GB1567106A - Creación de Inventos y Patentes con Inteligencia Artificial

GB1567106A – Microbial fractions
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GB1567106A – Microbial fractions
– Google Patents
Microbial fractions

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Publication number
GB1567106A

GB1567106A
GB3219/78A
GB321978A
GB1567106A
GB 1567106 A
GB1567106 A
GB 1567106A
GB 3219/78 A
GB3219/78 A
GB 3219/78A
GB 321978 A
GB321978 A
GB 321978A
GB 1567106 A
GB1567106 A
GB 1567106A
Authority
GB
United Kingdom
Prior art keywords
fraction
lysis
compositions
water
effected
Prior art date
1977-01-27
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

Application number
GB3219/78A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Sanofi Aventis France

Original Assignee
Roussel Uclaf SA
Priority date (The priority date 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 date listed.)
1977-01-27
Filing date
1978-01-26
Publication date
1980-05-08

1978-01-26
Application filed by Roussel Uclaf SA
filed
Critical
Roussel Uclaf SA

1980-05-08
Publication of GB1567106A
publication
Critical
patent/GB1567106A/en

Status
Expired
legal-status
Critical
Current

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Classifications

C—CHEMISTRY; METALLURGY

C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING

C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE

C12P21/00—Preparation of peptides or proteins

C12P21/005—Glycopeptides, glycoproteins

A—HUMAN NECESSITIES

A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE

A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS

A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]

A—HUMAN NECESSITIES

A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE

A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS

A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics

A61P31/04—Antibacterial agents

A—HUMAN NECESSITIES

A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE

A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS

A61P37/00—Drugs for immunological or allergic disorders

A61P37/02—Immunomodulators

A61P37/04—Immunostimulants

C—CHEMISTRY; METALLURGY

C07—ORGANIC CHEMISTRY

C07K—PEPTIDES

C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof

C07K14/195—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria

C07K14/24—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria from Enterobacteriaceae (F), e.g. Citrobacter, Serratia, Proteus, Providencia, Morganella, Yersinia

C07K14/275—Hafnia (G)

A—HUMAN NECESSITIES

A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE

A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES

A61K38/00—Medicinal preparations containing peptides

Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS

Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC

Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS

Y10S435/00—Chemistry: molecular biology and microbiology

Y10S435/8215—Microorganisms

Y10S435/822—Microorganisms using bacteria or actinomycetales

Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC

Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS

Y10S530/00—Chemistry: natural resins or derivatives; peptides or proteins; lignins or reaction products thereof

Y10S530/806—Antigenic peptides or proteins

Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC

Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS

Y10S530/00—Chemistry: natural resins or derivatives; peptides or proteins; lignins or reaction products thereof

Y10S530/82—Proteins from microorganisms

Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC

Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS

Y10S530/00—Chemistry: natural resins or derivatives; peptides or proteins; lignins or reaction products thereof

