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首页> 外文期刊>European journal of pharmaceutics and biopharmaceutics: official journal of Arbeitsgemeinschaft fuer Pharmazeutische Verfahrenstechnik e.V >Synthesis, characterization and assessment of suitability of trehalose fatty acid esters as alternatives for polysorbates in protein formulation.
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Synthesis, characterization and assessment of suitability of trehalose fatty acid esters as alternatives for polysorbates in protein formulation.

机译:海藻糖脂肪酸酯在蛋白质配方中作为聚山梨酯替代品的合成,表征和适用性评估。

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Nonionic polyethylene glycol-derived surfactants are today's choice as surfactants in protein formulations. Different groups discovered that although surface-induced stresses are reduced by these excipients, the long-term stability of different proteins decreased due to polyethylene glycol-related induction of oxidation processes under static storage conditions. In this paper, the potential of polyoxyethylene-free surfactants for protein formulation was evaluated. Three different sugar-based surfactants, 6-O-monocaprinoyl-alpha,alpha-trehalose, 6-O-monolauroyl-alpha,alpha-trehalose and 6-O-monopalmitoyl-alpha,alpha-trehalose, were synthesized in four reaction steps. These substances lack polyethylene glycol residues and can be produced from renewable resources. The chemical and physical properties of these three surfactants were investigated and compared with polysorbate 20 and 80. 6-O-monopalmitoyl-alpha,alpha-trehalose was insoluble in water at room temperature and was hence excluded from some of the further tests. The critical micellar concentration of all surfactants is in a comparable range of approximately 0.001-0.01% (m/V). The sugar-based surfactants showed slightly higher hemolytic activity than the polysorbate references. The surfactants with shorter chain length proved to be comparable to polysorbates in regard to physicochemical properties. Finally for human growth hormone, the protein-stabilizing properties against shaking-induced stress were tested and compared to polysorbate-containing formulations. Whereas in the absence of surfactant, dramatic monomer loss and aggregate formation occurred, it was found that 100% monomer content was maintained when 0.1% (m/V) 6-O-monocaprinoyl-alpha,alpha-trehalose or 6-O-monolauroyl-alpha,alpha-trehalose was added to the formulation. Polysorbate 80 at a concentration of 0.1% (m/V) also significantly stabilized the protein. Lower amounts of surfactants result in only partial stabilization. Furthermore, adsorption of human growth hormone to the container surface is reduced in the presence of the surfactants. Thus, the new sugar-based surfactants offer a promising alternative and have potential for application in protein formulations.
机译:如今,非离子型聚乙二醇衍生的表面活性剂已成为蛋白质制剂中的表面活性剂。不同的小组发现,尽管这些赋形剂降低了表面诱导的应力,但是由于聚乙二醇相关的静态存储条件下的氧化过程诱导,不同蛋白质的长期稳定性降低了。在本文中,评估了不含聚氧乙烯的表面活性剂用于蛋白质制剂的潜力。在四个反应步骤中合成了三种不同的基于糖的表面活性剂6-O-单己酰基-α,α-海藻糖,6-O-单月桂酰基-α,α-海藻糖和6-O-单棕榈酰基-α,α-海藻糖。这些物质没有聚乙二醇残留,可以从可再生资源中生产。对这三种表面活性剂的化学和物理性质进行了研究,并将其与聚山梨酯20和80进行了比较。6-O-单棕榈酰基-α,α-海藻糖在室温下不溶于水,因此从某些其他测试中排除。所有表面活性剂的临界胶束浓度在大约0.001-0.01%(m / V)的可比较范围内。糖基表面活性剂的溶血活性略高于聚山梨酸酯参考物。在理化性质方面,具有较短链长的表面活性剂被证明与聚山梨酯相当。最终,对于人类生长激素,测试了针对震动引起的压力的蛋白质稳定特性,并将其与含聚山梨酸酯的配方进行了比较。而在没有表面活性剂的情况下,发生了明显的单体损失和聚集体形成,发现当0.1%(m / V)6-O-单己酰基-α,α-海藻糖或6-O-单月桂酰酰基时,可以保持100%的单体含量将α-α,α-海藻糖加入制剂中。浓度为0.1%(m / V)的聚山梨酯80也可以显着稳定蛋白质。较少量的表面活性剂仅导致部分稳定。此外,在表面活性剂的存在下,人生长激素对容器表面的吸附减少。因此,新的基于糖的表面活性剂提供了有前途的替代方法,并具有在蛋白质制剂中的应用潜力。

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