Literature DB >> 12916940

Preparation of gelatin microbeads with a narrow size distribution using microchannel emulsification.

Satoshi Iwamoto1, Kei Nakagawa, Shinji Sugiura, Mitsutoshi Nakajima.   

Abstract

The purpose of this study was to prepare monodisperse gelatin microcapsules containing an active agent using microchannel (MC) emulsification, a novel technique for preparing water-in-oil (W/O) and oil-in-water (O/W) emulsions. As the first step in applying MC emulsification to the preparation of monodisperse gelatin microcapsules, simple gelatin microbeads were prepared using this technique. A W/O emulsion with a narrow size distribution containing gelatin in the aqueous phase was created as follows. First, the aqueous disperse phase was fed into the continuous phase through the MCs at 40 degrees C (operating pressure: 3.9 kPa). The emulsion droplets had an average particle diameter of 40.7 microm and a relative standard deviation of 5.1%. The temperature of the collected emulsion was reduced and maintained at 25 degrees C overnight. The gelatin microbeads had a smooth surface after overnight gelation; the average particle diameter was calculated to be 31.6 microm, and the relative standard deviation, 7.3%. The temperature was then lowered to 5 degrees C by rapid air cooling and finally dried. The gelatin beads were dried and could be resuspended well in iso-octane. They had an average particle diameter of 15.6 microm, and a relative standard deviation of 5.9%. Using MC emulsification, we were able to prepare gelatin microbeads with a narrow size distribution. Since this emulsification technique requires only a low-energy input, it may create desirable experimental conditions for microencapsulation of unstable substances such as peptides and proteins. This method is promising for making monodisperse microbeads.

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Year:  2002        PMID: 12916940      PMCID: PMC2784054          DOI: 10.1208/pt030325

Source DB:  PubMed          Journal:  AAPS PharmSciTech        ISSN: 1530-9932            Impact factor:   3.246


  13 in total

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5.  Incorporation of protein in PLG-microspheres with retention of bioactivity.

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Journal:  J Control Release       Date:  2000-07-03       Impact factor: 9.776

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Review 10.  Mucoadhesive nanoparticulate systems for peptide drug delivery.

Authors:  H Takeuchi; H Yamamoto; Y Kawashima
Journal:  Adv Drug Deliv Rev       Date:  2001-03-23       Impact factor: 15.470

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