Publications

2019
Nina Lidich, Garti-Levy, Sharon , Aserin, Abraham , and Garti, Nissim. . 2019. Potentiality Of Microemulsion Systems In Treatment Of Ophthalmic Disorders: Keratoconus And Dry Eye Syndrome - In Vivo Study.. Colloids And Surfaces, B: Biointerfaces, 173, Pp. 226–232. doi:10.1016/j.colsurfb.2018.09.063.
Microemulsions are widely studied as potential ocular drug delivery vehicles. In the present study we show the versatility of possible use microemulsions as ocular delivery vehicle. The ME is loaded with a hydrophilic drug, riboflavin phosphate (RFP) and a lipophilic, docosahexaenoic acid in triglyceride form (TG-DHA), each sep. These drugs treat keratoconus and dry eye syndrome, resp. The advantage of using ME loaded with RFP is in overcoming eye epithelium debridement during collagen crosslinking therapy for treatment of keratoconus. ME loaded with lipophilic TG-DHA provides convenient dosage in liq. aq. form of administration of highly lipophilic TG-DHA, which is known as a protective mol. in dry eye syndrome. The capability of RFP-loaded MEs was demonstrated in terms of improvement of biomech. strength of the rabbit cornea, as a result of successful penetration of RFP through the intact epithelium. TG-DHA-loaded microemulsion applied topically onto an eye with induced dry eye syndrome showed the significant relief of the dry eye condition. [on SciFinder(R)]
Eva Abramov, Ottaviani, Maria Francesca , Shames, Alexander I, Fattori, Alberto , and Garti, Nissim . 2019. Structural Characterization Of Reconstituted Bioactive-Loaded Nanodomains After Embedding In Films Using Electron Paramagnetic Resonance And Self-Diffusion Nuclear Magnetic Resonance Techniques. Langmuir, 35, 24, Pp. 7879–7886. doi:10.1021/acs.langmuir.9b00578.
Pharmaceutical applications of microemulsions (MEs) as drug delivery vehicles are recently gaining scientific and practical interests. Most MEs are able to solubilize bioactive molecules, but, at present, they cannot guarantee either controlled release of the drugs or significant advantage in the bioavailability of the bioactives. This study proposes to incorporate the modified ME structures, or nanodomains, into a natural polymeric film, to be used as a stable and capacious reservoir of drug-loaded nanodomains. These nanodomainloaded films may release the nanodroplets along with the drug molecules in a slow and controlled way. Gellan gum, an anionic polysaccharide, was used in aqueous solution as the film former, and curcumin, hydrophobic polyphenol, served as the guest molecule in the loaded systems. Films were prepared by using empty and curcumin-loaded MEs. It is imperative to verify the persistence of the ME structure upon the dissolution of the film mimicking its behavior when in contact with a human physiological aqueous environment via reaching the cell membranes. For this purpose, the films were dissolved, and the reconstituted ME structure was compared with the ME structure before film formation. Characterization of these structures, before and after dissolution, was achieved using electron paramagnetic resonance (EPR) and self-diffusion nuclear magnetic resonance (SD-NMR) techniques. Specific spin probes were inserted in the system, and a computer-aided analysis of the EPR spectra was performed to provide information on nanodomain microstructure assemblies. In addition, the SD-NMR profile of each component was analyzed to extract information on the diffusivity of the ME components before film formation and after ME reconstitution. The EPR and SD-NMR results were in good agreement to each other. The most important finding was that, after film dissolution, the ME nanodomains were reversibly and spontaneously reformed. It was also found that the film did not perturb the ME-nanodomain structure embedded in it. The film remained transparent and the bioactive curcumin was easily solubilized into the ME-droplet/water interface even after film dissolution. The combined techniques confirmed that the film constituted by bioactive-loaded MEs can serve as novel drug delivery vehicles.
נסים גרתי. 2019. שמנים צמחיים - מה חשוב לדעת ומה חדש / פרופ' נסים גרתי. מגזין מכון תנובה למחקר, 57 (יוני 2019), עמ' 13-17.
עד לפני כמה עשורים נחשבו השמנים הצמחיים לקבוצה הומוגנית, שהמשותף לה הוא היותם נוזליים בטמפרטורת החדר וממקור צמחי. צלילה לתוך עולם השמנים מעידה על כך שרב השונה והמיוחד על המשותף, הן בתכונות הכימיות והפיסיקליות, בתהליכי ההפקה, בשימושים בבישול ובתעשייה, והן בהשפעות הבריאותיות הנובעות מכל אלה. המאמר מתייחס להגדרות, הבדלים ומקורות של שמנים ושומנים, המקורות להם, שמנים בכבישה קרה ושמנים מיוחדים במזון וכתוספי תזונה.
