BHB LIPOSOMES AND PREPARATION METHODS THEREOF

Abstract

Among others, the present invention provides a liposome comprising an active ingredient and one membrane or one inner membrane and one outer membrane. Each membrane comprises a plurality of lipid molecules, and the active ingredient is entrapped inside the interior space defined by the membrane or the inner membrane, or embodied in the membrane or membranes and form a part of the membrane(s).

Claims

1. A liposome comprising an active ingredient and one membrane, or one inner membrane and one outer membrane, wherein the one membrane or each of the inner and outer membranes defines an interior space within the one membrane or the inner membrane, and/or between the inner and outer membranes, each membrane comprises a plurality of lipid molecules, and the active ingredient is entrapped inside the interior space or embodied in the membrane or membranes; wherein the active ingredient comprises -hydroxybutyrate acid (BHB), a physiologically acceptable salt, ester, or mixture thereof.

2. The liposome of claim 1, wherein the active ingredient is free acid form of BHB, and the lipid is phospholipid.

3. The liposome of claim 1, wherein the active ingredient is in R-form, S-form or a mixture of R- and S-forms.

4. The liposome of claim 1, wherein the liposome has a normal vesicle structure, and the active ingredient is entrapped inside the interior space defined by the membrane or the inner membrane.

5. The liposome of claim 1, wherein each membrane is a bilayer membrane.

6. The liposome of claim 1, wherein the liposome has a reverse vesicle structure, and the active ingredient is embodied in the membrane and forms a part of the membrane.

7. The liposome of claim 1, wherein the active ingredient further comprises one or more additional hydrophilic components, with a mass percentage ranging from 1% to 95% of the liposome's total mass.

8. The liposome of claim 2, wherein the phospholipid comprises phosphatidylcholine, phosphatidylethanolamine, phosphatidylserine, phosphatidylinositol, lysophosphatidylcholine, lysophosphatidylethanolamine, dipalmitoyl phosphatidylcholine, dioleoyl phosphatidylcholine, dilinoleoyl phosphatidylcholine, distearoyl phosphatidylcholine, or a combination thereof.

9. The liposome of claim 1, wherein the lipid has a mass percentage ranging from 1% to 40%, of the liposome's total mass.

10. The liposome of claim 1, further comprising a co-emulsifier, the co-emulsifier comprises polyethylene glycol 200-2000, glycerol, sorbitol, or a combination thereof,

11. The liposome of claim 10, wherein the co-emulsifier has a mass percentage ranging from 1% to 40%, of the liposome's total mass.

12. The liposome of claim 1, further comprising a stabilizer, the stabilizer comprises medium-chain fatty acid glyceride, soybean oil, sunflower oil, or a combination thereof,

13. The liposome of claim 12, wherein the stabilizer has a mass percentage ranging from 1% to 40%, of the liposome's total mass.

14. The liposome of claim 1, further comprising a solvent, the solvent is water.

15. The liposome of claim 1, comprising: (a) the active ingredient has a mass percentage ranging from 1% to 95% of the liposome's total mass; (b) a phospholipid has a mass percentage ranging from 1% to 40% of the liposome's total mass; (c) a co-emulsifier has a mass percentage ranging from 1% to 40% of the liposome's total mass; (d) a stabilizer has a mass percentage ranging from 1% to 40% of the liposome's total mass; and (e) water has a mass percentage ranging from 0.01% to 10% of the liposome's total mass.

16. A method for preparing a BHB liposome of claim 1, comprising the steps of: melting crystalline BHB, preparing a BHB coarse suspension, and preparing BHB liposomes.

17. The method of claim 16, wherein the step of melting crystalline BHB comprises heating crystalline BHB at 50-80 C. for 10-60 minutes till BHB is melted to a clear liquid state; preparation of the BHB coarse suspension comprises dissolving the molten BHB and the phospholipid in an organic solvent, removing the organic solvent by evaporation to form a uniformly-spread lipid film, then adding water, the co-emulsifier, and stabilizer to the lipid film, and dispersing for 5-30 minutes to obtain the BHB coarse suspension by using a mixing equipment; preparation of BHB liposomes comprises homogenizing the BHB coarse suspension to obtain BHB liposomes by using a liposomal preparation equipment.

