Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K9/00—Medicinal preparations characterised by special physical form
  • A61K9/10—Dispersions; Emulsions
  • A61K9/127—Liposomes
  • A61K9/1277—Processes for preparing; Proliposomes
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K9/00—Medicinal preparations characterised by special physical form
  • A61K9/10—Dispersions; Emulsions
  • A61K9/127—Liposomes
  • A61K9/1277—Processes for preparing; Proliposomes
  • A61K9/1278—Post-loading, e.g. by ion or pH gradient

Definitions

• the present invention is directed to a method for controlling the transbilayer distributions of ionizable lipids or ionizable proteins in a vesicle bilayer. More particularly, the invention describes methods for localizing ionizable lipids or ionizable proteins to either the inner or outer monolayer of unilamellar vesicles or to that of the outermost bilayer of multilamellar vesicles (MLV) in response to transmembrane ion gradients.
• MLV multilamellar vesicles
• Liposomes are completely closed lipid bilayer membranes containing an entrapped aqueous volume. Liposomes may be unilamellar vesicles (possessing a single membrane bilayer) or multilamellar vesicles (onion-like structures characterized by multiple membrane bilayers, each separated from the next by an aqueous layer) .
• the bilayer is composed of two lipid monolayers having a hydrophobic "tail” region and a hydrophilic "head” region.
• the structure of the membrane bilayer is such that the -hydrophobic (non-polar) "tails” of the lipid monolayers orient toward the center of the bilayer while the hydrophilic (polar) "heads” orient towards the aqueous phase.
• the original liposome preparation of Bangham et al. involves suspending phospholipids in an organic solvent which is then evaporated to dryness leaving a phospholipid film on the reaction vessel. Then an appropriate amount of aqueous phase is added, the mixture is allowed to "swell", and the resulting liposomes which consist of multilamellar vesicles (MLVs) are dispersed by mechanical means.
• MLVs multilamellar vesicles
• Large unilamellar vesicles may be produced using an extrusion apparatus by a method described in Cullis et al., PCT 87/00238, January 16, 1986, entitled “Extrusion Technique for Producing Unilamellar Vesicles,” relevant portions of which are incorporated herein by reference.
• Vesicles made by this technique are extruded under pressures of up to about 700 psi through a polycarbonate membrane filter. These vesicles may be exposed to at least one freeze and thaw cycle prior to the extrusion technique; this procedure is described in Bally et al., PCT 87/00043, January 15, 1987, entitled “Multilamellar Liposomes Having Improved Trapping Efficiencies", relevant portions of which are incorporated herein by reference.
• liposomes that may be used are those characterized as having substantially equal lamellar solute distribution.
• This class of liposomes is denominated as stable plurilamellar vesicles (SPLV) as defined in U.S. Patent No. 4,522,803 to Lenk, et al., monophasic vesicles as described in U.S. Patent No. 4558,579 to Fountain, et al., and frozen and thawed multilamellar vesicles (FATMLV) wherein the vesicles are exposed to at least one freeze and thaw cycle; this procedure is described in Bally et al., PCT Publication No. 87/00043, January 15, 1987, entitled “Multilamellar Liposomes Having Improved Trapping Efficiencies" and incorporated herein by reference.
• SPLV plurilamellar vesicles
• FATMLV frozen and thawed multilamellar ves
• the method for preparing the sterol vesicles involves adding to an aqueous buffer a salt form of an organic acid derivative of a sterol capable of forming closed bilayers in an amount sufficient to form completely closed bilayers which entrap an aqueous compartment.
• a suspension of multilamellar vesicles is formed by shaking the mixture. The formation of vesicles is facilitated if the aqueous buffer also contains the counterion of the salt in solution.
• the present invention provides a method for producing vesicles, preferably unilamellar vesicles, that exhibit transbilayer asymmetry of lipid in response to a transmembrane pH gradient.
• MLVs may also be made to exhibit this asymmetry in their outermost bilayer.
• the present invention describes methods for making liposomes in which the distribution of an ionizable lipid or protein component can be controlled between the monolayers of the outer bilayer of the liposomes. Such distribution may be made to be asymmetric.
• the liposomes of the invention have an outer bilayer which contains an ionizable lipid or an ionizable protein in an asymmetrical distribution between the monolayers of the outer bilayer.
• the ionizable lipid may be basic, as an amine such as sphingosine or stearylamine, or acidic, as in the phospholipids phosphatidylglycerol, phosphatidylinositol, or cardiolipin, a prostaglandin, or the fatty acids such as oleic acid or stearic acid.
• the ionizable protein may be basic.
• Several types of liposomes may be used in the practice of the invention, such as FATMLVs, MPVs, or SPLVs.
• the liposomes of the invention may also be exposed to an extrusion technique. Alternatively, the liposomes may be unilamellar.
• the liposomes may also contain a bioactive agent, and the bioactive agent itself may be ionizable.
• the liposomes may be administered to mammals such as humans.
• the liposomes of the invention are multilamellar or unilamellar.
• Multilamellar liposomes may be made by any method known in the art and include SPLVs, freeze and thaw MLVs, REVs, and MPVs.
• Unilamellar liposomes may be formed by a freeze and thaw technique followed by an extrusion through polycarbonate filters.
• the liposomes may contain bioactive agents, such as ionizable drugs. Such ionizable drugs may themselves be loaded into the liposomes according to an ion concentration gradient across the bilayer. Alternatively, drugs may simply be loaded during the aqueous entrapment step of the liposome-forming procedure.
• Liposomes of the invention may also be dehydrated for long term storage in stable form until rehydration and use. The liposomes may be administered to mammals such as humans.
• FIGURE 1 is a graph showing the time course for the reaction of TNBS with vesicles of DOPC containing 10 mol % DOPE. Labelling was determined by either chromatographic (closed circles) or spectrophotometric (open circles) methods.
• FIGURE 2A is a graph showing the labelling of stearylamine by TNBS in DOPC vesicles where both the interior entrapped aqueous medium and exterior bathing medium is pH 8.5
• FIGURE 2B is a graph showing the influence of a proton gradient across the vesicle bilayer (interior entrapped aqueous medium pH 5.0, exterior bathing medium pH 8.5) on the labelling of stearylamine to TNBS in DOPC vesicles.
• FIGURE 3A is a graph showing labelling of sphingosine to TNBS in DOPC vesicles where both the interior entrapped aqueous medium and exterior bathing medium is pH 8.5.
• FIGURE 3B is a graph showing the influence of a proton gradient across the vesicle bilayer (interior entrapped aqueous medium pH 5.0, exterior bathing medium pH 8.5) on the labelling of sphingosine to TNBS in DOPC vesicles.
• FIGURE 4A is a graph showing ability of BSA to extract [ 14C] oleic acid from LUVs when the interior entrapped aqueous medium is pH 10.0, and the external bathing medium is pH 7.0. The peak represents vesicles (closed circles) and oleic acid (open circles) .
• FIGURE 4B is a graph showing ability of BSA to remove [ 14C] oleic acid from LUVs when both the interior entrapped aqueous medium and the exterior bathing medium are both at pH 7.0.
• the peaks represent vesicles (closed circles) and oleic acid (open circles).
• DOPC dioleoyl phosphatidylcholine
• the liposomes of the present invention are unilamellar vesicles, preferably large unilamellar vesicles. However, small unilamellar vesicles and multilamellar vesicles may also be used.
• the lipids that may be used in the present invention are ionizable lipids.
• Ionizable lipids include those which are acidic and basic and may be deprotonated or protonated, at a pH of between about 2.0 and about 14.0 in an aqueous environment. Upon protonation or deprotonation, lipids become charged lipids.
• Such ionizable lipids include, but are not limited to phosphatidylglycerol, phosphatidic acid, and their derivatives, the amine-containing lipids phosphatidylserine, phosphatidylethanolamine and phosphatidylinositol; stearylamine, sphingosine, cardiolipin, and the fatty acids.
