CN100411610C - Liposome able to transmit blood and brain screen, medicinal compsns. using hiposome as carrier and its prepn. method - Google Patents
Liposome able to transmit blood and brain screen, medicinal compsns. using hiposome as carrier and its prepn. method Download PDFInfo
- Publication number
- CN100411610C CN100411610C CNB2005101205508A CN200510120550A CN100411610C CN 100411610 C CN100411610 C CN 100411610C CN B2005101205508 A CNB2005101205508 A CN B2005101205508A CN 200510120550 A CN200510120550 A CN 200510120550A CN 100411610 C CN100411610 C CN 100411610C
- Authority
- CN
- China
- Prior art keywords
- liposome
- brain barrier
- blood
- central nervous
- medicine
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
Images
Landscapes
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
Abstract
The present invention belongs to the technical field of medicine, particularly to a liposome which can pass through a blood-brain barrier, a medicinal compound which uses the liposome as a carrier and a preparation method thereof. The liposome comprises a blood-brain barrier anchor point with the mol content of 5 to 15 percent and also comprises high phase change temperature phosphatide, cholesterol and fusion agents, wherein the particle size range of the liposome is form 0.05 to 0.5 mu m. The liposome medicinal compound coats medicine with an effective amount for treating central nervous systems and has longer blood circulation time, and the coated medicine can be carried to pass through blood brain barriers to enter central nervous systems to achieve the function of treating central nervous system diseases.
Description
Technical field
The invention belongs to medical technical field, relate to a kind of liposome that can see through blood brain barrier, also relating to a kind of is the pharmaceutical composition and preparation method thereof of carrier with this liposome.Be specifically related to a kind of liposome that contains the blood brain barrier anchor point and a kind of be the pharmaceutical composition and preparation method thereof of the carrier medicine that is coated with treatment central nervous system effective dose with this liposome.This pharmaceutical composition has long blood circulation time and can initiatively see through blood brain barrier and enters the central nervous system and reach the effect for the treatment of central nervous system disease.
Background technology
Blood brain barrier (blood-brain barrier, be called for short BBB) is the blood that formed by capillary endothelial cell and the barrier between cerebral tissue.It provides a metastable interior environment for cerebral tissue, has ensured the head normal function.But because the existence of BBB makes 95% medicine to enter cerebral tissue from blood, some hydrophilic particularly, macromolecular drug, therefore most medicines for central nervous system all are difficult to reach ideal therapeutic effect through blood brain barrier, some fat-soluble micromolecule (Mw is less than 500D) are though see through BBB easily, but taken in the blood by the efficient efflux pump on the cell membrane again very soon (Begley DJ.The blood-brain barrier:principles for targeting peptides and drugs to the central nervous system[J] .J Pharm Pharmacol.1996,48 (2): 136-146.).Therefore, for central nervous system disease, find that a kind of energy sees through the active drug transmission method of BBB and find that a kind of new drug is of equal importance.
In order to overcome BBB, reported many methods, as: (1) makes brain capillary endothelial cell closely connect instantaneous opening by causing the blood height to ooze, and barrier action disappears; (2) medicine is made suitable lipotropy prodrug; (3) use the nanoparticle of polybutylcyanoacrylate (PACA), polylactic acid (PLA), poly lactic coglycolic acid materials such as (PLGA) medicine to be sent in the brain as carrier; (4) with the immunoliposome be carrier, the monoclonal antibody of surface of liposome goes up corresponding receptor generation specificity with BBB and combines, and starts receptor-mediated endocytosis transhipment, thereby makes medicine see through BBB; (5) change route of administration, for example by nasal-cavity administration etc.But method (1) may make some poisonous and harmful substances go into brain in the instantaneous operating period of tight connection, influence central nervous system function, method (2) is because the existence effect of efficient efflux pump is little, method (3) still is in conceptual phase, and complicated process of preparation, appointed condition requires high, method (4) then is not suitable for carrying out widespread usage (KREUTER J because of liposome stability is relatively poor with the cost costliness, ALYAUTDIN RN, KHARKEVICH DA, et al.Passage of peptides through theblood-brain barrier with colloidal polymer particles (nanoparticles) [J] .Brain Res, 1995,647 (1): 171-174.; SCHRODER U, SABEL BA..Nanoparticles, a drug carrier system to pass the blood-brain barrier, permit central analgesic effects of iv dalargin injections[J] .BrainRes, 1996,710 (122): 121-124.).Discover, in BBB, have the transportation system that absorbs the colloidal type material, therefore there is researcher to design the colloidal carrier of some medicines in view of the above, as nanoparticle and liposome etc., hope can by this colloidal carrier make the saturating BBB of medicine go into brain (A.Prokop.Bioartificial organs in the twenty-first century:nanobiological devices.Ann.NY Acad.Sci.2001,944:472-490.).Yet this type of colloidal carrier can be used as xenobiotic by reticuloendothelial system (RES) after being injected into blood be removed rapidly, mainly by the macrophage phagocytic of liver, spleen.As conventional liposome half-life 5～15min only in blood, the electronegative liposome half-life is shorter.
Conclusion to sum up, pharmaceutical carrier is gone into brain to the saturating BBB of medicine in order to realize, just must satisfy this several requirements: the first, strengthen carrier in stability in blood, prevent by absorption such as serum albumin and destroy; The second, avoid the scavenging action of RES, prolong carrier at blood circulation time; The 3rd, have with the effect of BBB specific bond and initiatively infiltrate through brain; The 4th, go into behind the brain can be rapidly and axoneure merge and discharge drug molecule generation therapeutical effect.Liposome is a kind of transmission system of first-selection, and the advantage of conventional liposome is more stable in the blood plasma, but systemic administration.Also develop simultaneously and long circulating liposomes, can obviously prolong the systemic circulation time, as U.S. Pat 4837028 disclosed pegylated liposomals etc.This shows, can on the conventional liposome basis, design a kind of medicine for central nervous system carrier that satisfies the BBB thoroughly of above-mentioned requirements.
