Drug Delivery System, its Preparation Process and Use

• US 20110064794A1
• Filed: 01/16/2009
• Published: 03/17/2011
• Est. Priority Date: 01/16/2008
• Status: Abandoned Application

• Current Assignee: Hangzhou Yuhong Pharmaceutical Science & Technology Co., Ltd., Shenyang Pharmaceutical University
• Original Assignee: Hangzhou Yuhong Pharmaceutical Science & Technology Co., Ltd., Shenyang Pharmaceutical University
• Inventors: Lu, Yi, Shi, Li, Dong, Xiaohui, Deng, Yihui
• Application Number:
  US12/863,130
• Publication Number:
  US 20110064794A1
• Time in Patent Office: Days
• US Class Current: 424/450
• CPC Class Codes: A61K 47/42 Proteins; Polypeptides; Degradation products thereof; Derivatives thereof, e.g. albumin, gelatin or zein oligopeptides having up to five amino acids A61K47/183; polyamino acids A61K47/34
• CPC Class Codes: A61K 47/44 Oils, fats or waxes according to two or more groups of A61K47/02-A61K47/42; Natural or modified natural oils, fats or waxes, e.g. castor oil, polyethoxylated castor oil, montan wax, lignite, shellac, rosin, beeswax or lanolin synthetic glycerides, e.g. medium-chain triglycerides, A61K47/14
• CPC Class Codes: A61K 9/1075 Microemulsions or submicron emulsions; Preconcentrates or solids thereof; Micelles, e.g. made of phospholipids or block copolymers A61K9/0026 takes precedence
• CPC Class Codes: A61K 9/19 lyophilised , i.e. freeze-dried, solutions or dispersions lyophilised products with subsequent particle size reduction A61K9/14; granules or pellets made by lyphilisation A61K9/1682; solid oral dosage forms made by lyophilisation A61K9/2095; lyophilisation additives A61K47/00

Abstract

A protein-phospholipid dispersion preparation in a drug delivery system is provided, in which the weight ratio of protein to phospholipid is 1:300-300:1 and the particle size is between 5 nm and 1000 nm. The preparation process of the said preparation contains the mixture of protein phase and phospholipid phase and the homogenization process. The said drug delivery system can be used in many different pharmaceutical agents.

Claims

1. A drug delivery system, characterized by comprising a protein-phospholipid dispersion, in which the weight ratio of protein to phospholipid is 1:

300 to 300;

1, and the particle size is between 5 nm and 1000 nm.

2. The drug delivery system according to claim 1, wherein, in the protein-phospholipid dispersion, the surface of phospholipids or the surface and interior of phospholipids are coated by protein layer, or the inner and outer parts of the liposome bilayer are coated by protein, or protein nanoparticles are formed in water phase of the liposomes.

3. The drug delivery system according to claim 1, wherein the protein is selected from at least one of human albumin, bovine serum albumin, egg albumin, zein, hemoglobin and derivatives thereof, galactose glycated albumin and modified porcine seralbumin.

4. The drug delivery system according to claim 1, wherein, the phospholipids are selected from at least one of soybean lecithin, egg yolk phosphatidylcholine (ovolecithin), EPG, diphosphatidylglycerol, sphingomyelin, phosphatidyl serine, phosphatidylinositol, phosphatidylethanolamine, hydrogenated soybean phosphatidylcholine, hydrogenated egg yolk phosphatidylcholine, distearoyl phosphatidylcholine, dipalmitoyl phosphatidylcholine, dioleoyl phosphatidylcholine, dimyristoyl phosphatidyl choline, dilauroyl phosphatidylcholine, dicaprinoyl phosphatidylcholine, dioctanoyl phosphatidylcholine, dicaproyl phosphatidylcholine, distearoyl phosphatidylglycerol and sodium salt thereof, dipalmitoyl phosphatidylglycerol and sodium salt thereof, L-α