• Fatty acids of all chain lengths and degrees of unsaturation may be used; for example those fatty acids having about 6 to about 22 carbon atoms, most preferably about 12 to about 18 carbon atoms and having about 0 to about 4 double bonds, most preferably having about 0 to about 1 double bond such as stearic acid and oleic acid.
• Other ionizable lipids (bilayer components) that may be used are the bile acids and prostaglandins.
• the prostaglandins include their precursor substances arachidonic acid and its metabolites as well as their structural analogs, and synthetic enzyme inhibitors.
• prostaglandin also includes synthetic compounds structurally related to the naturally occurring prostaglandins, as well as the prostacyclines and leukotrienes.
• Still other ionizable bilayer components that may be used are the salt forms of organic acid derivatives of sterols or tocopherols, preferably cholesterol or tocopherol hemisuccinates respectively.
• Neutral lipids being those that possess no net charge or are not ionizable at the pH employed, that may be used in the invention include, but are not limited to phospholipids such as phosphatidylcholine, dioleoylphosphatidylcholine, sphingomyelin, cholesterol, and their derivatives.
• Non-lipid materials, such as ionizable proteins (the term "protein” includes peptides or polypeptides) may also be used.
• Such proteins also include those with substituted amino acids, compared to the naturally occurring material, in their chains, as well as derivatives, analogs, and fragments of the proteins.
• Such proteins include those that are acidic or basic, and can be protonated or deprotonated.
• Such proteins include, but are not limited to, alpha, beta, and gamma interferons, interleukin 2, interleukin 1, colony-stimulating factors, tumor necrosis factor, the histone proteins, and the growth hormones such as bovine growth hormone, human growth hormone and porcine growth hormone. These proteins all have ionizable groups and are therefore useful for the practice of the present invention.
• Most preferably used in the present invention are the proteins oxytocin, vasopressin, arginine vasopressin, calcitonin, and alpha-atrial natriuritic factor.
• organic solvents may be used to suspend the lipids.
• Suitable organic solvents are those with a variety of polarities and dielectric properties, which solubilize the lipids, and include but are not limited to chloroform, methanol, ethanol, dimethylsulfoxide (DMSO) , methylene chloride, and solvent mixtures such as benzene:methanol (70:30).
• DMSO dimethylsulfoxide
• solvent mixtures such as benzene:methanol (70:30).
• Solvents are chosen on the basis of their biocompatability, low toxicity, and solubilization abilities.
• Liposomes entrap an aqueous medium which is enclosed by the lipid bilayers.
• the aqueous medium can be ' for example, water or water containing a dissolved salt or buffer.
• salts or buffers can be sodium chloride and phosphate buffered saline (PBS) .
• Other buffers include but are not limited to borate, citrate, Tris-HCl tris- (hydroxymethyl)- aminomethane hydrocholoride) , and HEPES (N-2-hydroxyethyl piperazine-N*- 2-ethane sulfonic acid).
• Buffers may be in the pH range of between about 2.0 and about 14.0.
• the preparations are hydrated with HEPES buffer (150 mM NaCl, 20 rriM HEPES), pH 7.0, borate buffer (100 mM Na 2 HC0 3 , 50 mM H 3 B0 3 , pH 8.5, or citrate buffer (150 mM Na-citrate), pH 8.5.
• HEPES buffer 150 mM NaCl, 20 rriM HEPES
• borate buffer 100 mM Na 2 HC0 3 , 50 mM H 3 B0 3 , pH 8.5
• citrate buffer 150 mM Na-citrate
• the medicament is entrapped in the liposome and then administered to the patient to be treated.
• the medicament is entrapped in the liposome and then administered to the patient to be treated.
• U.S. Patent No. 3,993,754 Sears, U.S. Patent No. 4,145,410; Papahadjopoulos et al., U.S. Patent No. 4,235,871; Schneider, U.S. Patent No. 4,224,179, Lenk, et al., U.S. Patent No. 4,522,803, and Fountain et al., U.S. Patent No. 4,588,578.