18. The method of claim 16, comprising the steps of melting crystalline BHB; dissolving phospholipids; preparing the BHB coarse suspension; and preparing BHB liposomes.

19. The method of claim 18, wherein the step of melting crystalline BHB comprises heating crystalline BHB at 50-80 C. for 10-60 minutes until BHB is melt into a clear liquid state; the step of dissolving phospholipid comprises mixing the phospholipid and the stabilizer together, heating the mixture of the phospholipid and stabilizer at 50-80 C. for 10-60 minutes to obtain a yellow liquid; the step of preparing the BHB coarse suspension comprises mixing water, co-emulsifier and the molten BHB together, then adding the yellow liquid of phospholipid and stabilizer to the mixture, and stirring the mixture for 5-30 minutes to obtain the BHB coarse suspension by using a mixing equipment; preparing BHB liposome comprises homogenizing the BHB coarse suspension to obtain BHB liposomes by using a liposomal preparation equipment.

20. A method for increasing or sustaining blood ketone level in a subject in need thereof, comprising administrating to the subject the BHB liposome of claim 1.

Description

BRIEF DESCRIPTIONS OF THE FIGURES

[0050] The following drawings illustrate by way of example and not limitation. For the sake of brevity and clarity, every feature of a given structure is not always labeled in every figure in which that structure appears. Identical reference numbers do not necessarily indicate an identical structure. Rather, the same reference number may be used to indicate a similar feature or a feature with similar functionality, as may non-identical reference numbers.

[0051] FIG. 1 shows a -hydroxybutyric acid (BHB) liposome according to one embodiment of this invention, in the form of normal vesicles.

[0052] FIG. 2 shows a BHB liposome according to another embodiment of this invention, in the form of reverse vesicles.

[0053] FIGS. 3A-3G show the stability of BHB liposomes after long term storage under cold condition (5 C.). Peaks labeled with BHB indicate BHB dry content, and peaks labeled with BHB dimers or BHB trimers indicate degradation products and impurities of BHB.

[0054] FIGS. 4A-4G show the stability of BHB liposomes after long term storage under conventional condition (20 C. and 60% relative humidity). Peaks labeled with BHB indicate BHB dry content, and peaks labeled with BHB dimers or BHB trimers indicate degradation products and impurities of BHB.

[0055] FIG. 5 shows blood ketone levels at different time points after oral administration of BHB free acid or BHB liposome respectively.

DETAILED DESCRIPTION OF THE INVENTION

[0056] Reference will now be made in detail to the preferred embodiments of the invention, examples of which are further illustrated. While the invention will be described in conjunction with the preferred embodiments, it will be understood that they are not intended to limit the invention to these embodiments. To the contrary, the invention is intended to cover alternatives, modifications and equivalents, which may be included within the spirit and scope of the invention as defined by the claims. Furthermore, in the detailed description of the present invention, numerous specific details are set forth in order to provide a thorough understanding of the present invention. However, it will be obvious to one of ordinary skill in the art that the present invention may be practiced without these specific details. In other instances, well known methods, procedures, components, and other features have not been described in detail as not to unnecessarily obscure aspects of the present invention.

Definitions

[0057] As used herein, the term subject or patient is used interchangeably and as used herein mean any mammal including but not limited to human beings including a human patient or subject to which the compositions of the invention can be administered. The term mammal includes human patients and non-human primates, as well as experimental animals such as rabbits, rats, and mice, and other animals.

[0058] Chemical structure of -hydroxybutyrate, also known as 3-hydroxybutyrate, -HB, BHB, or beta-hydroxybutyrate, is shown below.

##STR00001##

BHB is a chiral molecule at the 3 hydroxyl group, and there are two enantiomers, R/D and S/L.

[0059] The term Amphiphile refers to a molecule consisting of a water-soluble (hydrophilic) and an organic solvent-soluble (lipophilic) moiety. Amphipathic lipids are usually the major component of a lipid vesicle.

