DE202015101782U1 - Synergistic collagen hydrolyzate composition - Google Patents
Synergistic collagen hydrolyzate composition Download PDFInfo
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- DE202015101782U1 DE202015101782U1 DE202015101782.0U DE202015101782U DE202015101782U1 DE 202015101782 U1 DE202015101782 U1 DE 202015101782U1 DE 202015101782 U DE202015101782 U DE 202015101782U DE 202015101782 U1 DE202015101782 U1 DE 202015101782U1
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- 102000008186 Collagen Human genes 0.000 title claims abstract description 39
- 108010035532 Collagen Proteins 0.000 title claims abstract description 39
- 229920001436 collagen Polymers 0.000 title claims abstract description 39
- 239000000203 mixture Substances 0.000 title claims abstract description 33
- 230000002195 synergetic effect Effects 0.000 title description 5
- GHOKWGTUZJEAQD-ZETCQYMHSA-N (D)-(+)-Pantothenic acid Chemical compound OCC(C)(C)[C@@H](O)C(=O)NCCC(O)=O GHOKWGTUZJEAQD-ZETCQYMHSA-N 0.000 claims abstract description 44
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims abstract description 36
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims abstract description 25
- GHOKWGTUZJEAQD-UHFFFAOYSA-N Chick antidermatitis factor Natural products OCC(C)(C)C(O)C(=O)NCCC(O)=O GHOKWGTUZJEAQD-UHFFFAOYSA-N 0.000 claims abstract description 22
- 235000019161 pantothenic acid Nutrition 0.000 claims abstract description 22
- 229940055726 pantothenic acid Drugs 0.000 claims abstract description 22
- 239000011713 pantothenic acid Substances 0.000 claims abstract description 22
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims abstract description 21
- 235000001055 magnesium Nutrition 0.000 claims abstract description 21
- 239000011777 magnesium Substances 0.000 claims abstract description 21
- 229910052749 magnesium Inorganic materials 0.000 claims abstract description 21
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- 229910052725 zinc Inorganic materials 0.000 claims abstract description 21
- ZZZCUOFIHGPKAK-UHFFFAOYSA-N D-erythro-ascorbic acid Natural products OCC1OC(=O)C(O)=C1O ZZZCUOFIHGPKAK-UHFFFAOYSA-N 0.000 claims abstract description 18
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- 235000012239 silicon dioxide Nutrition 0.000 claims abstract description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 32
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- BUHVIAUBTBOHAG-FOYDDCNASA-N (2r,3r,4s,5r)-2-[6-[[2-(3,5-dimethoxyphenyl)-2-(2-methylphenyl)ethyl]amino]purin-9-yl]-5-(hydroxymethyl)oxolane-3,4-diol Chemical compound COC1=CC(OC)=CC(C(CNC=2C=3N=CN(C=3N=CN=2)[C@H]2[C@@H]([C@H](O)[C@@H](CO)O2)O)C=2C(=CC=CC=2)C)=C1 BUHVIAUBTBOHAG-FOYDDCNASA-N 0.000 description 1
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- 235000013619 trace mineral Nutrition 0.000 description 1
- 239000011573 trace mineral Substances 0.000 description 1
- 230000014616 translation Effects 0.000 description 1
- PLSARIKBYIPYPF-UHFFFAOYSA-H trimagnesium dicitrate Chemical compound [Mg+2].[Mg+2].[Mg+2].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O.[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O PLSARIKBYIPYPF-UHFFFAOYSA-H 0.000 description 1
- WGIWBXUNRXCYRA-UHFFFAOYSA-H trizinc;2-hydroxypropane-1,2,3-tricarboxylate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O.[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O WGIWBXUNRXCYRA-UHFFFAOYSA-H 0.000 description 1
- 238000000108 ultra-filtration Methods 0.000 description 1
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- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
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- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
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- A61K31/197—Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid or pantothenic acid
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Abstract
Zusammensetzung, umfassend Kollagenhydrolysat, Vitamin C, Kieselsäure, Magnesium, Pantothensäure und Zink, ggf. jeweils in Form einer physiologisch verträglichen Verbindung, insbesondere zur Erhaltung und/oder Verbesserung des Zustandes der Knochen in Gelenken und/oder des Knorpels und/oder der Bänder und/oder der Sehnen und/oder der Muskeln und Faszien des menschlichen Körpers.Composition comprising collagen hydrolyzate, vitamin C, silicic acid, magnesium, pantothenic acid and zinc, optionally in each case in the form of a physiologically tolerable compound, in particular for maintaining and / or improving the condition of the bones in joints and / or cartilage and / or ligaments and / or the tendons and / or muscles and fascia of the human body.
