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一种对活性药物成分生产在三个不同层面的资源消耗的系统评估。

A systematic evaluation of the resource consumption of active pharmaceutical ingredient production at three different levels.

机构信息

Research Group ENVOC, Ghent University, Coupure Links 653, Ghent, B-9000, Belgium.

出版信息

Environ Sci Technol. 2011 Apr 1;45(7):3040-6. doi: 10.1021/es1015907. Epub 2011 Mar 10.

DOI:10.1021/es1015907
PMID:21391625
Abstract

In this paper, the development and the advantages of a methodology which allows the systematic assessment of the environmental impact on the resource side of specific pharmaceutical production processes with limited data entry is presented. The quantification of the process-specific mass and energy balances over three different system boundaries (process, gate-to-gate, and cradle-to-gate) is based on the methodology explained in Van der Vorst et al. (Ind. Eng. Chem. Res.2009, 48(11), 5344-5350). These mass and energy balances are now coupled with the thermodynamic term exergy allowing the quantification of the resource efficiency at the process and gate-to-gate level and the environmental impact at the cradle-to-gate level. The advantages of such a calculation tool for the resource evaluation are illustrated with five consecutive pharmaceutical production steps which are part of the galantamine (anti-Alzheimer medication) pathway. It is shown that such a quantitative and systematic evaluation tool allows a detailed and relatively fast evaluation of the resource efficiency of active pharmaceutical ingredient (API) production processes at the three different levels. Combining thermodynamics and the systematic data inventory methodology for the quantification of the resource efficiency first allows results to be merged into a single impact value (exergy loss/mol API or CEENE/mol API) for fast benchmarking and evaluation of different API production processes. Second, it also allows results to be divided over different categories depending on the users' interest and make thorough analysis of processes in order to pinpoint process improvements and quantitatively justify the introduction of second generation production processes or production techniques.

摘要

本文介绍了一种方法的开发和优势,该方法允许在数据输入有限的情况下,系统地评估特定药物生产过程对资源方面的环境影响。通过 Van der Vorst 等人(Ind. Eng. Chem. Res.2009, 48(11), 5344-5350)中解释的方法,对三个不同系统边界(过程、门到门和摇篮到门)的特定过程的质量和能量平衡进行量化。这些质量和能量平衡现在与热力学术语“火用”相结合,允许在过程和门到门水平上量化资源效率,并在摇篮到门水平上量化环境影响。这种用于资源评估的计算工具的优点,通过五个连续的药物生产步骤来说明,这些步骤是加兰他敏(抗阿尔茨海默病药物)途径的一部分。结果表明,这种定量和系统的评估工具允许在三个不同水平上对活性药物成分(API)生产过程的资源效率进行详细和相对快速的评估。热力学和系统数据清单方法的结合用于量化资源效率,首先允许将结果合并为单个影响值(每摩尔 API 的火用损失或每摩尔 API 的 CEENE),以便快速基准测试和评估不同的 API 生产过程。其次,它还允许根据用户的兴趣将结果划分为不同类别,并对工艺进行彻底分析,以确定工艺改进并定量证明引入第二代生产工艺或生产技术的合理性。

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