Liposome Dispersions Research Articles

In vitro dissolution of encapsulated or dispersed vitamin E and cholesterol is correlated with preservation of refrigerated ovine sperm

BACKGROUND: Vitamin E (α‐tocopherol) and cholesterol are crucial components in cellular protection and physiological processes. Their uses in biological media face challenges due to their poor solubility and stability. OBJECTIVE: The study investigated the complex interactions of these bioactive compounds in various encapsulation systems of cyclodextrin and liposome, as well as dispersion in PEG-6000, in an attempt to improve the viability, motility, and preservation of ovine sperm cells. MATERIALS AND METHODS: The work explored the in vitro dissolution kinetics of vitamin E (α‐tocopherol) and cholesterol using semi-empirical models. RESULTS: The release profiles of VitE and Chl varied considerably, depending on the specific carrier systems. For liposome-loaded VitE and Chl, the Korsmeyer-Peppas model gave the best fit; for CD/VitE and CD/Chl, the Higuchi model provided the best fit, whereas for PEG-6000 dispersions (VitE and Chl) both the Higuchi and Korsmeyer-Peppas models demonstrated the excellent fit. All systems indicated a Fickian diffusion mechanism dictated by the concentration gradient. The delivery of VitE and Chl with CD, liposome and PEG dispersion significantly increased sperm mobility and motility. The effect on the VCL parameter was the greatest by liposome-loaded VitE and Chl, followed by CD encapsulation and PEG-6000 dispersion. CONCLUSION: The dynamics of vitamin E and cholesterol within innovative delivery systems offers valuable insights into the development of advanced solutions in reproductive health, particularly on improving the viability, motility of refrigerated ovine sperm cells.

Artificial magnetosomes: Molecularly restructured SPIONs with enhanced potential for magnetic imaging

Magnetosomes represent an elegant example of ultrastable nanomaterials that nature produces by encapsulating magnetic nanoparticles in liposomal sub-compartments of magnetotactic bacteria. Materials chemists continue to strive for ways to mimic the performance of natural systems, but the artificial synthesis of magnetosomes remains unrealized. Here, we report molecular restructuring of the surface of oleic-acid-capped superparamagnetic iron oxide nanoparticles (SPIONs) to produce magnetosomes. Our strategy involves the use of triethylamine as an amphiphilic surfactant that through a combination of ligand exchange and rearrangement mechanisms, facilitates an organic-to-aqueous phase transfer of SPIONs while turning them into magnetosomes. These liposome-encapsulated SPIONs showed dynamic aqueous stability alongside noticeably improved magnetic properties. This improved their performance as contrast agents for magnetic resonance imaging (MRI) and magnetic particle imaging (MPI), the latter revealing a 33.5 % improvement in signal sensitivity over the original SPIONs. The presented strategy is extendable to prepare liposomal dispersions of other biomedically important nanomaterials.

Manganese-Loaded Liposomes: An In Vitro Study for Possible Diagnostic Application.

The present study investigates the possible use of manganese (Mn)-based liposomal formulations for diagnostic applications in imaging techniques such as magnetic resonance imaging (MRI), with the aim of overcoming the toxicity limitations associated with the use of free Mn2+. Specifically, anionic liposomes carrying two model Mn(II)-based compounds, MnCl2 (MC) and Mn(HMTA) (MH), were prepared and characterised in terms of morphology, size, loading capacity, and in vitro activity. Homogeneous dispersions characterised mainly by unilamellar vesicles were obtained; furthermore, no differences in size and morphology were detected between unloaded and Mn-loaded vesicles. The encapsulation efficiency of MC and MH was evaluated on extruded liposomes by means of ICP-OES analysis. The obtained results showed that both MC and MH are almost completely retained by the lipid portion of liposomes (LPs), with encapsulation efficiencies of 99.7% for MC and 98.8% for MH. The magnetic imaging properties of the produced liposomal formulations were investigated for application in a potential preclinical scenario by collecting magnetic resonance images of a phantom designed to compare the paramagnetic contrast properties of free MC and MH compounds and the corresponding manganese-containing liposome dispersions. It was found that both LP-MC and LP-MH at low concentrations (0.5 mM) show better contrast (contrast-to-noise ratios of 194 and 209, respectively) than solutions containing free Mn at the same concentrations (117 and 134, respectively) and are safe to use on human cells at the selected dose. Taken together, the results of this comparative analysis suggest that these liposome-containing Mn compounds might be suitable for diagnostic purposes.

