Simulated gastrointestinal fate of lipids encapsulated in starch hydrogels: Impact of normal and high amylose corn starch

The influence of starch type (resistant starch (RS) versus native (NS) starch) and concentration (10 and 35 wt.%) on the potential gastrointestinal fate of digestible lipid (corn oil) droplets encapsulated within starch hydrogels was studied using a simulated gastrointestinal tract (GIT). The NS used was a normal corn starch, whereas the RS used was a high amylose corn starch. Changes in morphology, organization, size, and charge of the particles in the delivery systems were measured as they passed through each stage of the GIT model: mouth, stomach, and small intestine. The GIT fates of three types of delivery system were compared: free lipid droplets; lipid droplets in RS-hydrogels; and, lipid droplets in NS-hydrogels. Encapsulation of the lipid droplets in the hydrogels had a pronounced influence on their GIT behavior, with the effect depending strongly on starch type. The starch granules in the RS-hydrogels remained intact throughout the simulated GIT because their compact structure makes them resistant to enzyme digestion. The initial rate of lipid digestion in the small intestine phase also depended on delivery system type: emulsion > RS-hydrogels > NS-hydrogels. However, the lipid phase appeared to be fully digested at the end of the digestion period for all samples. These results provide useful information for designing functional foods for improved health. For example, food matrices could be developed that slowdown the rate of lipid digestion, and therefore prevent a spike in serum triacylglycerols in the blood, which may be advantageous for developing functional foods to tackle diabetes.     

Effects of Various Fiber Additions on Lipid Digestion during In Vitro Digestion of Beef Patties

ABSTRACT:  The purpose of this study was to examine the effect of various fiber additions on lipid digestion during the  in vitro  digestion of beef patties. The control patties were prepared with 90.5% lean meat and 9.5% tallow. Treatments consisted of 90% lean meat with 9.5% tallow and either 0.5% cellulose, 0.5% chitosan, or 0.5% pectin. The beef patties were then passed through an  in vitro  digestion model that simulated the composition of the mouth, stomach, and small intestine juices. The change in structure and properties of the lipid droplets was monitored by laser scanning confocal fluorescence microscopy. In general, there was a decrease in lipid droplet diameter as the droplets moved from mouth to stomach to small intestine. The amount of free fatty acid dramatically increased after  in vitro  digestion in all beef patties. The amount of free fatty acid was, however, lower in beef patties containing chitosan and pectin than other beef patties after  in vitro  digestion. Beef patties containing various fibers had lower thiobarbituric acid-reactive substances (TBARS) values than samples with no fibers. Among the samples to which fibers were added, chitosan and pectin had lower TBARS than beef patties with cellulose. The cholesterol content decreased after  in vitro  digestion in all beef patties but was not different among the beef patties before and after  in vitro  digestion. These results enhance our understanding of the physicochemical and structural changes that occur to ground beef within the gastrointestinal tract.     

赋形剂乳液粒径和油脂链长对橘子中β-胡萝卜素的物化特性及生物可给性的影响

利用体外模拟胃肠道(Gastrointestinal tract,GIT)消化模型,研究了粒径大小和油脂链长对赋形剂乳液/橘子混合体系在胃肠道消化过程中物化特性、微观形态的变化和对橘子中β-胡萝卜素生物可给性的影响。结果表明:相比于中等粒径(500 nm)乳液和大粒径(10 μm)乳液,小粒径(200 nm)乳液的物理特性(粒径和电位)和微观形态在各个模拟消化阶段中的变化趋势最明显;除小肠消化阶段之外,中链油脂(以MCT油为代表)制备的赋形剂乳液的物理特性与长链油脂(以玉米油为代表)制备的赋形剂乳液没有显著性差异(p>0.05);小粒径乳液的油脂消化速率最快,其生物可给性提升(38.13%)的效果显著大于中粒径(24.93%)和大粒径(26.23%)乳液(p<0.05);长链油脂与中链油脂的油脂消化速率的差异不显著(p>0.05);与中链油脂相比,长链油脂制备的赋形剂乳液对提高橘子中β-胡萝卜素的生物可给性具有更显著的影响(p<0.05)。研究结果对于科学设计赋形剂乳液来提高果蔬中亲脂性生物活性物质的生物可给性具有重要指导作用。     

