CS242310B1 - Ig-7s or igg,iga,igm containing agent for external use - Google Patents

Ig-7s or igg,iga,igm containing agent for external use Download PDF

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Publication number
CS242310B1
CS242310B1 CS118383A CS118383A CS242310B1 CS 242310 B1 CS242310 B1 CS 242310B1 CS 118383 A CS118383 A CS 118383A CS 118383 A CS118383 A CS 118383A CS 242310 B1 CS242310 B1 CS 242310B1
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CS
Czechoslovakia
Prior art keywords
iga
igg
parts
weight
igm
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CS118383A
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Czech (cs)
Slovak (sk)
Inventor
Alfred Stachy
Lydia Novotna
Anton Lucansky
Jozef Bulik
Imrich Banda
Original Assignee
Alfred Stachy
Lydia Novotna
Anton Lucansky
Jozef Bulik
Imrich Banda
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.)
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Application filed by Alfred Stachy, Lydia Novotna, Anton Lucansky, Jozef Bulik, Imrich Banda filed Critical Alfred Stachy
Priority to CS118383A priority Critical patent/CS242310B1/en
Publication of CS242310B1 publication Critical patent/CS242310B1/en

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Abstract

Vynález sa týká .přípravku pre vonkajšie použitie, ktorý obsahuje Ig-7S alebo zmesi IgG, IgA a IgM v methyleelulózovom základe. Zložky zmesi sú v nasledujúcom pomere: 5,0 až 20,0 hmotnostných dielov uvedených imunoglobulínoiv v 1 000 hmotnostných dielov uvedených základov. Lokálna aplikácia imunoglobulínov představuje nové liečebné možnosti zápalových ochorení tělesného povrchu.The invention relates to an external formulation use comprising Ig-7S or mixtures thereof IgG, IgA, and IgM in methyleululose base. The ingredients of the mixture are as follows: 5.0 to 20.0 parts by weight immunoglobulins in 1000 wt parts of the foundations. Topical application of immunoglobulins new therapeutic options for inflammatory body surface diseases.

Description

Vynález sa týká zloženia přípravku Ig-7S alebo zmesi IgG, IgA, IgM pre vonkajšie použitie, kde nosičem imunoglobulínov sú metylcelulózové hydrogély, alebo masťové základy. Imunoglobulíiny v uvedených nosičoch sú bud' čisté, alebo v ikombinácii s lokálně používanými antibiotikami.The invention relates to a composition of an Ig-7S preparation or a mixture of IgG, IgA, IgM for external use, wherein the carrier of the immunoglobulins is methylcellulose hydrogels or ointment bases. The immunoglobulins in said carriers are either pure or in combination with topically used antibiotics.

V súčasnoím období v kožnom lekárstve, septickej chirurgii použlvajú sa hydrogély a masti obsahujúce antibiotiká. Tvorba rezlstencle mikreorganizmev na lokálně podávané antibiotiká je značná. Lokálna apllkácia imunoglobulínov představuje nové liečebné možnosti zápalových ochorení tělesného povrchu mikrobiálně ekcémy, flegmóny róznej lokalizácie, bércové vředy, chronické osteomyeliitídy — nakolko dochádza ku synergickému účinku s antibiotikami. Potenciovanie účinku antibiotik imunoglobuUnami popisuje Ronmeberger a Zwisler 1982. (Ronneberg H. Zwisler O.: Fortschritte auf dem Gebiet der Antibiotika — und Immunotherapie, A. K. Klelnschmidt und S. Raptis vydav., Urban a Schwarzeinberg, Munchen 1982).At present, hydrogels and ointments containing antibiotics are used in dermatology, septic surgery. The formation of rezlstencle mikreorganizmev on topically administered antibiotics is considerable. Local application of immunoglobulins presents new treatment options for inflammatory diseases of the body surface by microbial eccemas, phlegmons of differentiated localization, leg ulcers, chronic osteomyeliitis - because of the synergistic effect with antibiotics. Potentiating the effect of immunoglobulin antibiotics is described by Ronmeberger and Zwisler 1982. (Ronneberg H. Zwisler O .: Fortschritte auf dem Gebiet der Antibiotik- und Immunotherapie, A.K. Klelnschmidt und S. Raptis ed., Urban and Schwarzeinberg, Munchen 1982).

Podstata vynálezu spočívá v tom, že přípravek obsahuje Ig v množstve 3,8—20,0 g opracovaných 1 000 g do 3—5 hmotnostných %! metylceilulózového alebo masťového základu.The present invention is characterized in that the composition comprises Ig in an amount of 3.8-20.0 g of treated 1000 g to 3-5% by weight . methylceilulose or ointment base.

