Publications

1999
Nissim Garti and Leser, Martin E. 1999. Natural Hydrocolloids As Food Emulsifiers.. Annual Surfactants Review, 2, Design and Selection of Performance Surfactants, Pp. 104–145.
A review with 83 refs. is given. Research activities carried out on various gums as emulsifiers are discussed and questions related to adsorption at interfaces of certain gums are clarified. Gum arabic, galactomannans (guar, locust bean, and fenugreek gum), xanthan gum, Portulaca oleracea and Opitus ficus gums, tragacanth gum, and pectins are included. Adsorption isotherms and the role of proteins in galactomannans, mechanistic considerations, protein-polysaccharide interactions, the stabilization by solid particles (colloidal microcryst. cellulose as emulsifier), and biosurfactants are discussed. [on SciFinder(R)]
N Garti, Slavin, Y, and Aserin, A. 1999. Portulaca Oleracea Gum And Casein Interactions And Emulsion Stability.. Food Hydrocolloids, 13, 2, Pp. 127–138. doi:10.1016/S0268-005X(98)00077-0.
It is well documented that weak or strong interactions between macromols. such as proteins or polysaccharides can synergistically improve the emulsifying capabilities of each of the biopolymers. A study was made to explore the nature of the adsorbed layer in emulsions formed in the presence of casein and a new anionic hydrocolloid extd. from Portulaca oleracea in several emulsification protocols. Electrophoretic mobility of medium chain triglyceride oil emulsion droplets and the corresponding adsorbing creamed phases were measured. The zeta potential magnitudes were calcd. in view of the possible pH dependent ionic-hydrogen bonding interactions between casein and a new ionic gum at the oil-water interfaces. Emulsions stability were detd. from the emulsification stability indexes and emulsification activity index. It was found that POG can adsorb by itself or together with casein onto the oil-water interface. Displacement of the POG from the interface by the casein will take place at pH values that will enhance repulsion forces between the biopolymers. However, complementary adsorption of a possible casein-POG complex will occur if the pH is enhancing the strong attraction interaction between the two biopolymers. The attraction forces between the two biopolymers will enhance the stability of oil-in-water emulsions formed in the presence of the two macromol. amphiphiles. [on SciFinder(R)]
Helga F Milhofer, Garti, Nissim , and Kamishny, Alexey. . 1999. Process For Preparation Of Novel Aspartame Crystals..
New crystal forms of aspartame were prepd. by using microemulsions comprising: (a) introducing aspartame into a microemulsion formed from an oil phase, an aq. phase and at least one emulsifier; (b) destabilizing the microemulsion to effect recrystn. of aspartame; (c) sepg. solid phase crystals from the liq. phase in which they are contained; and (d) cleaning the crystals to remove traces of the oil phase and surfactant. Thus, aspartame (22 g) was solubilized by mech. stirring in a microemulsion contg. 234 g (65%) of isooctane, 36 g (10%) of water and 90 g (25%) AOT at 65°. The microemulsion was then cooled at a rate of 1° per min with const. sirring to a final temp. of 5° and stirred at this temp. for an addnl. two hours to induce crystn. The crystal gave an X-ray pattern characteristic of form III aspartame. [on SciFinder(R)]
N Garti, Slavin, Y, and Aserin, A. 1999. Surface And Emulsification Properties Of A New Gum Extracted From Portulaca Oleracea L.. Food Hydrocolloids, 13, 2, Pp. 145–155. doi:10.1016/S0268-005X(98)00082-4.
The properties of a new gum extd. from the leaves of an edible herb (Portulaca oleracea) were studied. The biopolymer is a relatively small mol. wt. polysaccharide and exhibits significant charge d. at pH \textgreater 2. The extd. gum has surface and interfacial properties derived from its chem. compn. and structure. The Portulaca oleracea gum (POG) adsorbs onto the oil (n-tetradecane or soya) interfaces and stabilizes oil-in-water emulsions. Emulsions (5 wt% oil and 0.7 wt% gum) are stable to flocculation and coalescence at room temp. (for a year) but upon heating the gum desorbs and the emulsion coalesces. Mechanistic considerations regarding its adsorption isotherms, the role of the residual proteinaceous matter contaminating the polysaccharide and the charge are discussed. POG is a good example of a new gum that can be considered as a food emulsifier. [on SciFinder(R)]
N Garti. 1999. What Can Nature Offer From An Emulsifier Point Of View: Trends And Progress?. Colloids And Surfaces, A: Physicochemical And Engineering Aspects, 152, 1-2, Pp. 125–146. doi:10.1016/S0927-7757(98)00621-9.