GM1 is proved to be to see through one of minority glycolipid molecule of BBB up to now, it has been used to central nervous system's damage and reparation, be a kind of important neural reparative factor (WellsJM, Ventura RF, Ei senhauer PB, McKenna DC, Fine RE, Ullman MD.Transportof GM1 and GM1 inner ester across an in vitro model of the blood-brainbarrier.Neurosci Lett.1996.217:121-1244.).GM1 also is a kind of important lipid (Shoko Yokoyama that can be used for preparing liposome simultaneously, Tadahiro Takeda, Masahiko Abe, Preparation of ganglioside GM1 liposomes and their membrane properties.Colloids Surf.B:Biointerfaces.2002,27:181-187.).Also there are some researches show simultaneously, erythrocyte, platelet and lymphocyte can be in blood stable existence and be not taken as xenobiotic and removed by RES, the sialic acid of its film surface ganglioside and glycoprotein etc. have played important function, remove the erythrocyte of sialic acids groups, platelet and lymphocyte can be removed rapidly by liver, therefore sialic acid molecule has obvious anti-recognition reaction (Durocher JR in the RES reset procedure, Payne RC, Conrad ME.Role of sialic acid in erythrocytesurvival.Blood.1975,45 (1): 11-20.), therefore the liposome that contains sialic GM1 also can reduce the scavenging action of RES effectively and prolong blood circulation time, and is simultaneously very stable in serum.
Now existing many bibliographical informations a kind of lipid material that promotes that iuntercellular merges, i.e. N-acetyl PHOSPHATIDYL ETHANOLAMINE.Studies show that, in liposome, participate in N-palmityl PHOSPHATIDYL ETHANOLAMINE (NPPE) or N-stearoyl PHOSPHATIDYL ETHANOLAMINE (NSPE) can not only increase liposome membrane stability, more can promote liposome and cell fusion, thereby the lipid drug disposition is discharged into (J.C.Domingo in the cell, M.Mora, and M.A.De Madariaga.Incorporationof N-acylethanolamine pohospholipids into egg phosphatidylcholinevesicles:characterization and permeability properties of the binarysystems.Biochim.Biophys.Acta.1993.1148:308-316).
Common method for preparing lipidosome comprises thin film aquation method, organic solvent displacement method, detergent removal method and ethanol injection method etc.Some method has been used for suitability for industrialized production.But the liposome major part of these method gained is not suitable for filtering, unstable, can not fine removal residual organic solvent, also be difficult to obtain the even liposome that is fit to injection and has better bioavailability simultaneously.Therefore press for set up scalable, stablize, be convenient to the aseptic process cheap method for preparing lipidosome of all even expense of particle diameter simultaneously.
Summary of the invention
One of purpose of the present invention is to propose a kind of liposome of blood brain barrier thoroughly, makes it have the effect that blood brain barrier enters the central nervous system that obviously sees through, to satisfy the needs of medical field as the medicine for central nervous system carrier;
Two of purpose of the present invention is to propose more than one to state thoroughly that the liposome of blood brain barrier is the pharmaceutical composition of carrier, makes it can see through blood brain barrier and go into brain and reach the effect for the treatment of central nervous system disease;
Three of purpose of the present invention is the preparation methoies that propose aforementioned pharmaceutical compositions.
One of goal of the invention of the present invention is by selecting for use a kind of liposome that contains 5～15% molar content blood brain barrier anchor points to realize.
Furtherly, contain in the above-mentioned liposome:
High phase transition temperature phosphatidase 15 0～70% (molar content)
Blood brain barrier anchor point 5～15% (molar content)
Described high phase transition temperature phospholipid is sphingomyelin (being called for short SM, down together) and neutral synthetic phospholipid.Wherein said neutral synthetic phospholipid can (be called for short DPPC for dipalmitoyl phosphatidyl choline, down together), distearoyl phosphatidylcholine (is called for short DSPC, together following) or dimyristoyl phosphatidyl choline (abbreviation DMPC, down together), be the product that meets the cGMP requirement, can adopt the product of Lipoid company;
Described cholesterol is the product that meets cGMP, can adopt Lipoid company product;
Described blood brain barrier anchor point is that Monostalotetrahexosylgangliside (is called for short GM1, together following) and the GM1 slaine, be an oligosaccharide and the pure and mild chemical compound that sialic acid molecule links to each other and obtains by glucoside bond of nerve sheath amine, can adopt Folch, J., Lees, M.B., and Sloane Stanley, G.H. etc. are at (1957) J.Biol.Chem.226,497-509. the preparation of bibliographical information method, the structural formula of GM1 is:
The preferred GM1 sodium salt of the present invention is as the blood brain barrier anchor point.GM1 sodium is the glycolipid quasi-molecule, can be used as the lipid material and participate in the liposome membrane, by with blood brain barrier on specificity GM1 receptors bind and initiatively see through blood brain barrier and enter among the central nervous system.
Said flux is a N-acetyl PHOSPHATIDYL ETHANOLAMINE.
Said N-acetyl PHOSPHATIDYL ETHANOLAMINE can be N-palmityl PHOSPHATIDYL ETHANOLAMINE (abbreviation NPPE, down together) or N-stearoyl PHOSPHATIDYL ETHANOLAMINE (being called for short NSPE, down together), and the preferred NPPE of the present invention is as flux.