Influence of anionic dietary fibers (xanthan gum and pectin) on oxidative stability and lipid digestibility of wheat protein-stabilized fish oil-in-water emulsion

The influence of two anionic dietary fibers (xanthan gum and pectin) on the oxidative stability and lipid digestibility of fish oil emulsions stabilized by wheat protein (gliadin) was investigated. Lipid oxidation was determined by measuring lipid hydroperoxides and TBARS of the emulsions during storage, while protein oxidation was measured using fluorescence spectroscopy. Lipid and protein oxidation was faster at pH 3.5 than at pH 7, which may have been due to increased iron solubility under acidic conditions. Xanthan gum inhibited lipid and protein oxidation, which was attributed to its ability to bind iron ions. Conversely, pectin promoted oxidation, which was attributed to the presence of endogenous transition metals in the polysaccharide ingredient. In vitro digestion was carried out to evaluate the digestibility of oil droplets in emulsions with or without polysaccharides. Both xanthan gum and pectin significantly increased the rate of lipid digestion, which was attributed to their ability to inhibit droplet aggregation under gastrointestinal conditions. These results have important implications for designing emulsion-based functional foods with improved oxidative stability and lipid digestibility.     

Impact of salt and lipid type on in vitro digestion of emulsified lipids

This study examined the effects of oil type and NaCl addition on the micro-structural changes that occur to emulsified lipids as they pass through a model gastrointestinal tract (GIT). Oil-in-water emulsions stabilized by a non-ionic surfactant (Tween 20) were prepared using different kinds of lipids (3% soybean oil, corn oil, olive oil or lard). The emulsified lipids were passed through an in vitro digestion model that simulated the composition (pH, minerals, surface active components, and enzymes) of the human GIT. Prior to digestion, emulsified lipid droplets appear to be bridging flocculation in 1% NaCl added emulsified lipids, moreover lipid droplets of 1% NaCl added emulsified lipids seems to be more disrupted than no NaCl added emulsified lipids. Mean particle size prepared with lard was smaller than those of other emulsified lipids. Free fatty acid contents increased after in vitro digestion in all emulsified lipids. Especially, free fatty acid content of emulsified lipid made from lard and olive oil were significantly higher than those of other emulsions after in vitro digestion.     

Impact of amylose from maize starch on the microstructure,rheology and lipolysis of W/O emulsions during simulated semi-dynamic gastrointestinal digestion

This study aims to examine the microstructure, rheology and lipolysis of water-in-oil (W/O) emulsions (40 wt.%) prepared with or without (Control) the addition of normal (NAM) and high amylose (HAM) maize starch during simulated digestion in a semi-dynamic gastrointestinal tract (GIT) model. Microstructural examinations showed modification in initial W/O emulsion droplets to multiple W₁/O/W₂ droplets during in vitro digestion. This is in line with the rheological results, where the shear viscosity and moduli in the oral phase were remarkably reduced after entering the intestinal phase. In comparison to control and NAM emulsions, HAM emulsions showed a more compact and continuous network structure and greater viscosity and elastic modulus throughout GIT digestion. These results support lipolysis, where fewer free fatty acids were released in the HAM emulsion (70%) than in the control (86%) and NAM (78%) emulsions. This work has provided an in-depth understanding of the digestion of W/O emulsions as influenced by amylose content, which is meaningful for the development of low-fat products with reduced lipid digestibility.     

Effects of Biopolymers Encapsulations on the Lipid Digestibility of Emulsion-Type Sausages Using a Simulated Human Gastrointestinal Digestion Model

The purpose of this study is to examine the effects of biopolymers encapsulations on the digestion of lipid in emulsion-type sausages during simulated human gastrointestinal digestion. Emulsion-type sausages were prepared by incorporation of 1 % cellulose, pectin, or chitosan. The samples were then passed through a simulated human gastrointestinal digestion model that simulated the effects of the mouth, stomach, and small intestine. The change in digestion of the lipids was monitored by confocal fluorescence microscopy. The digestibility of lipid dramatically increased after simulated human gastrointestinal digestion for all emulsion-type sausage samples but was reduced by biopolymers encapsulations. Encapsulation with pectin and chitosan produced lower free fatty acid contents and lipid oxidation values than samples with no biopolymers encapsulations (p?<?0.05). Moreover, the lipase activity decreased after simulated human gastrointestinal digestion in emulsion-type sausages with encapsulated biopolymers (p?<?0.05). The effect of biopolymers encapsulation in the reduction of the lipid digestion can be ordered as pectin?>?chitosan?>?cellulose (p?<?0.05).     

