Cara Inaktivasi Virus

Perbedaan virus setelah inaktifasi

Inaktivasi Virus adalah bertujuan untuk mematikan daya pathogenitas virus tetapi tidak merusak sifat antigenitasnya, sehingga ketika virus/antigen dimasukan ke tubuh target, virus tersebut tidak menyebabkan  sakit tetapi tetap mampu merespon terbentuknya kekebalan (antibodi)
Berikut beberapa chemical dan prosedur proses inaktifasi virus  yang umum dipergunakan dalam proses inaktifasi virus dalam memproduksi  vaksin hewan dilengkapi dengan link journalnya


1. Formalin
  • Virus ND
Konsentrasi : 0,04 – 0,1%, Inkubasi 37˚C : 16 jam
American Association of Avian Pathologists : http://www.jstor.org/stable/1591214
Evaluation of Different Methods of Inactivation of Newcastle Disease Virus and Avian Influenza Virus in Egg Fluids and Serum

Konsentrasi : 0,04 %, Inkubasi 37˚C : 24 jam
Veterinary Research Communications, 12 (1988) 195-197 Geo Abstracts Ltd, Norwich-printed in England : https://eurekamag.com/pdf/001/001517990.pdf
A Premliminary Vaccine Potency Trial of A Newcastle Disease Virus Inactivated with Binary Ethylenimine

Konsentrasi : 0,025 %, 0,025 %, Room temperature (20 ˚C) 1 hari
NCBI-NIH
Inactivation of haemagglutinin and infectivity of influenza and Newcastle disease viruses by heat and by formalin


Konsentrasi : 0,1%, Inkubasi 37˚C : 16 jam
Immunogenicity of commercial , formaldehyde and binary ethylenimine inactivated Newcastle disease virus vaccines in specific pathogen free chickens
  • Virus AI H5N1
Konsentrasi : 0,04 – 0,1%, Inkubasi 37˚C : 16 jam
American Association of Avian Pathologists
Evaluation of Different Methods of Inactivation of Newcastle Disease Virus and Avian Influenza Virus in Egg Fluids and Serum
  • Virus AI H9N2

Konsentrasi : 0.1%, Inkubasi 20°C 10 jam
An_inactivated vaccine to control the current H9N2 low pathogenic avian influenza in Korea

Konsentrasi : 0,02%, Inkubasi 37°C 18 jam
Antigenic evolution of H9N2 chicken influenza viruses isolated in China during 2009–2013 and selection of a candidate vaccine strain with broad cross-reactivity

Konsentrasi : 0.025%, Inkubasi 4°C minimal 1 minggu
Vaccine Efficacy of Inactivated, Chimeric Hemagglutinin H9/H5N2 Avian Influenza Virus and Its Suitability for the Marker Vaccine Strategy

Konsentrasi : 0,1%, Inkubaasi 4°C, 24 jam
Assessment of the safety and efficacy of low pathogenic avian influenza (H9N2) virus in inactivated oil emulsion vaccine in laying hens

Konsentrasi : 0.12%, Inkubasi 37°C, 48 jam
Advacements in life Science: http://www.als-journal.com/427-17/:
Comparative efficacy of different adjuvant containing inactivated vaccines against low-pathogenicity Avian InfluenzaH9N2 virus

Konsentrasi : 0,04 – 0,1%; Inkubasi 37°C, 16 jam atau 48 jam
Evaluation of different inactivation methods for high and lowpathogenic avian influenza viruses in egg-fluids for antigenpreparationShailesh

Konsentrasi : 0.1%, Inkubasi 20°C, 10 jam
Genetic and antigenic evolution of H9N2 subtype avian influenza virus in domestic chickens in southwestern China, 2013±2016

Konsentrasi : 0.1%, Inkubasi 25°C, 24 jam
Archive Archives of Razi Institute: http://archrazi.areeo.ac.ir/article_107486_0.html
Optimizing the process of inactivating influenza virus subtype H9N2 by formalin in the production of killed avian influenza vaccine