The most complex emulsions are those of foods and, therefore, are difficult to stabilize. An infinite no. of microstructures of combinations of proteins, carbohydrates, fats and lipids are present in food systems. There is an increasing awareness of many investigators to the relevance of the principles of colloid and surface science to many of the technol. problems related to advanced foods. Amphiphilic mols. play a key role in the stabilization of many of the food colloids. It is, therefore, very important to understand the interfacial behavior of these mols. and to select the proper ones for the proper activity. Synthetic surfactants and emulsifiers are widely used in many of our foods, but, it becomes very important to replace them by natural mols. with good health records. The following review with 49 refs. discusses the main natural occurring mols. that are in use today and the future trends in this area. Monomeric emulsifiers such as mono- and diglycerides, lecithins and lysolecithins are still key players. Glycolipids are present only in very minor concns. in plants and animals and therefore are not com. available. Saponins are a very interesting group of materials with increasing potential. The polymeric amphiphilic compds. are "native" and enzymically modified proteins. However, in situ products chem. modified by a Maillard reaction can also be used as emulsifiers. The most interesting new emulsifiers are some selected hydrocolloids that exhibit surface properties and emulsification capabilities. Enzymically modified hydrocolloids show significant promise. Bio-surfactants have also been studied and considered as emulsifiers, but are not food grade products. New trends and progress will also be discussed. [on SciFinder(R)]
Nissim Garti, Aserin, Abraham , Madar, Zecharia , and Sternheim, Boaz. . 1999. Galactomannan Products And Compositions Containing The Same.. Germany DE69510920T.
A galactomannan isolated from fenugreek seed has ≥50 repeating units of mannose and galactose in a ratio of 0.5-1.0 and 1.8-1.0, a protein content of ≤20%, a saponin content of ≤5%, and a lipid content of ≤1%, and is useful as an active ingredient in nutraceutical and cosmetic products. [on SciFinder(R)]
N Garti, Lichtenberg, D, and Silberstein, T. 1999. The Hydrolysis Of Phosphatidylcholine By Phospholipase A2 In Microemulsion As Microreactor.. Journal Of Dispersion Science And Technology, 20, 1 & 2, Pp. 357–374. doi:10.1080/01932699908943796.
Phospholipase A2 (PLA2) was used to hydrolyze phosphatidylcholine (PC) in microemulsions. Phase diagrams were constructed for mixts. of alcs. (C2-C6), medium chain triglycerides (tricaprylin, TC) or vegetable oils, PC and water, and areas corresponding to isotropic systems were identified. The PC hydrolysis was carried out with high yields at various PC/(TC+alc.) compns. within the areas of isotropic systems at increasing amts. of solubilized water. The initial reaction rates depended on the aggregation state of the PC (size and nature of microemulsion structures), as well as on temp. and mode of calcium addn. At low enzyme concns., hydrolysis was preceded by a "lag phase" followed by an abrupt increase in rate. By contrast, no latency was obsd. at higher PLA2 PC ratios and the rate was significantly higher. The easy access of the enzyme to the substrate in the curved phospholipid-contg. microemulsion particles facilitate activation of the enzyme and "pushes" the reaction to completion. Hence, these microemulsions can serve as microreactors for the enzymic high yield hydrolysis. [on SciFinder(R)]
Nissim Garti, Berkovitz, Y. , and Aserin, A. . 1999. Methods For The Preparation Of Nanosized Material Particles. Eurasian Patent Organization 99905152.7, Based on PCT/IL99/00097. (European Patent Application ).
A Benichou, Aserin, A, and Garti, N. 1999. Steroid Saponins From Fenugreek Seeds: Extraction, Purification And Surface Properties.. Journal Of Dispersion Science And Technology, 20, 1 & 2, Pp. 581–605. doi:10.1080/01932699908943809.
