2006
DOI: 10.3168/jds.s0022-0302(06)72105-1
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Preparation of Liposomes from Milk Fat Globule Membrane Phospholipids Using a Microfluidizer

Abstract: The isolation of milk fat globule membrane (MFGM) material from buttermilk on a commercial scale has provided a new ingredient rich in phospholipids and sphingolipids. An MFGM-derived phospholipid fraction was used to produce liposomes via a high-pressure homogenizer (Microfluidizer). This technique does not require the use of solvents or detergents, and is suitable for use in the food industry. The liposome dispersion had an average hydrodynamic diameter of 95 nm, with a broad particle-size distribution. Incr… Show more

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Cited by 127 publications
(80 citation statements)
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“…These fractions have been comprehensively characterized in earlier publications [26][27][28][29], and contained similar overall levels of phospholipids (72-74% polar lipids), low levels of nitrogen (1.1-2.4%) and negligible amounts of triglycerides or cholesterol. The primary difference between the fractions was the distribution of phospholipid classes, with the MFGM-derived fraction containing approximately equal amounts of phosphatidyl choline, phosphatidyl ethanolamine and sphingomyelin; while the soya fraction contained twice the amount of phosphatidyl choline and had no sphingomyelin.…”
Section: Methodsmentioning
confidence: 99%
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“…These fractions have been comprehensively characterized in earlier publications [26][27][28][29], and contained similar overall levels of phospholipids (72-74% polar lipids), low levels of nitrogen (1.1-2.4%) and negligible amounts of triglycerides or cholesterol. The primary difference between the fractions was the distribution of phospholipid classes, with the MFGM-derived fraction containing approximately equal amounts of phosphatidyl choline, phosphatidyl ethanolamine and sphingomyelin; while the soya fraction contained twice the amount of phosphatidyl choline and had no sphingomyelin.…”
Section: Methodsmentioning
confidence: 99%
“…The techniques used included particle size analysis (as outlined below) and various forms of microscopy to provide images of the liposomes (negative staining transmission electron microscopy, thin section transmission electron microscopy, cryo-field emission scanning electron microscopy and atomic force microscopy [28,29]). …”
Section: Determination Of Liposome Formation and Structurementioning
confidence: 99%
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“…Dynamic high pressure microfluidization (DHPM) technology is an emerging homogenization technology which uses the combined forces of high-velocity impact, high-frequency vibration, instantaneous pressure drop, powerful shear, cavitation force and ultra-high pressures, up to 200 MPa, with a very short treatment time (less than 5 s) ). It has been applied for microbial reduction (Fantin et al 1996), preparation of mozzarella cheese (Tunick et al 2000), nanoemulsions (Jafari et al 2007) and liposomes (Thompson and Singh 2006) and improvement of whey protein and egg white protein (Iordache and Jelen 2003;Tu et al 2009). However, few reports exist on the effect of DHPM on dietary fibre.…”
Section: Introductionmentioning
confidence: 99%