Konsentrasi : 0.1%, Inkubasi 37°C, 18 jam
Optimizing the process of inactivating influenza virus subtype H9N2 by formalin in the production of killed avian influenza vaccine

Konsentrasi : 0.1%, Inkubasi 25°C 18 jam
Preparation and Evaluation of H9N2 Vaccine Adjuvated with Montanide ISA71 VG
  • Virus IB
Konsentrasi : 1:1000, Inkubasi 4˚C : 16 jam sambil disteerer
RESPON ANTIBODI DAN PROTEKSI VAKSIN INAKTIF INFECTIOUS BRONCHITIS ISOLAT LOKAL PADA AYAM PETELUR
BBalitvet
  • Virus IBD
Konsentrasi : 0.1 - 0.2%. Inkubasi 37 °C : 24 jam
Journal of Zhejiang University SCIENCE B : http://citeseerx.ist.psu.edu/viewdoc/download;jsessionid=9FBB35D7181AFAEB9111F401C8C7FC91?doi=10.1.1.521.9759&rep=rep1&type=pdf
Immunogenicity of formaldehyde and binary ethylenimine inactivated infectious bursal disease virus in broiler chicks*

2. BPL (Beta-propiolakton)

  • Virus ND
Konsentrasi : 0,025 – 0,1%, Inkubasi 4˚C : 18 jam kemudian Inkubasi 37˚C : 30 menit
American Association of Avian Pathologists : http://www.jstor.org/stable/1591214
Evaluation of Different Methods of Inactivation of Newcastle Disease Virus and Avian Influenza Virus in Egg Fluids and Serum
  • Virus AI H5N1
Konsentrasi : 0,025 – 0,1%, Inkubasi 4˚C : 18 jam kemudian Inkubasi 37˚C : 30 menit
American Association of Avian Pathologists : http://www.jstor.org/stable/1591214
Evaluation of Different Methods of Inactivation of Newcastle Disease Virus and Avian Influenza Virus in Egg Fluids and Serum

  • Virus AI H9N2

Konsentrasi : 0,1%., 38 bagian virus dikombinasikan + 1 bagian 0,5 M disodium fosfat (DSP), homoenkan, Tambahkan 1 bagian BPL (4%) Inkubasi 30 menit di atas es, diikuti oleh 2 jam inkubasipada 37 ° C untuk menghidrolisis BPL yang tersisa. PH larutan kemudian sesuaikan menjadi ~7,4 dengan 7% natrium bikarbonat. 
BMC Reseach :https://bmcresnotes.biomedcentral.com/articles/10.1186/s13104-018-3537-9
Induction of immune response in chickensprimed in ovo with an inactivated H9N2 avian influenza virus vaccine

Konsentrasi : 0,1%, Inkubasi 4°C, 16 jam
Elseiver
https://www.ncbi.nlm.nih.gov/pubmed/25997377
Evaluation of different inactivation methods for high and lowpathogenic avian influenza viruses in egg-fluids for antigenpreparationShailesh
  • Virus IB
Konsentrasi : 1:2000, Inkubasi 37˚C : 90 menit sambil disteerer
American Association of Avian Pathologists : http://www.jstor.org/stable/1588835
Avian Infectious Bronchitis Virus: Serologic Response of Chickens to Seven Beta-Propiolactione-Inactivated Strains

Konsentrasi : 0,025%, Inkubasi 37˚C : 2 jam sambil disteerer
American Association of Avian Pathologists : http://www.jstor.org/stable/1588835
Avian Infectious Bronchitis Virus: Serologic Response of Chickens to Seven Beta-Propiolactione-Inactivated Strains