Development of thermosensitive liposome-containing in-situ gel systems for intranasal administration of thiocolchicoside and in vivo evaluation in a rabbit model

Aim Thiocolchicoside (THC) is a drug under the category of BCS III. Due to its high molecular weight, it has poor oral bioavailability and low skin permeability. This study aims to find an alternative delivery method for THC that enhances its bioavailability through nasal application approach. In situ gels containing plain or liposomal THC with different combinations of Pluronic® F127 and PEG 400 were prepared. Method Liposome formulations were prepared using the thin film hydration method and tested for their characterization such as for drug content, particle size, and zeta potential. In vivo pharmacokinetic parameters of formulations such as Cmax, Tmax, and AUC were tested on the rabbit model. The formulations were also scrutinized for their cell viability properties. Result Formulation composition with 2% soybean phosphatidylcholine and 10 mg THC exhibited ∼94% entrapment efficiency, minimum particle size 101.32 nm, low polydispersity index 0.225 and +0.355 zeta potential. In situ liposomal dispersion containing 15% Pluronic® F127 turned into gel at nasal temperature. Cell lines were unharmed for 48 h. İn situ liposomal gels showed 1.5x higher blood concentration than the control formula. Conclusion In situ gels of liposomal THC formulations offer advantages over traditional nasal solutions, demonstrating comparable bioavailability to parenteral medication while also preserving the health of nasal mucosa cells.

Use of residual lipid fractions and protein hydrolysates from salmon skin cleaning processing for liposome production and their application in Pickering emulsions

In the salmon skin and scale cleaning process, several lipid fractions and protein materials were recovered as secondary by-products, presenting opportunities for the production of bioactive ingredients with high nutritional value. The predominant lipid component in all oil fractions was oleic acid.A protein hydrolysate was also obtained, consisting of ≈27% essential and ≈60% hydrophobic amino acids, below 3KDa (≈90.2%), and with significant antioxidant, ACE inhibitory and antidiabetic properties.Hydrolysate-loaded Liposomes (LH), prepared from partially purified phospholipids from recovered lipids, exhibited a slightly larger mean size (283 nm) than empty liposomes (226 nm) (L), and a very stable ζ potential for both. Stable oil-in-water emulsions (30/70) were produced using the oil fraction and replacing the aqueous phase by a dispersion of empty liposomes or hydrolysate-loaded liposomes. The presence of free or encapsulated hydrolysate resulted in poorer stabilisation compared to the empty liposomes, demonstrating that the latter are good Pickering agents.

Antiviral potential of rosuvastatin and hesperidin in combination with favipiravir liposomal nanoformulations in targeting the main protease (Mpro) of SARS-CoV-2: Molecular docking, molecular dynamics and in-vitro studies

Favipiravir (Fav) is a drug utilized to treat coronavirus disease 2019 (COVID-19) due its capacity to expedite the clearance of the SARS-CoV-2 virus through binding to its main protease (Mpro). However, the use of Fav has been associated with some adverse health effects. Meanwhile, numerous studies have highlighted the potential antiviral activities of specific phytochemicals and statins. Consequently, we thought to explore drug combination strategies involving certain statins and phytochemicals and their liposome nanoformulations either alone or with Fav, aiming to augment its efficacy and mitigate potential adverse effects. The molecular docking and molecular dynamic simulations analyses have revealed that hesperidin (HES) and rosuvastatin (ROS) have the best targeting potential for Mpro protein out of 10 phytochemicals and 6 statin compounds. The selected compounds were elaborated alone or with FAV into six nanoformulations FAV, ROS, HES, FAV/ROS, FAV/HES, and FAV/ROS/HES-loaded liposomes. Light and electron microscope evaluations confirmed the vesicular shape of all liposomal dispersions. The entrapment capacity and release extent from FAV/ROS/HES-loaded liposomes was the lowest compared to other nanoformulations. In vitro, the FAV/HES or FAV/ROS-loaded liposomes displayed the highest capacity to impede the replication of SARS-CoV-2 with IC50 of 0.738 and 3.28 μg/mL, respectively. These results confirmed the potential of hesperidin and rosuvastatin as adjuvant medications with Favipiravir to combat COVID-19 and suggest the preference of the combinatory treatments. Finally, our findings provide a rational for further in-vivo studies to evaluate the potential activities of these drug combinations to mitigate the adverse events of favipiravir and to boost its SARS-CoV-2 clearance efficacy.

Liposome Encapsulation of the Palmitoyl-KTTKS Peptide: Structural and Functional Characterization.

