Preparation of non-porous microspheres with high entrapment efficiency of proteins by a (water-in-oil)-in-oil emulsion technique

Author:

Viswanathan N.Badri,Thomas P.A,Pandit J.K,Kulkarni M.G,Mashelkar R.A

Publisher

Elsevier BV

Subject

Pharmaceutical Science

Reference22 articles.

1. Controlled release of lutinizing hormone-releasing analogue from poly(dl-lactide-co-glycolide) microspheres;Sanders;J. Pharm. Sci.,1984

2. A new technique to efficiently entrap leuprolide acetate into microcapsules of poly lactics or co-polylactic/glycolic acid;Ogawa;Chem. Pharm. Bull.,1988

3. F.G. Hutchinson, B.J.A. Furr, Biodegradable polymers for controlled release of peptides and proteins, in: F.H.D. Roerdink, A.M. Kroon (Eds.), Horizons in Biochemistry and Biophysics, Vol. 9. Drug Carrier Systems, John Wiley, 1989, pp. 11–29.

4. Biodegradable and biocompatible poly (dl-lactide-co-glycolide) microspheres as an adjuvant for Staphylococcal Enterotoxin B toxoid which enhances the level of toxin-neutralizing antibodies;Eldridge;Infection Immunity,1991

5. Biodegradable microparticles as controlled release antigen delivery systems;O'Hagan;Immunology,1991

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