Above-mentioned liposome particle size range is 0.05～0.5 μ m.
Two of goal of the invention of the present invention is achieved by the following technical solution, and a kind ofly utilizes the above-mentioned pharmaceutical composition that can see through the liposome of blood brain barrier for carrier, it is characterized in that, contains the medicine of treatment central nervous system effective dose in this pharmaceutical composition.
Furtherly, above-mentioned liposome as carrier, bag is by the medicine for central nervous system of treatment effective dose.
The medicine of described treatment central nervous system effective dose can be mecobalamin, C14H25N4NaO11P2 or nerve growth factor (being called for short NGF).
At present, the nervous system medicine above 95% can not directly enter the central nervous system by blood brain barrier, therefore can not reach good therapeutical effect, just more is difficult for having entered the central nervous system such as NGF albuminoid macromole.The liposome that contains the blood brain barrier anchor point of the present invention has following advantage (is that GM1 gives an example with the blood brain barrier anchor point):
1. prolong circulation time in blood, this is because sialic acid molecule (is called for short RES at reticuloendothelial system among the GM1, has obvious anti-recognition reaction in the reset procedure down together), therefore in blood, has longer circulation time, this has just increased the chance of liposome through blood brain barrier, reaches a kind of long lasting effect.
2. increased the targeting of blood brain barrier, this is initiatively to pass through blood brain barrier because the GM1 that surface of liposome participates in can combine with the blood brain barrier specific receptor.
3. promote the utilization of cell to drug molecule, this is because flux can promote liposome and cell fusion, thereby drug molecule is released in the cell rapidly.
These key advantage can produce better therapeutic effect to central nervous system disease, improve bioavailability of medicament and clinical indication scope.
The liposome that utilization of the present invention can see through blood brain barrier comprises the steps: for the drug combination preparation of carrier can adopt reverse phase evaporation to be prepared in conjunction with the high-pressure filteration method
(1) takes by weighing various lipids by liposome molar content percentage ratio, high phase transition temperature phosphatidase 15 0～70%, cholesterol 10～30%, blood brain barrier anchor point 5～15%, flux 15～25%, solvent with 5～10 times of volumes of liposome is dissolved as clear solution with above-mentioned lipid, and described solvent is chloroform, methanol or the two mixing;
(2) above-mentioned solution is put in the rotary evaporation flask, and the reduction vaporization solvent evaporated gets the adipose membrane of one deck attached to the evaporation flask walls;
(3) get above-mentioned steps (2) and contain the adipose membrane flask, fill nitrogen, to keep filling nitrogen down to step (6) operation always, adding organic solvent dissolution lipid to lipid final concentration is 100 μ m/ml, become organic phase solution, described organic solvent is ether, diethyl ether, chloroform, oxolane or diisopropyl ether;
(4) medicine of getting treatment central nervous system effective dose join for drug level be 0.05～50mg/ml aqueous phase solution;
(5) mix organic phase solution and aqueous phase solution, volume ratio was 2: 1～6: 1 when organic phase solution and aqueous phase solution mixed, supersound process;
(6) mixed solution in the step (5) is put in the rotary evaporation flask, the room temperature evaporated under reduced pressure is to gel; Adding equal-volume water reduction vaporization to sample again is suspension, finishes to fill nitrogen;
(7) the gained sample is put the processing of high-pressure homogenization squeezer and is got the uniform grading liposome by filtering with microporous membrane.
(8) liposomal samples adopts ion exchange chromatography, gel filtration chromatography or supercentrifugation to carry out separation and purification, and free principal agent is separated with liposome.
(9) maintenance of purification liposome and interior water etc. ooze condition, carry out preparation in isotonic buffer, are prepared into injection or lyophilized preparation.
Wherein, the microporous filter membrane aperture is preferably 0.2～0.5 μ m in the step (7), and high-pressure homogenization pressure is preferably 50～500psi.
Serum and the checking of cerebral tissue distribution test in external blood brain barrier model test checking and body, compare with drug coated not, medicine for central nervous system through liposome bag quilt of the present invention has the effect that obviously sees through blood brain barrier, and circulation time obviously prolongs in blood.
Description of drawings
Fig. 1 gets 20ul sample determination gained chromatogram after to be the NGF liposome with 1ml contain the solution dissolving of 1%Triton X-100.
Fig. 2 is that the NGF liposome is also got supernatant sample 20ul mensuration gained chromatogram behind the high speed centrifugation with the dissolving of 1m water for injection.
Fig. 3 investigates trend curve in the NGF liposome blood plasma.
Fig. 4 is that NGF and NGF liposome permeability in external blood brain barrier model compare.
Fig. 5 is
125I-NGF organizes serum, liver spleen and cerebral tissue distribution comparison diagram in vivo.
Fig. 6 is
125I-NGF liposome group is serum, liver spleen and cerebral tissue distribution comparison diagram in vivo.
