Intravenously injected cytomegalovirus human immune globulin and preparation method thereof

A human immunoglobulin, immunoglobulin technology, applied in the preparation methods of immunoglobulin, antiviral immunoglobulin, peptide, etc., can solve the problems of low efficiency and unstable properties, and improve the survival rate and specificity. high effect

Active Publication Date: 2016-05-25
哈尔滨派斯菲科生物制药有限公司
View PDF4 Cites 6 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] However, because giant cell human immunoglobulin has strict requirements on raw material selection and preparation co

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Intravenously injected cytomegalovirus human immune globulin and preparation method thereof
  • Intravenously injected cytomegalovirus human immune globulin and preparation method thereof
  • Intravenously injected cytomegalovirus human immune globulin and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0050] 1. Screening and collection of plasma from donors:

[0051] Select the plasma, and use the neutralization test method to detect the neutralizing titer of the giant cell antibody in the raw plasma should meet the following conditions: the neutralizing titer is not less than 1:20; L; Alanine aminotransferase (monitored by Lai's method) is not higher than 35 units; ELISA method to determine syphilis, hepatitis B surface antigen, HIV-1 / HIV-2 antibody, HCV antibody are all negative. Store in a freezer below -20°C, and the shelf life should not exceed 2 years.

[0052] 2. Determination of antibody titer in raw plasma by neutralization test:

[0053] (A) Pre-dilute the plasma sample with the MEM cell culture medium of the cell maintenance solution 1:4, inactivate at 56°C for 30 minutes, and then continue to dilute 5 times, that is, the final 1:20 times dilution; The cell maintenance medium was 5% fetal bovine serum by volume, and both the cell maintenance medium and the MEM ...

Embodiment 2

[0084] 1. Screening and collection of plasma from donors:

[0085] Select the plasma, and use the neutralization test method to detect the neutralizing titer of the giant cell antibody in the raw plasma should meet the following conditions: the neutralizing titer is not less than 1:20; L; Alanine aminotransferase (monitored by Lai's method) is not higher than 35 units; ELISA method to determine syphilis, hepatitis B surface antigen, HIV-1 / HIV-2 antibody, HCV antibody are all negative. Store in a freezer below -20°C, and the shelf life should not exceed 2 years.

[0086] 2. Determination of antibody titer in raw plasma by neutralization test:

[0087] (A) MEM cell culture medium (purchased from Gibco) of the plasma sample to be tested was pre-diluted 1:4 with cell maintenance medium (fetal bovine serum with a volume percentage of 5%, purchased from Gibco), and then extinguished at 56°C. Live for 30 minutes, then continue to 5-fold dilution, that is, the final 1:20-fold diluti...

Embodiment 3

[0110] 1. Screening and collection of plasma from donors:

[0111] Select the plasma, and use the neutralization test method to detect the neutralizing titer of the giant cell antibody in the raw plasma should meet the following conditions: the neutralizing titer is not less than 1:20; L; Alanine aminotransferase (monitored by Lai's method) is not higher than 35 units; ELISA method to determine syphilis, hepatitis B surface antigen, HIV-1 / HIV-2 antibody, HCV antibody are all negative. Store in a freezer below -20°C, and the shelf life should not exceed 2 years.

[0112] 2. Determination of antibody titer in raw plasma by neutralization test:

[0113] (A) MEM cell culture medium (purchased from Gibco) of the plasma sample to be tested was pre-diluted 1:4 with cell maintenance medium (5% fetal bovine serum by volume, purchased from Gibco), and then inactivated at 56°C for 30 Minutes, and then continue to 5-fold dilution, that is, the final 1:20-fold dilution.

[0114] (B) Tak...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

PropertyMeasurementUnit
Conductivityaaaaaaaaaa
Login to view more

Abstract

The invention relates to intravenously injected cytomegalovirus human immune globulin and a preparation method thereof, and the titer of a cytomegalovirus neutralizing antibody of the human immune globulin is larger than or equal to 1:500. The preparation method comprises the steps that 1, positive plasma with the titer of the cytomegalovirus neutralizing antibody larger than or equal to 1:20 is screened out; 2, the screened-out efficient positive plasma is mixed; 3, the mixed plasma is separated through a low-temperature ethanol filter-pressing method, an immune globulin component II is separated and purified by combining an ion-exchange column chromatography method, viruses are removed through filtration, chromatography, ultrafiltration, preparation, low-pH incubation virus inactivation and nanofilm filtration, the immune globulin with the purity of 98.5%-100% is obtained through subpackaging, and the antibody titer is not lower than 1:500. The cytomegalovirus human immune globulin prepared through the preparation and production method is high in antibody titer, purity and recovery rate and capable of conducting targeted treatment on cytomegalovirus, is an effectively drug for treating recessive and dominant infection caused by the cytomegalovirus in people, is safe and reliable and has larger social benefits and economic benefits.

Description

technical field [0001] The invention relates to therapeutic blood products in the field of biopharmaceuticals, in particular to a giant cell human immunoglobulin and a preparation method thereof. Background technique [0002] Human cytomegalovirus (HCMV), also known as human herpesvirus type 5 (HHV5), belongs to the betaherpesvirus subfamily. HCMV is one of the most common pathogens of human congenital virus infection, and the infection rate of this virus in adults in my country is as high as 95%. Ordinary people are usually recessive infection, but for immunocompromised populations, such as bone marrow and solid organ transplant recipients, HIV-infected patients and tumor patients, HCMV infection can lead to serious consequences. Primary or recurrent HCMV infection in pregnant women can cause neonatal intrauterine infection or perinatal infection to invade the fetus, which can cause central nervous system involvement, multiple organ damage, mental retardation or deafness i...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
IPC IPC(8): C07K16/08C07K1/36C07K1/34C07K1/18
CPCC07K16/088C07K2317/10C07K2317/90
Inventor 杨莉于引航李常禄杨金平陈东明孙晓东闫磊孙婷
Owner 哈尔滨派斯菲科生物制药有限公司
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap