Effect of Controlled Ice Nucleation on Primary Drying Stage and Protein Recovery in Vials Cooled in a Modified Freeze-DryerSource: Journal of Biomechanical Engineering:;2009:;volume( 131 ):;issue: 007::page 74511Author:Stéphanie Passot
,
Miquel Galan
,
G. John Morris
,
Fernanda Fonseca
,
Ioan Cristian Tréléa
,
Michèle Marin
DOI: 10.1115/1.3143034Publisher: The American Society of Mechanical Engineers (ASME)
Abstract: The freezing step influences lyophilization efficiency and protein stability. The main objective of this work was to investigate the impact on the primary drying stage of an ultrasound controlled ice nucleation technology, compared with usual freezing protocols. Lyophilization cycles involving different freezing protocols (applying a constant shelf cooling rate of 1°C/min or 0.2°C/min, putting vials on a precooled shelf, and controlling nucleation by ultrasounds or by addition of a nucleating agent) were performed in a prototype freeze-dryer. Three protective media including sucrose or maltodextrin and differing by their thermal properties and their ability to preserve a model protein (catalase) were used. The visual aspect of the lyophilized cake, residual water content, and enzymatic activity recovery of catalase were assessed after each lyophilization cycle and after 1 month of storage of the lyophilized product at 4°C and 25°C. The freezing protocols allowing increasing nucleation temperature (precooled shelf and controlled nucleation by using ultrasounds or a nucleating agent) induced a faster sublimation step and higher sublimation rate homogeneity. Whatever the composition of the protective medium, applying the ultrasound technology made it possible to decrease the sublimation time by 14%, compared with the freezing method involving a constant shelf cooling rate of 1°C/min. Concerning the enzyme activity recovery, the impact of the freezing protocol was observed only for the protective medium involving maltodextrin, a less effective protective agent than sucrose. Higher activity recovery results were obtained after storage when the ultrasound technology or the precooled shelf method was applied. Controlling ice nucleation during the freezing step of the lyophilization process improved the homogeneity of the sublimation rates, which will, in turn, reduce the intervial heterogeneity. The freeze-dryer prototype including the system of controlled nucleation by ultrasounds appears to be a promising tool in accelerating sublimation and improving intrabatch homogeneity.
keyword(s): Temperature , Freezing , Drying , Freeze drying equipment , Nucleation (Physics) , Ice , Proteins , Ultrasound , Water AND Cooling ,
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| contributor author | Stéphanie Passot | |
| contributor author | Miquel Galan | |
| contributor author | G. John Morris | |
| contributor author | Fernanda Fonseca | |
| contributor author | Ioan Cristian Tréléa | |
| contributor author | Michèle Marin | |
| date accessioned | 2017-05-09T00:31:37Z | |
| date available | 2017-05-09T00:31:37Z | |
| date copyright | July, 2009 | |
| date issued | 2009 | |
| identifier issn | 0148-0731 | |
| identifier other | JBENDY-26987#074511_1.pdf | |
| identifier uri | http://yetl.yabesh.ir/yetl/handle/yetl/139906 | |
| description abstract | The freezing step influences lyophilization efficiency and protein stability. The main objective of this work was to investigate the impact on the primary drying stage of an ultrasound controlled ice nucleation technology, compared with usual freezing protocols. Lyophilization cycles involving different freezing protocols (applying a constant shelf cooling rate of 1°C/min or 0.2°C/min, putting vials on a precooled shelf, and controlling nucleation by ultrasounds or by addition of a nucleating agent) were performed in a prototype freeze-dryer. Three protective media including sucrose or maltodextrin and differing by their thermal properties and their ability to preserve a model protein (catalase) were used. The visual aspect of the lyophilized cake, residual water content, and enzymatic activity recovery of catalase were assessed after each lyophilization cycle and after 1 month of storage of the lyophilized product at 4°C and 25°C. The freezing protocols allowing increasing nucleation temperature (precooled shelf and controlled nucleation by using ultrasounds or a nucleating agent) induced a faster sublimation step and higher sublimation rate homogeneity. Whatever the composition of the protective medium, applying the ultrasound technology made it possible to decrease the sublimation time by 14%, compared with the freezing method involving a constant shelf cooling rate of 1°C/min. Concerning the enzyme activity recovery, the impact of the freezing protocol was observed only for the protective medium involving maltodextrin, a less effective protective agent than sucrose. Higher activity recovery results were obtained after storage when the ultrasound technology or the precooled shelf method was applied. Controlling ice nucleation during the freezing step of the lyophilization process improved the homogeneity of the sublimation rates, which will, in turn, reduce the intervial heterogeneity. The freeze-dryer prototype including the system of controlled nucleation by ultrasounds appears to be a promising tool in accelerating sublimation and improving intrabatch homogeneity. | |
| publisher | The American Society of Mechanical Engineers (ASME) | |
| title | Effect of Controlled Ice Nucleation on Primary Drying Stage and Protein Recovery in Vials Cooled in a Modified Freeze-Dryer | |
| type | Journal Paper | |
| journal volume | 131 | |
| journal issue | 7 | |
| journal title | Journal of Biomechanical Engineering | |
| identifier doi | 10.1115/1.3143034 | |
| journal fristpage | 74511 | |
| identifier eissn | 1528-8951 | |
| keywords | Temperature | |
| keywords | Freezing | |
| keywords | Drying | |
| keywords | Freeze drying equipment | |
| keywords | Nucleation (Physics) | |
| keywords | Ice | |
| keywords | Proteins | |
| keywords | Ultrasound | |
| keywords | Water AND Cooling | |
| tree | Journal of Biomechanical Engineering:;2009:;volume( 131 ):;issue: 007 | |
| contenttype | Fulltext |