Pregled bibliografske jedinice broj: 566807
Optimization of Mumps Virus Production Process Using DoE
Optimization of Mumps Virus Production Process Using DoE // Program book- FEMS 2011 4th Congress of European Microbiologists / Schrentzel J., Zbinden R., Schink B. (ur.).
Ženeva, 2011. (poster, međunarodna recenzija, neobjavljeni rad, znanstveni)
CROSBI ID: 566807 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Optimization of Mumps Virus Production Process Using DoE
Autori
Markušić, Maja ; Šantak, Maja ; Marić, Gorana ; Kotarski, LJerka ; Forčić, Dubravko ; Pavlović, Nediljko
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, neobjavljeni rad, znanstveni
Izvornik
Program book- FEMS 2011 4th Congress of European Microbiologists
/ Schrentzel J., Zbinden R., Schink B. - Ženeva, 2011
Skup
4th Congress of European Microbiologists-FEMS 2011
Mjesto i datum
Ženeva, Švicarska, 26.06.2011. - 30.06.2011
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
mumps ; optimization ; design of experiments
Sažetak
Background: Traditional virus vaccine production process involves several steps ; virus replication on appropriate cell substrate, harvesting, clarification, virus purification by chromatography, stabilization, formulation and vaccine filling. In order to optimize entire production process with regards to productivity, critical process operations should be identified first. Objective: Optimization of mumps virus production process using process simulation tools, performing sensitivity analysis of process operation to global process productivity. Methods: For mumps virus vaccine production process we have identified virus replication step as the most contributing to overall process productivity. Based on preliminary studies on lab-scale production system, 25 cm2 T-flask, important process factors for optimization studies were found ; X1 – chicken fibroblast primary cell suspension preparation protocol (P-production scale “-“or L-lab-scale “+”) X2 – infection method (A-in cell monolayer “-“or B-in suspension “+”) X3 – harvest interval time (24 hours “-“or 48 hours “+”) Experiments were designed as full factorial experiment with two replicate runs (16 experiments in total). Five virus harvests were collected from each T-flask and virus titer was determined in each sample. Based on individual virus titers in harvests, cumulative virus titer and productivity were estimated as process responses. Main effects of selected factors on estimated process responses were calculated by STATISTICA 6.1 software. Conclusions: It was found that factors X1 and X2 have high positive effect on virus productivity as response variable. The effect of factor X3 is statistically not significant.
Izvorni jezik
Engleski
Znanstvena područja
Biologija
POVEZANOST RADA
Projekti:
021-0212432-3123 - Molekularna patogeneza virusa mumpsa (Šantak, Maja, MZOS ) ( CroRIS)
Ustanove:
Imunološki zavod d.d.
Profili:
Gorana Marić
(autor)
Nediljko Pavlović
(autor)
Maja Šantak
(autor)
Maja Jagušić
(autor)
Ljerka Kotarski
(autor)
Dubravko Forčić
(autor)