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International Journal of Pharmaceutics
Volume 335, Issues 1-2, 20 April 2007, Pages 176-179
 
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doi:10.1016/j.ijpharm.2006.11.011    How to Cite or Link Using DOI (Opens New Window)
Copyright © 2006 Elsevier B.V. All rights reserved.

Pharmaceutical Nanotechnology

The effect of monomers on the formulation of polymeric nanocapsules based on polyureas and polyamides

I. Montassera, b, 1, S. Briançona, b, Corresponding Author Contact Information, E-mail The Corresponding Author and H. Fessia, b

aUniversité Lyon 1, ISPB, Laboratoire de Génie Pharmacotechnique et Biogalénique, Lyon F-69003, France bCNRS, UMR5007, Laboratoire d’Automatique et de Génie des Procédés, Villeurbanne F-69622, France

Received 23 May 2006; 
revised 2 November 2006; 
accepted 3 November 2006. 
Available online 10 November 2006.

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Abstract

Formulation of nanocapsules based on polyureas and polyamides have been tested using a patented process. This method based on polycondensation reaction of two complementary monomers and spontaneous formation of oil in water emulsion, is an alternative concept to the known technique based on the same type of reaction used for the formulation of microcapsules, and in which the lipophilic monomer was emulsified in the organic phase before the formation of the polymeric membrane. Nanocapsules can be prepared from different monomers. Wall based on cross-linked polymer contributes to the stability of nanocapsules during and after formulation. The permeability of the polymeric wall is related to its crystallinity and contributes to the growth of nanocapsule membrane by the diffusion of the hydrophilic monomers to get stable colloidal suspensions.

Keywords: Nanocapsules; Spontaneous emulsification; Interfacial polycondensation; Polymers

Article Outline

1. Introduction
2. Materials and methods
2.1. Materials
2.2. Methods
2.2.1. Preparation of nanocapsules
2.2.2. Size of nanocapsules
2.2.3. Stability and formation of nanocapsules
3. Results and discussion
3.1. Polymeric nanocapsules based on polyamides
3.1.1. Formulation using phtaloylchloride “PTC” as lipophilic monomer and ethylenediamine “EDA”, 1,6-hexamethylenediamine “HMDA” or diethylenetriamine “DETA” as hydrophilic monomers
3.1.2. Formulation using sebacoyl chloride “SC” as lipophilic monomer and ethylenediamine “EDA”, 1,6-hexamethylenediamine “HMDA” or diethylenetriamine “DETA” hydrophilic monomers
3.2. Polymeric nanocapsules based on polyureas
3.2.1. Formulation using 2,4-tolyenediisocyanate “TDI” as lipophilic monomer and ethylenediamine “EDA”, 1,6-hexamethylenediamine “HMDA” or diethylenetriamine “DETA” as hydrophilic monomers
3.2.2. Formulation using hexamethyle-1,6 diisocyanate “HMDI” as lipophilic monomer and ethylenediamine “EDA”, 1,6-hexamethylenediamine “HMDA” or diethylenetriamine “DETA” as hydrophilic monomers
4. Conclusion
References






 
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