Literature DB >> 11465427

Study of the breakup under shear of a new thermally reversible water-in-oil-in-water (W/O/W) multiple emulsion.

L Olivieri1, M Seiller, L Bromberg, E Ron, P Couvreur, J L Grossiord.   

Abstract

PURPOSE: Thickening of the external aqueous phase of W/O/W multiple emulsions is essential to increase the release under shear. However, it leads to globules bursting during fabrication. To reduce this problem, we have tested a novel thermally reversible hydrogel, EMP hydrogel. This way, the corresponding multiple emulsion (EMPME) would gel only at skin temperature, which may increase the active ingredient delivery when topically applied.
METHODS: Samples were sheared at different shear rates and temperatures (20, 30, and 35 degrees C) with a controlled rheometer. A granulometric analysis was then performed with a laser diffraction granulometer, to assess the break up as a function of the shear rate at the three temperatures. Conductometric measurements (CDM 230 conductometer) provided the corresponding release curves.
RESULTS: As we expected, EMPME exhibited a thermally reversible behavior. Compared to a reference emulsion thickened by carbopol, this new thermo-sensitive multiple emulsion displayed higher break up and fraction released at 35 degrees C.
CONCLUSION: The first thermally reversible multiple emulsion has been developed in the present work. This one presents interesting advantages: (1) an easy fabrication process with a higher entrapment yield and (2) a higher fraction released at 35 degrees C compared with the reference emulsion.

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Year:  2001        PMID: 11465427     DOI: 10.1023/a:1011097713776

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


  7 in total

1.  W/O/W Multiple Emulsions Submitted to a Linear Shear Flow: Correlation between Fragmentation and Release.

Authors: 
Journal:  J Colloid Interface Sci       Date:  1999-10-01       Impact factor: 8.128

2.  Thermally reversible xyloglucan gels as vehicles for oral drug delivery.

Authors:  N Kawasaki; R Ohkura; S Miyazaki; Y Uno; S Sugimoto; D Attwood
Journal:  Int J Pharm       Date:  1999-04-30       Impact factor: 5.875

3.  Temperature-responsive gels and thermogelling polymer matrices for protein and peptide delivery.

Authors: 
Journal:  Adv Drug Deliv Rev       Date:  1998-05-04       Impact factor: 15.470

4.  Insulin in w/o/w multiple emulsions: preparation characterization and determination of stability towards proteases in vitro.

Authors:  A S Cunha; J L Grossiord; F Puisieux; M Seiller
Journal:  J Microencapsul       Date:  1997 May-Jun       Impact factor: 3.142

5.  Drug release from biodegradable injectable thermosensitive hydrogel of PEG-PLGA-PEG triblock copolymers.

Authors:  B Jeong; Y H Bae; S W Kim
Journal:  J Control Release       Date:  2000-01-03       Impact factor: 9.776

6.  Thermosensitive polymers as carriers for DNA delivery.

Authors:  W L Hinrichs; N M Schuurmans-Nieuwenbroek; P van de Wetering; W E Hennink
Journal:  J Control Release       Date:  1999-08-05       Impact factor: 9.776

7.  "On-off" thermocontrol of solute transport. I. Temperature dependence of swelling of N-isopropylacrylamide networks modified with hydrophobic components in water.

Authors:  Y H Bae; T Okano; S W Kim
Journal:  Pharm Res       Date:  1991-04       Impact factor: 4.200

  7 in total

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