HRP20191288T1 - Pripravak koji sadrži smjesu ekstrakata iz biljaka ili smjesu molekula koje se nalaze u tim biljkama, te upotreba namijenjena djelovanju na metabolizam glucida i/ili lipida - Google Patents

Pripravak koji sadrži smjesu ekstrakata iz biljaka ili smjesu molekula koje se nalaze u tim biljkama, te upotreba namijenjena djelovanju na metabolizam glucida i/ili lipida Download PDF

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HRP20191288T1
HRP20191288T1 HRP20191288T HRP20191288T1 HR P20191288 T1 HRP20191288 T1 HR P20191288T1 HR P20191288 T HRP20191288 T HR P20191288T HR P20191288 T1 HRP20191288 T1 HR P20191288T1
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Croatia
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preparation
plant
acid
intended
glucoside
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Sébastien Peltier
Pascal Sirvent
Thierry Maugard
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Valbiotis
Univ Clermont Auvergne
Univ La Rochelle
Centre Nat Rech Scient
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First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=52465501&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=HRP20191288(T1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Valbiotis, Univ Clermont Auvergne, Univ La Rochelle, Centre Nat Rech Scient filed Critical Valbiotis
Publication of HRP20191288T1 publication Critical patent/HRP20191288T1/hr

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Claims (23)