2019. Edible Oleogels : Structure And Health Implications 2Nd Edition. Champaign: American Oil Chemist Society Press.
Eliezer Goldmunz, Aserin, Abraham , and Garti, N. . 2019. Phase Inversion Characteristics Observed Upon Water Dilution Of A Bidiscontinuous Phase.. Colloids And Surfaces, A: Physicochemical And Engineering Aspects, Pp. Ahead of Print. doi:10.1016/j.colsurfa.2019.124213.
This study presents a directly aggregated pseudo-ternary system. The three apexes of the investigated system represent a surfactant phase [Tween 80:propylene glycol (9:1 wt ratio)], an oil phase [isopropyl myristate:benzyl alc. (7.5:2.5 wt ratio)], and water. Within the pseudo-ternary system, water diln. line, termed N91 (90 wt% surfactant phase and 10 wt% oil phase), was found to represent transparent and thermodynamically stable compns. from conc. to high water diln. (>95 wt% water). Despite that the system was found to be directly aggregated, diln. line N91 exhibited classical L2→L1 phase inversion characteristics (at 39 wt% water). To explain this phenomenon, a novel structural interpretation regarding the obsd. inversion as an obstruction of the bidiscontinuous phase, consisting of oil and water-segregated domains, is proposed. The evaluation of diln. line N91 was based on elec. cond., SAXS, SD-NMR, rheometry, DSC and cryo-TEM. The structural transitions along water diln. line N91 were found to be as follows: 'pseudo L1' (pseudo direct surfactant-oil aggregates) → bi-discontinuous structure (of which partial is a hexagonal H1 mesophase) → L1. We concluded that the high concn. of low CPP (crit. packing parameter) surfactant plays a major role in detg. the system's geometry throughout the water diln. line. As a result, the proposed interpretation of the structural inversion obsd. along diln. line N91 differs from the classical U-type inversion interpretation (L2 →bicontinuous →L1). [on SciFinder(R)]
2018
Tehila Mishraki-Berkowitz, Cohen, Guy , Aserin, Abraham , and Garti, Nissim . 2018. Controlling Insulin Release From Reverse Hexagonal (H-Ii) Liquid Crystalline Mesophase By Enzymatic Lipolysis. Colloids And Surfaces B-Biointerfaces, 161, Pp. 670–676. doi:10.1016/j.colsurfb.2017.11.031.
In the present study we aimed to control insulin release from the reverse hexagonal (H-II) mesophase using Thermomyces lanuginosa lipase (TLL) in the environment (outer TLL) or within the H-II cylinders (inner TLL). Two insulin-loaded systems differing by the presence (or absence) of phosphatidylcholine (PC) were examined. In general, incorporation of PC into the H-II interface (without TLL) increased insulin release, as a more cooperative system was formed. Addition of TLL to the systems' environments resulted in lipolysis of the H-II structure. In the absence of PC, the lipolysis was more dominant and led to a significant increase in insulin release (50% after 8 h). However, the presence of PC stabilized the interface, hindering the lipolysis, and therefore no impact on the release profile was detected during the first 8 h. Entrapment of TLL within the H-II cylinders (with and without PC) drastically increased insulin release in both systems up to 100%. In the presence of PC insulin released faster and the structure was more stable. Consequently, the presence of lipases (inner or outer) both enhanced the destruction of the carrier, and provided sustained release of the entrapped insulin. (C) 2017 Elsevier B.V. All rights reserved.
Nissim Garti, Garti Levi, Sharon , and Edri, Rotem. . 2018. Dilutable Formulations Of Cannabinoids And Processes For Their Preparation..
The present disclosure provides cannabinoid-loaded formulations, as well as processes for their prepn. [on SciFinder(R)]
Nissim Garti, Garti Levi, Sharon , and Edri, Rotem. . 2018. Method For Extraction Of An Agent From A Plant Source..
The present disclosure provides methods for extn. of various agents, e.g. active agent, from a plant source, specifically with the use of extn. formulations which are based on micellar liq. systems. [on SciFinder(R)]
Nissim Garti, Garti-Levi, Sharon , and Edri, Rotem. . 2018. Method For Selective Extraction Of Cannabinoids From A Plant Source..
The present disclosure provides methods for selective extn. of cannabinoids, for example cannabidiol (CBD), from a plant source, by using tailored extn. media. [on SciFinder(R)]
Nissim Garti. 2018. Topical Delivery Of Active Agents. United States of America (WO 2018/163176).