Description
Die vorliegende Erfindung betrifft eine Zusammensetzung, umfassend Kollagenhydrolysat, Vitamin C, Kieselsäure, Magnesium, Pantothensäure und Zink, ggf. jeweils in Form einer physiologisch verträglichen Verbindung, insbesondere zur Erhaltung und/oder Verbesserung des Zustandes der Knochen in Gelenken und/oder des Knorpels und/oder der Bänder und/oder der Sehnen und/oder der Muskeln und Faszien des menschlichen Körpers.The present invention relates to a composition comprising collagen hydrolyzate, vitamin C, silica, magnesium, pantothenic acid and zinc, optionally in each case in the form of a physiologically tolerable compound, in particular for maintaining and / or improving the condition of the bones in joints and / or cartilage and / or the ligaments and / or the tendons and / or the muscles and fascia of the human body.
Insbesondere kann die erfindungsgemäße Zusammensetzung ein Arzneimittel, ein diätetisches Lebensmittel, eine ergänzende bilanzierte Diät, ein Nahrungsergänzungsmittel, ein Nahrungsmittelzusatzstoff, ein speziell auf die Bedürfnisse von Sportlern ausgerichtetes Lebensmittel oder Nahrungsergänzungsmittel, oder ein funktionelles Nahrungsmittel sein.In particular, the composition according to the invention may be a pharmaceutical, a dietary supplement, a supplemented balanced diet, a dietary supplement, a food additive, a food or dietary supplement specially adapted to the needs of athletes, or a functional food.
Der Bewegungsapparat des menschlichen Körpers ist im Laufe des Lebens den unterschiedlichsten Anforderungen ausgesetzt. Gerade degenerative Veränderungen des menschlichen Bewegungsapparates und damit an Knochen in Gelenken, Knorpelgewebe, Bändern, Muskeln, Sehnen und Faszien sind in der Bevölkerung weit verbreitet. Die Ursachen hierfür sind unterschiedlich und können insbesondere in einer biologischen Prädisposition, mechanischer Überlastung, entzündlichen Veränderungen, Stoffwechselstörungen und Alterungsprozessen liegen.The musculoskeletal system of the human body is exposed to the most varied demands in the course of life. Especially degenerative changes of the human musculoskeletal system and thus of bones in joints, cartilage, ligaments, muscles, tendons and fascia are widespread in the population. The causes for this are different and may be in particular in a biological predisposition, mechanical overload, inflammatory changes, metabolic disorders and aging processes.
Es ist seit längerem bekannt, degenerative Veränderungen an Gelenken durch die orale Gabe von Kollagenhydrolysat zu behandeln (vgl.
Bekannt ist zudem, dass Vitamin C ein essentieller Begleiter des Kollagenhydrolysats ist, da es für den Aufbau des Kollagens im Körper erforderlich ist und zudem antioxidativ wirkt.It is also known that vitamin C is an essential companion of the collagen hydrolyzate, as it is required for building collagen in the body and also has an antioxidant effect.