General

[0060] Generally speaking, various embodiments of the present invention provide formulations of BHB liposome, comprising lipids (e.g., phospholipids), an active ingredient (e.g., -hydroxybutyric acid (BHB), physiologically acceptable salt, ester, or a mixture thereof, and optionally one or more additional hydrophilic active ingredients), a co-emulsifier, a stabilizer, and a solvent (e.g., water). In some embodiments, the BHB liposomes according to the present invention are made from the following raw materials by mass: (a) active ingredients: 195%; (b) phospholipids: 140%; (c) co-emulsifiers: 140%; (d) stabilizers: 140%; and (e) water: 0.0110%.

[0061] In some preferred embodiments, the BHB liposomes according to the present invention are preferably made from the following raw materials by mass: (a) active ingredients: 60-85%; (b) phospholipids: 510%; (c) co-emulsifiers: 510%; (d) stabilizers: 510%; and (e) water: 0.011%.

[0062] The BHB liposomes according to the present invention can be in the form of either normal vesicle structures or reverse vesicle structures, depending on the proportion of components. As shown in FIG. 1, for normal vesicles, the membranes are composed of one or more phospholipid bilayers, with the hydrophilic head groups arranged around the periphery. Accordingly, the hydrophilic BHB is located inside the aqueous core surrounded by the lipid bilayer membrane. Alternatively, as shown in FIG. 2, the BHB liposomes may form reverse vesicles, composed of a bilayer with the hydrophilic head groups arranged internally, surrounding a nonpolar core. Accordingly, the hydrophilic BHB is embedded in the lipid bilayer membrane, and form a part of the membrane.

[0063] The present invention also provides methods for producing such BHB liposomes, including, among other things, preparation of a BHB coarse suspension.

[0064] More specifically, one exemplary preparation method according to the present invention includes: (1) melting crystalline BHB: heating crystalline BHB free acid at 50-80 C. for 10-60 minutes till melting to a clear liquid state; (2) Phospholipid dissolution: mixing phospholipids and stabilizers, heating them at 50-80 C. for 10-60 minutes to obtain a yellow liquid; (3) preparation of the BHB coarse suspension: mixing water, co-emulsifiers and the molten BHB liquid from step 1, adding the solution of phospholipids and stabilizers from step 2 to the mixture, and stirring continuously for 5-30 minutes to obtain the BHB coarse suspension by using a mixing equipment; and (4) preparation of BHB liposomes: homogenizing the BHB coarse suspension to obtain BHB liposomes by using a conventional liposomal preparation equipment.

[0065] Another exemplary preparation method according to the present invention includes: (1) melting crystalline BHB: heating crystalline BHB at 50-80 C. for 10-60 minutes till melting to a clear liquid state; (2) preparation of the BHB coarse suspension: dissolving the molten BHB liquid from step 1 and phospholipids in an organic solvent, and then removing the organic solvent through evaporation to form a uniformly-spread lipid film, then adding water, co-emulsifiers, and stabilizers to the lipid film, and dispersing for 5-30 minutes to obtain the BHB coarse suspension by using a mixing equipment; (3) preparation of BHB liposomes: homogenizing the BHB coarse suspension to obtain BHB liposomes by using a conventional liposomal preparation equipment.

[0066] The following examples are illustrative of select embodiments of the present invention and are not meant to limit the scope of the invention.

Example 1

[0067] The BHB liposome formulation in Example 1 is made of the raw materials with the respective mass percentages as show in Table 1 below.

TABLE-US-00001 TABLE 1 Formulation ingredient Mass (kg) Mass percentage (%) BHB free acid 1.00 10.00 Phosphatidylcholine 2.00 20.00 Glycerol 2.00 20.00 Medium-chain fatty acid glycerides 4.00 40.00 Water 1.00 10.00

[0068] The above-mentioned BHB liposome formulation is prepared as follows: [0069] (1) Melting crystalline BHB: Heat 1 kg crystalline BHB in a 50 C. water bath for 60 minutes till melting to a clear liquid state; [0070] (2) Phospholipid dissolution: Mix 2 kg of phosphatidylcholine and 4 kg of medium-chain fatty acid glycerides, heat them in a 50 C. water bath for 60 minutes to obtain a yellow liquid; [0071] (3) Preparation of BHB coarse suspension: Mix 1 kg of water, 2 kg of glycerol, and 1 kg of BHB melting liquid, add the yellow liquid of 2 kg of phosphatidylcholine and 4 kg of medium-chain fatty acid glycerides from step 2 to the mixture, and then stir the mixture for minutes to obtain the BHB coarse suspension by using the high-shear emulsifier; [0072] (4) Preparation of BHB liposomes: Pass the BHB coarse suspension through a filter with defined pore size under high pressure (6000 psi) by using the liposome extruder system to obtain the uniform BHB liposome, in which the solid content of BHB is 10%.