• any bioactive agent can be entrapped within the liposomes for use according to the present invention.
• agents include but are not limited to antibacterial compounds such as gentamycin, antiviral compounds such as rifampacin, antifungal compounds such as amphdtericin B, anti-parasitic compounds such as antimony derivatives, antineoplastic compounds such as vinblastine, vincristine, mitomycin C, doxorubicin, daunomycin, methotrexate, and cisplatinum, among others, proteins such as albumin, toxins such as diptheria toxin, enzymes such as catalase, hormones such as estrogens, neurotransmitters such as acetylcholine, lipoproteins such as alpha-lipoprotein, glycoproteins such as hyaluronic acid, immunoglobulins such as IgG, immunomodulators such as the interferons or the interleukens, dyes such as Arsenazo III, radiolabels such as
• radio-opaque compounds such as 99Te
• fluorescent compounds such as carboxy fluoroscein
• polysaccharides such as glycogen
• cell receptor binding molecules such as estrogen receptor protein
• non-steroidal anti-inflammatories such as indomethacin, salicylic acid acetate, ibuprofen, sulindac, piroxicam, and naproxen
• anti- inflammatories such as dexamethasone, antiglaucomic agents such as timolol or pilocarpine, anesthetics such as dibucaine
• nucleic acids such as thymine
• polynucleotides such as RNA polymers.
• the liposomes of the present invention may be dehydrated, thereby enabling storage for extended periods of time until use. Standard freeze-drying equipment or equivalent apparatus may be used to dehydrate the liposomes. Liposomes may also be dehydrated simply by placing them under reduced pressure. Alternatively, the liposomes and their surrounding medium can be frozen in liquid nitrogen prior to dehydration. Dehydration with prior freezing may be performed in the presence of one or more protective sugars in the preparation, according to the procedures of Janoff et al., PCT 86/01103, February 27,
• protective sugars include but are not limited to trehalose, maltose, sucrose, glucose, lactose and dextran.
• multilamellar vesicles may be dehydrated with prior freezing with or without protective sugars.
• rehydration is accomplished by simply adding an aqueous solution, e.g., distilled water, to the liposomes and allowing them to rehydrate.
• vesicles containing ionizable lipids or ionizable proteins are made in an aqueous environment of controlled pH, then exposed to a bathing medium of a relatively more acidic or relatively more basic pH.
• a concentration gradient is formed across the membrane with the internal aqueous (entrapped) medium being of a different pH than that of the external aqueous (bathing) medium.
• lipids that can be protonated such as stearylamine and sphingosine are immediately sequestered into the inner monolayer.
• acidic lipids such as phosphatidylglycerol (PG) , phosphatidylinositol (PI), cardiolipin, the bile acids, prostaglandins, and the fatty acids oleic acid and stearic acid, to the inner monolayer are observed for vesicles whose internal aqueous media are basic with respect to the external aqueous medium.
• PG phosphatidylglycerol
• PI phosphatidylinositol
• cardiolipin the bile acids
• prostaglandins prostaglandins
• fatty acids oleic acid and stearic acid fatty acids oleic acid and stearic acid
• the distribution of weak acids and weak bases, including lipids and bioactive agents across the bilayer membrane is based on their abilities to permeate the membranes when in the neutral form, achieving transmembrane concentrations obeying the Henderson- Hasselbach equilibrium equation:
• AH + refers to a protonated lipid or bioactive agent such as one containing a protonated amine
• the subscripts i and o refer to the interior and exterior of the vesicle respectively.
• amine-containing lipids such as stearylamine and sphingosine, or basic bioactive agents
• their localization to the membrane results in similar redistributions where the transbilayer location of the protonated amine reflects the interior and exterior proton concentration at the membrane interfaces.
• transmembrane distributions of these amine-containing lipids demonstrate that the transmembrane distributions of lipids which are weak acids, such as some phospholipids and fatty acids, are also strongly dependent on transmembrane pH gradients. Since the neutral (protonated) form can permeate the membrane, this will result in transmembrane gradients according to:
• RCOO ⁇ refers to the unprotonated fatty acid.