Kieselsäure ist für viele Prozesse im Körper essentiell und dient vor allem der Stärkung von Knorpel, Sehnen und Bändern. Aber auch das Bindegewebe mit den Faszien und die Muskeln bedürfen einer ausreichenden Zufuhr von Kieselsäure. Die Knochenmasse und Knochendichte wird über die Knochenregeneration gesteuert, die durch Kieselsäure gesteigert wird (
Bekannt ist ebenfalls, dass Magnesium wichtig ist für die Energiestoffwechseleffizienz und die Proteinsynthese. Es ist ein wichtiges Strukturelement der Enzyme des Energiestoffwechsels im Körper. Als Elektrolyt dient es der Muskelentspannung und der Muskelregeneration. Magnesium trägt zu einem normalen Energiestoffwechsel, anhaltender Muskelleistung und einer Regeneration des gesamten Skelettapparats einschließlich der Knochen und des Knorpels bei. Dieses Mineral wird vor allem für die Aufnahme und Verwertung der Glucose als wichtigstem Energieträger benötigt (
Pantothensäure spielt eine entscheidende Rolle in der Regulation des Energiestoffwechsels. Das Vitamin steuert alle Auf- und Abbauvorgänge des Kohlenhydrat-, Fett- und Aminosäurestoffwechsels. Pantothensäure trägt damit zu einer Verminderung von Müdigkeit und Ermüdung auch und gerade bei sportlicher Aktivität bei; ein erhöhter Bedarf an diesem Vitamin beim Sport ist bekannt (
Zink wirkt vor allem als Antioxidans schützend bei körperlicher Belastung mit Bildung von freien Radikalen und andere reaktiven Verbindungen (
Der Erfindung liegt die Aufgabe zugrunde, eine synergistische Zusammensetzung mit Kollagenhydrolysat zur Erhaltung und/oder Verbesserung des Zustandes der Knochen in Gelenken und/oder des Knorpels und/oder der Bänder und/oder der Sehnen und/oder der Muskeln und Faszien des menschlichen Körpers mit einer verbesserten Wirksamkeit zur Verfügung zu stellen.The invention has for its object to provide a synergistic composition with collagen hydrolyzate for maintaining and / or improving the condition of the bones in joints and / or cartilage and / or ligaments and / or tendons and / or muscles and fasciae of the human body to provide improved efficacy.
Diese Aufgabe wird erfindungsgemäß gelöst durch eine Zusammensetzung, umfassend Kollagenhydrolysat, Vitamin C, Kieselsäure, Magnesium, Pantothensäure und Zink, ggf. jeweils in Form einer physiologisch verträglichen Verbindung. This object is achieved according to the invention by a composition comprising collagen hydrolyzate, vitamin C, silica, magnesium, pantothenic acid and zinc, if appropriate in each case in the form of a physiologically tolerable compound.
Es wurde überraschenderweise gefunden, dass die Wirkung von Kollagenhydrolysat auf die Kollagensynthese durch eine Kombination mit Vitamin C, Kieselsäure, Magnesium, Zink und Pantothensäure aufgrund der dadurch gesteigerten Energiestoffwechseleffizienz erheblich gesteigert werden kann. Dies gilt insbesondere auch in Belastungssituationen. Diese Wirkung beruht auf dem synergistischen Effekt der in der Zusammensetzung kombinierten Bestandteile und konnte für die Bestandteile der erfindungsgemäßen Zusammensetzung jeweils alleine so nicht beobachtet werden.It has surprisingly been found that the effect of collagen hydrolyzate on collagen synthesis by combination with vitamin C, silicic acid, magnesium, zinc and pantothenic acid can be significantly increased due to the increased energy metabolism efficiency. This is especially true in stress situations. This effect is based on the synergistic effect of the components combined in the composition and could not be observed alone for the constituents of the composition according to the invention in each case.
