Literature DB >> 18577008

Formation of biopolymer-coated liposomes by electrostatic deposition of chitosan.

C Laye1, D J McClements, J Weiss.   

Abstract

The purpose of this study was to prepare stable biopolymer-coated liposome suspensions using an electrostatic deposition method. Liposome suspensions were produced by homogenizing 1% soy lecithin in acetate buffer (0.1 M, pH 3). Cationic chitosan (Mw approximately 200 kDa) solutions were mixed with anionic liposome suspensions (d approximately 100 and 200 nm), and the effect of phospholipid concentration, chitosan concentration, and liposome size on the properties of the particles formed was determined. The particle size and charge (zeta-potential) were measured using dynamic light scattering and particle electrophoresis. The particle charge changed from -38 mV in the absence of chitosan to +60 mV in the presence of chitosan, indicating complex formation between the anionic liposomes and cationic chitosan molecules. Below a minimum critical chitosan concentration (c(min)), large aggregates were formed that phase separated within minutes, whose origin was attributed to formation of coacervates. On the other hand, above a maximum critical chitosan concentration (c(max)), large flocs were formed that sedimented within hours, whose formation was attributed to depletion flocculation. Minimum and maximum critical chitosan concentrations depended on liposomal concentration and size. At c(min) < c < c(max'), chitosan-coated liposomes were formed that did not aggregate and were stable to sedimentation. Coated liposomes had better stability to aggregation than uncoated liposomes when stored at ambient temperatures for 45 d. This study indicates that chitosan can be used to form biopolymer-coated liposomes with enhanced stability over uncoated liposomes.

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Year:  2008        PMID: 18577008     DOI: 10.1111/j.1750-3841.2008.00747.x

Source DB:  PubMed          Journal:  J Food Sci        ISSN: 0022-1147            Impact factor:   3.167


  13 in total

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4.  Chemical coupling of thiolated chitosan to preformed liposomes improves mucoadhesive properties.

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Journal:  Nanomaterials (Basel)       Date:  2020-12-05       Impact factor: 5.076

6.  Chitosan-covered liposomes as a promising drug transporter: nanoscale investigations.

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7.  Encapsulation of Liposomes within pH Responsive Microspheres for Oral Colonic Drug Delivery.

Authors:  M J Barea; M J Jenkins; Y S Lee; P Johnson; R H Bridson
Journal:  Int J Biomater       Date:  2012-06-27

8.  Physical and oxidative stability of uncoated and chitosan-coated liposomes containing grape seed extract.

Authors:  Monika Gibis; Nina Rahn; Jochen Weiss
Journal:  Pharmaceutics       Date:  2013-08-20       Impact factor: 6.321

9.  Effect of Charge on Separation of Liposomes upon Stagnation.

Authors:  Mahsa Narenji; Mohammad Reza Talaee; Hamid Reza Moghimi
Journal:  Iran J Pharm Res       Date:  2017       Impact factor: 1.696

10.  Mesoscopic Modeling of the Encapsulation of Capsaicin by Lecithin/Chitosan Liposomal Nanoparticles.

Authors:  Ketzasmin A Terrón-Mejía; Evelin Martínez-Benavidez; Inocencio Higuera-Ciapara; Claudia Virués; Javier Hernández; Zaira Domínguez; Waldo Argüelles-Monal; Francisco M Goycoolea; Roberto López-Rendón; Armando Gama Goicochea
Journal:  Nanomaterials (Basel)       Date:  2018-06-12       Impact factor: 5.076

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