（完整版）USP-1092-溶出度试验的开发和验证（中英文对照版）.docx
（ 1092）溶出度试验的开发和验证【中英文对照版】
INTRODUCTION
前言
Purpo
目的
The Dissolution Procedure: Developmentand Validation
<1092>provides a comprehensive approach covering items to considerfor developing and validating dissolution
procedures and the accompanyinganalytical procedures. It
address the u of automation throughout the testand
provides guidance and criteria for validation.It also address thetreatment of the data generated and the interpretation
of acceptance criteriafor immediate-and modified-relea
solid oral dosage forms.
溶出实验:开发和验证（1092）指导原则提供了在溶出度方法开发和验证过程
中以及采用相应分析方法时需要考虑的因素。本指导原则贯穿溶出度实验的全部过程，并对方法提供了指导和验证标准。同时它还涉及对普通制剂和缓释制剂所生成的数据和接受标准进行说明。
Scope
范围
Chapter<1092>address the development andvalidation
of dissolution procedures,with a focus on solid oral dosage forms.Many of the concepts prented, however, may be
老友记第五季
applicable to other dosageforms and routes of administration. General recommendations are given with theunderstanding
that modifications of the apparatus and procedures as given in USP general chapters need to be justified.
<1092>章节讨论了溶出度实验的开发和验证，重点是口服固体制剂。所提出的许多概念也可能适用于其他剂型和给药途径。关于设备和方法的修改部分在USP 通则中给出了合理的说明。
The organization of <1092>follows the quence of actions often performed inthe development and validation of a
开服装店如何选址
dissolution test. The ctions appear inthe following quence.
在进行溶解度实验的开发和验证时，常遵循指导原则<1092>，具体内容如
下：元音辅音
1. PRELIMINARY ASSESSMENT (FOR EARLY STAGES
softcore
OF PRODUCTDEVELOPMENT/DISSOLUTION METHOD DEVELOPMENT) 1.前期评估（对产品开发以及溶出度方法开发的前期研究评估）
1.1 Performing Filter Compatibility
1.1滤膜相容性研究
1.2Determining Solubility and Stability of DrugSubstance in Various Media
1.2原料药在不同溶出介质中溶解度测定和稳定性研究
1.3 Choosing a Medium and Volume
sooner or later1.3溶出介质和体积选择
1.4 Choosing an Apparatus
1.4溶出设备选择（桨法和篮法以及其他方法）
2.METHOD DEVELOPMENT
2.方法开发
2.1 Deaeration
2.1脱气
七夕快乐用英语怎么说
2.2 Sinkers
2.2沉降篮
2.3 Agitation
2.3转速
2.4 Study Design
2.4研究设计
2.4.1 TimePoints
2.4.1取样时间点
2.4.2 Obrvations
2.4.2观察
2.4.3Sampling
2.4.3取样
2.4.4Cleaning感谢生活
2.4.4清洗
2.5数据处理
2.6溶出方法评估
3.ANALYTICAL FINISH
3.完成分析
3.1Sample Processing
3.1样品处理
3.2Filters
3.2过滤
3.3Centrifugation
3.3离心
3.4Analytical Procedure
3.4分析方法
3.5Spectrophotometric Analysis 3.5光谱分析
3.6 HPLC
3.6HPLC法
4.AUTOMATION
4.自动化
4.1 Medium Preparation
4.1介质的配制
4.2 Sample Introduction and Timing 4.2定时进样
4.3 Sampling and Filtration
4.3取样和过滤
4.4 Cleaning
4.4清洗
condition是什么意思4.5 Operating Software and Computation of Results
4.5操作软件和计算的结果
5.VALIDATION
5.验证
5.1 Specificity/Placebo Interference
5.1专属性/安慰剂（辅料）干扰
5.2 Linearity and Range
5.2线性和范围
5.3 Accuracy/Recovery
5.3准确度/回收率
5.4 Precision
5.4精密度
5.4.1 REPEATABILITY OF ANALYSIS
5.4.1重复性
5.4.2 INTERMEDIATE PRECISION/RUGGEDNESS 5.4.2中间精密度/耐用性
5.4.3 REPRODUCIBILITY
5.4.3重现性
5.5 Robustness
5.5耐用性
5.6 Stability of Standard and Sample Solutions
5.6样品溶液和标准溶液的稳定性
5.7 Considerations for Automation
5.7自动操作注意事项
6.ACCEPTANCE CRITERIA
6.可接受标准
6.1 Immediate-Relea Dosage Forms
6.1速释剂型
6.2 Delayed-Relea Dosage Formsbrasrie
6.2延迟释放剂型
6.3 Extended-Relea Dosage Forms
6.3延长释放剂型
6.4 Multiple Dissolution Tests
6.4多个溶解度试验
6.5 Interpretation of Dissolution Results
6.5溶出结果说明
6.5.1 IMMEDIATE-RELEASE DOSAGE FORMS
6.5.1即时释放剂型
6.5.2 DELAYED-RELEASE DOSAGE FORMS
6.5.2延迟释放剂型
6.5.3 EXTENDED-RELEASE DOSAGE FORMS
6.5.3延长释放剂型
1. PRELIMINARYASSESSMENT (FOR EARLY STAGES OF PRODUCT DEVELOPMENT/DISSOLUTION METHODDEVELOPMENT)
1.前期评估（产品开发 / 溶出度方法开发的初期阶段）
Beforemethod development can begin, it is important to
characterize the molecule sothat the filter, medium, volume of medium, and apparatus can be chon properlyin order to evaluate the performance of the dosage form.
在开始溶出方法开发之前，我们对用以评价制剂溶出行为的滤膜、溶出介质、溶出介质体积和溶出设备进行适当的筛选是非常重要的。
1.1 Performing Filter Compatibility
1.1滤膜相容性研究
Filtrationis a key sample-preparation step in achieving
accurate test results. Thepurpo of filtration is to remove
undissolved drug and excipients from thewithdrawn solution.
If not removed from the sample solution,particles of thedrug will continue to dissolve and can bias the results.Therefore, filteringthe dissolution samples is usually necessary and
should be done immediately ifthe filter is not positioned on the cannula.
为获得准确试验结果，过滤是样品制备的一个关键步骤。过滤的目的是为了除去溶出液中未溶解的药物和辅料。如果不把未溶解的药物和辅料从样品溶液中除去，那么未溶解的药物颗粒将会继续溶解使试验结果出现偏差，因此，如果取样管中没有过滤器，应立即对溶出度样品进行过滤。
Filtration also removes insolubleexcipients that may otherwi interfere with the analytical finish.Selectionof the proper filter material is important and should be accomplished,