A nano-delivery technology for topical delivery of a plurality of active agents such as diclofenac, lidocaine, clonidine, fentanyl, and more.

Pending in US, EP, Australia, Canada, China, India, Israel, Japan and Russia

Licensed to an International Big Pharma company.

Nissim Garti and Garti Levi, Sharon. . 2018. Topical Delivery Systems For Active Compounds..
The disclosure concerns viscous or gelled delivery systems based on oily nano-domains dispersed in a viscosified/gelled continuous aq. phase, and suitable for prolonged and/or sustained topical delivery of various active compds. [on SciFinder(R)]
2017
Shifra Rokach, Aserin, Abraham , Garti, Nissim , Rokach, Shifra , Ottaviani, Maria Francesca , and Shames, Alexander I. 2017. Behavior Of Ppi-G2 Dendrimer In A Microemulsion. The Journal Of Physical Chemistry. B, 121, 10, Pp. 2339–2349.
Dendrimer nanostructures are of eminent interest in biomedical applications because of their uniform and well-defined molecular size and shape, and their ability to cross cell membranes and reduce the risk of premature clearance from the human body. Dendrimers perform as gene and drug carriers and have also shown significant therapeutic properties for treating cancer and neurodegenerative diseases. A complex drug delivery system, based on a dendrimer solubilized in the aqueous core of a water-in-oil (W/O) microemulsion (ME) along with the drug may combine the advantages of both dendrimers and MEs to provide better control of drug release. We propose a new microemulsion composed of drug-permitted surfactants and dendrimer that can be used as a potential controlled drug delivery nanosystem. The influence of second generation poly(propyleneimine) (PPI-G2) dendrimer; solubilized in (W/O) ME with a capacity of up to 25 wt% PPI-G2 at various pHs; and their interactions with the surfactant phosphatidylcholine (PC), cosurfactant (butanol), and water was studied. SAXS and EPR measurements indicated that increasing PPI-G2 concentration reduces droplet curvature and increases droplet size thus increasing macro-(SAXS) and micro-(EPR) order degree. Furthermore, SD-NMR and ATR-FTIR show stronger interactions between PPI-G2 and water molecules at the expense of PC and butanol headgroups hydration, which increases microviscosity (EPR). PPI-G2's effect is somewhat opposite to the increasing water phase effect, thus reducing the amount of free water (DSC) and slowing the mobility of all ME components (SD-NMR).[on SciFinder (R)]
Nissim Garti. 2017. One Pot Process For Extracting Lipophilic Agent Plant Material. United States of America WO 2018/061011.

 

Process for extracting and delivery a lipophilic agents using the same medium. Delivery can be by all forms of administration.