Überraschenderweise wurde weiter gefunden, dass die erfindungsgemäße Zusammensetzung insbesondere in der Lage ist, nachlassender körperlicher Belastbarkeit, insbesondere degenerativen Veränderungen am Bewegungsapparat, insbesondere in den Gelenken einschließlich Knochen, Knorpel, Sehnen, Muskeln, Bändern und Faszien effektiv entgegenzuwirken. So kann gerade Fehlbelastungen und Überbelastungen im Rahmen von körperlicher Aktivität wie Sport durch die verbesserte Kolllagensynthese effektiv entgegen gewirkt werden. Zudem hat sich gezeigt, dass die synergistische Wirkung der erfindungsgemäßen Zusammensetzung einen positiven Einfluss auf die die Belastbarkeit, Elastizität und Beweglichkeit von Bindegewebe, Muskeln, Bändern und Sehnen hat. Auch die Struktur, Elastizität und Beweglichkeit der Faszien wird durch die erfindungsgemäße Zusammensetzung deutlich verbessert. Surprisingly, it has also been found that the composition according to the invention is in particular capable of effectively counteracting decreasing exercise capacity, in particular degenerative changes to the musculoskeletal system, in particular in the joints including bones, cartilage, tendons, muscles, ligaments and fascia. Thus, it is possible to effectively counterbalance inappropriate loading and overloading in the context of physical activity, such as exercise, through improved collagen synthesis. In addition, it has been found that the synergistic effect of the composition according to the invention has a positive influence on the resilience, elasticity and mobility of connective tissue, muscles, ligaments and tendons. The structure, elasticity and mobility of the fascia is also significantly improved by the composition according to the invention.
Das erfindungsgemäße Kollagenhydrolysat ist wasserlöslich und entspricht vorzugsweise dem in der
Das im Rahmen der vorliegenden Erfindung verwendete Kollagenhydrolysat geliert aufgrund eines ausreichend geringen Molekulargewichts unter den Bedingungen des Standard-Bloomtests nicht mehr, weist also eine Gelstärke von 0 g Bloom auf. Vorzugsweise ist das Kollagenhydrolysat durch enzymatische Hydrolyse von Kollagen des Typs I und/oder des Typs II gewonnen. Es hat sich gezeigt, dass der stimulierende Effekt auf die Biosynthese der extrazellulären Matrix des Knorpelgewebes (welches überwiegend aus Kollagen des Typs II besteht) im Wesentlichen unabhängig ist vom Typ des Kollagenhydrolysats, was darauf hindeutet, dass die Peptidfragmente in Kollagenhydrolysat des Typs I und des Typs II die gleiche oder eine ähnliche Struktur aufweisen. The collagen hydrolyzate used in the context of the present invention no longer gels due to a sufficiently low molecular weight under the conditions of the standard Bloom test, and therefore has a gel strength of 0 g Bloom. Preferably, the collagen hydrolyzate is obtained by enzymatic hydrolysis of Type I and / or Type II collagen. It has been found that the stimulating effect on the extracellular matrix biosynthesis of cartilaginous tissue (which consists predominantly of type II collagen) is essentially independent of the type of collagen hydrolyzate, suggesting that the peptide fragments are present in type I and II collagen hydrolyzate Type II have the same or a similar structure.
Für die Herstellung von Kollagenhydrolysat eignen sich insbesondere Knochen, Haut, Bindegewebe (jeweils Typ I) oder Knorpel (Typ II) verschiedener Wirbeltiere, geeignet sind insbesondere Rinderknochen, Rinderspalt, Schweineschwarte, Geflügel und Fische. Das Herstellungsverfahren für das Kollagenhydrolysat kann dabei sowohl von nativem Kollagen ausgehen als auch von Gelatine, also extrahiertem und denaturiertem Kollagen. Bone, skin, connective tissue (in each case type I) or cartilage (type II) of various vertebrates are particularly suitable for the production of collagen hydrolyzate; bovine bone, bovine cleft, pork rind, poultry and fish are particularly suitable. The production process for the collagen hydrolyzate can be based on both native collagen and gelatin, ie extracted and denatured collagen.