• fatty acids In vesicles exhibiting pH gradients where the interior is basic, fatty acids therefore move to the interior monolayer.
• Ionizable lipids or proteins are also translocated and ionizable agents loaded into liposomes according to a Na + /K + concentration gradient. In such cases, " Na + /K + diffusion potentials existing across the membrane allow an ionized species to go into the membrane in place of a K + ion that diffuses out.
• the method of the invention requires the formation of liposomes at a controlled pH, including an ionizable lipid or ionizable protein.
• an ionizable lipid or ionizable protein may be stearylamine or sphingosine, or phospholipids or fatty acids such as oleic or stearic acid.
• the ionizable lipids may be in a proportion of from about 1 mol% to about 50 mol% of the total lipid used to form the liposomes, preferably 5-10 mol%.
• the ionizable lipids may be in a proportion of up to about a 1:1 mol ratio.
• the labeling agent TNBS may be used to trace the transbilayer migration of the ionizable lipids.
• TNBS-labelled liposomes containing charged lipid were exposed to bathing media of differing pH than that of the formation buffer (relatively more acidic or basic) .
• the formation buffer will be basic, at pH from about 8.0 to about pH 14.0 preferably about pH 8.0 to about pH 11.0, most preferably about pH 10.0.
• the liposomes are exposed to buffer of more acidic pH, at pH about 2.0 to about pH 7.5 preferably about pH 2.0 to about pH 6.0, most preferably about pH 5.0.
• the formation buffer used was acidic, at pH about 2.0 to about pH 7.5, most preferably pH 5.0.
• the liposomes were exposed to buffer of more basic pH, about pH 7.5 to about pH 14.0, most preferably about pH 8.0.
• Such exposure of the liposomes to the alternate pH buffer may take place either on a gel filtration column, or directly, by immersion of vesicles directly in the buffer.
• the lipid to .be translocated across the bilayer is a phospholipid, such as phosphatidylclycerol, phosphatidylinositol, or cardiolipin
• a phospholipid such as phosphatidylclycerol, phosphatidylinositol, or cardiolipin
• the liposomes are formed, containing the ionizable phospholipids, by any of the above-mentioned methods in the art for forming liposomes, preferably unilamellar liposomes, and containing buffer at pH 8.0, for example, 300mM phosphate buffer.
• the thus-labeled liposomes containing the charged (ionizable) lipid were then exposed to bathing media of differing pH than that of the formation medium.
• the formation buffer is basic, at a pH of about 6.0 to about 10.0, preferably about pH 8.0.
• the liposomes are exposed to buffer of more acidic pH, i.e., about pH 3.0 to about 6.0, preferably about pH 4.0.
• the liposome suspension is heated to about 30°C to about 60°C, preferably 60°C, for about 10 minutes.
• the suspension is held at that temperature for about 12 hours.
• the suspension is then cooled to about 25°C.
• translocating ionizable lipids can be employed for ionizable proteins.
• Preferantial translocation of the charged lipid to one or the other monolayers was spectrophotometrically detected by labelling of the amino-containing lipid by TNBS.
• the asymmetry may be demonstrated by ion exchange using DEAE sephacel ion exchange (see Example 8).
• the liposomes of the present invention may also be remote loaded with ionizable agents according to the disclosure of Bally et al., PCT 86/01102, February 26, 1986, entitled "Encapsulation of Antineoplastic Agents in Liposomes", relevant portions of which are incorporated herein by reference.
• a transmembrane potential is created across the bilayers of the liposomes during formation, and the ionizable agent is loaded into the liposomes by means of the transmembrane potential.
• This potential is generated by creating a concentration gradient for one or more charged species (e.g., Na + , K + and/or H + ) across the liposome membranes.
• the inner monolayer of the liposome may already be charged due to transmembrane migration of a ionizable lipid or ionizable protein to the inner monolayer.
