Literature DB >> 7724486

Structures of nanoparticles prepared from oil-in-water emulsions.

B Sjöström1, A Kaplun, Y Talmon, B Cabane.   

Abstract

Hydrophobic substances were dissolved in an organic solvent and emulsified with an aqueous solution at very high shear. Droplets of very small sizes (50-100 nm) were obtained by using surfactants which were combinations of lecithins and bile salts. After emulsification, the organic solvent was removed by evaporation, yielding stable dispersions of solid particles. The sizes, shapes, and structures of the particles were examined through quasi-elastic light scattering, small-angle neutron scattering and cryotransmission electron microscopy. Cholesterol acetate particles stabilized by lecithin and bile salts were found to be platelets of 10-20 nm thickness and 80 nm diameter. Cholesteryl acetate particles stabilized with POE-(20)-sorbitan monolaurate were dense spherical globules of diameter 100 nm. Particles with a composition similar to the endogenously occurring, lipoprotein, LDL, were large spherical globules studded with small vesicles. The subsequent evolution of the cholesteryl acetate dispersion upon aging was examined. There was no transfer of cholesteryl acetate between particles nor to large crystals. However, some aggregation of the particles was observed when the volume fraction of the particles in the aqueous dispersion exceeded 0.05. Thus, the structure of the nanoparticles obtained through deswelling of emulsion droplets changes according to the nature of the emulsifiers and to the composition of the hydrophobic substances which they contain.

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Year:  1995        PMID: 7724486     DOI: 10.1023/a:1016278302046

Source DB:  PubMed          Journal:  Pharm Res        ISSN: 0724-8741            Impact factor:   4.200


  8 in total

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4.  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.

Authors:  B Sjöström; B Kronberg; J Carlfors
Journal:  J Pharm Sci       Date:  1993-06       Impact factor: 3.534

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Journal:  J Lipid Res       Date:  1980-09       Impact factor: 5.922

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Authors:  O von Dardel; C Mebius; T Mossberg
Journal:  Acta Anaesthesiol Scand       Date:  1976       Impact factor: 2.105

7.  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.

Authors:  B Sjöström; B Bergenståhl; B Kronberg
Journal:  J Pharm Sci       Date:  1993-06       Impact factor: 3.534

8.  Intermediate structures in the cholate-phosphatidylcholine vesicle-micelle transition.

Authors:  A Walter; P K Vinson; A Kaplun; Y Talmon
Journal:  Biophys J       Date:  1991-12       Impact factor: 4.033

  8 in total
  4 in total

Review 1.  Biopolymeric nanoparticles.

Authors:  Sushmitha Sundar; Joydip Kundu; Subhas C Kundu
Journal:  Sci Technol Adv Mater       Date:  2010-02-26       Impact factor: 8.090

Review 2.  Recent advances in lipid nanoparticle formulations with solid matrix for oral drug delivery.

Authors:  Surajit Das; Anumita Chaudhury
Journal:  AAPS PharmSciTech       Date:  2010-12-21       Impact factor: 3.246

3.  Formulation of tenofovir-loaded functionalized solid lipid nanoparticles intended for HIV prevention.

Authors:  Dima Alukda; Timothy Sturgis; Bi-Botti C Youan
Journal:  J Pharm Sci       Date:  2011-03-15       Impact factor: 3.534

Review 4.  Preparation of Solid Lipid Nanoparticles and Nanostructured Lipid Carriers for Drug Delivery and the Effects of Preparation Parameters of Solvent Injection Method.

Authors:  Van-An Duong; Thi-Thao-Linh Nguyen; Han-Joo Maeng
Journal:  Molecules       Date:  2020-10-18       Impact factor: 4.411

  4 in total

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