Y10S530/82—Proteins from microorganisms

Y10S530/825—Bacteria

Description

PATENT SPECIFICATION
( 21) Application No 3219/78 ( 22) Filed 26 Jan 1978 ( 31) Convention Application No 7702267 ( 32) Filed 27 Jan 1977 in ( 33) France (FR) ( 44) Complete Specification published 8 May 1980 ( 51) INT CL 3 C 07 C 7/00 ( 52) Index at acceptance C 3 H C 2 ( 11) 1 567 106 ( 19) ( 54) MICROBIAL FRACTIONS ( 71) We, ROUSSEL UCLAF, a French Body Corporate of 35 Boulevard des Invalides, Paris 7 eme, France, do hereby declare the invention for which we pray that a patent may be granted to us, and the method by which it is to be performed, to be particularly described in and by the
following statement:-
This invention relates to new watersoluble glycoprotein fractions derived from Hafnia, to processes for their preparation and to pharmaceutical compositions containing them.
Numerous preparations derived from lysed microbial substances have been described in the literature, see, for example, French Special Medicament Patent Specification Nos 5 488 M (Canadian
Patents and Development Limited), 6 495 M (Institut de Recherches Scientifiques) and 6 513 M (Institut de Recherches Scientifiques).
These microbial lysates, either alone or in association with an antibiotic, serve to initiate a quick immunisation reaction or to increase the defences of the body system against microbial attack These lysates come, in general, from a definite microbial species and bring about immunisation which is more specific than general They have the disadvantage of being generally allergenic and thus their repeated use cannot be recommended.
In French Patent Specification No.
2,043,475 there is described a glycoprotein fraction derived from one or more saprophytes or pathogenic strains and possessing an immunising capacity and a certain amount of anti-inflammatory activity.
The present invention is based on the discovery that certain glycoprotein fractions derived from Hafnia exhibit interesting pharmacological activity and in particular, in general, anti-inflammatory and immunostimulant activity as well as good tolerance levels.
Thus, according to one feature of the present invention, we provide a watersoluble glycoprotein fraction derived from lysed Hafnia, said fraction having an apparent molecular weight greater than or equal to 300,000.
The term «apparent molecular weight» as used herein refers to the molecular weight as determined by means of a porous gel standardised with known macromolecular solutions Such standarised porous gels include, for example, «Sepharose» (registered Trade Mark) gels and expecially the «Sepharose» 6 B gels.
In general the fractions according to the invention will have an apparent molecular weight greater than or equal to 1 million.
Preferred fractions are those containing substantialy no diaminopimelic acid, the absence of diaminopimelic acid being indicative of a non-membranous origin.
Especially preferred are fractions containing from 40 to 50 %/ of proteins having biuretogenic activity and from 25 to % of neutral monosaccharides, e g.
hexoses such as glucose, galactose or mannose, said fraction further having ultraviolet absorption maxima at about 215 and 260 mu An ultra-violet absorption maximum at about 215 mutis characteristic of the peptide bond whilst a weaker absorption maximum at about 260 mui is characteristic of the nucleic acids and of proteins.
Proteins having biuretogenic acitivity are defined herein as proteins giving the coloured biuret reaction (characteristic of peptidic bonds).
Particular glycoprotein fractions according to the invention which may be mentioned are those derived from the Hafnia strain desposited at the Institut Pasteur in Paris under No 5 731.
Thus Hafnia strain, which is an enterobacterium mobile at 22 C but only slightly mobile at 37 C, has the following characteristics:
Glucose Mannose Rhamnose Arabinose Sorbitol Saccharose + + 95 variable p O 5 P-4 k_ 1,567,106 Raffinose Urease Indole Lysine decarboxylase + Ornithine decarboxylase + Arginine d.
hydrolase Gelatine I 370 C Citrate l 48 hours at 22 C + Particularly preferred glycoprotein fraetions according to the invention are in the form of a slightly beige-coloured, odourless, neutral powder which is soluble in water up to a concentration of 25 mg/ml but substantially insoluble in solvents such as ethanol, methanol, acetone, ether and benzene The fractions according to the invention may also be in the form of a solution in water.
The infra-red absorption spectrum, as well as an ultra-violet absorption as mentioned above, confirm the partial peptidic nature of the fractions according to the invention.