The specific embodiment
Embodiment 1: the liposome that contains the GM1 sodium salt is a carrier, and bag is by the pharmaceutical composition of NGF
Take by weighing various lipids by liposome molar content percentage ratio, DMPC 50%, and CH 20%, GM1 sodium salt 10%, and NPPE 20%, and wherein, DMPC, NPPE and CH purchase the company to Lipoid, and the GM1 sodium salt is own purification gained.Solvent (chloroform: methanol, volume ratio 2: 1) with 5 times of volumes of liposome is dissolved as clear solution.Above-mentioned solution is put in the rotary evaporation flask, and the reduction vaporization solvent evaporated is the adipose membrane of one deck attached to the evaporation flask walls.Get and contain the adipose membrane flask, fill nitrogen (following operation keeps filling nitrogen always), adding organic solvent (ether) to lipid final concentration is 100 μ m/ml, and dissolve limpid is organic phase solution afterwards.Get nerve growth factor, be dissolved in 10mMNaCL, 10mM Tris-Cl, in the buffer of pH 7.4, final concentration is that 0.1mg/ml is aqueous phase solution.By organic facies: water, 4: 1 mixed of volume ratio the two, supersound process, 5min/4 ℃.Above-mentioned mixed solution is put in the rotary evaporation flask, and 20 ℃/10～50mmHg is to gel; Adding 30 ℃/10～50mmHg/15min of equal-volume water again, to be evaporated to sample be suspension, finishes to fill nitrogen.Above-mentioned liposomal samples is put the high-pressure homogenization squeezer and is handled, and filter membrane is selected 0.45 μ m for use, and pressure 100psi circulates 3 times.Above-mentioned sample allows liposomal samples pass through chromatography media under this condition according to crossing CM SepharoseFast Flow cation-exchange chromatography medium, and liposome sees through, and free NGF is adsorbed on the medium, reaches free principal agent and separates with liposome.Purification liposomal samples 10mM NaCL, 10mM Tris-Cl, pH 7.4 suspends and is diluted to suitable concn, adds packing lyophilizing after 4% mannitol, lyophilized preparation.
Embodiment 2: the liposome that contains the GM1 sodium salt is a carrier, and bag is by the pharmaceutical composition of mecobalamin
Take by weighing various lipids by liposome molar content percentage ratio, DMPC 50%, and CH 30%, GM1 sodium salt 5%, and NPPE 15%, and wherein, DMPC, NPPE and CH purchase the company to Lipoid, and the GM1 sodium salt is own purification gained.Solvent (chloroform: methanol, volume ratio 1: 1) with 7.5 times of volumes of liposome is dissolved as clear solution.Above-mentioned solution is put in the rotary evaporation flask, and the reduction vaporization solvent evaporated is the adipose membrane of one deck attached to the evaporation flask walls.Get and contain the adipose membrane flask, fill nitrogen (following operation keeps filling nitrogen always), adding organic solvent (diethyl ether) to lipid final concentration is 100 μ m/ml, and dissolve limpid is organic phase solution afterwards.Get mecobalamin, be dissolved in the water for injection, final concentration is that 10mg/ml is aqueous phase solution.By organic facies: water, 6: 1 mixed of volume ratio the two, supersound process, 5min/4 ℃.Above-mentioned mixed solution is put in the rotary evaporation flask, and 20 ℃/10～50mmHg is to gel; Adding 30 ℃/10～50mmHg/15min of equal-volume water again, to be evaporated to sample be suspension, finishes to fill nitrogen.Above-mentioned liposomal samples is put the high-pressure homogenization squeezer and is handled, and filter membrane is selected 0.5 μ m for use, and pressure 50psi circulates 3 times.Above-mentioned sample is crossed the gel filtration chromatography post, reaches free principal agent and separates with liposome.Purification liposomal samples 10mMNaCL, 10mM PB, pH 6.8 suspends and is diluted to suitable concn, adds packing after 5% mannitol, injection.
Embodiment 3: the liposome that contains the GM1 sodium salt is a carrier, and bag is by the pharmaceutical composition of C14H25N4NaO11P2
Take by weighing various lipids by liposome molar content percentage ratio, DMPC 60%, and CH 10%, GM1 sodium salt 5%, NPPE 25%, wherein, DMPC, NPPE and CH purchase the company to Lipoid, and the GM1 sodium salt is own purification gained, are dissolved as clear solution with the solvent (chloroform) of 10 times of volumes of liposome.Above-mentioned solution is put in the rotary evaporation flask, and the reduction vaporization solvent evaporated is the adipose membrane of one deck attached to the evaporation flask walls.Get and contain the adipose membrane flask, fill nitrogen (following operation keeps filling nitrogen always), adding organic solvent (oxolane) to lipid final concentration is 100 μ m/ml, and dissolve limpid is organic phase solution afterwards.Get C14H25N4NaO11P2, be dissolved in the water for injection, final concentration is that 2.5mg/ml is aqueous phase solution.By organic facies: water, 2: 1 mixed of volume ratio the two, supersound process, 5min/4 ℃.Above-mentioned mixed solution is put in the rotary evaporation flask, and 20 ℃/10～50mmHg is to gel; Adding 30 ℃/10～50mmHg/15min of equal-volume water again, to be evaporated to sample be suspension, finishes to fill nitrogen.Above-mentioned liposomal samples is put the high-pressure homogenization squeezer and is handled, and filter membrane is selected 0.2 μ m for use, and pressure 500psi circulates 3 times.Above-mentioned sample reaches free principal agent and separates with liposome through ultracentrifugation.Purification liposomal samples 10mM NaCL, 10mM PB, pH 6.8 suspends and is diluted to suitable concn, adds packing after 5% mannitol, injection.