Influence of lipid type on gastrointestinal fate of oil-in-water emulsions: In vitro digestion study

The potential gastrointestinal fate of oil-in-water emulsions containing lipid phases from different sources was examined: vegetable oils (corn, olive, sunflower, and canola oil); marine oils (fish and krill oil); flavor oils (orange and lemon oil); and, medium chain triglycerides (MCT). The lowest rates and extents of lipid digestion were observed for emulsified flavor oil, followed by emulsified krill oil. There was no appreciable difference between the final amounts of free fatty acids released for emulsified digestible oils. Differences in the digestibility of emulsions prepared using different oils were attributed to differences in their compositions, e.g., fatty acid chain length and unsaturation. The particle size distribution, particle charge, microstructure, and macroscopic appearance of the emulsions during passage through the simulated GIT depended on oil type. The results of this study may facilitate the design of functional foods that control the digestion and absorption of triglycerides, as well as the bioaccessibility of hydrophobic bioactives.     

Role of calcium and calcium-binding agents on the lipase digestibility of emulsified lipids using an in vitro digestion model

Controlling the digestibility of lipids within the gastrointestinal tract is important for developing food and pharmaceutical products. In vitro digestion methods are commonly used to study the influence of formulation composition and microstructure on lipid digestibility. In this paper, we focus on the impact of calcium and calcium-binding agents on the rate of lipid droplet digestion in corn oil-in-water emulsions monitored using a pH-stat method. The rate of fatty acid production increased with increasing calcium, e.g., the free fatty acids released after 20 min digestion was <12% for 0 mM CaCl2, but >95% for 20 mM CaCl2. The ability of calcium to increase the digestion rate was found for three different emulsifiers used to stabilize the initial lipid droplets: lyso-lecithin, caseinate and β-lactoglobulin. For these three systems, the initial rate of lipid digestion increased in the following order lyso-lecithin > β-lactoglobulin > caseinate at both 0 and 20 mM CaCl2, but the rate was considerably faster at higher calcium levels for all systems. The addition of EDTA, a calcium chelating agent, to emulsions containing 20 mM CaCl2 caused an appreciable decrease in lipid digestion rate, reducing the amount of free fatty acids produced after 20 min from around 97% to 32% when the EDTA level was increased from 0 to 5 mM. Finally, we examined the impact of two anionic polysaccharides (pectin and alginate) on the rate of lipid digestion in emulsions containing 20 mM CaCl2. High methoxy pectin, which does not bind calcium strongly, did not have a major effect on the rate of digestion, whereas alginate, which does bind calcium strongly, depressed the rate considerably. This study has important implications for designing and testing delivery systems that control lipid digestion.     

Improvement of physicochemical stabilities of emulsions containing oil droplets coated by non-globular protein-beet pectin complex membranes

The potential of beet pectin for improving the physical and chemical stabilities of emulsions containing silk fibroin coated droplets was investigated. Five wt.% corn oil-in-water emulsions containing fibroin-coated droplets (0.5 wt.% fibroin) and anionic pectin (0.05 wt.%) were prepared at pH 7. The pH of these emulsions was then adjusted to pH 4, so that the anionic pectin molecules electrostatically deposited to the fibroin-coated droplets. The influence of pH (3 to 7) and sodium chloride concentrations (0 to 500 mM) on the properties of primary (0 wt.% pectin) and secondary (0.05 wt.% pectin) emulsions was studied. Pectin was deposited to the droplet surfaces at pH 3, 4, and 5, but not at pH 6 and 7. In addition, secondary emulsions were stable up to higher ionic strengths (< 500 mM) than primary emulsions (< 200 mM). The addition of beet pectin also prolonged the lag phase of lipid oxidation in the emulsions as determined by the formation of lipid hydroperoxides and headspace hexanal. The controlled electrostatic deposition method utilized in this study could be used to extend the range of application of silk fibroin in the industry.     

