• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

运用实验设计方法于稳定性研究:评价药物稳定性的偏最小二乘方法。

Applying the methodology of Design of Experiments to stability studies: a Partial Least Squares approach for evaluation of drug stability.

机构信息

a Lek Pharmaceuticals d.d. , Ljubljana , Slovenia.

b Faculty of Pharmacy , University of Ljubljana , Ljubljana , Slovenia.

出版信息

Drug Dev Ind Pharm. 2018 May;44(5):778-786. doi: 10.1080/03639045.2017.1412459. Epub 2017 Dec 14.

DOI:10.1080/03639045.2017.1412459
PMID:29192517
Abstract

The aim of the present research is to show that the methodology of Design of Experiments can be applied to stability data evaluation, as they can be seen as multi-factor and multi-level experimental designs. Linear regression analysis is usually an approach for analyzing stability data, but multivariate statistical methods could also be used to assess drug stability during the development phase. Data from a stability study for a pharmaceutical product with hydrochlorothiazide (HCTZ) as an unstable drug substance was used as a case example in this paper. The design space of the stability study was modeled using Umetrics MODDE 10.1 software. We showed that a Partial Least Squares model could be used for a multi-dimensional presentation of all data generated in a stability study and for determination of the relationship among factors that influence drug stability. It might also be used for stability predictions and potentially for the optimization of the extent of stability testing needed to determine shelf life and storage conditions, which would be time and cost-effective for the pharmaceutical industry.

摘要

本研究旨在表明,实验设计方法可应用于稳定性数据评估,因为它们可以被视为多因素和多层次的实验设计。线性回归分析通常是一种用于分析稳定性数据的方法,但多元统计方法也可用于评估药物在开发阶段的稳定性。本文以含有不稳定药物成分氢氯噻嗪 (HCTZ) 的药物产品的稳定性研究数据为例。使用 Umetrics MODDE 10.1 软件对稳定性研究的设计空间进行建模。我们表明,偏最小二乘模型可用于多维呈现稳定性研究中生成的所有数据,并确定影响药物稳定性的因素之间的关系。它也可用于稳定性预测,并有可能优化确定保质期和存储条件所需的稳定性测试程度,这将对制药行业具有时间和成本效益。

相似文献

1
Applying the methodology of Design of Experiments to stability studies: a Partial Least Squares approach for evaluation of drug stability.运用实验设计方法于稳定性研究:评价药物稳定性的偏最小二乘方法。
Drug Dev Ind Pharm. 2018 May;44(5):778-786. doi: 10.1080/03639045.2017.1412459. Epub 2017 Dec 14.
2
Prediction of saxagliptin stability using a new approach based on Partial Least Squares and Design of Experiments.基于偏最小二乘法和实验设计的新型方法预测沙格列汀稳定性。
Pharm Dev Technol. 2020 Dec;25(10):1260-1270. doi: 10.1080/10837450.2020.1817073. Epub 2020 Sep 9.
3
Linear support vector regression and partial least squares chemometric models for determination of Hydrochlorothiazide and Benazepril hydrochloride in presence of related impurities: a comparative study.用于在存在相关杂质的情况下测定氢氯噻嗪和盐酸贝那普利的线性支持向量回归和偏最小二乘化学计量学模型:一项比较研究。
Spectrochim Acta A Mol Biomol Spectrosc. 2014 Sep 15;130:350-6. doi: 10.1016/j.saa.2014.04.024. Epub 2014 Apr 18.
4
Design of experiments and multivariate analysis approach to study dissolution stability of a modified-release drug product to support lean design strategies.采用实验设计和多变量分析方法研究缓释制剂的溶出稳定性以支持精益设计策略。
Drug Dev Ind Pharm. 2021 Sep;47(9):1481-1488. doi: 10.1080/03639045.2021.2001491. Epub 2021 Nov 17.
5
Stability-indicating LC method for the simultaneous determination of lisinopril and hydrochlorothiazide.同时测定赖诺普利和氢氯噻嗪的稳定性指示液相色谱法。
J Chromatogr Sci. 2014 Nov-Dec;52(10):1193-7. doi: 10.1093/chromsci/bmt176. Epub 2013 Dec 1.
6
Stability study of losartan/hydrochlorothiazide tablets.氯沙坦/氢氯噻嗪片的稳定性研究。
Int J Pharm. 2005 Mar 3;291(1-2):127-37. doi: 10.1016/j.ijpharm.2004.07.050. Epub 2004 Dec 28.
7
Development and validation of multivariate calibration methods for simultaneous estimation of Paracetamol, Enalapril maleate and hydrochlorothiazide in pharmaceutical dosage form.建立并验证了多变量校准方法,可同时测定药物制剂中的扑热息痛、马来酸依那普利和氢氯噻嗪的含量。
Spectrochim Acta A Mol Biomol Spectrosc. 2017 Jan 15;171:369-375. doi: 10.1016/j.saa.2016.08.028. Epub 2016 Aug 20.
8
Simultaneous quantitative analysis of olmesartan, amlodipine and hydrochlorothiazide in their combined dosage form utilizing classical and alternating least squares based chemometric methods.利用基于经典和交替最小二乘法的化学计量学方法同时定量分析奥美沙坦、氨氯地平和氢氯噻嗪的复方制剂。
Acta Pharm. 2016 Mar;66(1):83-95. doi: 10.1515/acph-2016-0004.
9
Influence of pH modifiers on the dissolution and stability of hydrochlorothiazide in the bi- and three-layer tablets.pH调节剂对氢氯噻嗪在双层和三层片剂中的溶出度及稳定性的影响
Acta Pharm. 2015 Dec;65(4):383-97. doi: 10.1515/acph-2015-0031.
10
Stability-Indicating Liquid Chromatographic Methods with Photodiode Array Detection and Light Scattering Detection for Simultaneous Determination of Candesartan and Hydrochlorothiazide.采用光电二极管阵列检测和光散射检测的稳定性指示液相色谱法同时测定坎地沙坦和氢氯噻嗪
J Chromatogr Sci. 2018 Feb 1;56(2):99-107. doi: 10.1093/chromsci/bmx068.

引用本文的文献

1
Use of Factorial Designs to Reduce Stability Studies for Parenteral Drug Products: Determination of Factor Effects via Accelerated Stability Data Analysis.使用析因设计减少注射用药品的稳定性研究:通过加速稳定性数据分析确定因素效应
Pharmaceutics. 2025 Aug 18;17(8):1067. doi: 10.3390/pharmaceutics17081067.