Further confirmation is provided by the positive reaction of the fractions according to the invention to the biuret Lowry and ninhydrin reactions, all characteristic of peptidic bonds The fractions according to the invention also give a positive results in sugar characterisation reactions, for example reaction with orcinol and with carbazole.
The glycoprotein fractions according to the invention has proved to be nonodialysable, pharmacologically heatstable ( 1 hour at 105 C) and p H stable (p H 3 and p H 10, 15 hours at + 4 C), as well as resistant to the action of proteolytic enzymes such as pronase ( 24 hours at + 37 C).
The glycoprotein fractions according to the invention, may be prepared, for example, by cultivating a microbial Hafnia strain on or in a suitable culture medium therefor; harvesting the fully developed microbial substances thereby obtained and subjecting them to lysis; extracting the lysate thus obtained with one or more organic solvents; subjecting the extraction product thus obtained, in aqueous solution, to diafiltration through a porous membrane having a retention threshold for molecules having a molecular weight greater than or equal to 300,000, and if desired lyophilising the solution thus obtained.
According to a preferred embodiment, the microbial strains are cultivated in a liquid culture medium under aerobic conditions Any culture media suitable for such strains may, be used Such media may, for example, contain meat extracts, casein peptone, soya papainic peptone, yeast autolysates, sugars, mineral elements and/or distilled water.
Lysis of the harvested microbial substances may be effected enzymatically, physically and/or chemically, enzymatic lysis being preferred.
Enzymatic lysis is preferably effected by means of an enzyme such as lysozyme, trypsin, pronase, papain and/or achymotrypsin, the use of lysozyme being particularly preferred Physical lysis is preferably effected by means of ultrasonics, penetrating radiation and/or heating whilst chemical lysis is preferably effected by means of a surface-active agents, e g.
polyethylene glycol sorbate, an organomercury antiseptic, e g sodium mercurothiolate and/or mineral or organic acid, e g trichloracetic acid By whatever method it is carried out, lysis is preferably effected over a period of from 7 to 60 days.
If desired the lysate obtained may be lyophilized before the extraction with one or more organic solvents.
The lysate, according to a preferred embodiment, is extracted with two organic solvents, most preferably acetone and methanol used sequentially The purpose of the extraction is to eliminte lipids and pigments and, to this end, the extraction should be carried out by agitating the lysate vigorously with the organic solvent for several hours.
Diafiltration of the extraction product, in aqueous solution, may be carried out according to conventional methods The porous membrane is preferably the membrane XM 300 sold by the companies Romicon and Amicon (Amicon Corporation, Lexington, Massachusetts 0 2713, U S A) If desired, the porous membrane may be in the form of hollow fibres and a particular membrane of this type which may be mentioned is that sold under the name HIP 100 by the aforementioned Amicon.
According to a further embodiment of the present invention the extraction product, in aqueous solution, may be subjected to a preliminary diafiltration through a porous membrane having a retention threshold for molecules having a molecular weight which is less than 300,000, for example about 100,000 e g the membrane sold under the name XM 100 by Amicon, before diafiltration through the porous membrane having a retention threshold for molecules greater than or equal to 300,000.
The retentate is isolated generally in the form of an aqueous solution which may, if desired, by lyophilised.
As mentioned above, the glycoprotein fractions according to the invention possess intersting pharmacological activity Those fractions which we have tested show not only remarkable anti-inflammatory and immunostimulant properties, but also good tolerance levels Such fractions are thus useful, for example, in the treatment of inflammations of the skin and mucous membranes; as anti-pruriginous agents in dermatology, oto-rhino-laryngology, ophthalmology, proctology and gynaecology; and in the treatment of chronic or acute intestinal infections such as colon bacillus infections; toxin infections of the alimentary tract caused by Salmonella and by enterotoxic staphyloccoci; dysenteric syndromes of microbial origin such as shigelloses; candidoses of the digestive tract; and urinary infections caused by Proteus and by Pseudomonas.
According to a yet further feature of the present invention there are provided pharmaceutical compositions comprising, as active ingredient, a water-soluble glycoprotein fraction as hereinbefore defined in association with a pharmaceutical carrier or excipient.