Embodiment 4: the liposome that contains the GM1 sodium salt is a carrier, and bag is by the pharmaceutical composition of NGF
Take by weighing various lipids by liposome molar content percentage ratio, DMPC 60%, and CH 15%, GM1 sodium salt 15%, and NPPE 10%, and wherein, DMPC, NPPE and CH purchase the company to Lipoid, and the GM1 sodium salt is own purification gained.Solvent (methanol) with 5 times of volumes of liposome is dissolved as clear solution.Above-mentioned solution is put in the rotary evaporation flask, and the reduction vaporization solvent evaporated is the adipose membrane of one deck attached to the evaporation flask walls.Get and contain the adipose membrane flask, fill nitrogen (following operation keeps filling nitrogen always), adding organic solvent (diisopropyl ether) to lipid final concentration is 100 μ m/ml, and dissolve limpid is organic phase solution afterwards.Get nerve growth factor, be dissolved in 10mM NaCL, 10mM Tris-Cl, in the buffer of pH7.4, final concentration is that 0.8mg/ml is aqueous phase solution.By organic facies: water, 6: 1 mixed of volume ratio the two, supersound process, 5min/4 ℃.Above-mentioned mixed solution is put in the rotary evaporation flask, and 20 ℃/10～50mmHg is to gel; Adding 30 ℃/10～50mmHg/15min of equal-volume water again, to be evaporated to sample be suspension, finishes to fill nitrogen.Above-mentioned liposomal samples is put the high-pressure homogenization squeezer and is handled, and filter membrane is selected 0.2 μ m for use, and pressure 300psi circulates 3 times.Above-mentioned sample allows liposomal samples pass through chromatography media under this condition according to crossing CM Sepharose Fast Flow cation-exchange chromatography medium, and liposome sees through, and free NGF is adsorbed on the medium, reaches free principal agent and separates with liposome.Purification liposomal samples 10mM NaCL, 10mM Tris-Cl, pH 7.4 suspends and is diluted to suitable concn, adds packing lyophilizing after 4% mannitol, lyophilized preparation.
Embodiment 5: the liposome that contains the GM1 sodium salt is a carrier, and bag is by the pharmaceutical composition of C14H25N4NaO11P2
Take by weighing various lipids by liposome molar content percentage ratio, DMPC 70%, and CH 10%, GM1 sodium salt 5%, and NPPE 15%, and wherein, DMPC, NPPE and CH purchase the company to Lipoid, and the GM1 sodium salt is own purification gained.Solvent (chloroform: methanol, volume ratio 1: 1) with 10 times of volumes of liposome is dissolved as clear solution.Above-mentioned solution is put in the rotary evaporation flask, and the reduction vaporization solvent evaporated is the adipose membrane of one deck attached to the evaporation flask walls.Get and contain the adipose membrane flask, fill nitrogen (following operation keeps filling nitrogen always), adding organic solvent (chloroform) to lipid final concentration is 100 μ m/ml, and dissolve limpid is organic phase solution afterwards.Get C14H25N4NaO11P2, be dissolved in the water for injection, final concentration is that 4mg/ml is aqueous phase solution.By organic facies: water, 4: 1 mixed of volume ratio the two, supersound process, 5min/4 ℃.Above-mentioned mixed solution is put in the rotary evaporation flask, and 20 ℃/10～50mmHg is to gel; Adding 30 ℃/10～50mmHg/15min of equal-volume water again, to be evaporated to sample be suspension, finishes to fill nitrogen.Above-mentioned liposomal samples is put the high-pressure homogenization squeezer and is handled, and filter membrane is selected 0.2 μ m for use, and pressure 250psi circulates 3 times.Above-mentioned sample reaches free principal agent and separates with liposome through ultracentrifugation.Purification liposomal samples 10mM NaCL, 10mM PB, pH 6.8 suspends and is diluted to suitable concn, adds packing after 5% mannitol, lyophilizing, lyophilized preparation.
The applicant has been made following property research and compliance test result to bag of the present invention by the pharmaceutical composition of NGF (NGF liposome):
1, property research
(1) NGF assay
Get 1 NGF lipid freeze-dry powder, add the dissolving of 0.9ml water for injection, add 0.1ml10%Triton X-100 again, the centrifuging and taking supernatant is as the assay sample solution behind the vibration mixing.Get NGF stock solution, be mixed with the NGF standard solution of variable concentrations.With Shodex PROTEINKW-82.5 gel chromatographic columns standard solution and sample solution are analyzed, according to standard solution chromatograph NGF concentration in the calculation sample solution as a result.Result such as table 1, the linear regression equation of peak area and protein concentration are " C (μ g/ml)=0.0004A-1.2691, R
2=0.9984 ", as calculated, the NGF drug content is 77.8 μ g/ml.
Table 1 high-efficient liquid phase technique is measured NGF liposome drug content result
(2) form and particle size distribution
The liposome that takes a morsel is with 1% phosphotungstic acid negative staining, transmission electron microscope observing.As seen the liposome bag that participates in GM1 and NPPE by NGF after form do not change, and be evenly distributed, be typical dactylotype.Measuring the liposome mean diameter through the laser particle size scatterometer is 97.3 ± 10.4nm.
(3) entrapment efficiency determination
Get 2 NGF lipid freeze-dry powders, wherein 1 photograph " assay " method is measured the NGF total amount; 1 adds the dissolving of 1.0ml water for injection in addition, gets supernatant behind the high speed centrifugation and measures NGF content with method, calculates the envelop rate of liposome.As calculated, NGF content is 77.36 μ g/ml, and NGF content is 2.55 μ g/ml in the centrifugal supernatant, and the NGF liposome encapsulation is 96.7%.Fig. 1 and Fig. 2 are respectively supernatant sample HPLC chromatogram behind NGF liposome content working sample and the high speed centrifugation.
(4) percolation ratio is measured
Get the NGF liposome, respectively at 4 ℃ and 37 ℃ of placements, carry out percolation ratio in different time points sampling then and measure, determine NGF liposome stability and storage condition according to percolation ratio, measurement result sees Table 2 and table 3.The result shows that under 4 ℃ of conditions, the NGF liposome stability is fine, and percolation ratio is lower than 5% when placing 12 months.But can not long preservation under 37 ℃ of conditions, place 1 month percolation ratio and just surpass 5%, place and reached 17.5% in 3 months.