• Ionizable bioactive agents may be loaded in response to this charge, while the membrane asymmetry of the liposomes entrapping these agents changes in response to this charge imposed by the gradient.
• both processes simultaneously i.e.: loading of the liposomes with ionizable agent and inducing asymmetry in the liposome membrane. Both processes may be controlled by the pH gradient applied to the liposomes.
• Ionizable lipids or proteins or entrapped ionizable agents are translocated to the inner monolayer of the bilayer in question (i.e.: the single bilayer of a unilamellar liposomes, or the outermost bilayer of a multilamellar liposome) in response to this gradient.
• the medicaments are administered within liposomes, in admixture with a pharmaceutically-acceptable carrier selected with regard to the intended route of administration and standard pharmaceutical practice. Dosages for these medicaments when entrapped in liposomes will be about that of the drugs alone; dosages will be set by the prescribing physician with regard to the age, weight, and condition of the patient. The proportional ratio of active ingredient to carrier will naturally depend on the chemical nature, solubility, and stability of the active ingredient, as well as the dosage contemplated.
• a liposome composition of this invention can be used in the form of tablets, capsules, lozenges, troches, powders, syrups, elixirs, aqueous solutions and suspensions, and the like.
• carriers which can be used include lactose, sodium citrate, and salts of phosphoric acid.
• Various disintegrants such as starch, and lubricating agents such as magnesium stearate, sodium lauryl sulfate and talc, are commonly used in tablets.
• useful diluents are lactose and high molecular weight polyethylene glycols.
• aqueous suspensions are required for oral use, certain sweetening and/or flavoring agents can be added.
• parenteral administration or injection via intravenous, intraperitoneal, intramuscular, subcutaneous, or intra-mammary route sterile solutions of the liposome composition are prepared.
• the total concentration of solutes should be controlled to render the preparation isotoni ⁇ .
• vesicle-entrapped compounds may be incorporated into a broad range of topical dosage forms including but not limited to gels, oils, emulsions and the like.
• the suspension containing the entrapped compound may be added ' to the aqueous phase as an ingredient in the liposome preparation.
• Such preparations may be administered as topical creams, pastes, ointments, gels, lotions and the like for direct application.
• the liposomes of the present invention may be used as in vitro diagnostic agents.
• DOPC dioleoylphosphatidylcholine
• DOPE dioleoylphosphatidyl- ethanolamine
• [ 14C]-labelled DOPE was prepared from DOPC and [ 14C]- ethanolamine (both obtained from New England Nuclear (NEN) , Boston, MA) using phospholipase D to exchange the choline head group for ethanolamine.
• the resulting [ 14C]-labelled DOPE was purified on CM cellulose. Cholesterol, stearylamine, sphingosine, stearic acid and oleic acid were obtained from Sigma (St. Louis) and used without further purification.
• the resulting LUVs exhibited an average diameter of 100 nm (as determined by light scattering techniques) and a trapped volume of approximately 1.5 ul/umol phospholipid.
• DOPC and DOPE (1:9 mol ratio containing trace amounts of [ 14C]-DOPE) were mixed in chloroform and LUVs prepared as described in Example 1.
• Two umoles of the vesicle suspension (200 ul) were added to 800 ul of 0.5 mM Trinitrobenzene sulphonic acid (TNBS) (Sigma) in 100 mM sodium bicarbonate (NaHC0 3 ), 50 mM hydrogen borate (H 2 B0_), pH 8.5.
• TNBS Trinitrobenzene sulphonic acid
• NaHC0 3 sodium bicarbonate
• H 2 B0_ hydrogen borate
• TNP-PE trintrophenylated phosphatidylethanolamine
• the silica pellet was extracted once more and the combined solvent dried under nitrogen at 50°C.