For pharmaceutical administration the glycoprotein fractions according to the invention may be incorporated into the conventional pharmaceutical preparations in either solid or liquid form, optionally in combination with other active ingredients.
The compositions may, for example, be presented in a form suitable for oral, rectal or parenteral (including topical and vaginal) administration Preferred forms include, for example, tablets, coated tablets, gelatin, granules, suppositories, syrups, ovules, creams, ointments, lotions and solutions e g.
for injection, drops or eye washes.
The active ingredient may be incorporated in excipients customarily employed in pharmaceutical compositions such as, for example, talc, gum arabic, lactose, starch, magnesium stearate, cocoa butter, aqueous or non-aqueous vehicles, fatty substances of animal or vegetable origin, paraffin derivatives, glycols, various wetting, dispersing or emulsifying agents and/or preservatives.
Advantageously the compositions may be formulated as dosage units, each unit being adapted to supply a fixed dose of active ingredient Suitable dosage units for adults contain from 1 to 15, preferably from 2 to 10 mg of active ingredient The oral daily dosage, which may be varied according to the compound used, the subject treatment and the complaint concerned, may, for example, be from 0 5 to 20 mg per day in adults.
The following non-limiting examples serve to illustrate the present invention.
Example 1:
Stage A: culture A culture medium is prepared corresponding to the following formulation:
meat extract sodium chloride casein peptone yeast autolysate dipotassium phosphate monopotassium phosphate glucose soya papainic peptone distilled water q s v.
690 g 690 g 690 g 690 g 483 g 207 g 4104 g 2760 g 138 litres A culture medium is prepared by mixing successively the meat extract, the sodium chloride, the casein peptone, the yeast autolysate, the dipotassium phosphate and the monopotassium phosphate in about 20 litres of distilled water The p H of the medium obtained is adjusted to about 7 and then the medium is sterilised at 120 C for 40 minutes The solutions of glucose and of soya papainic peptone are introduced into the sterilised culture medium at the moment of inoculation, themselves having been previously sterilised.
The Hafnia strain (Institut Pasteur No 5 731) cultivated on medium containing agar, is inolculated into 50 cm 3 of the culture medium This solution, serving as the inoculum is introduced into the remainder of the culture broth The total volume of the culture medium is adjusted to 138 litres by the addition of sterile distilled water.
The culture medium is subsequently maintained at 37 C and the p H is adjusted automatically to 7 (by the addition of the solution of ammonia or by the addition of a solution of hydrochloric acid).
The growth of the micro-organisms is estimated with a photometer; the number of micro-organisms is calculated as a function of the observed optical density by comparison with a standard curve.
After complete development, that is after about 7 hours, the medium contains about 1 thousand million micro-organisms per cm 3.
Stage B: lysis To the 138 litres of culture broth obtained in Stage A above is added an aqueous solution of lysozyme hydrochloride (sterilised by filtration on a 0 22,u millipore membrane), so as to give a final concentration of 160 y of lysozyme hydrochloride per cm 3 of culture medium.
The broth and solution are left in contact for one hour at 560 C in the presence of 0.25 g of EDTA per litre of broth, 862 5 g of sodium mercurothiolate and 80 g of polysorbate (sold under the name of Tween» lregistered Trade Markl 80) per litre 3 1,567,106 1,567,106 of culture broth Lysis is then continued for 7 days at 37 C under sterile conditions.
The lysate is then isolated, homogenised by agitation and lyophilised.
7,900 g of a brown powder are obtained.
Analyses:
-C/O 37 9 -H% 6 -N% 7 5 Stage C: treatment a) With acetone All of the powder obtained in Stage B above is suspended in 138 litres of cold acetone, then agitated vigorously for 3 hours at 3,500 revolutions per minute.
After 3 hours the resultant suspension is filtered on fritted glass A yellow powder is recovered which is vacuum-filtered quickly.
b) With methanol The powder obtained above ( 7,295 g) is suspended in 138 litres of cold methanol and agitated vigorously for 3 hours at 1,500 revolutions per minute After 3 hours the resultant suspension is decanted off, the major part of the supernatant liquid is siphoned off and the remainder of the solution is filtered on fritted glass.