Table 2NGF liposome percolation ratio measurement result (4 ℃)
Table 3NGF liposome percolation ratio measurement result (37 ℃)
(5) phase transition temperature is measured
Get the NGF liposome, measure phase change temperature of liposome with water for injection dissolving back with conductance method, the result is 38.3 ± 0.9 ℃.
(6) stability is measured in the blood plasma
Get the NGF liposome, hatch for 37 ℃ in Dialysis tubing after adding the 1.0ml human plasma, measures 24 hours in the seepage situation, assay method carries out the gel high-efficient liquid phase analysis for get supernatant behind different time points sampling high speed centrifugation, mensuration NGF liposome percolation ratio.Measurement result sees Table 4.The result shows that NGF liposome stability in blood plasma is fine, and percolation ratio is lower than 5% in 24 hours.Fig. 2 is a stable trend curve in the NGF liposome blood plasma.
Percolation ratio is investigated measurement result (37 ℃) in the table 4NGF liposome blood plasma
(7) organic solvent residual
Get the NGF liposome, with chloroform, methanol, ether residual quantity in the gas chromatography determination sample solution, measurement result sees Table 5.The result shows that NGF liposome Determination of Residual Organic Solvents is very low, meets the Chinese Pharmacopoeia relevant regulations.
Table 5NGF liposome Determination of Residual Organic Solvents measurement result
2, NGF liposome permeability in the blood brain barrier external model is measured
According to list of references (Wells JM, Ventura RF, Eisenhauer PB, McKennaDC, Fine RE, Ul lman MD.Transport of GM1 and GM1 inner esteracross an in vitro model of the blood-brain barrier.NeurosciLett.1996.217:121-1244.) method cultivation CBEC formation blood brain barrier external model.Cell culture is got NGF liposome and NGF stock solution after converging, be 1.0 μ g/ml with test with the culture medium dilution respectively, respectively get 1ml and add 1 for the examination pond, tried to add in the pond test culture medium 2ml, make the inside and outside liquid level of cell inserter equal, to eliminate the influence of static pressure that the liquid level difference produces to permeability.Then in 24 hours in different time points from being tried the pond 50 μ l that take a sample, sampling finishes the back and measures the sample thief NGF of institute content with the NGF enzyme linked immunological kit.Measurement result sees Table 6.The result shows, compares with NGF stock solution, and the NGF liposome has the effect that obviously sees through blood brain barrier.Fig. 4 shows that NGF solution and NGF liposome see through the trend of blood brain barrier model.
The external blood brain barrier model of table 6 is to NGF solution and NGF liposome permeability measurement result
3, NGF liposome measure of spread in serum, liver spleen and the cerebral tissue in vivo
Get NGF stock solution, according to list of references (Poduslo JF, Curran GL, Dyck PJ.Increase in albumin,
IgG, and IgM blood-nerve barrier indices in human diabeticneuropathy[J] .Proc Natl Acad Sci USA, 1988,85 (13): 4879-4883.) narration method, adopt chloramine-t method labelling NGF preparation
125I-NGF.Press the preparation of embodiment 2 methods
125The I-NGF liposome.
Get 40 of SD male rats, be divided into two groups, promptly
125I-NGF solution group and
125I-NGF liposome group.Separate its one-sided carotid artery and femoral vein with 15% urethane anesthesia back, the ligation of carotid artery proximal part, distal end is done the carotid artery intubate.The femoral vein administration, dosage is
125I-NGF 0.5 μ g/g.Respectively at after the administration 15,30 and 60min get blood 1mL from intubate, with peristaltic pump perfusion normal saline 20min, cut off opposing carotid at last then, continue perfusion 15min, eliminate the influence that medicine residual in the brain blood capillary distributes to cerebral tissue with this.Blood sample 3000 * g is centrifugal, and 5min obtains serum, measures radioactivity with γ-calculating instrument; Simultaneously also after administration 15,30 and 60min put to death rat, get liver spleen and cerebral tissue with 0.5%Triton X-100 homogenate after the centrifugal 10min of 10,000 * g get supernatant and measure radioactivity.Measurement result sees Table 7.Result's demonstration,
125I-NGF group radioactivity mainly is distributed in the blood regulating liver-QI spleen, and cerebral tissue content is very little, and blood drug level descends rapidly, is mainly absorbed by the liver spleen; And
125I-NGF liposome group is kept higher blood drug level always, and the liver spleen absorbs very little, is mainly absorbed by cerebral tissue.Can obviously reflect thus
125The I-NGF liposome has the effect that longer blood circulation time and saturating blood brain barrier are gone into brain.
Serum, liver spleen and cerebral tissue measure of spread result in table 7NGF and the NGF liposome body
Claims (8)
1. liposome that can see through blood brain barrier, it is characterized in that, described liposome contains: synthetic neutral phospholipid 50～70% (molar content), cholesterol 10～30% (molar content), the slaine 5～15% (molar content) of ganglioside GMI of monosialic acid tetrahexose or GM1, flux 15～25% (molar content), described synthetic neutral phospholipid is dipalmitoyl phosphatidyl choline, distearoyl phosphatidylcholine or dimyristoyl phosphatidyl choline; Described flux is a N-acetyl PHOSPHATIDYL ETHANOLAMINE.
2. according to the described a kind of liposome that can see through blood brain barrier of claim 1, it is characterized in that described GM1 slaine is the GM1 sodium salt.
3. according to the described a kind of liposome that can see through blood brain barrier of claim 1, it is characterized in that described N-acetyl PHOSPHATIDYL ETHANOLAMINE is N-palmityl PHOSPHATIDYL ETHANOLAMINE or N-stearoyl PHOSPHATIDYL ETHANOLAMINE.