Získaná zmes sa homogeinizuje a rozplňuje do balení po 10 a 50 g.The mixture obtained is homogenized and filled into packs of 10 and 50 g.

V případe, že do zmesi přidáváme aj antibiotiká použijeme tieto koncentrácie na 100 g masťového základu, alebo metylcelulózového hydrogélu.If antibiotics are added to the mixture we use these concentrations per 100 g ointment base or methylcellulose hydrogel.

Bacltracín Chlor ampheinicol Neomycín Nystatin Trichomycin Tyrothricin Gentamycin Příklad prevedenia:Bacltracin Chlorine ampheinicol Neomycin Nystatin Trichomycin Tyrothricin Gentamycin Example:

575 000 j. 0,25-2,5 g 0,25-2,0 g575,000 0.25-2.5 g 0.25-2.0 g

5—15 000 000 j. 10—20 000 000 j. 25-75 mg5—15 000 000 units 10—20 000 000 units 25-75 mg

80—240 mg80—240 mg

500 mg imunoglobulínov 7S alebo zmesi IgG, IgA, IgM sa rozpustí v 10 g aqua pri inj. ČsL—3 a zmieša s 30 g masťového základu č. III pre antibiotiká o zložení:500 mg of 7S immunoglobulins or a mixture of IgG, IgA, IgM are dissolved in 10 g of aqua at injection. ČsL — 3 and mixed with 30 g ointment base no. III for antibiotics containing:

Alkohol cetylicus 1,0 gAlcohol cetylicus 1.0 g

Cera alba 1,0 gCera alba 1.0 g

Cera lané 10,0 gCereal rope 10.0 g

Vaselina alba 20,0 gVaselina alba 20.0 g

1000 mg imunoglobulínu 7S alebo zmesi IgG, IgA, IgM sa rozpustí v 20 g aqua pre inj. GsL—3 a přidá sa do 80 g 3—5 % metyle elulózovéhio hydrogélu.1000 mg of immunoglobulin 7S or a mixture of IgG, IgA, IgM is dissolved in 20 g of aqua for inj. GsL-3 and added to 80 g of 3-5% methyl cellulose hydrogel.

Obe získané zmesi sa homogenizujú a rozplňujú do balení po 10 a 50 g.The two mixtures obtained are homogenized and filled into packages of 10 and 50 g, respectively.

Claims (2)

PREDMETSUBJECT 1. Prípravok pre vonkajšie použitie obsahujúcl Ig-7S alebo zmesi IgG, IgA, IgM v methylcelulózoívom hydrogéle alebo masťovom základe, vyznačujúci sa tým, že ako účininú zložku obsahuje 3,8 až 20,0 hmoitnostných dielov uvedených imunoglobulínov v 1 000 hmotnostných dielov masťového alebo hydrogélového základu.An external preparation comprising Ig-7S or mixtures of IgG, IgA, IgM in a methylcellulose hydrogel or ointment base, characterized in that it contains as active ingredient 3.8 to 20.0 parts by weight of said immunoglobulins per 1000 parts by weight of ointment. or a hydrogel base. VYNALEZUWe claim: 2. Přípravek podl'a bodu 1, vyznačujúci sa tým, že obsahuje 2,6 až 5,2 hmotnostných dielov IgG, 1,0 až 2,0 hmotnostných dielov IgA, 0,25 až 0,5 hmotnostných dielov IgM na 1 000 hmotnostných dielov masťového alebo hydrogélovéhoi základu.2. A composition according to claim 1 comprising 2.6 to 5.2 parts by weight of IgG, 1.0 to 2.0 parts by weight of IgA, 0.25 to 0.5 parts by weight of IgM per 1000 parts by weight of an ointment or hydrogel base.
CS118383A 1983-02-22 1983-02-22 Ig-7s or igg,iga,igm containing agent for external use CS242310B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CS118383A CS242310B1 (en) 1983-02-22 1983-02-22 Ig-7s or igg,iga,igm containing agent for external use

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CS118383A CS242310B1 (en) 1983-02-22 1983-02-22 Ig-7s or igg,iga,igm containing agent for external use

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CS242310B1 true CS242310B1 (en) 1986-04-17

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AT402789B (en) * 1991-03-25 1997-08-25 Immuno Ag PHARMACEUTICAL PREPARATION BASED ON PLASMA PROTEINS

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AT402789B (en) * 1991-03-25 1997-08-25 Immuno Ag PHARMACEUTICAL PREPARATION BASED ON PLASMA PROTEINS

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