• the activity of each sample was determined employing a Packard 2000CA scintillation analyzer (United Technologies, California). This procedure established the validity of the TNBS labelling procedures for assaying transmembrane distributions of lipids containing primary amino groups in large unilamellar vesicle systems. Fifty percent of the PE in DOPE:DOPC (1:9 mol ratio) LUVs in the absence of pH gradients were labelled employing this chromatographic assay procedure. As shown in FIG. 1, the TNBS-PE reaction was essentially complete within 10 minutes and proceeds to an equilibrium value of 52 +/- 4%, consistent with an equilibrium transmembrane distribution of PE.
• DOPC was mixed in chloroform with 10 mol% DOPE, and dried under vacuum.
• the lipids were resuspended in buffer to a concentration of 20 umoles/ml at pH 8.5 (100 mM NaHCO-, 50 mM H 2 B0 3 ) .
• the vesicles were produced as in Example 1 and were passed down gel filtration columns (15 X 1.5 cm) containing Sephadex G50 (Pharmacia or Sigma) equilibrated with 100 mM NaHCOg, 50 mM H 2 B0 3 at pH 8.5.
• a double beam spectrophotometer (Pye Unicam SP8-500, Philips) was employed to follow the TNBS labelling of available primary amine groups on the vesicles.
• a reference cuvette containing 2.5 ml of buffer (pH 8.5) was placed in the reference beam.
• the sample cuvette contained 2.5 ml of buffer (pH 8.5) containing 0.5 mM TNBS.
• Absorbance at 420 nm was followed to establish a base line and subsequently 0.1 to 0.5 ml aliquots of vesicles were added to each cuvette. The increase in absorbance at 420 nm was recorded until the reaction was complete. .Two hundred ul of Triton X-100 detergent (0.5%). was added to both cuvettes to solubilize the vesicles and thus expose all amino groups present to TNBS. The absorbance in the presence of detergent was taken as 100% labelling. The above procedure was repeated for lipids resuspended in buffer of pH 5.0 (150 mM sodium-citrate).
• FIG. 1 shows the time course for the vesicle-TNBS reaction where the DOPC vesicles contain 10 mol% DOPE, as determined spectrophotometrically.
• Example 1 The materials and procedures of Example 1 were employed using DOPC-stearylamine (5 mol%) vesicles.
• FIG. 2A shows the TNBS labelling of stearylamine proceeding to completion as assayed spectrophotometrically (see Example 1), when the pH of the entrapped aqueous solution and the bathing medium were both pH 8.5. This demonstrates the rapid redistribution of inner monolayer stearylamine to the outer monolayer as the outer monolayer stearylamine is depleted on reaction with TNBS.
• FIG. 2B shows labelling in the presence of a pH gradient, (entrapped aqueous solution pH 5.0, bathing medium pH 8.5). No labelling of stearylamine could be detected within 10 minutes. Subsequent addition of 200 ul of Triton X-100 detergent (TX-100) to solubilize the vesicles resulted in complete labelling within 20 seconds. These results are consistent with a localization of stearylamine to the inner monolayer in response to the pH gradient.
• a pH gradient entrapped aqueous solution pH 5.0, bathing medium pH 8.5
• Example 3 The materials and procedures of Example 3 were employed using DOPC-sphingosine (5 mol%) vesicles.
• Figure 3A shows the result of LUVs that do not exhibit a proton gradient (pH 8.5: both internal and external buffer) . This demonstrates the rapid redistribution of inner monolayer sphingosine to the outer monolayer as the outer monolayer sphingosine is depleted on reaction with TNBS.
• Figure 3B shows the result of LUVs that exhibit a proton gradient, pH 5.0 inside and pH 8.5 outside. These results are consistent with a localization of sphingosine to the inner monolayer in response to the pH gradient.
• DOPC was mixed with 10 mol% [ 14C]-oleic acid and trace 3 amounts of [ H]-DPPC, in chloroform. The mixture was dried under vacuum and the lipid resuspended in 150 mM NaCl,
• the liposomes were freeze-thawed and vesicles produced as in Example 1.
• the vesicles were passed down Sephadex G50 columns pre-equilibrated with 150 mM NaCl, 20 mM HEPES at pH 7.0.