4. according to the described a kind of liposome that can see through blood brain barrier of arbitrary claim in the claim 1 to 3, it is characterized in that described liposome particle size range is 0.05～0.5 μ m.
5. one kind is utilized the described pharmaceutical composition that can see through the liposome of blood brain barrier for carrier of claim 1, it is characterized in that, contain the medicine of treatment central nervous system effective dose in this pharmaceutical composition, described treatment central nervous system's medicine is mecobalamin, C14H25N4NaO11P2 or nerve growth factor.
6. according to the described pharmaceutical composition of claim 5, it is characterized in that the medicine of described treatment central nervous system effective dose is by described liposome bag quilt.
7. one kind prepares the described preparation of drug combination method of claim 5, it is characterized in that this method comprises the steps:
(1) takes by weighing synthetic neutral phospholipid 50～70% by liposome molar content percentage ratio, cholesterol 10～30%, the slaine 5～15% of ganglioside GMI of monosialic acid tetrahexose or GM1, flux 15～25%, solvent with 5～10 times of volumes of liposome is dissolved as clear solution with above-mentioned lipid, described solvent is chloroform, methanol or the two mixing, described synthetic neutral phospholipid is dipalmitoyl phosphatidyl choline, distearoyl phosphatidylcholine or dimyristoyl phosphatidyl choline, and described flux is a N-acetyl PHOSPHATIDYL ETHANOLAMINE;
(2) above-mentioned solution is put in the rotary evaporation flask, and the reduction vaporization solvent evaporated gets the adipose membrane of one deck attached to the evaporation flask walls;
(3) get above-mentioned steps (2) and contain the adipose membrane flask, fill nitrogen, to keep filling nitrogen down to step (6) operation always, adding organic solvent dissolution lipid to lipid final concentration is 100 μ m/ml, become organic phase solution, described organic solvent is ether, diethyl ether, chloroform, oxolane or diisopropyl ether;
(4) medicine of getting treatment central nervous system effective dose is joined for drug level is 0.05～50mg/ml aqueous phase solution, and described treatment central nervous system's medicine is mecobalamin, C14H25N4NaO11P2 or nerve growth factor;
(5) mix organic phase solution and aqueous phase solution, volume ratio was 2: 1～6: 1 when organic phase solution and aqueous phase solution mixed, supersound process;
(6) mixed solution in the step (5) is put in the rotary evaporation flask, the room temperature evaporated under reduced pressure is to gel; Adding equal-volume water reduction vaporization to sample again is suspension, finishes to fill nitrogen;
(7) the gained sample is put the processing of high-pressure homogenization squeezer and is got the uniform grading liposome by filtering with microporous membrane;
(8) liposomal samples adopts ion exchange chromatography, gel filtration chromatography or supercentrifugation to carry out separation and purification, and free principal agent is separated with liposome;
(9) ooze under the condition at maintenance of purification liposomal samples and interior water etc., be diluted to suitable concn, be prepared into injection or lyophilized preparation.
8. according to the described preparation of drug combination method of claim 7, it is characterized in that the microporous filter membrane aperture is 0.2～0.5 μ m in the described step (7), high-pressure homogenization pressure is 50～500psi.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2005101205508A CN100411610C (en) | 2005-12-29 | 2005-12-29 | Liposome able to transmit blood and brain screen, medicinal compsns. using hiposome as carrier and its prepn. method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2005101205508A CN100411610C (en) | 2005-12-29 | 2005-12-29 | Liposome able to transmit blood and brain screen, medicinal compsns. using hiposome as carrier and its prepn. method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1833633A CN1833633A (en) | 2006-09-20 |
| CN100411610C true CN100411610C (en) | 2008-08-20 |
Family
ID=37001624
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB2005101205508A Expired - Fee Related CN100411610C (en) | 2005-12-29 | 2005-12-29 | Liposome able to transmit blood and brain screen, medicinal compsns. using hiposome as carrier and its prepn. method |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN100411610C (en) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102078299B (en) * | 2011-01-04 | 2012-09-26 | 海南美大制药有限公司 | Citicoline sodium liposome solid preparation |
| CN102366408B (en) * | 2011-09-14 | 2013-03-20 | 海南灵康制药有限公司 | Monosialotetrahexosyl ganglioside sodium liposome injection |
| CN106974889A (en) * | 2017-03-14 | 2017-07-25 | 重庆大学 | Carry medicine gangliosides micella and its preparation method and application |
| EP3501495A1 (en) | 2017-12-21 | 2019-06-26 | InnoMedica Holding AG | Liposomes comprising sphingomyelin |
| CN114588109B (en) * | 2020-12-07 | 2023-09-12 | 沈阳药科大学 | Coenzyme Q 10 Emulsion, preparation method and application thereof |
| CN114642634A (en) * | 2020-12-17 | 2022-06-21 | 中国科学院深圳先进技术研究院 | Blood brain barrier penetrating drug-carrying micelle and preparation method and application thereof |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5073543A (en) * | 1988-07-21 | 1991-12-17 | G. D. Searle & Co. | Controlled release formulations of trophic factors in ganglioside-lipsome vehicle |
| CN1517094A (en) * | 2003-01-13 | 2004-08-04 | 重庆富进生物医药有限公司 | Monosialic acid tetrahexose ganglioside liposome complex preparation |
