IDENTIFICATION AND QUANTITATION OF IMPURITIES & RESIDUAL

杂质的鉴定和定量

• 批准号: 6435082
• 负责人: ALFRED DEL GROSSO
• 金额: --
• 依托单位国家: 美国
• 资助国家: 美国
• 起止时间: 至
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/6435082
• 关键词: analytical method; biological products; chelating agents; chemical standardization; chemical synthesis; drug quality /standard; gas chromatography; glutaraldehyde; high performance liquid chromatography; mass spectrometry; method development; pollen; squalene

The objectives of this project are to develop and validate methodologies for chemical impurities and residual manufacturing agents in biological products whose presence may affect product safety or efficacy. These include: 1) residual glutaraldehyde used as inactivating or conjugating agent in vaccines, 2) residual tetrachloroethylene in pollen allergenic extracts and allergenic source materials, 3) inactive components of crude allergenic extracts and allergen patch test materials and 4) squalene in anthrax vaccine. Current work in progress, or that performed in the past year includes: 1) The development and validation of methods for the determination of tetrachloroethylene, used in the processing of pollen source materials for allergenic extracts. A purge-and-trap gas chromatographic method for tetrachloroethylene in allergenic extracts has been developed and validated, data has been obtained for a representative sampling of final products. The determination of this same compound in allergenic source materials by gas chromatography/mass spectrometry is in the process of validation, interim data on a representative sampling of pollen source materials have been collected. 2) An HPLC method for the determination of glutaraldehyde, involving pre-column derivatization with p-nitrobenzyl-hydroxylamine and UV detection has been developed, validatation studies are in progress. 3) Gas chromatographic and gas chromatographic-mass spectrometric methods have been developed and applied to anthrax vaccine for the determination of squalene as an alledged adulterant. 4) A recently acquired ion-trap HPLC/mass spectrometer will be used along with gas chromatography/mass spectrometry to develop a general procedure for impurities screening in a variety of products as well as the characterization of low-molecular weight compounds in allergenic extracts and allergen patch test products.

该项目的目标是开发和验证生物制品中可能影响产品安全或功效的化学杂质和残留制造剂的方法学。这些问题包括：1)疫苗中用作灭活剂或结合剂的残留戊二醛；2)花粉变应原提取物和致敏源材料中的残留四氯乙烯；3)变应原粗提物和变应原斑贴试验材料中的非活性成分；4)炭疽疫苗中的角鲨烯。目前正在进行的工作或过去一年进行的工作包括：1)开发和验证四氯乙烯的测定方法，用于加工过敏原提取物的花粉来源材料。建立了一种吹扫捕集气相色谱测定致敏原提取物中四氯乙烯的方法，并对其进行了验证，获得了具有代表性的最终产品采样数据。用气相色谱/质谱仪测定致敏源材料中的这种化合物正在验证过程中，已经收集了具有代表性的花粉来源材料样本的中期数据。2)建立了高效液相色谱测定戊二醛的方法，包括柱前衍生化和紫外检测，验证研究正在进行中。3)建立了气相色谱和气相色谱-质谱法，并将其应用于炭疽疫苗中掺入的角鲨烯的检测。4)最近获得的离子陷阱高效液相色谱/质谱仪将与气相色谱/质谱仪一起使用，以开发一种通用程序，用于筛选各种产品中的杂质，以及表征过敏原提取物和过敏原斑贴测试产品中的低分子化合物。