IP Library › Granted Patent US 12,624,128
Granted Patent B2
US 12,624,128 · App. 18/092,051 · Granted May 12, 2026

Low molecular weight chondroitin sulfate, composition, preparation method and use thereof

Inventors: Haoning Zhang (Qixia District, CN); Song Chen (Qixia District, CN); Bo Jin (Qixia District, CN); Yonggang Xu (Qixia District, CN); Chuangen Tang (Qixia District, CN)
Assignee: Nanjing Hanxin Pharmaceutical Technology Co., Ltd.
C08B37/0069A61K31/737A61P19/02C07H5/06
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Quick Facts
Patent No.
US 12,624,128
App. No.
18/092,051
Granted
May 12, 2026
Kind
B2
Abstract

The invention relates to a low molecular weight sulfate chondroitin and a preparation method thereof. A low molecular weight chondroitin sulfate with the average molecular weight of less than 1000 Dalton can be obtained by a production process of chondroitin sulfate lyase degradation, deproteinization, filtration and sterilization and drying using macromolecular sulfate chondroitin as a raw material. The low molecular weight Chondroitin sulfate has a narrow molecular weight distribution range, the ratio of chondroitin sulfate disaccharide is 43˜60% and the ratio of chondroitin sulfate tetrasaccharide is 30˜45%, the sum of chondroitin sulfate disaccharide and chondroitin sulfate tetrasaccharide is more than 87%, the total oligosaccharide content of low molecular weight chondroitin sulfate is more than 97% and the protein content is less than 0.5%; Compared with the general market macromolecule chondroitin sulfate, the product has more remarkable repair effect at the concentration of 50˜100 μg/mL on chondrocytes damaged by 1 mM hydrogen peroxide, with strong repair ability and repair rate of 14%˜23%. The low molecular weight chondroitin sulfate can be used to treat joint injury and is an important raw material for medical products, health care products, cosmetics and food.

Claims (35)

1 . A composition containing 50 mg˜800 mg of low molecular weight chondroitin sulfate, wherein the average molecular weight of the low molecular weight chondroitin sulfate is less than 1000 Dalton, comprising chondroitin sulfate disaccharide and chondroitin sulfate tetrasaccharide as main components, of which the content of chondroitin sulfate tetrasaccharide is about 30%˜about 45% and the sum of chondroitin sulfate disaccharide and chondroitin sulfate tetrasaccharide is more than 87%; and wherein the general formula of the structure of the low molecular weight chondroitin sulfate is shown in the following formula I:

wherein n=0˜5, and n is an integer, R 1 , R 2 , R 3 =—H or —SO 3 Na.

2 . The composition according to claim 1 , wherein the average molecular weight of the low molecular weight chondroitin sulfate is 590˜830 Da.

3 . A method for preparing the composition according to claim 1 , the method comprising:

depolymerizing macromolecular chondroitin sulfate as raw material with chondroitin sulfate lyase through enzymatic depolymerization to obtain a mixture;

obtaining from the mixture a low molecular weight chondroitin sulfate product with the average molecular weight stably controlled to less than 1000 Dalton;

wherein the low molecular weight chondroitin sulfate comprising chondroitin sulfate disaccharide and chondroitin sulfate tetrasaccharide as main components, of which the content of chondroitin sulfate tetrasaccharide is about 30%˜about 45% and the sum of chondroitin sulfate disaccharide and chondroitin sulfate tetrasaccharide is more than 87%; and wherein the general formula of the structure of the low molecular weight chondroitin sulfate is shown in the following formula I:

wherein n=0˜5, and n is an integer, R 1 , R 2 , R 3 =—H or —SO 3 Na.

4 . The method for preparing the composition according to claim 3 , wherein the chondroitin sulfate lyase is obtained by the following steps:

screening and identifying the chondroitin sulfate lyase from: soil samples, sewage or silt from coastal areas, river banks, farmers' markets, slaughterhouses and dining halls, and

expressing the chondroitin sulfate lyase in Escherichia coli or Bacillus subtilis.

5 . The method for preparing the composition according to claim 3 , wherein the macromolecule chondroitin sulfate as raw material is derived from the cartilaginous tissue of terrestrial and marine animals selected from one or more of chicken cartilage, pig cartilage, bovine cartilage or shark bone.

6 . The method for preparing the composition according to claim 5 , wherein the macromolecule chondroitin sulfate as raw material is derived from shark bone.

7 . The method for preparing the composition according to claim 3 , wherein the addition amount of the chondroitin sulfate lyase relative to fermentation broth per liter is about 100˜300 U/L.

8 . The method for preparing the composition according to claim 3 , wherein the concentration of the macromolecule chondroitin sulfate as raw material is about 100˜700 g/L.