Das Kollagenhydrolysat in der erfindungsgemäßen Zusammensetzung weist bevorzugt ein mittleres Molekulargewicht von ca. 0,3 kDa bis ca. 30 kDa auf, insbesondere von ca. 2 kDa bis ca. 10 kDa, besonders bevorzugt von ca 3 kDa. Die Molekulargewichtsverteilung des Kollagenhydrolysats kann durch die Auswahl geeigneter proteolytischer Enzyme (meist bakterielle Proteasen) gesteuert werden. Zusätzlich können gegebenenfalls einzelne Molekulargewichtsfraktionen des Hydrolysats durch Ultrafiltration oder chromatographische Verfahren abgetrennt werden. Das erfindungsgemäße Kollagenhydrolysat hat ein Molekulargewicht von ca. 3 kDa und wird durch Hydrolyse tierischen Kollagens des Typs I mit Hilfe von bakteriellen Proteasen hergestellt und von der Anmelderin unter den Namen Fortigel® vertrieben.The collagen hydrolyzate in the composition according to the invention preferably has an average molecular weight of about 0.3 kDa to about 30 kDa, in particular from about 2 kDa to about 10 kDa, particularly preferably about 3 kDa. The molecular weight distribution of the collagen hydrolyzate can be controlled by the selection of suitable proteolytic enzymes (usually bacterial proteases). In addition, optionally, individual molecular weight fractions of the hydrolyzate can be separated by ultrafiltration or chromatographic methods. The collagen hydrolyzate according to the invention has a molecular weight of about 3 kDa and is produced by hydrolysis of animal collagen type I with the aid of bacterial proteases and sold by the applicant under the name of Fort hedgehog ®.
Die in der erfindungsgemäßen Zusammensetzung weiter enthaltenen Bestandteile liegen ggf. jeweils in einer physiolosgisch verträglichen Verbindung vor, insbesondere das Magnesium als Magnesium-Citrat, das Zink als Zink-Citrat und die Pantothensäure als Calcium-D-Pantothenat.The constituents further contained in the composition according to the invention may be present in each case in a physiologically tolerable compound, in particular magnesium as magnesium citrate, zinc as zinc citrate and pantothenic acid as calcium D-pantothenate.
Gegenstand der vorliegenden Erfindung ist ferner ein Arzneimittel oder Nahrungsergänzungsmittel, welches die erfindungsgemäße Zusammensetzung umfassend Kollagenhydrolysat, Vitamin C, Kieselsäure, Magnesium, Zink und Pantothensäure umfasst. Insbesondere betrifft die Erfindung ein Arzneimittel oder Nahrungsergänzungsmittel oder ein diätetisches Lebensmittel zur Vorbeugung und/oder Behandlung degenerativer Gelenkveränderungen, zur Stimulierung der Knorpelbildung und zur Stimulierung des Bindegewebes.The present invention furthermore relates to a medicament or dietary supplement which comprises the composition according to the invention comprising collagen hydrolyzate, vitamin C, silica, magnesium, zinc and pantothenic acid. In particular, the invention relates to a pharmaceutical or dietary supplement or dietetic food for the prevention and / or treatment of degenerative articular changes, for the stimulation of cartilage formation and for the stimulation of the connective tissue.
Vorzugsweise sind in der erfindungsgemäßen Zusammensetzung 1 g bis 10 g Kollagenhydrolysat, 40 mg bis 400 mg Vitamin C, 100 mg bis 1000 mg Kieselsäure, 50 mg bis 500 mg Magnesium, 1 mg bis 10 mg Zink und 3 mg bis 30 mg Pantothensäure pro Dosiseinheit enthalten; besonders bevorzugt 1 g bis 8 g Kollagenhydrolysat, 40 mg bis 250 mg Vitamin C, 100 mg bis 600 mg Kieselsäure, 50 mg bis 250 mg Magnesium, 1 mg bis 5 mg Zink und 3 mg bis 22 mg Pantothensäure pro Dosiseinheit; am meisten bevorzugt sind in der erfindungsgemäßen Zusammensetzung 5 g Kollagenhydrolysat, 80 mg Vitamin C, 420 mg Kieselsäure, 125 mg Magnesium, 2 mg Zink und 18 mg Pantothensäure pro Dosiseinheit enthalten.Preferably in the composition according to the invention 1 g to 10 g of collagen, 40 mg to 400 mg of vitamin C, 100 mg to 1000 mg of silica, 50 mg to 500 mg of magnesium, 1 mg to 10 mg of zinc and 3 mg to 30 mg pantothenic acid per dose unit contain; particularly preferably 1 g to 8 g of collagen hydrolyzate, 40 mg to 250 mg of vitamin C, 100 mg to 600 mg of silica, 50 mg to 250 mg of magnesium, 1 mg to 5 mg of zinc and 3 mg to 22 mg of pantothenic acid per dose unit; 5 g collagen hydrolyzate, 80 mg vitamin C, 420 are most preferred in the composition according to the invention mg of silica, 125 mg of magnesium, 2 mg of zinc and 18 mg of pantothenic acid per dose unit.