• Two hundred ul of a solution of fat-free bovine serum albumin (BSA), (Sigma) was added to 1 ml of the resulting vesicle preparation to give a final protein concentration of 5 mg/ml.
• BSA fat-free bovine serum albumin
• the vesicle-albumin mixture was applied to a 15 X 1.5 cm column containing Sepaharose 4B gel (Pharmacia) pre-equilibrated in buffer at pH 7.0.
• FIG. 4A shows removal of only a small amount of oleic acid by BSA when a transmembrane pH gradient (entrapped aqueous medium pH 10.0, exterior bathing medium pH 7.0) is present.
• FIG. 4B shows almost complete removal of oleic acid by BSA when both the interior entrapped medium and the exterior bathing medium are the same (pH 7.0). This is consistent with a localization of the oleic acid to the inner monolayer in the presence of a proton gradient (interior basic).
• Example 5 The procedures of Example 5 were employed using DOPC mixed with 10 mol% of [ 14C]-stearic acid and trace amounts 3 of [ H]-DPPC, in chloroform. Results similar to those of
• Example 4 employing oleic acid, were observed.
• Liposomes containing 20 mg/ml EPC and 5 mol% PG were formed according to the procedures of Example 1.
• the lipid film was hydrated in 2.0 ml of 300mM phosphate buffer at pH 8.0.
• the external buffer was then changed to pH 4.0 by titration with 6M sulphuric acid or by gel filtration to exchange the external buffer for 150mM citrate pH 4.0.
• the liposome suspension was heated at 60°C for 30 minutes and the first external medium was simultaneously replaced by the more acidic external medium. Following the 30 minute heating step, the liposome suspension was cooled to 25°C. Results similar to those obtained in Example 4 employing oleic acid, were observed.
• Liposomes that do not exhibit PG asymmetry bind to the DEAE and are not eluted until the column is washed with high ionic strength buffer (see Example 8).
• the liposomes of Example 7 were passed down a gel filtration column (15 X 1.5 cm.) containing Sephadex G-50 equilibrated with 10 mM HEPES (pH 7.0). The liposomes were added to DEAE-Sephacel (Pharmacia), the flow rate adjusted to 1-2 ml/min., and 1.0 ml fractions collected. Liposomes bound to the column material were eluted employing 0.5 M NaCl, 10 mM HEPES ao pH 7.0. Fractions were counted in a Packard 2000CA scintillation analyzer.
• Liposome pH gradients were dissipated employing nigericin and valinomycin each at a concentration of 1 ug/umol lipid followed by the addition of 100 mM KC1 to a final concentration of ImM.
• Example 3 The procedures and materials of Example 3 were employed, and ion exchange chromatography was used to determine the migration of the lipid to the inner monolayer, as in Example 8.
• the liposomes of Example 3 (0.5 ml, having 50 umol/ml phospholipid) were passed down a gel filtration column (10 X 1.5 cm.) containing Sephadex G-50 equilibrated ' with 10 mM HEPES (pH 7.0). The liposomes were added to CM-Sepharose, CL-6B (Pharmacia), the flow rate adjusted to 1-2 ml/min. , and 1.0 ml fractions collected. Liposomes bound to the column material were eluted employing 0.5 M NaCl, 10 mM HEPES at pH 8.5. Fractions were counted in a Packard 2000CA scintillation analyzer.
• Liposome pH gradients were dissipated by subjecting the vesicles to to five cycles of freezing and thawing followed by resizing using the LUVET process.

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• 1987
  • 1987-06-12 JP JP62503863A patent/JP2760355B2/ja not_active Expired - Fee Related
  • 1987-06-12 WO PCT/US1987/001401 patent/WO1987007530A1/en active IP Right Grant
  • 1987-06-12 EP EP19870904192 patent/EP0269720B1/en not_active Expired - Lifetime
  • 1987-06-12 DE DE87904192T patent/DE3776763D1/de not_active Expired - Fee Related
• 1992
  • 1992-07-28 SG SG769/92A patent/SG76992G/en unknown

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