9 . The method for preparing the composition according to claim 3 , wherein the time of enzymatic depolymerization is about 6˜40 h.

10 . The method for preparing the composition according to claim 3 , wherein the temperature of enzymatic depolymerization is about 25˜35° C.

11 . The method for preparing the composition according to claim 3 , wherein the pH of the enzymatic depolymerization is about 6.5˜8.5.

12 . The method for preparing the composition according to claim 3 , wherein enzymatic protein is removed from the mixture by mixed solvents after enzymolysis reaction in a reaction, in which the volume ratio of the mixture to mixed solvents is 2˜5:1, and the volume ratio of dichloromethane and isopropyl alcohol in the mixed solvents is 3˜5:1; and wherein the reaction is stirred at 100˜500 rpm for 10˜40 min, centrifuged at 3000˜5000 rpm for 10˜30 min, and the top layer of the reaction solution is taken.

13 . The method for preparing the composition according to claim 3 , wherein the enzymatic protein is removed from the mixture after enzymolysis reaction by ultrafiltration to obtain reaction solution.

14 . The method for preparing the composition according to claim 12 , wherein the upper reaction solution is filtered and sterilized through a 0.22 μm capsule filter after removing the enzymatic protein, and then the reaction solution is added into 8˜12 times volume of anhydrous ethanol for precipitation and dried in vacuum.

15 . The method for preparing the composition of according to claim 13 , wherein the reaction solution is filtered and sterilized through a 0.22 μm capsule filter after removing the enzymatic protein and then dried in spray.

16 . The composition according to claim 1 , wherein compared with the macromolecule chondroitin sulfate from shark bone, the low molecular weight chondroitin sulfate obtained by enzymatic depolymerization from one or more of shark bone and chicken cartilage has the repair rate is 14%˜23% at the concentration of 50-100 μg/mL on chondrocytes damaged by 1 mM hydrogen peroxide; or the low molecular weight chondroitin sulfate with specific content range of disaccharide and tetrasaccharide mentioned in claim 1 in the concentration range of 50˜1600 μg/mL repair chondrocytes damaged by 1 mM hydrogen peroxide, and the repair rate is 20%˜62.4%.

17 . The composition containing the low molecular weight chondroitin sulfate according to claim 1 , wherein the composition contains glucosamine.

18 . The composition containing the low molecular weight chondroitin sulfate according to claim 17 , wherein the glucosamine is glucosamine hydrochloride, glucosamine sulfate or a mixture thereof.

19 . The composition containing the low molecular weight chondroitin sulfate according to claim 1 , wherein the hydrolyzed chondroitin sulfate is a mixture of hydrolyzed chondroitin sulfate with various molecular weights.

20 . The composition containing the low molecular weight chondroitin sulfate according to claim 1 , wherein the composition comprises pharmaceutically acceptable excipients selected from fillers, disintegrants, adhesives, odorants, lubricants and film coating agents.

21 . The composition containing the low molecular weight chondroitin sulfate according to claim 20 , wherein the fillers are selected from microcrystalline cellulose, starch, dextrin, mannitol, and lactose; wherein the disintegrants are selected from crospovidone, croscarmellose sodium, carboxymethyl starch sodium, hydroxypropyl starch, pregelatinized starch, low substituted hydroxypropyl cellulose, sodium bicarbonate, citric acid, and tartaric acid; wherein the adhesives are selected from carboxymethylcellulose sodium, hydroxypropyl cellulose, methyl cellulose, ethyl cellulose, hydroxypropyl methyl cellulose, and polyvinylpyrrolidone; wherein the lubricants are selected from magnesium stearate, colloidal silicon dioxide, talc, hydrogenated vegetable oil, polyethylene glycol, and stearic acid; and wherein the film coating agents are selected from hydroxypropyl methyl cellulose, polyethylene glycol and colour lake.

22 . The composition containing the low molecular weight chondroitin sulfate according to claim 1 , wherein the composition is in the dosage forms selected from tablets, granules, capsules and pills.

23 . A method of reducing joint inflammation, relieving pain and/or relieving and treating osteoporosis in an administration target, wherein the method comprising administering to an administration target in need thereof a therapeutically effective amount of the composition containing low molecular weight chondroitin sulfate according to claim 1 .

24 . A method according to claims 23 wherein the method for reducing joint inflammation by declining the level of inflammatory cytokines or complement in serum or reducing the pathological score upon safranin O-fast green staining, wherein the inflammatory cytokines is one of the following: IL-6, IL-1β or TNF-α; wherein the complement is C5b-9.

