release of salbutamol sulphate from poly (lactide-co-glycolide) microspheres prepared by water-in-oil-in-water emulsion technique | |
| Chandy et al. | Development of polylactide microspheres for protein encapsulation and delivery | |
| Jain et al. | Comparison of various injectable protein-loaded biodegradable poly (lactide-co-glycolide)(PLGA) devices: in-situ-formed implant versus in-situ-formed microspheres versus isolated microspheres | |
| Javiya et al. | Physicochemical characterization of spray-dried PLGA/PEG microspheres, and preliminary assessment of biological response | |
| Thakare et al. | Formulation parameters and release mechanism of theophylline loaded ethyl cellulose microspheres: effect of different dual surfactant ratios |