Example 2

[0073] The BHB liposome formulation in Example 2 is made of the raw materials with the respective mass percentages in Table 2 below.

TABLE-US-00002 TABLE 2 Formulation Ingredient Mass (kg) Mass percentage (%) BHB free acid 1.00 10.00 Phosphatidylcholine 2.00 20.00 Glycerol 2.00 20.00 Medium-chain fatty acid glycerides 4.00 40.00 Water 1.00 10.00

[0074] The above-mentioned BHB liposome formulation is prepared as follows: [0075] (1) Melting crystalline BHB: Heat 1 kg crystalline BHB in a 50 C. water bath for 60 minutes till melting to a clear liquid state; [0076] (2) Preparation of BHB coarse suspension: Mix 1 kg BHB melting liquid and 2 kg of phosphatidylcholine, dissolve them in 10 kg ethanol, and then remove the ethanol through evaporation to form a uniformly-spread lipid film, then add 1 kg water, 2 kg glycerol, 4 kg medium-chain fatty acid glyceride to the lipid film, disperse for 30 minutes to obtain the BHB coarse suspension by using a high-shear emulsifier; [0077] (3) Preparation of BHB liposomes: Pass the BHB coarse suspension through a filter with defined pore size under high pressure (6000 psi) by using a liposome extruder system to obtain the uniform BHB liposome, in which the solid content of BHB is 10%.

Example 3

[0078] The BHB liposome formulation in Example 3 is made of the raw materials with the respective mass percentages as shown in Table 3 below.

TABLE-US-00003 TABLE 3 Formulation ingredient Mass (kg) Mass percentage (%) BHB free acid 3.00 30.00 Phosphatidylethanolamine 1.00 10.00 Polyethylene glycol 400 1.00 10.00 Soybean oil 4.00 40.00 Water 1.00 10.00

[0079] The above-mentioned formulation of BHB liposome is prepared as follows: [0080] (1) Melting crystalline BHB: Heat 3 kg crystalline BHB in a 50 C. water bath for 60 minutes till melting to a clear liquid state; [0081] (2) Phospholipid dissolution: Mix 1 kg of phosphatidylethanolamine and 4 kg of soybean oil, heat them in a 50 C. water bath for 60 minutes to obtain a yellow liquid; [0082] (3) Preparation of BHB coarse suspension: Mix 1 kg of water, 1 kg of polyethylene glycol 400, and 3 kg of BHB melting liquid, and add the yellow liquid of 1 kg of phosphatidylethanolamine and 4 kg of soybean oil from step 2 to the mixture, and disperse the mixture for 30 minutes to obtain the BHB coarse suspension by using a high-speed disperser; [0083] (4) Preparation of BHB liposomal: Pressurize the BHB coarse suspension (6000 psi) by using the high-pressure microfluidic system to obtain homogenized BHB liposome, in which the solid content of BHB is 30%.

Example 4

[0084] The BHB liposome formulation in Example 4 is made of the raw materials with the respective mass percentages as shown in Table 4 below.

TABLE-US-00004 TABLE 4 Formulation Ingredient Mass (kg) Mass percentage (%) BHB free acid 5.00 50.00 Phosphatidylserine 1.00 10.00 Sorbitol 1.00 10.00 Sunflower oil 2.90 29.00 Water 0.10 1.00