In this study, the amphiphilic N-palmitoyl-KTTKS peptide was integrated in the bilayer of egg-derived phosphatidylcholine (PC) vesicles using two different preparation methods, namely thin-film evaporation (TLE) and reverse-phase evaporation (REV). Both the REV and TLE methods allowed for the formation of homogeneous liposome dispersions (PdI < 0.20) with mean hydrodynamic diameters of <100 nm and <200 nm, respectively, a net negative surface charge and a percentage of structured phospholipids higher than 90%. The inclusion of the amphiphilic N-palmitoyl-KTTKS peptide within phospholipid-based vesicles could improve peptide stability and skin delivery. Therefore, the obtained liposomes were evaluated via experiments assessing the synthesis of collagen and the ECM in 3T3-NIH fibroblasts. The obtained results showed that, when delivered with PC liposomes, pal-KTTKS stimulated collagen production more than free pentapeptide and 1 mM ascorbic acid, used as a positive control.

Modification and Improvement of the Liposome Composition of Preputial Gland Extract of Siberian Musk Deer

In this work, we set out to characterize the liposomal form of a new original product based on the preputial gland extract of Siberian musk deer whose composition was modified by an inclusion complex with β-cy- clodextrin. Musk deer liposomes were obtained by an efficient and scalable high-pressure homogenization method. The resulting liposomal product was characterized by transmission electron microscopy, dynamic light scattering, preparative and analytical chromatography, and gas chromatography-mass spectrometry. A specification for the liposomal form of Siberian musk deer extract was developed, which includes all critical indicators of product quality. Homogeneous dispersions of musk deer liposomes with a uniform size distribution were obtained, with the distribution maxima observed at 50 and 240 nm. The high physicochemical stability of the liposomal dispersion was established with the zeta potential value of the obtained nanoparticles ranging from –5 to –35 mV. According to size-exclusion chromatography and mass spectrometry, the incorporation of deer musk target components into liposomes reached 58–75% for musk liposomes in terms of steroid components and total protein. The revealed quality indicators of the studied liposomal product indicate the possibility of obtaining highly effective products based on the liposomal form of musk deer extract, modified with cyclodextrin, as an adaptogen of natural origin with an enhanced and pronounced activity in laboratory performance tests.

Viscoelasticity of Liposomal Dispersions.

Janus-faced viscoelastic gelling agents-possessing both elastic and viscous characteristics-provide materials with unique features including strengthening ability under stress and a liquid-like character with lower viscosities under relaxed conditions. The mentioned multifunctional character is manifested in several body fluids such as human tears, synovial liquids, skin tissues and mucins, endowing the fluids with a special physical resistance property that can be analyzed by dynamic oscillatory rheology. Therefore, during the development of pharmaceutical or cosmetical formulations-with the intention of mimicking the physiological conditions-rheological studies on viscoelasticity are strongly recommended and the selection of viscoelastic preparations is highlighted. In our study, we aimed to determine the viscoelasticity of various liposomal dispersions. We intended to evaluate the impact of lipid concentration, the presence of cholesterol or 1,2-distearoyl-sn-glycero-3-phosphocholine (DSPC) and the gelling agents polyvinyl alcohol (PVA) and hydroxyethylcellulose (HEC) on the viscoelasticity of vesicular systems. Furthermore, the effect of two model drugs (phenyl salicylate and caffeine) on the viscoelastic behavior of liposomal systems was studied. Based on our measurements, the oscillation rheological properties of the liposomal formulations were influenced both by the composition and the lamellarity/size of the lipid vesicles.

Gas‐Liquid Flow‐Induced Characteristics of Dispersed Liposome‐Based Particles

AbstractLiposomes are closed bilayers of phospholipids formed in aqueous media. The hydrodynamic property of colloidal dispersions of liposomes is one of the factors which alter the structure of liposomes. The present review article discusses the mechanistic aspects of the deformation, breakage, and fusion of liposomes in different liquid shear flows. Then, characteristic features reported with respect to the particles consisting of liposomes and bubbles are discussed to explore the role of shear flows induced by the acoustically active bubbles. Furthermore, the gas‐liquid flow‐induced characteristics of liposomes are described for their application to kinetically controllable enzymatic reactions in bubble‐column bioreactors.