| CN1621092A (en) * | 2003-11-25 | 2005-06-01 | 杨正茂 | Folic acid receptor targeted liposome medicine carrier, its preparation and application |
-
2005
- 2005-12-29 CN CNB2005101205508A patent/CN100411610C/en not_active Expired - Fee Related
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5073543A (en) * | 1988-07-21 | 1991-12-17 | G. D. Searle & Co. | Controlled release formulations of trophic factors in ganglioside-lipsome vehicle |
| CN1517094A (en) * | 2003-01-13 | 2004-08-04 | 重庆富进生物医药有限公司 | Monosialic acid tetrahexose ganglioside liposome complex preparation |
| CN1621092A (en) * | 2003-11-25 | 2005-06-01 | 杨正茂 | Folic acid receptor targeted liposome medicine carrier, its preparation and application |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1833633A (en) | 2006-09-20 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CA2193502C (en) | Sphingosomes for enhanced drug delivery | |
| Gao et al. | Bioorthogonal supramolecular cell-conjugation for targeted hitchhiking drug delivery | |
| JP4885715B2 (en) | Irinotecan formulation | |
| EP1389089B1 (en) | Method and composition for solubilising a biologically active compound with low water solubility | |
| RU2391966C1 (en) | Based on botanical phospholipids nanosystem for actuation of biologically active compounds, and method of its manufacture (versions) | |
| CN100411610C (en) | Liposome able to transmit blood and brain screen, medicinal compsns. using hiposome as carrier and its prepn. method | |
| Sou et al. | Selective uptake of surface-modified phospholipid vesicles by bone marrow macrophages in vivo | |
| ES2964413T3 (en) | Sustained release inhalable liposomal composition for use in the treatment of lung diseases | |
| CN103501766A (en) | Advanced active liposomal loading of poorly water-soluble substances | |
| CN101579310A (en) | Decataxel self-microemulsifying composition and preparation method thereof | |
| CN101325947A (en) | Liposome combination | |
| Xiong et al. | Preparation, characterization and evaluation of breviscapine lipid emulsions coated with monooleate–PEG–COOH | |
| US20210093721A1 (en) | Colloidal particles for use in medicine | |
| CN106821987B (en) | Liposome carrying phenol hydroxyl group-containing insoluble drug, and preparation method and application thereof | |
| Sharma et al. | A Review on Novel Vesicular Drug Delivery System: Transfersomes. | |
| Fahr et al. | Liposomal formulations of cyclosporin A: a biophysical approach to pharmacokinetics and pharmacodynamics | |
| US20080089928A1 (en) | Liposome drug carriers with ph-sensitivity | |
| CN102905693A (en) | Water-soluble pharmaceutical composition comprising at least one therapeutically active substance having hydrophobic properties and at least one compound selected from among sialoglycosphingolipids, glycosphingolipids or a mixture of sialoglycosphingolipids and glycosphingolipids | |
| CN103415283A (en) | Liposome formulation comprising an anti-tumour active substance, method for its preparation and pharmaceutical compositions comprising it | |
| CN112773776B (en) | Drug-loaded nanoparticle system | |
| CN103040764A (en) | Bleomycin hydrocloride lipidosome injection | |
| US10925831B2 (en) | Liposomal formulations of platinum-acridine anticancer agents and methods thereof | |
| Wang et al. | Enhanced Pharmacokinetics of Celastrol via Long-Circulating Liposomal Delivery for Intravenous Administration | |
| Lin et al. | Comprehensive analysis of the influence of physicochemical properties and tumor-associated environments on liposome intratumoral penetration | |
| Spanjer | Targeting of liposomes to liver cells in vivo. |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| ASS | Succession or assignment of patent right |
Owner name: WUHAN SCIENCE AND TECHNOLOGY INNOVATION BIO-TECHNO Free format text: FORMER OWNER: WUHAN HAITE BIO-PHARMACEUTICAL CO., LTD. Effective date: 20090918 |
|
| C41 | Transfer of patent application or patent right or utility model | ||
| TR01 | Transfer of patent right |
Effective date of registration: 20090918 Address after: Hanyang hanqiang Wuhan economic and Technological Development Zone, Hubei province Wuhan City Street No. 74 Patentee after: Wuhan science and technology innovation Biological Technology Co Ltd Address before: Hubei Province, Wuhan City, Hanyang economic and Technological Development Zone of Wuhan science and technology park. Patentee before: Wuhan Haite Biological Pharmaceutical Co., Ltd. |
|
| ASS | Succession or assignment of patent right |
Owner name: SIHUAN BIO INDUSTRY GROUP CO., LTD. Free format text: FORMER OWNER: WUHAN SCIENCE AND TECHNOLOGY INNOVATION BIO-TECHNOLOGY CO., LTD. Effective date: 20100318 |
|
| C41 | Transfer of patent application or patent right or utility model | ||
| COR | Change of bibliographic data |
Free format text: CORRECT: ADDRESS; FROM: 430056 NO.74, HANQIANG STREET, HANYANG WUHAN ECONOMIC AND TECHNOLOGICAL DEVELOPMENT ZONE, WUHAN CITY, HUBEI PROVINCE TO: 100037 8/F, DONGRUN SHIDAI BUILDING, NO.3, FUWAI AVENUE, XICHENG DISTRICT, BEIJING CITY |
|
| TR01 | Transfer of patent right |
Effective date of registration: 20100318 Address after: 100037 Beijing City, Xicheng District Fuwai Street No. 3 Dongrun Times Building 8 Patentee after: Four ring Biological Industry Group Co Ltd Address before: Hanyang hanqiang Wuhan economic and Technological Development Zone of Hubei Province, Wuhan City, 430056 street, No. 74 Patentee before: Wuhan science and technology innovation Biological Technology Co Ltd |
|
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20080820 Termination date: 20201229 |
|
| CF01 | Termination of patent right due to non-payment of annual fee |