DK3010537T3 - Fremgangsmåde til forebyggelse af aggregation af viruskomponenter - Google Patents

Fremgangsmåde til forebyggelse af aggregation af viruskomponenter Download PDF

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DK3010537T3
DK3010537T3 DK14734942.7T DK14734942T DK3010537T3 DK 3010537 T3 DK3010537 T3 DK 3010537T3 DK 14734942 T DK14734942 T DK 14734942T DK 3010537 T3 DK3010537 T3 DK 3010537T3
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basic amino
hrv
amino acid
virus
arginine
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DK14734942.7T
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't Oever Arend Gesinus Van
Wilfridus Adrianus Maria Bakker
Yvonne Elisabeth Thomassen
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De Staat Der Nederlanden Vert Door De Mini Van Vws Mini Van Volksgezondheit Welzijn En Sport
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Claims (15)

1. Fremgangsmåde til fremstilling afen sammensætning omfattende enterovi-ruspartikler, hvor fremgangsmåden omfatter trinnene: a) fremstilling af et medium indeholdende enteroviruspartiklerne; b) oprensning af enteroviruspartiklerne fra mediet, hvor en basisk aminosyre eller et derivat deraf under mindst en del af oprensningen er til stede i en slut-koncentration på mindst 1 mM og er tilstrækkelig til at forhindre eller reducere aggregation af enteroviruspartiklerne; og c) inaktivering af enteroviruspartiklerne; hvor den basiske aminosyre eller derivatet deraf er udvalgt fra gruppen bestående af: arginin, lysin, histidin, arginin-HCI, lysin-HCI, histidin-HCI, agmatin, L-argininethylesterdihydrochlorid, tranexamsyre, DL-5-hydroxylysinhydrochlo-rid, L-lysinmethylesterdihydrochlorid, 3-methyl-L-histidin, salte deraf og kombinationer deraf.
2. Fremgangsmåde ifølge krav 1, yderligere omfattende et trin d), hvor enteroviruspartiklerne formuleres.
3. Fremgangsmåde ifølge krav 1 eller 2, hvor den basiske aminosyre eller derivatet deraf er til stede i en slutkoncentration på mindst 1 mM og er tilstrækkelig til at forhindre eller reducere aggregation af enteroviruspartiklerne under mindst en del af trin c).
4. Fremgangsmåde ifølge krav 3, hvor den basiske aminosyre eller derivatet deraf også under trin d) er til stede i en slutkoncentration på mindst 1 mM og er tilstrækkelig til at forhindre eller reducere aggregation af enteroviruspartiklerne.
5. Fremgangsmåde ifølge et hvilket som helst af kravene 1 - 4, hvor koncentrationen af den basiske aminosyre eller derivatet deraf er mindst 1 mM og tilstrækkelig til at forhindre eller reducere aggregation af enteroviruspartiklerne og opretholdes under hele varigheden af mindst et blandt trin b), c) og d).
6. Fremgangsmåde ifølge et hvilket som helst af kravene 1 - 5, hvor slutkon-centrationen af den basiske aminosyre eller derivatet deraf er mindst 5 mM, 10 mM, 25 mM, 50 mM eller 100 mM og er tilstrækkelig til at forhindre eller reducere aggregation af enteroviruspartiklerne.
7. Fremgangsmåde ifølge et hvilket som helst af kravene 1 - 6, hvor enteroviruspartiklerne er viruslignende partikler af en enterovirus.
8. Fremgangsmåde ifølge et hvilket som helst af kravene 1 - 7, hvor enteroviruspartiklerne er af en Enterovirus udvalgt fra gruppen bestående af poliovira, coxsackie A-vira, coxsackie B-vira, echovira, rhinovira og enterovirus 68, 69, 70, 71 og 73 .
9. Fremgangsmåde ifølge krav 8, hvor enteroviruspartiklerne omfatter poliovira af serotyperne 1,2 og 3.
10. Fremgangsmåde ifølge et hvilket som helst af kravene 1 til 9, hvor sammensætningen omfattende enteroviruspartikler er en vaccine.
11. Fremgangsmåde ifølge krav 10, hvor vaccinen er en inaktiveret poliovaccine (IPV).
12. Anvendelse afen basisk aminosyre eller et derivat deraf til forhindring eller reduktion af aggregation af enteroviruspartikler under oprensning af enteroviruspartikler fra et medium, hvor en basisk aminosyre eller et derivat deraf under mindst en del af oprensningen er til stede i en slutkoncentration på mindst 1 mM og er tilstrækkelig til at forhindre eller reducere aggregation af enteroviruspartiklerne, og hvor den basiske aminosyre eller derivatet deraf er udvalgt fra gruppen bestående af: arginin, lysin, histidin, arginin-HCI, lysin-HCI, hi-stidin-HCI, agmatin, L-argininethylesterdihydrochlorid, tranexamsyre, DL-5-hy-droxylysinhydrochlorid, L-lysinmethylesterdihydrochlorid, 3-methyl-L-histidin, salte deraf og kombinationer deraf.
13. Anvendelse ifølge krav 12, hvor enteroviruspartiklerne er af en Enterovirus udvalgt fra gruppen bestående af poliovira, coxsackie A-vira, coxsackie B-vira, echovira, rhinovira og enterovirus 68, 69, 70, 71 og 73.
14. Fremgangsmåde ifølge krav 13, hvor enteroviruspartiklerne er poliovira af mindst en af serotyperne 1, 2 og 3.
15. Anvendelse ifølge krav 13, hvor enteroviruspartiklerne er en inaktiveret poliovaccine (IPV).
DK14734942.7T 2013-06-17 2014-06-17 Fremgangsmåde til forebyggelse af aggregation af viruskomponenter DK3010537T3 (da)

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PCT/NL2014/050395 WO2014204303A2 (en) 2013-06-17 2014-06-17 Methods for the prevention of aggregation of viral components

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CN108578399B (zh) * 2018-07-10 2020-01-07 湖北工业大学 氨基酸酯化合物在制备抗cvb3病毒药物中的应用
CA3152838A1 (en) * 2019-08-30 2021-03-04 Kashiv Biosciences, Llc Novel formulation of highly concentrated pharmacologically active antibody

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HK1223845A1 (zh) 2017-08-11
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CN105517568A (zh) 2016-04-20
CN105517568B (zh) 2020-07-07
HUE040108T2 (hu) 2019-02-28
KR20160019477A (ko) 2016-02-19
EP3010537B1 (en) 2018-07-11
HRP20181606T1 (hr) 2018-11-30
BR112015031541A2 (pt) 2017-07-25
SI3010537T1 (sl) 2018-09-28
KR102219672B1 (ko) 2021-02-25
LT3010537T (lt) 2018-10-25
PL3010537T3 (pl) 2019-03-29
ES2689150T3 (es) 2018-11-08
WO2014204303A2 (en) 2014-12-24
WO2014204303A3 (en) 2015-10-08
US20160184423A1 (en) 2016-06-30
RS57864B1 (sr) 2018-12-31
PT3010537T (pt) 2019-12-03

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