Design and characterization of dual‐pronged liposome‐embedded gel for enhanced dermal delivery

AbstractThe present study aims to develop a combination of Nigella sativa seed oil (NSO) and virgin coconut oil (VCO)‐loaded liposomal gel as a topical drug delivery system for vitiligo. A 3 × 3 factorial design approach was adopted to study the effect of variables on liposome characteristics and performance. A total of nine batches were formed. The cholesterol: phospholipid (wt/wt) and drug (NSO:VCO) ratios (vol/vol) were marked as two independent variables, X1 and X2. The dependent variables selected were entrapment efficiency, vesicle size, and polydispersity index. Liposomes were fabricated by thin‐film hydration technology. A carbopol gel matrix was used to embed the optimized liposome vesicles, which were then tested for pH, viscosity, ability to spread, and stability. Better stability for topical drug delivery systems was demonstrated by the incorporation of liposomes in gel prepared from cross‐linked polyacrylate. In vitro drug release, ex vivo drug permeation and drug retention were compared between liposomal and conventional preparations. Skin permeation and skin retention studies demonstrated that the prepared liposomal gel significantly extended the penetration of drugs into the skin and retained more drugs in the skin when compared to liposomal dispersion and conventional gel formulations. The stability of the developed liposomal gel was assured at 5 ± 3°C and 25 ± 2°C. From the studies described above, it is concluded that liposomal gel is the best‐suited formulation among all the preparations examined. The enhanced epidermal localization and accumulation of therapeutic moiety on the disease site could improve the effectiveness of the treatment.

Study on development and tissue permeation of different formulations of Fasudil.

The study is intended to formulate Fasudil loaded vesicular system for application in the management of angina. Fasudil was made into a complex with phospholipid, and other different formulations were made, including Fasudil solution, liposomal form, and Fasudil loaded into the gel. A drug characterization study was conducted and noted. Drug release was quantified and analyzed and, finally, inoculated in Sprague-Dawley rats. These rats underwent anginal induction, and each formulation's effect on angina was evaluated. Drug solution (F-Phos) and F-Phos-Lipo (liposomal dispersion form of the drug) have shown that more than half percent of them have been released within 1.5 hours, and the rapid release occurred from liposomal dispersion in the first hour. The study determined the viscosity of the different formulations, which was significantly (p<0.05) higher than the theoretical sum of the viscosity of each formulation. The study found that the F-Phos-Lipo+P-407HMS formulation is the most effective as its application has the minimum infarct area percentage compared to the other formulations and can also reduce creatine kinase levels significantly as compared to the different formulations (p<0.05). The study concluded that the typical gel formulation (liposomal Fasudil dispersed in hydroxypropyl methylcellulose solution, which is added to blank poloxamer 407) had been shown to have significantly anti-anginal properties, including easy administration, its application on the infarct area percentage and subsequently its pharmacological effect on the cardiac tissue.

Review of Proliposomal Gel for Transdermal drug delivery system

Proliposomes are an innovative kind of carrier-mediated drug delivery that offers numerous advantages over traditional liposomes. The conventional liposomes are susceptible to oxidation or hydrolysis, as well as sedimentation, aggregation, or fusion with other substances. While, proliposomes are far more stable than liposomes, making them better suited for the delivery of pharmaceuticals. They are a dry, free-flowing, granular substance that, when it comes in touch with water or a biological fluid inside the body, instantly transforms into a liposomal dispersion. Future systems for delivering medications could be proliposomes. They have achieved a considerable improvement in resolving the stability, bioavailability, and solubility of poorly soluble medicines difficulties associated with liposomes with their non-invasive drug administration into or across the skin. They are a better alternative to the liposomal vesicular system because of their increased physical and chemical stability and potential for scalability for commercial viability. Because they are in dry powder form, they can be manufactured into unit dose forms like tablets, capsules, and beads, among other things. Because of all these advantages, proliposomes have been used for a variety of medical applications.

High-shear wet agglomeration process for enriching cornstarch with curcumin and vitamin D3 co-loaded lyophilized liposomes

Curcumin and vitamin D3 are bioactive molecules of great importance for the food industry. However, their low stability in several processing conditions hampers their proper incorporation into powdered food formulations. This study proposes the enrichment of a common raw material (cornstarch) with curcumin and vitamin D3 by using high-shear wet agglomeration. The bioactives were initially encapsulated into liposome dispersions and then subjected to lyophilization. The resulting dried vesicles were later incorporated into cornstarch by wet agglomeration using maltodextrin as the binder solution. The phospholipid content and the amount of added liposomes were evaluated to characterize the enriched cornstarch samples. The lyophilized vesicles showed a high retention rate of 99 % for curcumin and vitamin D3, while the enriched cornstarch samples retained above 96 % (curcumin) and 98 % (vitamin D3) after 30 days of controlled storage. All in all, the presence of dried liposomes improved the flowability and delayed retrogradation phenomenon in agglomerated cornstarch. Therefore, this study introduced a novel and reliable method of incorporating hydrophobic and thermosensitive molecules into powdered food formulations by using readily available materials and a straightforward high-shear wet agglomeration process.