The vacuum-filtered powder is dried at ambient temperature under vacuum for 24 hours 3,988 g of a pale beige powder are obtained.
Stage D: diafiltration 6 times 600 g of the powder obtained in Stage C above are dissolved in 6 times 10 litres of distilled water containing I g/l of mercurothiolate The solution obtained is maintained under agitation at + 4 C for 24 hours then centrifuged for 2 hours at 4,000 revolutions per minute, then at 90,000 g in a continuous centrifuge with an output of 6 1/hour The solution thus obtained is made up to 10 litres with filtered distilled water (through a 0 22 u millipore membrane) and introduced into a diafiltration apparatus provided with porous membranes of which the retention threshold is at 300,000 and the apparent diameter of the pores is approximately 2 A (membranes sold by the company Amicon or by the company Romicon under the name XM 300.
volumes of distilled water, that is a volume of 500 litres, are circulated in the apparatus The duration of the operation is about 48 hours.
The diafiltered solution is recovered then centrifuged continuously at 90,000 g with an output of 6 litres/hour.
9.5 litres of a solution are obtained which is then lyophilised.
Finally 105 g of glycoprotein are obtained in the form of a beige-white, woolly and very hygroscopic powder.
Contents of:
-water -phosphorus -chlorine -proteins -sugars Spectra U V:
9 % 0.01 % 0 % -biuret 51 % -orcinol 29 % (neutral hexoses) -carbazole 1 5 % (uronic acids) -a maximum at 216 my -a maximum at 258 my I.R: confirms the partial peptidic nature of the products.
Hydrolysis with 6 N hydrochloric acid at C for 24 hours of the glycoprotein fraction obtained above, followed by chromatography on a layer of cellulose with one of the following solvent systems: nbutanol/acetic acid/water, ( 60:30:30), isopropanol/ammonia ( 2/3:1/3) or methanol/pyridine/acetic acid/water ( 18:50:4:28), shows the absence of diaminopimelic acid in these hydrolysates.
This absence of diaminopimelic acid in the hydrolysates indicates the nonmembranous origin of the glycoproteins obtained according to the invention.
Study of the change in optical density at 280 mtn of the eluate of chromatography on Sepharose 6 B of the glycoprotein fraction obtained in Example 1 as a function of the Ve/Vo shows that the proteins of the fraction have a molecular weight greater than 1 million.
(The Vo corresponds to the volume of elution of a dextran of molecular weight greater than 1 million, totally retained on Sepharose 6 B of which the molecular weight retention limit is I million.
The Ve corresponds to the volume of elution of the Hafnia glycoprotein fraction obtained) Example 2:
Operating as in Stages A and B of Example 1 90 litres of lysate are prepared which are then lyophilised 4,750 g of a brownish yellow powder are obtained.
Stage C: treatment a) With acetone The powder obtained above is extracted 1,567,106 by means of 90 litres of cold acetone as indicated in Stage C a) of Example 1.
b) With methanol The product obtained above is extracted by means of 90 litres of cold methanol as indicated in Stage C b) of Example 1 The product obtained is dried cold under vacuum 1,765 g of a beige powder are obtained.
Stage D: diafiltration 600 g of the powder in Stage C above are suspended in 15 litres of distilled water The suspension obtained is agitated at + 40 C for hours, then centrifuged at 4,000 revolutions per minute for 2 hours and then continuously at 90,000 g with an output of 6 litres/hour 14 litres of solution are obtained which are introduced into a diafiltration apparatus provided with porous membranes of which the retention threshold is at 300,000 and of which the apparent diameter of the pores is approximately 2 A (membranes sold by the company Amicon or by the company Romicon under the name XM 300) The 14 litres of solution are washed with 40 volumes of distilled water.
The duration of the operation is about 48 hours.
The final solution is centrifuged at 90,000 g, then lyophilised 55 6 g of a beige-white, woolly and very hygroscopic powder are obtained.
Analyses -C% 40 3 -H% 6 -N% 8 3 Content of:
-water 10 % -phosphorous 0 025 % -chlorine 0 / -proteins -biuret 4 11 % -sugars -orcinol 26 % (neutral hexoses).
Spectra U V: maxima at 215 and 257 mpu I R: confirms the partial peptidic nature of the product.
-Absence of diaminopimelic acid.
-Molecular weight on Sepharose 6 B greater than I million.
Example 3:
Compressed tablets were prepared according to the formulation:
glycoprotein fraction obtained in Example 1 5 mg excipient q s for one compressed tablet up to 200 mg (Detail of the excipient: lactose, talc, starch, magnesium stearate).
Example 4:
An ointment was prepared according to the formulation:
glycoprotein fraction obtained in Example 2 200 mg excipient q s v 100 g

