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收缩期血浆分离的动力学

The dynamics of contract plasma fractionation.

作者信息

Farrugia Albert, Scaramuccia Daniela

机构信息

School of Surgery, QEII Medical Centre, The University of Western Australia (M509), Stirling Highway, Crawley WA 6009, Australia.

Value Partners Management Consulting SpA, Via Vespri Siciliani, 9, 20146, Milan, Italy.

出版信息

Biologicals. 2017 Mar;46:159-167. doi: 10.1016/j.biologicals.2017.02.007. Epub 2017 Feb 21.

Abstract

Plasma Derived Medicinal Products (PMDPs) are an essential component of the modern therapeutic armamentarium. They are differentiated from most other medicines in several ways, particularly the unique nature of the raw material used for their manufacture. Human plasma has been fractionated to PDMPs for the past 75 years, and the economics of manufacturing requires currently that as many products are harvested from each litre as is feasible and reflective of clinical needs. PDMPs may be purchased on the open market from the various commercial and not-for-profit (NFP) manufacturers. They may also be manufactured under contract (CM) from plasma supplied by government and similar agencies as a product of blood transfusion services. Clients for CM aspire to make full use of donated plasma, hence maximizing the donors' gift after the standard components of transfusion have been harvested. Many such countries also aspire to making their national clinical needs self-sufficient in PDMPs, attempting to acquire strategic independence from the vagaries of the commercial open market. The increasing commercial imperatives operating in the PMDP sector generate a tension with such ethical aspirations which are not easily resolved. In particular, the need to harvest as many proteins as possible may generate products which are surplus to national needs, necessitating an ethical paradigm for the optimal provision of such products. In addition, traditional relationships between blood services and domestic fractionation agencies may come under stress as a result of the competitive processes underpinning such transactions, which are now subject to international norms of free trade. Blood services engaged in the supply of hospital transfusion components are detached from the pharmaceutical Good Manufacturing Practices (GMP) culture needed for the production of plasma for CM, while the generation of such plasma through extraction from whole blood donations deflects the focus from that of a dedicated raw material for CM to a byproduct of the donation process. We review the field of CM, assess the current tensions within the sector, and offer suggestions for the strategic positioning of governments and other clients to ensure optimal outcomes for all the stakeholders involved.

摘要

血浆衍生药物产品(PMDPs)是现代治疗药物库的重要组成部分。它们在几个方面与大多数其他药物有所不同,特别是其制造所用原材料的独特性质。在过去75年里,人类血浆已被分离成PMDPs,目前制造的经济性要求从每升血浆中尽可能多地收获符合临床需求的产品。PMDPs可以从各种商业和非营利(NFP)制造商处在公开市场上购买。它们也可以根据合同(CM)由政府和类似机构提供的血浆制造,作为输血服务的一种产品。CM的客户希望充分利用捐赠的血浆,从而在采集输血的标准成分后使捐赠者的馈赠最大化。许多这样的国家还希望在PMDPs方面实现国家临床需求的自给自足,试图从商业公开市场的变幻莫测中获得战略独立性。PMDP部门日益增长的商业需求与这些不易解决的道德愿望产生了矛盾。特别是,尽可能多地收获蛋白质的需求可能会产生超出国家需求的产品,因此需要一种道德范式来优化此类产品的供应。此外,由于此类交易背后的竞争过程,血液服务机构与国内分离机构之间的传统关系可能会受到压力,而这些交易现在受制于自由贸易的国际规范。从事医院输血成分供应的血液服务机构与CM生产血浆所需的药品生产质量管理规范(GMP)文化脱节,而通过从全血捐赠中提取产生此类血浆,将重点从CM的专用原材料转移到捐赠过程的副产品上。我们回顾了CM领域,评估了该部门目前的矛盾,并为政府和其他客户的战略定位提供建议,以确保所有相关利益者都能获得最佳结果。

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