Two techniques for extn. and purifn. were used in order to obtain a purified saponins ext. from several sources (fenugreek, soybean, locust bean and sesame). The results indicate that fenugreek steroid saponins ext. has the best surface properties and reduces the surface tension to 33.3 mN/m and the tetradecane-water interfacial tension from 44 mN/m to 7.5 mN/m. The HLB value was 18. Three different types of oil (n-tetradecane, soybean oil, tricaprylin) were emulsified with a 6 wt% aq. soln. of saponins to give an av. droplet size of 0.7 $μ$m (stable after month). An effective synergism is seen when these emulsions were prepd. with sucrose fatty acid esters as co-surfactant. Foaming power was also evaluated. [on SciFinder(R)]
N Garti, Clement, V, Leser, M, Aserin, A, and Fanun, M. 1999. Sucrose Ester Microemulsions.. Journal Of Molecular Liquids, 80, 2,3, Pp. 253–296. doi:10.1016/S0167-7322(99)80010-5.
A review with 95 refs. Sucrose esters are biodegradable surfactants that can be manufd. in various hydrophilic-lipophilic properties using different fatty acids varying in their lipophilic chain length. These surfactants are used in different industries including pharmaceutical, food processing, detergents, agricultural and others. Few no. of works had been done using sucrose esters in microemulsions. In this review we tried to introduce the relevant works that enlighten the behavior of sucrose esters in phase diagrams prepd. using different oils and medium chain alcs. We hope that this review article can be an aid to those researchers interested in microemulsions based on sucrose esters and their applications. [on SciFinder(R)]
N Garti, Clement, V. , and Leser, M. . 1999. Water-In-Oil Microemulsions Based On Hydrophilic Sugar Ester Surfactants As Microreactorsv. United States of America 000-100 401 (Nestle patent disclosure). doi:10.1007/BF02719011.
1998
L Tunik, Fueredi-Milhofer, H, and Garti, N. 1998. Adsorption Of Sodium Diisooctyl Sulfosuccinate Onto Calcium Oxalate Crystals.. Langmuir, 14, 12, Pp. 3351–3355. doi:10.1021/LA9708041.
The adsorption of diisooctyl sulfosuccinate (AOT) from high ionic strength soln. onto well-defined calcium oxalate monohydrate (COM) and dihydrate (COD) crystals was studied. Adsorption at the COM/soln. interface is characterized by a two-step (LS type) isotherm, starting at low equil. concns. (5 mg dm-3). At ceq = 15-30 mg dm-3 it reaches a plateau which is followed by a relatively steep inflection (ceq = 30-50 mg dm-3) and a further slow increase of the adsorption as a function of increasing AOT concn. In suspensions without surfactant the particles were neg. charged. Upon adsorption an initial slight decrease of the neg. $\zeta$-potential, coinciding with the first plateau, occurred which was followed by a sharp increase in concordance with the increasing surface concn. of the surfactant. In contrast, adsorption onto COD is characterized by a sigmoid isotherm. It commenced at 14 mg dm-3 of AOT and increased abruptly up to a plateau. The max. adsorbed amt. was about half the max. amt. adsorbed on COM, the corresponding adsorption densities in mols. per square nanometer being 7.45 for COD and 14.22 for COM, resp. COD crystals suspended in electrolyte soln. without surfactant were almost uncharged, and the neg. $\zeta$-potential increased in concordance with AOT adsorption. The results are discussed in accordance with literature data and by considering the ionic structure of the different crystal faces. It is assumed that the first adsorption step in the COM/surfactant system is due to electrostatic interactions causing head-on adsorption of the surfactant mols. at high-energy sites, while in the second step a bilayer is formed. In the COD/surfactant system the hydration layers covering the COD crystal faces are shielding them from electrostatic interactions. Consequently AOT adsorption at the COD/soln. interface proceeds only through surface aggregation, resulting in a bilayer of intertwined surfactant mols. [on SciFinder(R)]
A system of coating comprises applying a primary coating having a surface energy 22-28 dynes/cm2 of polymeric material having nonstick and hardness properties and applying a top coating having surface energy ∼18-21 dynes/cm2 of a silicon polymer, and in between a bi- or polyfunctional org. compd. to wet the surface of the primary coating and chem. or phys. bond and couple the primary coating and top coating together. The coated substrates are resistant to marking by graffiti, to marine fouling organisms, and adhesion by ice. Steel substrates were coated with a primary coating of epoxy-siloxane emulsion compn., and top coated with poly(di-Me siloxane) contg. Tween 80 coupling agent. [on SciFinder(R)]
Nissim Garti and Bisperink, Chris. . 1998. Double Emulsions: Progress And Applications.. Current Opinion In Colloid & Interface Science, 3, 6, Pp. 657–667. doi:10.1016/S1359-0294(98)80096-4.
