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10.1111/jam.12654

http://scihub22266oqcxt.onion/10.1111/jam.12654
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25250638!7166340!25250638
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suck abstract from ncbi


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pmid25250638      J+Appl+Microbiol 2014 ; 117 (6): 1810-9
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  • The influence of stabilizers and rates of freezing on preserving of structurally different animal viruses during lyophilization and subsequent storage #MMPMID25250638
  • Malenovska H
  • J Appl Microbiol 2014[Dec]; 117 (6): 1810-9 PMID25250638show ga
  • AIMS: To make a comparative evaluation of the effects of different stabilizers and freezing rates on structurally different viruses during lyophilization and storage. METHODS AND RESULTS: Two virus strains from each of six animal virus families, including both enveloped and nonenveloped viruses, were lyophilized in (i) culture medium, (ii) with the addition of gelatine-sucrose and (iii) skim milk-sodium glutamate. All the virus suspensions were frozen (i) at -80 degrees C or (ii) in liquid nitrogen before lyophilization. Virus titre assay after lyophilization and after 8 months storage at 4 degrees C revealed that the efficacy of stabilizers depended on virus structure. Generally, the best protective quality for enveloped viruses was achieved with gelatine-sucrose, which best maintained their infectivity and envelope morphology. Even additive-free culture medium proved adequate for nonenveloped viruses. Differences in stabilizer efficacy were also found between virus families and were expressed immediately after lyophilization; the activity of stabilizers in the course of storage was very similar. Freezing in liquid nitrogen proved beneficial for picornaviruses. CONCLUSIONS: The choice of an appropriate stabilizer with respect to virus type is crucial for effective lyophilization. SIGNIFICANCE AND IMPACT OF THE STUDY: This study contributes to the establishment of general guidelines for animal virus lyophilization, with particular respect to differences in virus structure.
  • |*Freezing[MESH]
  • |*Viruses/ultrastructure[MESH]
  • |Culture Media[MESH]


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