1. Pripravak, naznačen time što u najmanju ruku sadrži smjesu molekula koja u najmanju ruku sadrži: – ekstrakt biljke Chrysanthellum indicum, te – ekstrakt biljke Cynara scolymus, te – ekstrakt biljke Vaccinium mirtillus, te – sintetski piperin i/ili ekstrakt biljke Piper koji sadrži piperin, gdje navedena smjesa molekula sadrži: – najmanje jednu molekulu koju se bira između apigenin-7-O-glukuronida, krisantelina A, krisantelina B, kavene kiseline, luteolina, maritimetina, eriodiktiola, izookanina, apigenina, luteolin-7-O-glukozida, maritimeina, marein, eriodiktiol-7-O-glukozida, flavomarein, apigenin-8-C-α-l-arabinozid-6-C-β-d-glukozida (šaftozida), apigenin-6,8-C-di-β-d-glukopiranozida (vicenina-2), te – najmanje jednu molekulu koju se bira između dikafeoilkinske kiseline, sulfomonokafeoilkinske kiseline, luteolina, luteolin-7-O-glukozida, luteolin-7-O-glukuronid, apigenin-7-O-glukozida, cinaropikrina, te – najmanje jednu molekulu koju se bira između monokafeoilkinske kiseline, delfinidin-3-galaktozida, delfinidin-3-glukozida, cijanidin-3-galaktozida, delfinidin-3-arabinozida, cijanidin-3-glukozida, petunidin-3-galaktozida, cijanidin-3-arabinozida, petunidin-3-glukozida, peonidin-3-galaktozida, petunidin-3-arabinozida, peonidin-3-glukozida, malvidin-3-galaktozida, malvidin-3-glukozida, malvidin-3-arabinozida, te – u najmanju ruku piperin.
2. Pripravak u skladu s patentnim zahtjevom 1, naznačen time što smjesa molekula također sadrži ekstrakt biljke Olea europaea.
3. Pripravak u skladu s bilo kojim od prethodnih patentnih zahtjeva, naznačen time što se Piper bira između Piper nigrum, Piper aduncum i/ili Piper longum.
4. Pripravak u skladu s bilo kojim od prethodnih patentnih zahtjeva, naznačen time što se ekstrakt biljke Chrysanthellum indicum dobiva iz cijele biljke i/ili nadzemnih dijelova biljke Chrysanthellum indicum.
5. Pripravak u skladu s bilo kojim od prethodnih patentnih zahtjeva, naznačen time što se ekstrakt biljke Cynara scolymus dobiva iz cijele biljke i/ili iz listova biljke Cynara scolymus.
6. Pripravak u skladu s bilo kojim od prethodnih patentnih zahtjeva, naznačen time što se ekstrakt biljke Vaccinum mirtillus dobiva iz cijele biljke i/ili iz plodova biljke Vaccinum mirtillus.
7. Pripravak u skladu s bilo kojim od prethodnih patentnih zahtjeva, naznačen time što ima najmanje jednu od sljedećih karakteristika: – sadrži količinu ekstrakta biljke Chrysanthellum indicum koja omogućuje primjenu najmanje 0,00001 g ekstrakta biljke Chrysanthellum indicum po kg tjelesne težine osobe na kojoj se primijenjuje pripravak i dnevno, te/ili – sadrži količinu ekstrakta biljke Cynara scolymus koja omogućuje primjenu najmanje 0,00001 g ekstrakta biljke Cynara scolymus po kg tjelesne težine osobe na kojoj se primijenjuje pripravak i dnevno, te/ili – sadrži količinu ekstrakta biljke Vaccinium mirtillus koja omogućuje primjenu najmanje 0,00001 g ekstrakta biljke Vaccinium mirtillus po kg tjelesne težine osobe na kojoj se primijenjuje pripravak i dnevno, te/ili – sadrži količinu piperina koja omogućuje primjenu najmanje 0,001 mg piperina po kg tjelesne težine osobe na kojoj se primijenjuje pripravak i dnevno.
8. Pripravak u skladu s patentnim zahtjevom 2, naznačen time što sadrži količinu ekstrakta biljke Olea europaea koja omogućuje primjenu najmanje 0,00001 g ekstrakta biljke Olea europaea po kg tjelesne težine osobe na kojoj se primijenjuje pripravak i dnevno.
9. Pripravak u skladu s bilo kojim od prethodnih patentnih zahtjeva, naznačen time što pripravak također u najmanju ruku sadrži jednu molekulu koju se bira između oleuropeina i hidroksitirosola.
10. Pripravak, naznačen time što u najmanju ruku sadrži smjesu molekula, naznačen time što navedena smjesa u najmanju ruku sadrži dikafeoilkinsku kiselinu, apigenin-7-O-glukuronid, monokafeoilkinsku kiselinu, piperin i oleuropein.