A review with 75 refs. Research work and progress on several major issues related to double emulsions have taken place recently. Such developments include the intrinsic thermodn. instability derived from the droplets size of the double emulsion; how the release of active ingredients entrapped within the inner phase can be prolonged and controlled; new advanced methods for studying the structure and nature of double emulsion droplets and their interfaces; new possible applications of double emulsions for sustained and prolonged release of active ingredients in cosmetics, food, agriculture and pharmaceuticals; double emulsions as intermediate systems in the prepn. of microspheres or nanospheres; and the scope and limitations of possible new applications of multicompartment microspheres prepd. from double emulsions. [on SciFinder(R)]
VD Fedotov, Vylegzhanina, Natalija N, Altshuler, AE , Shlenkin, VI , Zuev, Yu. F, and Garti, N. 1998. An Electron Spin Resonance Study Of The Soy Bean Phosphatidylcholine-Based Reversed Micelles.. Applied Magnetic Resonance, 14, 4, Pp. 497–512. doi:10.1007/BF03161858.
The ESR spectra of 1-palmitoyl-2-stearoyl-(n-doxyl)-glycero-3-phosphocholine spin label positional isomers (n = 5, 7, 10, 12 and 16) were studied in soy bean phosphatidylcholine (SPC)-based microemulsions with various vol. fractions of disperse phase over the wide temp. range. The max. hyperfine splitting 2Amax and the order parameters S were taken as indexes of the rotational mobility and the motion spatial restrictions of the labeled lipid chain segments. The temps. Ttr at which sharp enhancements of 2Amax and S occur depend on concn. and size of the reversed micelles in solns. To explain this, a plausible model, taking into account capability of the SPC mol. hydrocarbon chains to change a tilt angle with respect to the surface of a polar head group as temp. varies, is proposed. The estns. of the correlation times $\tau$sl obtained from the lineshape characteristics of the ESR spectra provided the possibility to suggest that these correlation times characterize the reorientations of the SPC chain axis about the normal to the surface of a polar head group of a reversed micelle. [on SciFinder(R)]
N. Garti and Aserin, A. . 1998. Ester Oils. Israel 123367.
S Ezrahi, Aserin, A, and Garti, N. 1998. An Excursion Into Phase Tetrahedra-Where Physical Chemistry And Geometry Meet.. Journal Of Chemical Education, 75, 12, Pp. 1648–1652. doi:10.1021/ed075p1648.
The authors have shown how triangles and tetrahedra can be used to represent the compn. and phase behavior of three- and four-component systems. The relationship between such triangular representations and the full tetrahedron is explained by geometric considerations of the cross-sections through the tetrahedron. [on SciFinder(R)]
N. Garti, Aserin, A. , Svitov, I. , and Friedman, M. . 1998. Hydroxylation And Derivatization Of Fatty Acid Derivatives To Obtain New Surfactants. Israel.
N. Garti, Shani, A. , and Aserin, A. . 1998. Lubricious Coating Compositions Based On Jojoba Oil. United States of America 5713995.
Abraham Aserin, Garti, Nissim , and Shani, Arnon. . 1998. Lubricous Coating Compositions Containing Jojoba Oil..
Coating compns. comprise natural or synthetic jojoba oil which is optionally partially or completely hydrogenated and/or isomerized, a solvent, or a dispersing system (an immiscible org. liq. and dispersing agent). The coating compns. are for polymers or plastics or naturally occurring macromols. with high hydrophobicity or with low or medium surface energy. Thus, a coating contained GKF 8-10 (octane-decane) 46.5%, pentane-hexane 46.5%, jojoba oil 5.8%, glycerol 0.5, and fragrances 0.7%. [on SciFinder(R)]

Pages