-dimyristoyl phosphatidylglycerol and sodium salt thereof, dilauroyl phosphatidylglycerol, dicaprinoyl phosphatidylglycerol, dioctanoyl phosphatidylglycerol, dicaproyl phosphatidylglycerol, distearoyl phosphatidylethanolamine, dipalmitoyl phosphatidylethanolamine, dioleoyl phosphatidylethanolamine, dimyristoyl phosphatidylethanolamine, dilauroyl phosphatidylethanolamine, bi-distearoyl phosphatidylglycerol and sodium salt thereof, bi-dipalmitoyl phosphatidylglycerol and sodium salt thereof, bi-dimyristoyl phosphatidylglycerol and sodium salt thereof, bi-dilauroyl phosphatidylglycerol, distearoyl phosphatidylinositol, dipalmitoyl phosphatidylinositol, dioleoyl phosphatidylinositol, dimyristoyl phosphatidylinositol, dilauroyl phosphatidylinositol, palmitoyl oleoyl phosphatidylcholine, palmitoyl linoleoyl phosphatidylcholine, stearyl linoleoyl phosphatidylcholine, stearyl oleoyl phosphatidylcholine, arachidonic stearoyl phosphatidylcholine, DSPE-PEG, DPPE-PEG, DMPE-PEG and DLPE-PEG, wherein the molecular weight of PEG in DSPE-PEG, DPPE-PEG, DMPE-PEG and DLPE-PEG is from 100 to 10000.

5. The drug delivery system according to claim 1, wherein the said delivery system further comprises organic solvents selected from at least one of ethanol, methanol, propanol, propylene glycol, methyl-2-pyrrolidone, n-butanol, tert butyl alcohol, acetone, ethyl acetate and isopropyl ether.

6. The drug delivery system according to claim 1, wherein the said delivery system further comprises oils, and the weight ratio between the oils and phospholipid is between 1:

0.1 and 1;

10, the said oils are selected from at least one of MCT, structured-oil, tocopherol, tocopheryl acetate, oleinic acid, ethyl oleate, soybean oil, safflower oil, olive oil, octanoic acid, decanoic acid, lauric acid, palmitinic acid, linoleic acid, linolenic acid, docosahexaenoic acid, deep-sea fish oil and plant volatile oil.

7. The drug delivery system according to claim 1, wherein, the said drug delivery system further comprises ligand and antibody, the said ligand is selected from galactose derivates, transferrin derivates, folic acid and derivates thereof, glucosamine derivates and RGD and derivates thereof and so on, the said antibody is selected from murine, humanized, recombine murine or recombine humanized antibody.

8. The drug delivery system according to claim 1, wherein, the said drug delivery system further comprises cholesterol and/or sitosterol.

9. The drug delivery system according to claim 1, wherein, the said drug delivery system further comprises positively charged substances selected from chitosan, octadecylamine, fatty amine, cholesterol-based polyamine cationic lipids or derivatives thereof.

10. The drug delivery system according to claim 1, wherein, the said drug delivery system further comprises pH regulator.

11. The drug delivery system according to claim 1, wherein, the said pH regulator is selected from at least one of organic acid, organic base, inorganic acid or inorganic base, such as citric acid, lactic acid, fumaric acid, tartaric acid, acetic acid, glucanic acid, lactobionic acid, sorbic acid, succinic acid, maleic acid, ascorbic acid, oxalic acid, formic acid, benzenesulfonic acid, benzoic acid, aspartic acid, hydrochloric acid, sulphuric acid, phosphoric acid, nitric acid, sodium hydroxide, arginine, lysine.

12. A method for manufacturing the drug delivery system according to claim 1, comprising the following steps:

1) preparing the phospholipid-containing phase;

2) preparing the protein-containing aqueous phase; and

3) mixing the phospholipid-containing phase and the protein-containing aqueous phase, and extruding optionally at 0-60°

C. under a pressure of 400-40000 psi, and then homogenizing.

13. The method according to claim 12, wherein the said protein-containing aqueous phase is 0.005-50% (g/ml) protein aqueous solution.

14. The method according to claim 12, wherein the said homogenization is high press homogenization or microfluidic homogenization.

15. The method according to claim 12, wherein the said method further comprises freeze drying or spray drying.

16. The method according to claim 15, wherein an additive used in the freeze drying or spray drying method is selected from at least one of sucrose, lactose, glucose, mannitol, dextran, trehalose, xylitol, maltose, fructose, protein, chitosan, glycine, citral and sodium chloride.

17. The method according to claim 12, wherein the said method further comprises filtration sterilization.

18. Use of the protein-phospholipid dispersion in the manufacture of a drug delivery system according to claim 1.