[0085] The above-mentioned BHB liposome formulation is prepared as follows: [0086] (1) Melting crystalline BHB: Heat 5 kg of crystalline BHB in a 50 C. water bath for 60 minutes till melting to a clear liquid state; [0087] (2) Phospholipid dissolution: Mix 1 kg phosphatidylserine and 2.9 kg sunflower oil, heat them in a 50 C. water bath for 60 minutes to obtain a yellow liquid; [0088] (3) Preparation of BHB coarse suspension: Mix 0.1 kg water, 1 kg sorbitol, and 5 kg BHB melting liquid, and add the yellow liquid of 1 kg phosphatidylserine and 2.9 kg sunflower oil from step 2 to the mixture, and stir the mixture for 30 minutes to obtain the BHB coarse suspension by using the high-shear emulsifier; [0089] (4) Preparation of BHB liposome: Homogenize the BHB coarse suspension twice using a high-pressure homogenizer at the pressure of 35-45 MPa for the first time and 60-70 MPa for the second time to obtain the uniform BHB liposome, in which the solid content of BHB is 50%.

Example 5

[0090] The BHB liposome formulation in Example 5 is made of the raw materials with the respective mass percentages as shown in Table 5 below.

TABLE-US-00005 TABLE 5 Formulation Ingredient Mass (kg) Mass percentage (%) BHB free acid 5.00 50.00 Phosphatidylserine 1.00 10.00 Sorbitol 1.00 10.00 Sunflower oil 2.90 29.00 Water 0.10 1.00

[0091] The above-mentioned BHB liposome formulation is prepared as follows: [0092] (1) Melting crystalline BHB: Heat 5 kg crystalline BHB in a 50 C. water bath for 60 minutes till melting to a clear liquid state. [0093] (2) Preparation of BHB coarse suspension: Mix 5 kg BHB melting liquid and 1 kg phosphatidylcholine, dissolve them in 10 kg ethanol, and then remove the ethanol by evaporation to form a uniformly-spread lipid film, then add 0.1 kg water, 1 kg sorbitol and 2.9 kg sunflower oil to the lipid film, and disperse for 30 minutes to obtain the BHB coarse suspension by using the high-shear emulsifier; [0094] (3) Preparation of BHB liposomal: Homogenize the BHB coarse suspension twice using a high-pressure homogenizer at the pressure of 35-45 MPa for the first time and 60-70 MPa for the second time to obtain the uniform BHB liposome, in which the solid content of BHB is 50%.

Example 6

[0095] The BHB liposome formulation in Example 6 is made of the raw materials with the respective mass percentages as shown in Table 6 below.

TABLE-US-00006 TABLE 6 Formulation ingredient Mass (kg) Mass percentage (%) BHB free acid 7.00 70.00 Phosphatidylcholine 0.60 6.00 Polyethylene glycol 400 0.60 6.00 Medium-chain fatty acid glycerides 1.74 17.40 Water 0.06 0.60

[0096] The above-mentioned BHB liposome formulation is prepared as follows: [0097] (1) Melting crystalline BHB: Heat 7 kg crystalline BHB in an 80 C. water bath for 20 minutes till melting to a clear liquid state; [0098] (2) Phospholipid dissolution: Mix 0.6 kg of phosphatidylcholine and 1.74 kg of medium-chain fatty acid glycerides, heat them in the 80 C. water bath for 20 minutes to obtain a yellow liquid; [0099] (3) Preparation of BHB coarse suspension: Mix 0.06 kg of water, 0.6 kg of polyethylene glycol 400, 7 kg of BHB melting liquid, and add the yellow liquid of 0.6 kg of phosphatidylcholine and 1.74 kg of medium-chain fatty acid glycerides from step 2 to the mixture, and stir for 30 minutes to obtain the BHB coarse suspension by using a high-shear emulsifier; [0100] (4) Preparation of BHB liposome: Pass the BHB coarse suspension through a filter with defined pore size under high pressure (6000 psi) by using a liposome extruder system to obtain the uniform BHB liposome, in which the solid content of BHB is 70%.

Example 7

[0101] The BHB liposome formulation in Example 7 is made of the raw materials with the respective mass percentages as shown in Table 7 below.

