Effect of Terminal (Dry) Heat Treatment on Non-Enveloped Viruses in Coagulation Factor Concentrates

Vox Sanguinis ◽  
1994 ◽  
Vol 67 (4) ◽  
pp. 345-350 ◽  
Author(s):  
H.F. (a) Hart ◽  
W.G. (a) Hart ◽  
J. (a) Crossley ◽  
A.-M. (b) Wood ◽  
A. (c) John ◽  
...  
Vox Sanguinis ◽  
1994 ◽  
Vol 67 (4) ◽  
pp. 345-350 ◽  
Author(s):  
H.F. Hart ◽  
W.G. Hart ◽  
J. Crossley ◽  
A.-M. Perrie ◽  
D.J. Wood ◽  
...  

Blood ◽  
2005 ◽  
Vol 106 (11) ◽  
pp. 4066-4066
Author(s):  
Christoph Kannicht ◽  
Monika Stadler ◽  
Andrea Neisser-Svae ◽  
Gerhard Gruber

Abstract Purpose: Wilate® is a novel, human plasma-derived, high purity, double virus inactivated coagulation factor concentrate. The safe and effective treatment of von Willebrand disease patients and haemophilia A has been demonstrated in clinical trials. The very high virus safety is achieved by an optimised solvent/detergent (S/D) method and terminal dry-heat treatment (PermaHeat) of the lyophilised product, not affecting the integrity of the proteins, which was investigated in this study. Methods: Analyses of PermaHeat treated (+100°C for 120 min) Wilate® samples with different residual moisture (RM) contents were performed in order to evaluate the upper RM limit in lyophilised samples. Samples with RM up to 7.3% were subjected to SDS-PAGE, immunoblotting and peptide mapping. Further investigations were based on FVIII:C activity testing and phospholipid binding properties, VWF multimer analysis, Ristocetin cofactor (VWF:RCo) activity and collagen binding (VWF:CB). Summary of results: The analyses confirmed that the structural and functional integrities of both VWF and FVIII were maintained during PermaHeat of Wilate® at +100°C for 120 minutes when the RM was kept at or below 1.8% during the heating procedure. Changes of protein-biochemical properties were detectable only for RM values exceeding 2%. Denaturation of samples occurred at RM of more than 3.5%. Conclusion: Beside S/D treatment, optimised PermaHeat treatment of the lyophilised VWF/FVIII product ensures the high viral safety margin of Wilate®. According to the results, the RM content during PermaHeat treatment was specified with a great safety margin to a maximum of 1.6%. This limit is carefully controlled in each vial before heating by RM testing utilising near infrared (NIR). At or below this RM no structural or functional changes of VWF and FVIII were detected after PermaHeat treatment.


Vox Sanguinis ◽  
1994 ◽  
Vol 66 (2) ◽  
pp. 96-103 ◽  
Author(s):  
A. Knevelman ◽  
H.J.C. Wit ◽  
B. Griffin ◽  
H. Hart ◽  
R.V. McIntosh

Vox Sanguinis ◽  
1994 ◽  
Vol 66 (2) ◽  
pp. 96-103
Author(s):  
A. Knevelman ◽  
H.J.C. de Wit ◽  
B. Griffin ◽  
H. Hart ◽  
R.V. McIntosh

Transfusion ◽  
2008 ◽  
Vol 48 (4) ◽  
pp. 790-790 ◽  
Author(s):  
Johannes Blümel ◽  
Albert Stühler ◽  
Herbert Dichtelmüller

2017 ◽  
Vol 112 ◽  
pp. 489-493
Author(s):  
K.M. Tabi ◽  
G.F. Ngando Ebongue ◽  
G.N. Ntsomboh ◽  
E. Youmbi

2018 ◽  
Vol 84 (7) ◽  
Author(s):  
Lin He ◽  
Zhan Chen ◽  
Shiwei Wang ◽  
Muying Wu ◽  
Peter Setlow ◽  
...  

ABSTRACTDNA damage kills dry-heated spores ofBacillus subtilis, but dry-heat-treatment effects on spore germination and outgrowth have not been studied. This is important, since if dry-heat-killed spores germinate and undergo outgrowth, toxic proteins could be synthesized. Here, Raman spectroscopy and differential interference contrast microscopy were used to study germination and outgrowth of individual dry-heat-treatedB. subtilisandBacillus megateriumspores. The major findings in this work were as follows: (i) spores dry-heat-treated at 140°C for 20 min lost nearly all viability but retained their Ca2+-dipicolinic acid (CaDPA) depot; (ii) in most cases, dry-heat treatment increased the average times and variability of all major germination events inB. subtilisspore germination with nutrient germinants or CaDPA, and in one nutrient germination event withB. megateriumspores; (iii)B. subtilisspore germination with dodecylamine, which activates the spore CaDPA release channel, was unaffected by dry-heat treatment; (iv) these results indicate that dry-heat treatment likely damages spore proteins important in nutrient germinant recognition and cortex peptidoglycan hydrolysis, but not CaDPA release itself; and (v) analysis of single spores incubated on nutrient-rich agar showed that while dry-heat-treated spores that are dead can complete germination, they cannot proceed into outgrowth and thus not to vegetative growth. The results of this study provide new information on the effects of dry heat on bacterial spores and indicate that dry-heat sterilization regimens should produce spores that cannot outgrow and thus cannot synthesize potentially dangerous proteins.IMPORTANCEMuch research has shown that high-temperature dry heat is a promising means for the inactivation of spores on medical devices and spacecraft decontamination. Dry heat is known to killBacillus subtilisspores by DNA damage. However, knowledge about the effects of dry-heat treatment on spore germination and outgrowth is limited, especially at the single spore level. In the current work, Raman spectroscopy and differential interference contrast microscopy were used to analyze CaDPA levels in and kinetics of nutrient- and non-nutrient germination of multiple individual dry-heat-treatedB. subtilisandBacillus megateriumspores that were largely dead. The outgrowth and subsequent cell division of these germinated but dead dry-heat-treated spores were also examined. The knowledge obtained in this study will help understand the effects of dry heat on spores both on Earth and in space, and indicates that dry heat can be safely used for sterilization purposes.


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