Claims (1)

WHAT WE CLAIM IS:-
1 A water-soluble glycoprotein fraction derived from lysed Hafnia, said fraction having an apparent molecular weight greater than or equal to 300,000.
2 A fraction as claimed in claim 1 having an apparent molecular weight greater than or equal to I million.
3 A fraction as claimed in claim I or claim 2 containing substantially no diaminopimelic acid.
4 A fraction as claimed in claim 3 containing from 40 to 50 % of proteins having biuretogenic activity and from 25 to 35 % of neutral monosaccharides, said fraction further having ultra-violet absorption maxima at about 215 and 260 m Au.
A fraction as claimed in any of the preceding claims derived from the Hafnia strain deposited at the Institut Pasteur in Paris under No 5 731.
6 A fraction as claimed in any of the preceding claims in the form of a slightly beige-coloured, odourless, neutral powder which is soluble in water up to a concentration of 25 mg/ml but substantially insoluble in ethanol, methanol, acetone, ether and benzene.
7 A fraction as claimed in any of claims 1 to 6 in the form of a solution in water.
8 A water-soluble glycoprotein fraction as claimed in claim 1 substantially as herein described.
9 A water-soluble glycoprotein fraction substantially as herein described in Example I or Example 2.
A process for the preparation of water-soluble glycoprotein fraction as defined in claim 1 which comprises cultivating a microbial Hafnia strain on or in a suitable culture medium therefor:
harvesting the fully developed microbial substances thereby obtained and subjecting them to lysis; extracting the lysate thus obtained with one or more organic solvents:
subjecting the extraction product thus obtained, in aqueous solution, to diafiltration through a porous membrane having a retention threshold for molecules having a molecular weight greater than or equal to 300,000, and if desired lyophilising the solution thus obtained.
11 A process as claimed in claim 10 wherein the retentate obtained is subsequently lyophilised.
12 A process as claimed in claim 10 or claim 11 wherein the microbial strains are 6 57 O the Hafnia strain deposited at the Institut Pasteur in Paris under No 5 731.
13 A process as claimed in any of claims to 12 wherein the microbial strains are cultivated in a liquid culture medium under aerobic conditions.
14 A process as claimed in any of claims to 13 wherein lysis of the microbial substances is effected enzymatically.
15 A process as claimed in claim 14 wherein lysis is effected by means of lysozyme, trysin, pronase, papain and/or achymotrypsin.
16 A process as claimed in any of claims 10 to 13 wherein lysis of the microbial substances is effected physically.
17 A process as claimed in claim 16 wherein lysis is effected by means of ultrasonics, penetrating radiation and/or heating.
18 A process as claimed in any of claims to 13 wherein lysis of the microbial substances is effected chemically.
19 A process as claimed in claim 18 wherein lysis is effected by means of a surface active agent, organo-mercury antiseptic and/or acid.
A process as claimed in claim 19 wherein lysis is effected by means of polyethylene glycol sorbate, sodium mercurothiolate and/or trichloroacetic acid.
21 A process as claimed in any of claims to 20 wherein lysis of the microbial substances is carried out for from 7 to 60 days.
22 A process as claimed in any of claims to 21 wherein the lysate obtained is lyophilised before extraction with one or more organic solvents.
23 A process as claimed in any of claims to 22 wherein the lysate is extracted with two organic solvents.
24 A process as claimed in claim 23 wherein the lysate is extracted sequentially with acetone and methanol.
A process as claimed in any of claims to 24 wherein the porous membrane is in the form of hollow fibres.
26 A process as claimed in any of claims 10 to 25 wherein the extraction product, in aqueous solution, is subjected to a preliminary diafiltration through a porous membrane having a retention threshold for molecules having a molecular weight which is less than 300,000, before diafiltration through the porous membrane having a retention threshold for molecules greater than or equal to 300,000.
27 A process as claimed in claim 26 wherein the porous membrane having a retention threshold for molecules having a molecular weight which is less than 300,000 has a retention threshold for molecules having a molecular weight of about 100,000.
28 A process for the preparation of a water-soluble glycoprotein fraction as defined in claim 1 substantially as herein described.
29 A process for the preparation of a water-soluble glycoprotein fraction as defined in claim 1 substantially as herein described in Example I or Example 2.
Water-soluble glycoprotein fractions as defined in claim 1 whenever prepared by a process as claimed in any of claims 10 to 29.
31 Pharmaceutical compositions comprising, as active ingredient, a watersoluble glycoprotein fraction as defined in claim I in association with a pharmaceutical carrier on excipient.
32 Compositions as claimed in claim 31 in a form suitable for oral, rectal, topical or parenteral administration.
33 Compositions as claimed in claim 31 or claim 32 in the form of tablets, coated tablets, gelatin caples, granules, suppositories, solutions, ointments, creams, syrups, ovules, lotions and aerosols.
34 Compositions as claimed in any of claims 31 to 33 in the form of dosage units.
Compositions as claimed in claim 34 wherein each dosage unit contains from 1 to mg of active ingredient.
36 Compositions as claimed in claim 35 wherein each dosage unit contains from 2 to mg of active ingredient.
37 Compositions as claimed in any of claims 31 to 36 wherein the active ingredient comprises a compound as claimed in any of claims 2 to 8.
38 compositions as claimed in claim 37 wherein the active ingredient comprises a compound as claimed in claim 5.
39 Compositions as claimed in claim 37 wherein the active ingredient comprises a compound as claimed in claim 6.
Pharmaceutical compositions as claimed in claim 31 substantially as herein described.
41 Pharmaceutical compositions substantially as herein described in Example 3 or Example 4.
For the Applicants, FRANK B DEHN & CO, Chartered Patent Agents, Imperial House, 15-19 Kingsway, London, W C 2.
Printed for Her Majesty’s Stationery Office, by the Courier Press, Leamington Spa, 1980 Published by The Patent Office, 25 Southampton Buildings, London, WC 2 A l AY, from which copies may be obtained.
1,567,106