Modulation of physicochemical properties of lipid droplets using β-lactoglobulin and/or lactoferrin interfacial coatings

There is considerable interest in the development of food-grade delivery systems to encapsulate, protect and release bioactive lipids. In this study, emulsion-based delivery systems were prepared consisting of lipid droplets covered by β-lactoglobulin (BLG) and/or lactoferrin (LF) coatings. BLG and LF are globular proteins with relatively low (pI ∼ 5) and high (pI ∼ 8) isoelectric points, respectively. Mixed systems were prepared by adding LF to BLG-stabilized corn oil-in-water emulsions (BLG/LF-coated droplets) or by adding BLG to LF-stabilized corn oil-in-water emulsions (LF/BLG-coated droplets) at pH 7, where there is an electrostatic attraction between the proteins. The influence of pH (3–7), ionic strength (0–60 mM CaCl₂ or 0–200 mM NaCl, pH 7), and thermal treatment (21–90 °C, pH 7, 20 min) on the physical stability of the resulting emulsions was examined. Emulsions with good stability to pH, salt, and thermal processing could be created using mixed interfacial coatings. In addition, we found that the lipids in these emulsions could still be digested using an in vitro digestion model to simulate small intestine conditions. This work may lead to the formation of emulsion-based delivery systems with improved physicochemical and functional performance.     

负载葡萄皮粉花色苷提取物的W/O/W型复乳制备及其体外消化评价

以葡萄皮花色苷(ACNs)提取物为内水相(W1),玉米油为油相,乳清蛋白(WPI)溶液为外水相(W2)制备水包油包水(W/O/W)型复乳.复乳的包埋率高达(93.19±2.78)％,平均粒径为(287.90±3.12)nm.经口腔消化后,乳液未发现有明显变化;模拟胃部消化后,乳液液滴相互融合形成具有双层结构的较大微粒,...     

Effects of water-soluble soybean polysaccharide on rheological properties,stability and lipid digestibility of oil-in-water emulsion during in vitro gastrointestinal digestion

Water-soluble soybean polysaccharide (SSPS) is a naturally occurring emulsifier. SSPS was used as the sole emulsifier to stabilize an oil-in-water (O/W) emulsion. The effects were investigated of different SSPS concentrations (3–20% (w/w)) on the lipid digestibility, rheological properties and stability of O/W emulsions during in vitro digestion model. The droplet size of the emulsions tended to increase during the oral phase because the emulsions were unstable and droplets coalesced, except with a SSPS concentration of 20% (w/w). The presence of SSPS markedly reduced the free fatty acid (FFA) content after its stabilized O/W emulsion passed through in vitro gastrointestinal digestion. The amount of FFA significantly decreased as the concentration of SSPS increased due to SSPS stabilization film on oil droplet surface and high viscous system. SSPS may be an attractive alternative ingredient to control the lipid digestibility of emulsions for various food products.     

The effect of pectin concentration and degree of methyl-esterification on the in vitro bioaccessibility of β-carotene-enriched emulsions

Soluble fibers, like pectin, are known to influence the physicochemical processes during the digestion of dietary fat and may therefore affect the absorption of lipophilic micronutrients such as carotenoids. The objective of the current work was to investigate whether the pectin concentration and degree of methyl-esterification (DM) influence the bioaccessibility of carotenoids loaded in the oil phase of oil-in-water emulsions. The in vitro β-carotene bioaccessibility was determined for different oil-in-water emulsions in which 1 or 2% citrus pectin with a DM of 99%, 66% and 14% was present. Results show that pectin concentration and DM influence the initial emulsion properties. The most stable emulsions with the smallest oil droplets (D(v,0.9) of 15–16 μm) were obtained when medium or high methyl-esterified pectin was present in a 2% concentration while gel-like pectin structures (D(v,0.9) of 114 μm), entrapping oil droplets, were observed in the case where low methyl-esterified pectin was present in the aqueous emulsion phase. During in vitro stomach digestion, these gel-like structures, entrapping β-carotene loaded oil droplets, significantly enlarged (D(v,0.9) of 738 μm), whereas the emulsion structure could be preserved when the medium or high methyl-esterified pectin was present. Initial emulsion viscosity differences, due to pectin concentration and especially due to pectin DM, largely disappeared during in vitro digestion, but were still significant after the stomach digestion phase. The observed differences in emulsion structure before and during in vitro digestion only resulted in a significant difference between emulsions containing low methyl-esterified pectin (β-carotene bioaccessibility of 33–37%) and medium/high methyl-esterified pectin (β-carotene bioaccessibility of 56–62%).     