Die pro Dosiseinheit aufgeführten Mengen sind für die ein- bis fünfmalige Anwendung täglich, bevorzugt für die ein- bis dreimalige Anwendung täglich und besonders bevorzugt für die einmal tägliche Anwendung vorgesehen.The amounts listed per unit dose are daily for the one to five applications, preferably for once to three applications daily and particularly preferably for once daily use.
Die erfindungsgemäße Zusammensetzung kann in der für Arzneimittel, Nahrungsergänzungsmittel und diätische Lebensmittel üblichen weise oral appliziert werden, insbesondere in Form von Tabletten, Kautabletten, Braustabletten, Dragees, Kapseln, Pastillen, Lutschtabletten, Riegeln, Lösungen, Suspension, Trinkzubereitungen, Pulvern oder Granulaten. The composition according to the invention can be administered orally in the manner customary for medicines, dietary supplements and dietary foods, in particular in the form of tablets, chewable tablets, effervescent tablets, dragees, capsules, lozenges, lozenges, bars, solutions, suspensions, drink preparations, powders or granules.
Die nachstehenden Beispiele sollen die Erfindung näher erläutern:The following examples are intended to explain the invention in more detail:
Beispiel 1:Example 1:
Jeweils 10 g Kollagenhydrolysat, 160 mg Vitamin C, 840 mg Kieselsäure, 250 mg Magnesium, 10 mg Zink und 30 mg Pantothensäure werden als Pulver in einen Portionsbeutel gefüllt.Each 10 g of collagen hydrolyzate, 160 mg of vitamin C, 840 mg of silica, 250 mg of magnesium, 10 mg of zinc and 30 mg of pantothenic acid are filled as a powder into a sachet.
Beispiel 2: Example 2:
Jeweils 8 g Kollagenhydrolysat, 120 mg Vitamin C, 800 mg Kieselsäure, 200 mg Magnesium, 5 mg Zink und 30 mg Pantothensäure werden als Granulat in einen Portionsbeutel gefüllt.Each 8 g of collagen hydrolyzate, 120 mg of vitamin C, 800 mg of silica, 200 mg of magnesium, 5 mg of zinc and 30 mg of pantothenic acid are filled as granules into a sachet.
Beispiel 3:Example 3:
Jeweils 1 g Kollagenhydrolysat, 40 mg Vitamin C, 105 mg Kieselsäure, 50 mg Magnesium, 1 mg Zink und 4 mg Pantothensäure werden in einer Filmtablette verpresst.Each 1 g of collagen hydrolyzate, 40 mg of vitamin C, 105 mg of silica, 50 mg of magnesium, 1 mg of zinc and 4 mg of pantothenic acid are compressed in a film-coated tablet.
Beispiel 4:Example 4:
Jeweils 2,5 g Kollagenhydrolysat, 40 mg Vitamin C, 210 mg Kieselsäure, 60 mg Magnesium, 1 mg Zink und 9 mg Pantothensäure werden als Lutschtablette verpresst.In each case 2.5 g of collagen hydrolyzate, 40 mg of vitamin C, 210 mg of silica, 60 mg of magnesium, 1 mg of zinc and 9 mg of pantothenic acid are compressed as a lozenge.