GB3219/78A
1977-01-27
1978-01-26
Microbial fractions

Expired

GB1567106A
(en)

Applications Claiming Priority (1)

Application Number
Priority Date
Filing Date
Title

FR7702267A

FR2378855A1
(en)

1977-01-27
1977-01-27

NEW GLYCOPROTEINS ISOLATED FROM HAFNIA, METHOD OF PREPARATION AND APPLICATION AS MEDICINAL PRODUCTS

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GB1567106A
true

GB1567106A
(en)

1980-05-08

Family
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Application Number
Title
Priority Date
Filing Date

GB3219/78A
Expired

GB1567106A
(en)

1977-01-27
1978-01-26
Microbial fractions

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US
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US4154821A
(en)

JP
(1)

JPS5396000A
(en)

BE
(1)

BE863359A
(en)

CA
(1)

CA1092041A
(en)

CH
(1)

CH639395A5
(en)

DE
(1)

DE2803001A1
(en)

DK
(1)

DK150497C
(en)

FR
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FR2378855A1
(en)

GB
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GB1567106A
(en)

IE
(1)

IE46195B1
(en)

LU
(1)

LU78953A1
(en)

NL
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NL7801024A
(en)

Cited By (1)

* Cited by examiner, † Cited by third party

Publication number
Priority date
Publication date
Assignee
Title

GB2237740A
(en)

1989-10-17
1991-05-15
Roussel Uclaf
Hair treatment compositions containing glycoprotein extracts of gram (-) bacteria

Families Citing this family (8)

* Cited by examiner, † Cited by third party

Publication number
Priority date
Publication date
Assignee
Title

US4243582A
(en)

1979-04-26
1981-01-06
Monsanto Company
Novel glycoproteins from bovine cartilage

US4313934A
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1979-05-08
1982-02-02
Kirin Beer Kabushiki Kaisha
Physiologically active polysaccharides, production and uses thereof

FR2490496A1
(en)

1980-09-19
1982-03-26
Roussel Uclaf

NEW IMMUNOSTIMULANT GLYCOPROTEINS EXTRACTED FROM KLEBSIELLA PNEUMONIAE, PROCESS FOR OBTAINING THEM, THEIR APPLICATION AS MEDICAMENTS AND COMPOSITIONS COMPRISING THE SAME

FR2490495A1
(en)