Characterization of Phase Separation Behavior, Emulsion Stability, Rheology, and Microstructure of Egg White–Polysaccharide Mixtures

ABSTRACT:  Phase separation behavior of egg white-pectin/guar gum mixtures was investigated. These systems led to phase separation arisen by either depletion flocculation or thermodynamic incompatibility. The influence of polysaccharides on the emulsifying activity index (EAI), emulsifying stability index (ESI), creaming stability, microstructure, and rheological properties was also studied at different polysaccharide concentrations (0% to 0.5%, [w/v]). Increasing pectin and guar gum concentration from 0.01% to 0.5% significantly improved EAI by 51% and 25%, respectively. The highest ESI and EAI values were obtained in the presence of 0.5% (w/v) pectin/guar gum. Microscopic images showed that emulsions containing polysaccharides had small droplets as compared to that of emulsions without polysaccharides. The addition of polysaccharides improved emulsion stability against creaming. Egg white-stabilized emulsions with and without polysaccharides reflect the pseudoplastic behavior with  n  < 1.0. Polysaccharides, especially at high concentrations, affected the viscoelastic behavior of the emulsions; storage ( G ') and loss modulus ( G ") crossed-over at lower frequency values as compared to that of emulsions containing no polysaccharide.     

Influence of particle size on lipid digestion and β-carotene bioaccessibility in emulsions and nanoemulsions

The interest in incorporating carotenoids, such as β-carotene, into foods and beverages is growing due to their potential health benefits. However, the poor water-solubility and low bioavailability of carotenoids is currently a challenge to their incorporation into many foods. The aim of this work was to study the influence of particle size on lipid digestion and β-carotene bioaccessibility using corn oil-in-water emulsions with different initial droplet diameters: large (d₄₃ ≈ 23 μm); medium (d₄₃ ≈ 0.4 μm); and small (d₄₃ ≈ 0.2 μm). There was a progressive increase in the mean particle size of all the emulsions as they passed through a simulated gastrointestinal tract (GIT) consisting of mouth, stomach, and small intestine phases, which was attributed to droplet coalescence, flocculation, and digestion. The electrical charge on all the lipid particles became highly negative after passage through the GIT due to accumulation of anionic bile salts, phospholipids, and free fatty acids at their surfaces. The rate and extent of lipid digestion increased with decreasing mean droplet diameter (small ≈ medium ? large), which was attributed to the increase in lipid surface area exposed to pancreatic lipase with decreasing droplet size. There was also an appreciable increase in β-carotene bioaccessibility with decreasing droplet diameter (small > medium > large). These results provide useful information for designing emulsion-based delivery systems for carotenoids for food and pharmaceutical uses.     

Influence of initial emulsifier type on microstructural changes occurring in emulsified lipids during in vitro digestion

The purpose of this study was to examine the impact of emulsifier type on the micro-structural changes that occur to emulsified lipids as they pass through a model gastrointestinal system. Lipid droplets initially coated by different kinds of emulsifiers (lecithin, Tween 20, whey protein isolate and sodium caseinate) were prepared using a high speed blender. The emulsified lipids were then passed through an in vitro digestion model that simulated the composition (pH, minerals, surface active components, and enzymes) of mouth, stomach and small intestine juices. The change in structure and properties of the lipid droplets were monitored by laser scanning confocal fluorescence microscopy, conventional optical microscopy, light scattering, and micro-electrophoresis. In general, there was a decrease in mean droplet diameter (d₃₂) as the droplets moved from mouth to stomach to small intestine. The electrical charge on the droplets stabilized by lecithin, Tween 20 and sodium caseinate were negative throughout the model GI system, while those stabilized by whey protein were positive in the stomach. This suggests that at least some of this globular protein remained attached to the droplet surfaces. The data was interpreted in terms of the competitive adsorption of phospholipids/bile salts with the adsorbed emulsifiers, as well as the enzymatic digestion of proteins and lipids. These results enhance our understanding of the physicochemical and structural changes that may occur to emulsified lipids within the gastrointestinal tract, which may have important consequences for the design of functional foods that alter lipid bioavailability. Nevertheless, there were appreciable differences between the behavior of emulsions within the in vitro model used in this study and literature reports of their behavior within in vivo studies, which highlights the need for more realistic in vitro digestion models.     

