| Literature DB >> 24928131 |
Jenni Pessi1, Hélder A Santos2, Inna Miroshnyk3, David A Weitz4, Sabiruddin Mirza4.
Abstract
In this study, microfluidic technology was employed to develop protein formulations. The microcapsules were produced with a biphasic flow to create water-oil-water (W/O/W) double emulsion droplets with ultrathin shells. Optimized microcapsule formulations containing 1% (w/w) bovine serum albumin (BSA) in the inner phase were prepared with poly(vinyl alcohol), polycaprolactone and polyethylene glycol. All the particles were found to be intact and with a particle size of 23-47 μm. Furthermore, the particles were monodisperse, non-porous and stable up to 4 weeks. The encapsulation efficiency of BSA in the microcapsules was 84%. The microcapsules released 30% of their content within 168 h. This study demonstrates that microfluidics is a powerful technique for engineering formulations for therapeutic proteins.Entities:
Keywords: Drug delivery; Ethyl acetate (PubChem CID 8857); Microcapsules; Microfluidics; Poly(vinyl alcohol) (PubChem CID 11199); Polycaprolactone; Polycaprolactone (PubChem CID 10401); Polyethylene glycol (PubChem CID 174); Therapeutic proteins
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Year: 2014 PMID: 24928131 DOI: 10.1016/j.ijpharm.2014.06.012
Source DB: PubMed Journal: Int J Pharm ISSN: 0378-5173 Impact factor: 5.875