In Vitro Evaluation of Aerosol Therapy with Pentamidine-Loaded Liposomes Coated with Chondroitin Sulfate or Heparin for the Treatment of Leishmaniasis.

The second-line antileishmanial compound pentamidine is administered intramuscularly or, preferably, by intravenous infusion, with its use limited by severe adverse effects, including diabetes, severe hypoglycemia, myocarditis and renal toxicity. We sought to test the potential of phospholipid vesicles to improve the patient compliance and efficacy of this drug for the treatment of leishmaniasis by means of aerosol therapy. The targeting to macrophages of pentamidine-loaded liposomes coated with chondroitin sulfate or heparin increased about twofold (up to ca. 90%) relative to noncoated liposomes. The encapsulation of pentamidine in liposomes ameliorated its activity on the amastigote and promastigote forms of Leishmania infantum and Leishmania pifanoi, and it significantly reduced cytotoxicity on human umbilical endothelial cells, for which the concentration inhibiting 50% of cell viability was 144.2 ± 12.7 µM for pentamidine-containing heparin-coated liposomes vs. 59.3 ± 4.9 µM for free pentamidine. The deposition of liposome dispersions after nebulization was evaluated with the Next Generation Impactor, which mimics human airways. Approximately 53% of total initial pentamidine in solution reached the deeper stages of the impactor, with a median aerodynamic diameter of ~2.8 µm, supporting a partial deposition on the lung alveoli. Upon loading pentamidine in phospholipid vesicles, its deposition in the deeper stages significantly increased up to ~68%, and the median aerodynamic diameter decreased to a range between 1.4 and 1.8 µm, suggesting a better aptitude to reach the deeper lung airways in higher amounts. In all, nebulization of liposome-encapsulated pentamidine improved the bioavailability of this neglected drug by a patient-friendly delivery route amenable to self-administration, paving the way for the treatment of leishmaniasis and other infections where pentamidine is active.

Lubricating Performance of Polymer-Coated Liposomes

Dry mouth is a troublesome condition linked to lubrication failure and leads to other diseases such as fungal infections and wounds in the oral cavity. There are many commercial salivary substitutes in the market, but none with a long-lasting lubrication effect. Polymer-coated liposomes can be an interesting formulation strategy for retrieving the symptoms of dry mouth by mimicking the micelles of saliva. In the present study, polymer coated-liposomes were prepared by the conventional thin film method and subsequently coated with three different polymers with different charge densities; alginate, chitosan and hydrophobically modified ethyl hydroxyethyl cellulose (HM-EHEC). The prepared polymer-coated liposomes were studied concerning their lubricating properties using a ball-on-disc tribometer at 2 N load at 37 °C, and their flow behaviours were also measured. Solutions of the pure polymers and dispersions of the uncoated liposomes were also studied to investigate any contributions from the individual components. A commercial dry mouth product based on HEC (hydroxyethyl cellulose) and glycerol was also included. The formulations were measured as soon as possible after preparation and some of them after >4 weeks. Results demonstrated that all the positively-charged formulations (chitosan, positive liposomes and chitosan-coated liposomes) had superior lubricating properties with friction coefficients (μ < 0.1) at orally relevant speeds (50 mm/s) as compared to the neutral or negatively-charged systems. At boundary lubrication conditions (3 mm/s), the chitosan-coated liposomes obtained an even lower friction force than the individual components, thus indicating a synergistic effect between the polymer and the liposome.

Influence of iontophoresis on delivery of NSAID-loaded deformable liposomal dispersions: in vitro and in vivo evaluation.

Aim: Negatively charged deformable liposomes (DL) of ketoprofen were formulated to enhance transdermal delivery of ketoprofen (KP) under the influence of iontophoresis for intraarticular delivery. Methods: Conventional and deformable KP liposomes were prepared using thin film hydration, characterized and intraarticular delivery of KP was evaluated using Sprague-Dawley rats. Results: Vesicles displayed entrapment efficiency (>71%); zeta potential <-25mV; size between 152.4±12.42nm to 220.4±6.22nm, KP-DL were stable under iontophoresis. Conventional and deformable liposomes exhibited relatively higher iontophoretic flux values than passive flux; Iontophoretic delivery enhanced KP availability in the synovial fluid (1.34±0.12μg.h/ml) fourfold over passive delivery (0.329±0.15μg.h/ml). Conclusion: Iontophoretic mediated transport of deformable liposomes could improve transdermal delivery of ketoprofen into the synovial joints than conventional liposomes.