Pending in US, EP and Israel

 

Nissim Garti. 2017. One Pot Process For Extraction Of Cannabinoids From A Plant Source.. United States of America WO 2018/061009.

Process for extraction and delivery of cannabinoids, using the same medium.
Pending in US, EP, Australia, Brazil, Canada, China, Japan, Mexico, New Zealand and Korea.
Licensed to a cannabis-based US company

Delphine Hagage-Dobensky, Aserin, Abraham , and Garti, Nissim. . 2017. Progesterone Solubilization Within Reverse Hexagonal Mesophase.. Colloids And Surfaces, A: Physicochemical And Engineering Aspects, 516, Pp. 254–261. doi:10.1016/j.colsurfa.2016.12.015.
The present work reports on the prepn. and characterization of progesterone-loaded reverse hexagonal (HII) mesophase based on a glycerol monooleate (GMO)/tricaprylin (TAG)/water mixt. for transdermal application. Several compns. into which progesterone was quant. solubilized were selected and used in the present study in order to evaluate the effect of the hormone on structural transitions and characteristics. A GMO/TAG of 90:1 wt ratio with 20 wt% water was found to form HII mesophases with relative high solubilization capacity of 4 wt% progesterone and a shelf life of over one year. The structures were identified by cross-polarized light microscopy (CPLM). Structural confirmations were obtained from small-angle X-ray scattering (SAXS) measurements. The hormone is solubilized at the interface of the HII mesophase as confirmed by SAXS, rheol., FTIR, and DSC. The progesterone, which is loaded onto reverse hexagonal cylinders, leads to strengthening the hydrogen bonding and to better packing of the HII mesophase, suggesting that progesterone is a kosmotropic agent. The reverse hexagonal mesophase seems to be a promising carrier for solubilization of progesterone. [on SciFinder(R)]
Nissim Garti. 2017. Water Dilutable Nano Delivery Technology Of Cannabinoids. United States of America WO 2018/061007.

 

A concentrated formulation having high loads of cannabinoids that can be diluted in water in any ratio or physiological liquid.

 

Pending in US, EP, Australia, Brazil, Canada, China, Japan, Mexico, New Zealand and Korea

Licensed to a cannabis-based US company.

 

 

Nissim Garti, Garti Levi, Sharon , Aserin, Abraham , and Perlstein, My. . 2017. Delivery Systems For Propofol..
The present invention concerns novel dilutable delivery systems and propofol microemulsions suitable for i.v. delivery of propofol. [on SciFinder(R)]
Tehila Mishraki-Berkowitz, Aserin, Abraham , and Garti, Nissim. . 2017. Structural Properties And Release Of Insulin-Loaded Reverse Hexagonal (Hii) Liquid Crystalline Mesophase.. Journal Of Colloid And Interface Science, 486, Pp. 184–193. doi:10.1016/j.jcis.2016.09.074.
Insulin loading into the HII mesophases was examd. as a function of its concn., with addn. of glycerol as a cosolvent and with addn. of phosphatidylcholine (PC) as a structural stabilizer. The structural properties, the mol. interactions, the viscoelastic properties, and the dynamic behavior were investigated by SAXS, ATR-FTIR, and rheol. measurements. Insulin release was then monitored and analyzed. Insulin incorporation into the HII systems shrank the cylinders as it competed with the lipids in water-bonding. Insulin interrupted the interface while increasing $\tau$max and creating a more solid-like response. Upon addn. of PC, cooperative flow behavior was detected, which is probably the reason for increase in insulin cumulative release from 28% to 52% after 300 min. In the presence of glycerol, the system was less cooperative but insulin was more compactly folded, resulting in a slight improvement in insulin release (up to 6%). Addn. of both PC and glycerol caused the max. release (55%). The addn. of additives into the HII system demonstrates how structural modifications can improve insulin release, and influence future design of encapsulated drug delivery systems. [on SciFinder(R)]

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