Influence of chitosan on stability and lipase digestibility of lecithin-stabilized tuna oil-in-water emulsions

The influence of chitosan concentration (0–0.3 wt%) and molecular weight (120, 250 and 342.5 kDa) on the physical stability and lipase digestibility of lecithin-stabilized tuna oil-in-water emulsions was studied. The ζ-potential, droplet size, creaming stability, free fatty acids and glucosamine released was measured for the emulsions when they were subjected to an in vitro digestion model. The ζ-potential of the oil droplets in lecithin-chitosan stabilized emulsions changed from positive (≈+53 mV) to negative and the emulsions were unstable to droplet aggregation for all chitosan concentrations and molecular weights used after being subjected to the digestion model. The amount of free fatty acid and glucosamine released per unit amount of emulsion was higher when pancreatic lipase was included in the digestion model. These results suggest that lecithin-chitosan coated droplets can be degraded by lipase under simulated gastrointestinal conditions. Consequently, chitosan coated lipid droplets may serve as useful carriers for the delivery of bioactive lipophilic nutraceuticals.     

Encapsulation,protection, and release of polyunsaturated lipids using biopolymer-based hydrogel particles

Delivery systems are needed to encapsulate polyunsaturated lipids, protect them within food products, and ensure their bioavailability within the gastrointestinal tract. Hydrogel particles assembled from food-grade biopolymers are particularly suitable for this purpose. In this study, hydrogel microspheres were fabricated by electrostatic complexation of low methoxy pectin and caseinate by decreasing the solution pH from 7 to 4.5. After hydrogel particle formation, the caseinate was enzymatically cross-linked using transglutaminase to improve the stability of the biopolymer matrix. The effect of hydrogel particle encapsulation on the physical location, chemical stability, and lipase digestibility of emulsified polyunsaturated lipids (fish oil) was investigated. The cross-linked hydrogel particles formed using this process were relatively small (D₄₃ = 4.6 μm), negatively charged (ζ = − 37 mV), and evenly distributed within the system. Confocal microscopy confirmed that the fish oil droplets were trapped within casein-rich hydrogel microspheres. Encapsulation of the fish oil droplets improved their stability to lipid oxidation compared to conventional emulsions, which was attributed to a high local concentration of antioxidant protein around the emulsified lipids. The rate and extent of digestion of the encapsulated lipid droplets within a simulated small intestine were similar to those of non-encapsulated ones. These results suggest that casein-rich hydrogel microspheres may protect polyunsaturated lipids in foods and beverages, but release them after ingestion.     

In vitro β‐Carotene Bioaccessibility and Lipid Digestion in Emulsions: Influence of Pectin Type and Degree of Methyl‐Esterification

Citrus pectin (CP) and sugar beet pectin (SBP) were demethoxylated and fully characterized in terms of pectin properties in order to investigate the influence of the pectin degree of methyl‐esterification (DM) and the pectin type on the in vitro β‐carotene bioaccessibility and lipid digestion in emulsions. For the CP based emulsions containing β‐carotene enriched oil, water and pectin, the β‐carotene bioaccessibility, and lipid digestion were higher in the emulsions with pectin with a higher DM (57%; “CP57 emulsion”) compared to the emulsions with pectin with a lower DM (30%; “CP30 emulsion”) showing that the DM plays an important role. In contrast, in SBP‐based emulsions, nor β‐carotene bioaccessibility nor lipid digestion were dependent on pectin DM. Probably here, other pectin properties are more important factors. It was observed that β‐carotene bioaccessibility and lipid digestion were lower in the CP30 emulsion in comparison with the CP57, SBP32, and SBP58 emulsions. However, the β‐carotene bioaccessibility of CP57 emulsion was similar to that of the SBP emulsions, whereas the lipid digestion was not. It seems that pectin type and pectin DM (in case of CP) are determining which components can be incorporated into micelles. Because carotenoids and lipids have different structures and polarities, their incorporation may be different. This knowledge can be used to engineer targeted (digestive) functionalities in food products. If both high β‐carotene bioaccessibility and high lipid digestion are targeted, SBP emulsions are the best options. The CP57 emulsion can be chosen if high β‐carotene bioaccessibility but lower lipid digestion is desired.