25 . A method according to claims 23 , wherein the method for reducing joint inflammation by improving the level of bone hydroxyprolinic acid in femur.

26 . A method according to claims 23 , wherein the method for relieving and treating osteoporosis by improving the level one of the following: bone weight coefficient, bone density, ash level, bone phosphorus, serum alkaline phosphatase, bone morphogenetic protein, calcitonin, femoral trabecula area, percentage of trabecula area or number of trabeculae or by reducing the level of parathyroid hormone.

27 . A method according to claims 23 , wherein said composition is administrated in the dosage forms of tablets, granules, capsules or pills.

28 . A method according to claims 23 , wherein said composition is administered once daily or twice daily.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 20, 2023
From: ZHANG, HAONING; CHEN, SONG; JIN, BO; XU, YONGGANG; TANG, CHUANGEN
To: NANJING HANXIN PHARMACEUTICAL TECHNOLOGY CO., LTD.
Reel/Frame 062743/0852 →
Priority Claims (3)
WO PCT/CN2019/115120 · Nov 1, 2019 · international
WO PCT/CN2020/079335 · Mar 13, 2020 · international
CN 202011070381.2 · Sep 30, 2020 · national
Continuity (3)
Continuation In Part 17335837 · Jun 1, 2021
Continuation PCTCN2020126003 · Nov 2, 2020
Related Publication 20230250199A1 · Aug 10, 2023
References Cited (36)
US 3405120A · Kawano et al. · 1968 [cited by applicant]
US 5344451A · Dayton · 1994 [cited by applicant]
US 11572421B2 · Zhang et al. · 2023 [cited by applicant]
US 20150152198A1 · Miraglia et al. · 2015 [cited by applicant]
CN 1513471A · 2004 [cited by applicant]
CN 1262277C · 2006 [cited by applicant]
CN 101057862A · 2007 [cited by applicant]
CN 101658482A · 2010 [cited by applicant]
CN 102228466A · 2011 [cited by applicant]
CN 102676613A · 2012 [cited by applicant]
CN 103602711A · 2014 [cited by applicant]
CN 103602771A · 2014 [cited by applicant]
CN 103623006A · 2014 [cited by applicant]
CN 104411363A · 2015 [cited by applicant]
CN 108070627A · 2018 [cited by applicant]
CN 108979627A · 2018 [cited by applicant]
CN 109913437A · 2019 [cited by applicant]
JP 2000273102A · 2000 [cited by applicant]
JP 3278629B2 · 2002 [cited by applicant]
JP 2002262900A · 2002 [cited by applicant]
JP 2003339393A · 2003 [cited by applicant]
JP 2010260846A · 2010 [cited by applicant]
JP 201168605A · 2011 [cited by applicant]
JP 5262783B2 · 2013 [cited by applicant]
JP 5341411B2 · 2013 [cited by applicant]
KR 20060100894A · 2006 [cited by applicant]
WO 2013174847A1 · 2013 [cited by applicant]
Uebelhart et al., Osteoarthritis and Cartilage, 1998, 6(Supplement A), p. 39-46. (Year: 1998). [cited by examiner]
U.S. Appl. No. 17/335,837, filed Jun. 1, 2021, U.S. Pat. No. 11,572,421, Issued. [cited by applicant]
Zhang et al., “Chondroitin Sulfate Oligosaccharides Prepared by Chondroitinase and its Antioxidant Activities,” Science and Technology Food Industry, 20178, 38(13):48-52 (7 pages with English Abstract). [cited by applicant]
PCT International Search Report for PCT Application No. PCT/CN2020/079335 mailed Dec. 14, 2020 (4 pages). [cited by applicant]
Extended European Search Report dated 14.12.2023 for EP Application No. 20882136.3 (56 pages). [cited by applicant]
Akio Hamai, et al., “Two Distinct Chondroitin Sulfate ABC Lyases: An Endoeliminase Yielding Tetrasaccharides and an Exoeliminase Preferentially Acting on Ogligosaccharides”, The Journal of Biological Chemistry, 1997, 27… [cited by applicant]
Lian Li, et al., “Preparation of Low Molecular Weight Chondroitin Sulfates, Screening of a High Anti-Complement Capacity of Low Molecular Weight Chrondroitin Sulfate and Its Biological Activity Studies in Attenuating Os… [cited by applicant]
First Office Action of the corresponding Russian Application No. 2022112645/04(026349) dated Feb. 27, 2024 (11 pages including English Translation). [cited by applicant]
Ju. A. Kuchina et al., “Properties of of chondroitin sulfate from marine aquatic organisms.” X All-Russian Scientific Conference and School of Young Scientists “Chemistry and Technology of Plant Substances” (Kazan, 2017… [cited by applicant]