TABLE-US-00007 TABLE 7 Formulation Ingredient Mass (kg) Mass percentage (%) BHB free acid 8.00 80.00 Phosphatidylinositol 0.60 6.00 Polyethylene glycol 400 0.60 6.00 Soybean oil 0.74 7.40 Water 0.06 0.60

[0102] The above-mentioned BHB liposome formulation is prepared as follows: [0103] (1) Melting crystalline BHB: Heat 8 kg of BHB free acid crystals in an 80 C. water bath for 20 minutes till melting to a clear liquid state; [0104] (2) Preparation of BHB coarse suspension: Mix 8 kg of BHB melting liquid and 0.6 kg of phosphatidylcholine, dissolve them in 10 kg ethanol, and then remove the ethanol by evaporation to form a uniformly-spread lipid film, then add 0.06 kg of water, 0.6 kg of polyethylene glycol 400, 0.74 kg of soybean oil to the lipid film, and stir for 30 minutes to obtain the BHB coarse suspension by using the high-shear emulsifier; [0105] (3) Preparation of BHB liposomal: Pass the BHB coarse suspension through a filter with defined pore size under high pressure (6000 psi) by using the liposome extruder system to obtain the uniform BHB liposome, in which the solid content of BHB is 80%.

Example 8

[0106] The BHB liposome formulation in Example 8 is made of the raw materials with the respective mass percentages as shown in Table 8 below.

TABLE-US-00008 TABLE 8 Formulation Ingredient Mass (kg) Mass percentage (%) BHB free acid 8.00 80.00 Phosphatidylinositol 0.60 6.00 Polyethylene glycol 400 0.60 6.00 Soybean oil 0.74 7.40 Water 0.06 0.60

[0107] The above-mentioned BHB liposome formulation is prepared as follows: [0108] (1) Melting crystalline BHB: Heat 8 kg of BHB free acid crystals in an 80 C. water bath for 20 minutes till melting to a clear liquid state; [0109] (2) Phospholipid dissolution: Mix 0.6 kg of phosphatidylinositol with 0.74 kg of soybean oil, heat them in the 80 C. water bath for 20 minutes to obtain a yellow liquid; [0110] (3) Preparation of BHB coarse suspension: Mix 0.06 kg of water, 0.6 kg of polyethylene glycol 400, 8 kg of BHB melting liquid, then add the yellow liquid of 0.6 kg of phosphatidylinositol and 0.74 kg of soybean oil from step 2 to the mixture, and stir for 30 minutes to obtain the BHB coarse suspension by using the high-shear emulsifier; [0111] (4) Preparation of BHB liposomal: Pass the BHB coarse suspension through a filter with defined pore size under high pressure (6000 psi) by using a liposome extruder system to obtain the uniform BHB liposome, in which the solid content of BHB is 80%.

Example 9 Stability Analysis of the BHB Liposomes

[0112] We performed this study to evaluate the stability of BHB liposomes after long-term storage under conventional condition (20 C. and 60% relative humidity) and under cold condition (5 C.). This study was conducted by measuring the sample of BHB liposome using HPLC method initially and at week 1, week 2, week 3, week 4. FIGS. 3 and 4 show the results of the stability analysis. As shown in the Figures, peaks labeled with BHB indicate BHB dry content, and peaks labeled with BHB dimers or BHB trimers indicate degradation products and impurities of BHB.

[0113] FIGS. 3A-3G show the stability of BHB liposome after long-term storage under cold condition (5 C.). More specifically, FIG. 3A shows HPLC analysis results of the initial BHB liposome (week 0). FIG. 3B shows HPLC analysis results of BHB liposome after 1-week storage under cold condition (5 C.). FIG. 3C shows HPLC analysis results of BHB liposome after 2-week storage under cold condition (5 C.). FIG. 3D shows HPLC analysis results of BHB liposome after 3-week storage under cold condition (5 C.). FIG. 3E shows HPLC analysis results of BHB liposome after 4-week storage under cold condition (5 C.). FIG. 3F shows BHB dry content (%) of BHB liposome stored under cold condition. FIG. 3G shows BHB dimer content (%) of BHB liposome stored under cold condition (BHB dimer indicates the degradation product of BHB).