11. Pripravak u skladu s bilo kojim od prethodnih patentnih zahtjeva, naznačen time što također u najmanju ruku sadrži jedan dodatni element, dodatno dodan u smjesu molekula, gdje se navedeni dodatni element bira između: – sljedećih vitamina: B1, B2, B3, B5, B6, B8, B9, B12, C, A, D, E, K1 i K2; – sljedećih spojeva: obetikolne kiseline, korosolne kiseline, višestruko nezasićenih masnih kiselina iz porodice omega-6 i/ili omega-3, orotinske kiseline, pangamičnr kiseline, para-aminobenzojeve kiseline, amigdalina, β-glukana, karnitina, dimetilglicina, imeglimina, izoflavona, l-arginina, oksitocina, pektina, piridoksamina, rezveratrola, viniferina, l-citrulina; – sljedećih oligoelemenata i minerala: arsena, bora, kalcija, bakra, željeza, fluora, joda, litija, mangana, magnezija, molibdena, nikla, fosfora, selenija, vanadija i cinka; – sljedećih mikrosastojaka neesencijalne prirode: konjugirane linolenske kiseline, lipoične kiseline, karotenoida, karnitina, kolina, koenzima Q10, fitosterola, polifenola iz porodice tanina i lignana, te taurina; – frukto-oligosaharida, galakto-oligosaharida; – fermentiranih mliječnih proizvoda; – kvasaca; – gljiva; – proizvoda dobivenih iz kukaca kompatibilnih sa prehrambenim i farmaceutskim sektorom; – marihuane i hašiša; – sredstava za oblaganje; – aroma; – sredstava za zakiseljavanje; – antikoagulansi; – ugušćivača; – stabilizatora; – emulgatora; – punila; – pomoćnih tvari.
12. Pripravak u skladu s bilo kojim od prethodnih patentnih zahtjeva, naznačen time što je u obliku praha, gela ili emulzije, ili u tekućem obliku.
13. Pripravak u skladu s bilo kojim od prethodnih patentnih zahtjeva, naznačen time što je u obliku tableta, pilula, kapsula, štapića, vrećica, ampula ili kapaljki, ili u injektibilnom obliku.
14. Pripravak u skladu s bilo kojim od prethodnih patentnih zahtjeva, naznačen time što je namijenjen upotrebi kao medikament.
15. Pripravak u skladu s bilo kojim od patentnih zahtjeva 1 do 14, naznačen time što je namijenjen upotrebi kao medikament ili nutritivni proizvod u sprječavanju i/ili u borbi protiv patoloških poremećaja metabolizma šećera i/ili lipida kod ljudi ili životinja.
16. Pripravak namijenjen upotrebi u skladu s patentnim zahtjevom 14 ili 15, naznačen time što je namijenjen sprječavanju i/ili u borbi protiv dijabetesa tip 1 i 2 i/ili nealkoholnih bolesti masne jetre i/ili kardiovaskularnih patoloških pojava i/ili patoloških pojava povezanih s otpornošću na inzulin.
17. Pripravak namijenjen upotrebi u skladu s patentnim zahtjevom 16, naznačen time što je nealkoholna bolest masne jetre nealkoholna steatoza jetre.
18. Pripravak namijenjen upotrebi u skladu s patentnim zahtjevom 16, naznačen time što su kardiovaskularne patološke pojave koronarne kardiopatije, cerebrovaskularne bolesti, periferne arteriopatije i tromboze dubokih vena.
19. Pripravak namijenjen upotrebi u skladu s patentnim zahtjevom 16, naznačen time što je patološka pojava povezana s otpornošću na inzulin Alzheimerova bolest.
20. Pripravak namijenjen upotrebi u skladu s bilo kojim od patentnih zahtjeva 16 do 19, naznačen time što se upotrebljava u kombinaciji s najmanje jednim antidiabetičkim terapijskim sredstvom, kojeg se bira između bigvanida, uključujući metformin, inhibitora dipeptidil-peptidaze-IV (DPP-IV), analoga glukagonu sličnod peptida-1 (GLP-1), tiazolidindiona (TZD), sulfonilurea, brzih i sporih inzulina, inhibitora natrijsko-glukoznog sutransportera-2 (SGLT2), inhibitora glikozidase (akarboze, miglitola, vogliboze, peptida koji sadrže slijed alanin-prolin ili prolin-alanin), molekula iz porodice fibranor, poput elafibranora, ili molekula koje ciljaju na nuklearne receptore, a osobito na receptore ROR (α, β, γ) i receptore Rev-Erb (α, β).
21. Pripravak namijenjen upotrebi u skladu s patentnim zahtjevom 14 ili 15, naznačen time što je namijenjen sprječavanju i/ili borbi protiv dislipidemije.
22. Pripravak namijenjen upotrebi u skladu s prethodnih patentnim zahtjevom, naznačen time što se upotrebljava u kombinaciji s hipolipidemijskim terapijskim sredstvom, kojeg se bira između: statina, fibrata, nikotinske kiseline, ionsko-izmjenjivačkih smola, inhibitora apsorpije kolesterola, višestruko nezasićenih omega-3 masnih kiselina, tiadenola, te agonista nuklearnog receptora FXR (farnezoidnog X receptora).
23. Pripravak namijenjen upotrebi u skladu s patentnim zahtjevom 14 ili 15, naznačen time što je namijenjen sprječavanju i/ili borbi protiv pretilosti i prekomjerne težine i/ili metaboličkog sindroma i/ili patoloških problema s krvnim tlakom.
HRP20191288 2014-10-20 2019-07-17 Pripravak koji sadrži smjesu ekstrakata iz biljaka ili smjesu molekula koje se nalaze u tim biljkama, te upotreba namijenjena djelovanju na metabolizam glucida i/ili lipida HRP20191288T1 (hr)

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