一种新的单粒子计数器重合模型,第一部分:理论与实验验证。

J Z Knapp, L R Abramson
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引用次数: 0

摘要

定义了在通过光消粒子计数器实施usp 788污染粒子分析时估计信号重合对粒子计数不足和注入错误计数的影响的先决条件。其中包括随粒径变化的颗粒浓度测量和计数过程的新模型。这两个先决条件都得到了经验验证:一个归一化方程描述了所有单粒子计数器中的重合效应。归一化方程的单个参数是每毫升有效检测器体积的数量。在充分悬浮粒子的基础上,提出了5%的最大计数不足限制。使用SVP usp XXII每个容器10,000个颗粒的验收限制或PMA建议usp XXIII中> 10微米的颗粒每个容器最大6,000个颗粒,估计最小容器尺寸的漏计误差。已记录的注射溶液中低于10微米粒径控制的大浓度颗粒可造成额外的788测量危害。用泊松模型通过粒子重合来估计和控制假粒子计数注入到强制测量中。通过了解颗粒计数器测量系统的能力和适当时使用稀释技术,现有颗粒计数系统可以达到可接受的计数精度限制。新的计数过程模型和新的颗粒浓度测量方法可使药典污染检测和GLP用户评价试验中使用的仪器规范标准、保守。本文的第一部分包括重合效应对颗粒计数的理论和测量的粒度分布。总结了用于确定符合计数损失作为单粒子计数器的粒子浓度的函数的实验验证。本文的第二部分描述了一种实用的协议,用于确定操作限制,以实现单个粒子计数器的选定巧合计数不足限制。
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A new coincidence model for single particle counters, Part I: Theory and experimental verification.

The prerequisites for estimating the effect of signal coincidence on both particle undercounting and the injection of false counts in the implementation of U.S.P. 788 contaminating particle assays by light extinction particle counters are defined. These include a particle concentration measure that varies with particle size and a new model of the counting process. Both prerequisites have been verified empirically: a single normalized equation describes the coincidence effect in all single particle counters. The single parameter of the normalized equation is the number of effective detector volumes per milliliter. A maximum undercount limit of 5% is proposed based on adequately suspended particles. Using the SVP U.S.P. XXII acceptance limits of 10,000 particles per container or the PMA propose 6,000 particles per container maximum for particles > 10 microns in U.S.P. XXIII, undercount errors are estimated for the smallest container sizes. The large concentration of particles below the controlled 10 microns particle size, that has been documented in injectable solutions, can pose an additional 788 measurement hazard. A Poisson model is used to estimate and control the injection of false particle counts into the mandated measurement through particle coincidence. Acceptable counting accuracy limits with present particle counting systems can be achieved by understanding the capabilities of the particle counter measurement system and using a dilution technique when appropriate. The new model of the counting process and the new particle concentration measures can result in standard, conservative, instrument specifications for use in Pharmacopeial contamination testing and in GLP user evaluation tests. Part I of this paper includes the theory of the coincidence effect on particle counting and the particle size distribution measured. A summary of the experimental verification employed to determine coincidence count loss as a function of particle concentration for single particle counters is reported. Part II of this paper describes a practical protocol for the determination of operating limits to achieve a selected coincidence undercount limit for single particle counters.

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Ethylene oxide sterilization: III--Influence of carrier nature in a biological monitor performance. Solid state chemical instability of an asparaginyl residue in a model hexapeptide. Low temperature properties of lyophilized solutions and their influence on lyophilization cycle design: pentamidine isethionate. Parameters governing steam sterilization of deadlegs. A new coincidence model for single particle counters, Part I: Theory and experimental verification.
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