Konsentrasi : 0,05%, Inkubasi 37˚C : 1,5 jam sambil disteerer
Arc". Raz; Ins. 56 (2003) 13-35: http://archrazi.areeo.ac.ir/article_109025_455d22bbc2a9b8ce0b3a779d4ca92b20.pdf
Efficacy of Experimental Inactivated Vaccine for Infectious Bronchitis Disease

3. BEI (Binary Ethylenimine)
  • Virus ND
Konsentrasi : 0,01 M, Inkubasi 37˚C : 5 - 8 jam
American Association of Avian Pathologists : http://www.jstor.org/stable/1591214
Evaluation of Different Methods of Inactivation of Newcastle Disease Virus and Avian Influenza Virus in Egg Fluids and Serum

Konsentrasi : 0,001 M, Inkubasi 37˚C : 24 jam
Research Gate : https://www.researchgate.net/publication/233231064
_Avian_Influenza_Virus_H5N1_Inactivation_by_Binary_Ethylenimine/download Avian Influenza Virus (H5N1) Inactivation by Binary Ethylenimine

Konsentrasi : 4 mM, Inkubasi 30˚C : 21 jam
Semantic Scholar : https://www.semanticscholar.org/paper/Immunogenicity-of-commercial-%2C-formaldehyde-and-in-Toroghi-Babaei/21f4f22022c582eacf3c8a6fe71a863cd363e2f6
Immunogenicity of commercial , formaldehyde and binary ethylenimine inactivated Newcastle disease virus vaccines in specific pathogen free chickens

Konsentrasi : 0.001 M (1% v/v).
Veterinary Research Communications, 12 (1988) 195-197 Geo Abstracts Ltd, Norwich-printed in England : https://eurekamag.com/pdf/001/001517990.pdf
A Premliminary Vaccine Potency Trial of A Newcastle Disease Virus Inactivated with Binary Ethylenimine

Konsentrasi : 4 mM, Inkubasi 30˚C : 21 jam
Razi Vaccine & Serum Research Institute ; https://www.semanticscholar.org/paper/Immunogenicity-of-commercial-%2C-formaldehyde-and-in-Toroghi-Babaei/21f4f22022c582eacf3c8a6fe71a863cd363e2f6
Immunogenicity of commercial , formaldehyde and binary ethylenimine inactivated Newcastle disease virus vaccines in specific pathogen free chickens
  • Virus AI H5N1
Konsentrasi : 0,01 M, Inkubasi 37˚C : 5 - 8 jam
American Association of Avian Pathologists : http://www.jstor.org/stable/1591214 Evaluation of Different Methods of Inactivation of Newcastle Disease Virus and Avian Influenza Virus in Egg Fluids and Serum
  • Virus IBD
Konsentrasi : 0,001 - 0,002 mol / L,  0,1 mol/L 2-bromoethylamine hydrobromide larutkan kedalam 0.175 mol/L NaOH, inkubasi di at 37°C 1 jam, Masukan campuran larutan diatas 1 s/d 2 % ke dalam virus, inkubssi di 37°C 36 jam, Residu BEI dihidrolisis dengan menambahan larutan 1 mol / L steril Na-tiosulfat 10% dari volume BEI yang digunakan
Journal of Zhejiang University SCIENCE B : http://citeseerx.ist.psu.edu/viewdoc/download;jsessionid
=9FBB35D7181AFAEB9111F401C8C7FC91?oi=10.1.1.521.9759&rep=rep1&type=pdf
Immunogenicity of formaldehyde and binary ethylenimine inactivated infectious bursal disease virus in broiler chicks*

Nah itulah artikel mengenai inaktifasi virus sebagai referensi  untuk melakukan optimasi inaktifasi virus skala produksi

Untuk mendapatkan artikel/journal-journal yang ada dalam tabel diatas, silahkan baca artikel "cara amudah download artikel/journal berbayarkarena tidak semua journal dapat diakses dengan lengkap atau bahkan kita harus membelinya

Dan untuk proses pengujian inaktifasinya silahkan baca "cara uji inaktivasi virus"

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