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首页> 外文期刊>Journal of pharmaceutical sciences. >Effects of buffer composition and processing conditions on aggregation of bovine IgG during freeze-drying.
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Effects of buffer composition and processing conditions on aggregation of bovine IgG during freeze-drying.

机译:缓冲液组成和加工条件对冻干过程中牛IgG聚集的影响。

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摘要

The objective of this study was to identify critical formulation and processing variables affecting aggregation of bovine IgG during freeze-drying when no lyoprotective solute is used. Parameters examined were phosphate buffer concentration and counterion (Na versus K phosphate), added salts, cooling rate, IgG concentration, residual moisture level, and presence of a surfactant. No soluble aggregates were detected in any formulation after either freezing/thawing or freeze-drying. No insoluble aggregates were detected in any formulation after freezing, but insoluble aggregate levels were always detectable after freeze-drying. The data are consistent with a mechanism of aggregate formation involving denaturation of IgG at the ice/freeze-concentrate interface which is reversible upon freeze-thawing, but becomes irreversible after freeze-drying and reconstitution. Rapid cooling (by quenching in liquid nitrogen) results in more and larger aggregates than slow cooling on the shelf of the freeze-dryer. This observation is consistent with surface area measurements and environmental electron microscopic data showing a higher surface area of freeze-dried solids after fast cooling. Annealing of rapidly cooled solutions results in significantly less aggregation in reconstituted freeze-dried solids than in nonannealed controls, with a corresponding decrease in specific surface area of the freeze-dried, annealed system. Increasing the concentration of IgG significantly improves the stability of IgG against freeze-drying-induced aggregation, which may be explained by a smaller percentage of the protein residing at the ice/freeze-concentrate interface as IgG concentration is increased. A sodium phosphate buffer system consistently results in more turbid reconstituted solids than a potassium phosphate buffer system at the same concentration, but this effect is not attributable to a pH shift during freezing. Added salts such as NaCl or KCl contribute markedly to insoluble aggregate formation. Both sodium and potassium chloride contribute more to turbidity of the reconstituted solid than either sodium or potassium phosphate buffers at similar ionic strength, with sodium chloride resulting in a substantially higher level of aggregates than potassium chloride. At a given cooling rate, the specific surface area of dried solids is approximately a factor of 2 higher for the formulation containing sodium chloride than the formulation containing potassium chloride. Turbidity is also influenced by the extent of secondary drying, which underscores the importance of minimizing secondary drying of this system. Including a surfactant such as polysorbate 80, either in the formulation or in the water used for reconstitution, decreased, but did not eliminate, insoluble aggregates. There was no correlation between pharmaceutically acceptability of the freeze-dried cake and insoluble aggregate levels in the reconstituted product.
机译:这项研究的目的是确定在不使用冻干保护性溶质的情况下,影响冷冻干燥过程中牛IgG聚集的关键配方和加工变量。检查的参数是磷酸盐缓冲液浓度和抗衡离子(Na对K磷酸盐),添加的盐,冷却速率,IgG浓度,残留水分含量和表面活性剂的存在。冷冻/解冻或冷冻干燥后,在任何配方中均未检测到可溶性聚集体。冷冻后在任何制剂中均未检测到不溶性聚集体,但冻干后始终可检测到不溶性聚集体水平。该数据与聚集体形成的机制有关,该机制涉及在冰/冷冻剂-浓缩物界面处的IgG变性,其在冻融时是可逆的,但是在冻干和重构后变得不可逆。与在冷冻干燥机架子上缓慢冷却相比,快速冷却(通过在液氮中淬火)可产生更多和更大的聚集体。该观察结果与表面积测量和环境电子显微镜数据一致,该数据显示快速冷却后冷冻干燥的固体具有较高的表面积。与未退火的对照相比,快速冷却的溶液的退火导致重构的冷冻干燥固体中的聚集明显减少,并且冷冻干燥的退火系统的比表面积相应降低。 IgG浓度的增加显着提高了IgG对冻干诱导的凝集的稳定性,这可以解释为随着IgG浓度的增加,存在于冰/冰冻浓缩物界面的蛋白质百分比降低。与相同浓度的磷酸钾缓冲液系统相比,磷酸钠缓冲液系统始终能产生更多的浑浊的重构固体,但这种效果并不归因于冷冻过程中的pH值变化。添加的盐(例如NaCl或KCl)显着促进了不溶性聚集体的形成。氯化钠和氯化钾在离子强度相近的情况下,比磷酸钠或磷酸钾缓冲液对重构固体的浊度贡献更大,氯化钠比氯化钾产生的聚集体含量高得多。在给定的冷却速率下,含氯化钠的制剂的干燥固体的比表面积大约比含氯化钾的制剂高约2倍。浊度还受二次干燥程度的影响,这强调了最小化该系统的二次干燥的重要性。在制剂或用于重构的水中包括表面活性剂如聚山梨酯80,可减少但不能消除不溶性聚集体。冻干饼的药学可接受性与重构产品中不溶性聚集物的含量之间没有相关性。

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