Beispiel 5:Example 5:
Jeweils 5 g Kollagenhydrolysat, 80 mg Vitamin C, 420 mg Kieselsäure, 125 mg Magnesium, 2 mg Zink und 18 mg Pantothensäure sind Bestandteil einer wässrigen Lösung von 25 ml. Each 5 g of collagen hydrolyzate, 80 mg of vitamin C, 420 mg of silica, 125 mg of magnesium, 2 mg of zinc and 18 mg of pantothenic acid are part of an aqueous solution of 25 ml.
ZITATE ENTHALTEN IN DER BESCHREIBUNG QUOTES INCLUDE IN THE DESCRIPTION
Diese Liste der vom Anmelder aufgeführten Dokumente wurde automatisiert erzeugt und ist ausschließlich zur besseren Information des Lesers aufgenommen. Die Liste ist nicht Bestandteil der deutschen Patent- bzw. Gebrauchsmusteranmeldung. Das DPMA übernimmt keinerlei Haftung für etwaige Fehler oder Auslassungen.This list of the documents listed by the applicant has been generated automatically and is included solely for the better information of the reader. The list is not part of the German patent or utility model application. The DPMA assumes no liability for any errors or omissions.
Zitierte PatentliteraturCited patent literature
- WO 2010/149596 A1 [0004] WO 2010/149596 A1 [0004]
- DE 102009030351 A1 [0014] DE 102009030351 A1 [0014]
Zitierte Nicht-PatentliteraturCited non-patent literature
- A. Bello und S. Oesser (2006), Current Medical Research and Opinion (22) 2221–2232 [0004] A. Bello and S. Oesser (2006), Current Medical Research and Opinion (22) 2221-2232 [0004]
- Rodell et al., 2014, Macdonald et al., 2012, Jugdaohsingh et al., 2005, Eisinger et al., 1993, Moukarzel et al. 1992 [0006] Rodell et al., 2014, Macdonald et al., 2012, Jugdaohsingh et al., 2005, Eisinger et al., 1993, Moukarzel et al. 1992 [0006]
- Eisinger et al., 1993, Schiano et al., 1979 [0006] Eisinger et al., 1993, Schiano et al., 1979 [0006]
- Spector et al., 2005 [0006] Spector et al., 2005 [0006]
- Bohl et al., 2002, Saur et al., 2002, Rayssignuier et al., 1990 [0007] Bohl et al., 2002, Saur et al., 2002, Rayssignuier et al., 1990 [0007]
- Neumann, 1996 [0008] Neumann, 1996 [0008]
- Kara et al., 2010, De Olivera et al., 2009 [0009] Kara et al., 2010, De Olivera et al., 2009 [0009]
- Khaled et al., 1999 [0009] Khaled et al., 1999 [0009]
Claims (17)
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DE102009030351A1 (en) | 2009-06-22 | 2010-12-23 | Gelita Ag | Composition for the treatment of degenerative joint diseases |
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DE102009030351A1 (en) | 2009-06-22 | 2010-12-23 | Gelita Ag | Composition for the treatment of degenerative joint diseases |
WO2010149596A1 (en) | 2009-06-22 | 2010-12-29 | Gelita Ag | Compositions for treating degenerative joint diseases |
Non-Patent Citations (8)
Title |
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A. Bello und S. Oesser (2006), Current Medical Research and Opinion (22) 2221-2232 |
Bohl et al., 2002, Saur et al., 2002, Rayssignuier et al., 1990 |
Eisinger et al., 1993, Schiano et al., 1979 |
Kara et al., 2010, De Olivera et al., 2009 |
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EP3381457A1 (en) * | 2017-03-28 | 2018-10-03 | Natural Products & Drugs GmbH | Physiologically active composition comprising n-acetylglucosamine for the treatment of back pain |
WO2018178146A1 (en) * | 2017-03-28 | 2018-10-04 | Natural Products & Drugs Gmbh | Physiologically active preparation comprising n-acetyl-glucosamine for the treatment of back pain |
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