Modification of liposomes composed of a cationic lipid TMAG and an anionic lipid DSPG with a PEGylated lipid based on the investigation of lipid structures

Charged lipids are widely utilized in functional liposomes for controlled release and targeting of drugs. In this study, we prepared the liposomes composed of a cationic lipid N-(α-trimethylammonioacetyl)-distearoyl-D-glutamate chloride (TMAG) and an anionic lipid 1,2-dioctadecanoyl-sn-glycero-3-phospho-1′-rac-glycerol (DSPG) with the molar ratio of TMAG/DSPG = 0:10–10:0 by hydration and extrusion methods. SAXS study for the lipid thin films revealed the formation of lamellar structures of TMAG and DSPG. The lipid thin film, except for the composition of 5:5 and 6:4, formed a liposome with a size of ∼100 nm that could encapsulate riboflavin in the inner aqueous phase. The zeta potentials of liposomes with the composition of 0:10–4:6 showed negative charges, while those of 7:3–10:0 showed positive charges. As the composition approached from 0:10 or 10:0 to 5:5, the phase transition temperature of the lipid bilayer from liquid crystalline phase to gel phase became higher, and the extent of fluorescence anisotropy increased. Thus, the lipid bilayer around the equimolar mixture could form a rigid structure with low fluidity of lipid alkyl chains. The surface charge cancellation by the opposite ionic head groups and the less curvature of the rigid lipid bilayer should prevent the liposomal formation at the composition of 5:5 and 6:4. However, the equimolar composition of 5:5 could form a liposome by the modification of distearoylphosphatidylethanolamine-polyethyleneglycol 2000 (DSPE-PEG2000) into the lipid bilayer at the molar ratio of 4% because it can reduce the rigidity of the lipid bilayer, provide positive curvature to the lipid bilayer, and stabilize the liposome dispersion in water through steric hindrance.

The Impact of Propanol, N-Butanol and Pentanol on Aqueous Dispersions of Sonicated Liposomes. EPR Study

Abstract This paper presents the effect of selected alcohols on the fluidity of liposome membranes obtained in sonication of DPPC lecithin. Using the EPR technique, the duality of propanol, n-butanol and pentanol on the behaviour of the aqueous dispersion of liposomes was demonstrated. It was shown that after exceeding a certain concentration, these alcohols initiate dispersion foaming, leading to phase separation: liposome dispersion - lipid foam. The influence of the shape of the molecule and the length of hydrocarbon chains on the effectiveness of destabilisation of the structure of lipid membranes was indicated.

Physical and Oxidative Water-in-Oil Emulsion Stability by the Addition of Liposomes from Shrimp Waste Oil with Antioxidant and Anti-Inflammatory Properties.

Liposomes made of partially purified phospholipids (PL) from Argentine red shrimp waste oil were loaded with two antioxidant lipid co-extracts (hexane-soluble, Hx and acetone-soluble, Ac) to provide a higher content of omega-3 fatty acids. The physical properties of the liposomes were characterized by Transmission Electron Microscopy (TEM), Dynamic Light Scattering (DLS) and Differential Scanning Calorimetry (DSC). The antioxidant and anti-inflammatory activity of the lipid extracts and liposomal suspensions were evaluated in terms of Superoxide and ABTS radical scavenging capacities and TNF-α inhibition. Uni-lamellar spherical liposomes (z-average ≈ 145 nm) with strong negative ζ potential (≈ -67 mV) were obtained in all cases. The high content of neutral lipids in the Hx extract caused structural changes in the bilayer membrane and decreased entrapment efficiency regarding astaxanthin and EPA + DHA contents. The liposomes loaded with the Hx/Ac extracts showed higher antioxidant and anti-inflammatory activity compared with empty liposomes. The liposomal dispersions improved the physical and oxidative stability of water-in-oil emulsions as compared with the PL extract, inducing pronounced close packing of water droplets. The liposomes decreased hydroperoxide formation in freshly made emulsions and prevented thio-barbituric acid-reactive substances (TBARS) accumulation during chilled storage. Liposomes from shrimp waste could be valuable nanocarriers and stabilizers in functional food emulsions.