1980-09-19
1982-03-26
Roussel Uclaf

NOVEL HYDROSOLUBLE IMMUNOSTIMULANT GLYCOPROTEINS EXTRACTED FROM KLEBSIELLA PNEUMONIAE, PROCESS FOR OBTAINING THEM, USE THEREOF AS MEDICAMENTS AND COMPOSITIONS CONTAINING THEM

FR2523154A1
(en)

1982-03-09
1983-09-16
Fabre Sa Pierre

PROCESS FOR THE PREPARATION OF INTERFERON-INDUCING IMMUNOSTIMULATING PROTEOGLYCANS, PROTEOGLYCANS OBTAINED AND MEDICAMENTS CONTAINING THEM

US4503149A
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1983-06-06
1985-03-05
Conoco Inc.
Method of microbial assay

FR2563431B1
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1984-04-26
1987-03-06
Roussel Uclaf

NEW COSMETIC COMPOSITIONS CONTAINING LYSED EXTRACTS FROM HAFNIA

FR2648351A1
(en)

1989-06-20
1990-12-21
Roussel Uclaf

USE OF GLYCOPROTEIC COMPLEXES EXTRACTED FROM GRAM (-) BACTERIA FOR THE MANUFACTURE OF A MEDICAMENT FOR FACILITATING THE HEALING OF THE SKIN AND PREPARATION METHOD

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James Harrison Stanton
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1971-11-26
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water-soluble immunological adjuvants

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1971-11-19
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Anvar

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1971-12-14
1977-06-28
Kumiai Chemical Industry Co., Ltd.
Process for using cell wall-lysing enzymes

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Lysis of yeast cell walls

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1976-08-24
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1974-05-06
1978-03-24
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1977

1977-01-27
FR
FR7702267A
patent/FR2378855A1/en
active
Granted

1978

1978-01-23
US
US05/871,408
patent/US4154821A/en
not_active
Expired – Lifetime

1978-01-24
DE
DE19782803001
patent/DE2803001A1/en
active
Granted

1978-01-26
DK
DK037578A
patent/DK150497C/en
not_active
IP Right Cessation

1978-01-26
CA
CA295,753A
patent/CA1092041A/en
not_active
Expired

1978-01-26
IE
IE183/78A
patent/IE46195B1/en
not_active
IP Right Cessation

1978-01-26
LU
LU78953A
patent/LU78953A1/en
unknown

1978-01-26
BE
BE184666A
patent/BE863359A/en
not_active
IP Right Cessation

1978-01-26
GB
GB3219/78A
patent/GB1567106A/en
not_active
Expired

1978-01-27
NL
NL7801024A
patent/NL7801024A/en
not_active
Application Discontinuation

1978-01-27
CH
CH93478A
patent/CH639395A5/en
not_active
IP Right Cessation

1978-01-27
JP
JP745178A
patent/JPS5396000A/en
active
Granted

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Publication number
Priority date
Publication date
Assignee
Title

GB2237740A
(en)

1989-10-17
1991-05-15
Roussel Uclaf
Hair treatment compositions containing glycoprotein extracts of gram (-) bacteria

GB2237740B
(en)

1989-10-17
1994-04-13
Roussel Uclaf
Use of compositions containing glycoprotein extracts of gram (-) bacteria for the stimulation of hair growth

Also Published As

Publication number
Publication date

IE780183L
(en)

1978-07-27

DK37578A
(en)

1978-07-28

JPS5396000A
(en)

1978-08-22

FR2378855B1
(en)

1979-05-11

DK150497C
(en)

1987-11-16

LU78953A1
(en)

1978-09-28

DE2803001A1
(en)

1978-08-03

US4154821A
(en)

1979-05-15

CH639395A5
(en)

1983-11-15

NL7801024A
(en)

1978-07-31

DE2803001C2
(en)

1990-07-05

BE863359A
(en)

1978-07-26

IE46195B1
(en)

1983-03-23

FR2378855A1
(en)

1978-08-25

DK150497B
(en)

1987-03-09

CA1092041A
(en)

1980-12-23

JPS6133840B2
(en)

1986-08-04

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