[0114] FIGS. 4A-4G show the stability of BHB liposome after long-term storage under conventional condition at 20 C. and 60% relative humidity. More specifically, FIG. 4A shows HPLC analysis of initial BHB liposome (week 0). FIG. 4B shows HPLC analysis results of BHB liposome after 1-week storage (20 C./60%). FIG. 4C shows HPLC analysis results of BHB liposome after 2-week storage (20 C./60%). FIG. 4D shows HPLC analysis results of BHB liposome after 3-week storage (20 C./60%). FIG. 4E shows HPLC analysis results of BHB liposome after 4-week storage. FIG. 4F shows BHB dry content (%) of BHB liposome stored under conventional condition. FIG. 4G shows BHB dimer content (%) of BHB liposome stored under conventional condition (BHB dimer indicates the degradation product of BHB).

[0115] As shown in FIGS. 3A-3G, after the long-term storage under cold condition (5 C.), there was no significant change in the contents of BHB liposomes. As shown in FIGS. 4A-4G, after long-term storage at 20 C. and 60% relative humidity, the BHB dry content decreased slightly from 70.1% to 68.8%, and the impurity (as indicated by BHB dimers) increased slightly from 3.0% to 4.7%, both of which are within the acceptable range. Accordingly, stability analysis showed that the BHB liposomes of the present invention demonstrate great stability.

Example 10 Effects of BHB Acid and BHB Liposomes on Blood Ketone Levels

[0116] The ketogenic potential of BHB Acid and BHB Liposome was analyzed according to Csilla's method with slight modifications (Nutrients. 2019 October; 11(10): 2330).

[0117] Specific Pathogen Free (SPF) male Institute of Cancer Research (ICR) mice were purchased from Qinglongshan Animal Breeding Center. All mice were on standard diet, and housed individually in a steel cage under standard photoperiod (12:12 h light-dark cycle) in a room at 24 C., and tap water was freely available. Prior to treatments, the mice fasted for 16 hours.

[0118] For treatments, a number of 30 mice were randomly divided into three groupscontrol group, BHB group, and BHB liposome group. The mice were treated via oral gavage at 0.1 ml/10 g body weight as shown in Table 9. The BHB group mice were treated with free acid form of R-BHB in water (once daily) at 9.92 mmol/kg, the BHB liposome group mice were treated with liposomal R-BHB free acid in water (once daily) at 9.92 mmol/kg, and the control group mice were treated with water. The pH of the administrated treatment solutions or water were all adjusted to 7 before administration. And the blood ketone levels were measured using a blood ketone meter at 0, 10, 20, 30, 45, 60, 90, 120, and 240 min after administration.

TABLE-US-00009 TABLE 9 Treatment Plan Dose (mg/kg BHB content Dose (mmol/kg Gavage Group body weight) (w/w) body weight) volume Control / / / 0.1 mL/10 g BHB 1860.7 mg/kg 55.5% 9.92 mmol/kg 0.1 mL/10 g BHB 1516.4 mg/kg 68.1% 9.92 mmol/kg 0.1 mL/10 g liposomes
FIG. 5 shows blood ketone levels at different time points after oral administration of BHB acid or BHB liposome as shown in Table 9. The highest blood ketone level is 2.8 mmol/L for BHB acid treatment group and 4.1 mmol/L for BHB liposome treatment group. The highest blood ketone level of R-BHB liposome was 1.41 times of that of R-BHB free acid. And the area under the curve of R-BHB liposome is 1.25 times that of R-BHB free acid, thus, the bioavailability of BHB liposome is significantly higher than that of R-BHB. In conclusion, BHB liposome demonstrated higher ketogenic potential, better bioavailability, and achieved better nutritional ketosis as compared to BHB free acid.

[0119] Although specific embodiments and examples of this invention have been illustrated herein, it will be appreciated by those skilled in the art that any modifications and variations can be made without departing from the spirit of the invention. The examples and illustrations above are not intended to limit the scope of this invention. Any combination of embodiments of this invention, along with any obvious their extension or analogs, are within the scope of this invention. Further, it is intended that this invention encompass any arrangement, which is calculated to achieve that same purpose, and all such variations and modifications as fall within the scope of the appended claims.

[0120] All the features disclosed in this specification (including any accompanying claims, abstract and drawings) may be replaced by alternative features serving the same, equivalent or similar purpose, unless expressly stated otherwise. Thus, unless expressly stated otherwise, each feature disclosed is one example of a generic series of equivalent or similar features.