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Surfactant-free microspheres of Poly(ε-caprolactone)/poly (ethylene glyco I )/poly(ε-caprolactone) triblock copolymers as a protein carrier
41/41 checkable references clean · checked 2026-08-11
Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.
5 without a DOI — not checked. A reference deposited without a DOI is never matched by title or guessed at; it stays outside the checked set, and this line discloses that.
The 41 checked references that resolve
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Protein encapsulation in biodegradable amphiphilic microspheres
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Bovine serum albumin release from poly(α-hydroxy acid) microspheres: effects of polymer molecular weight and surface properties
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The preparation and evaluation of salbutamol sulphate containing poly(lactic acid-co-glycolic acid) microspheres with factorial design-based studies
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Polyether-polyester block copolymers by non-catalysed polymerization of ɛ-caprolactone with poly(ethylene glycol)
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In vitro and in vivo evaluation of PLAGA (50/50) microspheres containing 5-fluorouracil prepared by a solvent evaporation method
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Effects of solvent selection and fabrication method on the characteristics of biodegradable poly(lactide-co-glycolide) microspheres containing ovalbumin
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PLGA nanoparticles prepared by nanoprecipitation: drug loading and release studies of a water soluble drug
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Public Health Hazards from Environmental Chemical Carcinogens, Mutagens and Teratogens
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The preparation and characterisation of poly(lactide-co-glycolide) microparticles. I: Oil-in-water emulsion solvent evaporation
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The Preparation and Characterization of Poly(lactide-co-glycolide) Microparticles. II. The Entrapment of a Model Protein Using a (Water-in-Oil)-in-Water Emulsion Solvent Evaporation Technique
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Controlled delivery of therapeutics from microporous membranes. II. In vitro degradation and release of heparin-loaded poly(d,l-lactide-co-glycolide)
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Release of the fluorescent marker Prodan® from poly(D,L-lactic acid) nanoparticles coated with albumin or polyvinyl alcohol in model digestive fluids (USP XXII)
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The importance of gastrointestinal uptake of particles in the design of oral delivery systems
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Quantitative analysis of polyvinyl alcohol on the surface of poly(d,l-lactide-co-glycolide) microparticles prepared by solvent evaporation method: effect of particle size and PVA concentration
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The immunogenicity of a model protein entrapped in poly(lactide-co-glycolide) microparticles prepared by a novel phase separation technique
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Peptide containing microspheres from low molecular weight and hydrophilic poly(d,l-lactide-co-glycolide)
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The preparation and characterization ofpoly(lactide-co-glycolide) microparticles: III. Microparticle/polymer degradation rates and the in vitro release of a model protein
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A new technique to efficiently entrap leuprolide acetate into microcapsules of polylactic acid or copoly(lactic/glycolic) acid.
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Protein-loaded poly(dl-lactide-co-glycolide) microparticles for oral administration: formulation, structural and release characteristics
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The preparation of sub-200 nm poly(lactide-co-glycolide) microspheres for site-specific drug delivery
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The Adsorption of Poly(vinyl alcohol) to Biodegradable Microparticles Studied by X-Ray Photoelectron Spectroscopy (XPS)
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Mechanistic studies of macromolecular drug release from macroporous polymers. II. Models for the slow kinetics of drug release
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A Method for the Preparation of Submicron Particles of Sparingly Water-Soluble Drugs by Precipitation in Oil-in-Water Emulsions. I: Influence of Emulsification and Surfactant Concentration
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Opioid-Induced Respiratory Depression and Analgesia May Be Mediated by Different Subreceptors
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Preparation, purification and morphology of polymeric nanoparticles as drug carriers
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Comparison of Body Distribution of Poly(vinyl alcohol) with Other Water-soluble Polymers after Intravenous Administration
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Morphology, drug distribution, and in vitro release profiles of biodegradable polymeric microspheres containing protein fabricated by double-emulsion solvent extraction/evaporation method
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A novel emulsification-solvent extraction technique for production of protein loaded biodegradable microparticles for vaccine and drug delivery
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no DOI — not checkedBradford, M. M., A rapid and sensitive method for the quantitation of microgram Quantities of protein utilizing for the principle of protein-dye binding.Biochemistry, 72, 248–254 (1976).
no DOI — not checkedDunn, R., Hardee, G., Poison, A., Bennet, A., Martin, S., Wardley, R., Moseley, W., Krinick, N., Foster, T., Frank, K., and Cox, S.,In-situ forming biodegradable implants for controlled release veterinary applications.Proc. Int. Symp. Control. Release Bioact. Mater., 22, 91–92 (1995).
no DOI — not checkedLeach, K. J. and Mathiowitz, E., Degradation of double-walled polymer microspheres of PLLA and P(CPP:SA) 20:80. I.In vitro degradation.Biomaterials, 19, 1973–1980 (1998).
no DOI — not checkedRadomsky, M. L., Brouwer, G., Floy, B. J., Loury, D. J., Chu, F., Tipon, A. J., and Sanders, L. M., The controlled release of ganirelix from the Artigel injectable implant system.Proc. Int. Symp. Control. Release Bioact. Mater., 20, 458–459 (1993).
no DOI — not checkedSjostrom, B., Bergenstahl, B., and Kronberg, B., A method for the preparation of submicron particles of sparingly water-soluble drugs by precipitation in oil-in water emulsions. II: Influence of the emulsifier, the solvent, and the drug substance.J. Pharm. Sci., 82, 585–589 (1993b).
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