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本文引用的文献

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ICH Q10 Pharmaceutical Quality System Guidance: Understanding Its Impact on Pharmaceutical Quality.ICH Q10 药物质量体系指南:理解其对药物质量的影响。
AAPS J. 2021 Nov 12;23(6):117. doi: 10.1208/s12248-021-00657-y.
2
Quality-by-Design II: Application of Quantitative Risk Analysis to the Formulation of Ciprofloxacin Tablets.质量源于设计II:定量风险分析在环丙沙星片制剂中的应用
AAPS PharmSciTech. 2016 Apr;17(2):233-44. doi: 10.1208/s12249-015-0349-2. Epub 2015 Jul 23.
3
Quality by design I: Application of failure mode effect analysis (FMEA) and Plackett-Burman design of experiments in the identification of "main factors" in the formulation and process design space for roller-compacted ciprofloxacin hydrochloride immediate-release tablets.基于质量源于设计理念 I:应用失效模式与影响分析(FMEA)和 Plackett-Burman 实验设计,识别盐酸环丙沙星干法制粒速释片制剂和工艺设计空间中“主要因素”。
AAPS PharmSciTech. 2012 Dec;13(4):1243-54. doi: 10.1208/s12249-012-9844-x. Epub 2012 Sep 20.
4
Eudragit(®) RS PO/RL PO as rate-controlling matrix-formers via roller compaction: Influence of formulation and process variables on functional attributes of granules and tablets.Eudragit(®) RS PO/RL PO 作为控释骨架材料的制粒:配方和工艺变量对颗粒和片剂功能特性的影响。
Drug Dev Ind Pharm. 2012 Oct;38(10):1240-53. doi: 10.3109/03639045.2011.645831. Epub 2012 Jan 19.
5
Assessment of the critical factors affecting the porosity of roller compacted ribbons and the feasibility of using NIR chemical imaging to evaluate the porosity distribution.评估影响辊压制带状物孔隙率的关键因素,以及使用近红外化学成像技术评估孔隙率分布的可行性。
Int J Pharm. 2011 May 30;410(1-2):1-8. doi: 10.1016/j.ijpharm.2011.02.028. Epub 2011 Mar 1.
6
NIR spectroscopy applications in the development of a compacted multiparticulate system for modified release.近红外光谱在开发用于改良释放的紧凑型多颗粒系统中的应用。
AAPS PharmSciTech. 2011 Mar;12(1):262-78. doi: 10.1208/s12249-010-9580-z. Epub 2011 Jan 15.
7
Biowaiver monographs for immediate release solid oral dosage forms: ciprofloxacin hydrochloride.速释固体口服剂型的生物豁免说明书:盐酸环丙沙星。
J Pharm Sci. 2011 Jan;100(1):22-33. doi: 10.1002/jps.22259.
8
Systematical approach of formulation and process development using roller compaction.采用滚压法进行制剂和工艺开发的系统方法。
Eur J Pharm Biopharm. 2009 Oct;73(2):219-29. doi: 10.1016/j.ejpb.2009.04.008. Epub 2009 May 4.
9
Quality by design, part II: application of NIR spectroscopy to monitor the coating process for a pharmaceutical sustained release product.质量源于设计,第二部分:近红外光谱法在监测药物缓释产品包衣过程中的应用
J Pharm Sci. 2008 Sep;97(9):4052-66. doi: 10.1002/jps.21307.
10
Quality by design, part I: application of NIR spectroscopy to monitor tablet manufacturing process.质量源于设计,第一部分:近红外光谱法在片剂生产过程监测中的应用。
J Pharm Sci. 2008 Sep;97(9):4040-51. doi: 10.1002/jps.21303.

设计质量III:近红外光谱法在监测直接压片过程中的滚压及速释片剂产品质量属性方面的应用。

Quality-by-design III: application of near-infrared spectroscopy to monitor roller compaction in-process and product quality attributes of immediate release tablets.

作者信息

Kona Ravikanth, Fahmy Raafat M, Claycamp Gregg, Polli James E, Martinez Marilyn, Hoag Stephen W

机构信息

School of Pharmacy, University of Maryland, 20 N. Pine Street, Baltimore, Maryland, 21201, USA.

出版信息

AAPS PharmSciTech. 2015 Feb;16(1):202-16. doi: 10.1208/s12249-014-0180-1. Epub 2014 Oct 16.

DOI:10.1208/s12249-014-0180-1
PMID:25319052
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4309813/
Abstract

The objective of this study is to use near-infrared spectroscopy (NIRS) coupled with multivariate chemometric models to monitor granule and tablet quality attributes in the formulation development and manufacturing of ciprofloxacin hydrochloride (CIP) immediate release tablets. Critical roller compaction process parameters, compression force (CFt), and formulation variables identified from our earlier studies were evaluated in more detail. Multivariate principal component analysis (PCA) and partial least square (PLS) models were developed during the development stage and used as a control tool to predict the quality of granules and tablets. Validated models were used to monitor and control batches manufactured at different sites to assess their robustness to change. The results showed that roll pressure (RP) and CFt played a critical role in the quality of the granules and the finished product within the range tested. Replacing binder source did not statistically influence the quality attributes of the granules and tablets. However, lubricant type has significantly impacted the granule size. Blend uniformity, crushing force, disintegration time during the manufacturing was predicted using validated PLS regression models with acceptable standard error of prediction (SEP) values, whereas the models resulted in higher SEP for batches obtained from different manufacturing site. From this study, we were able to identify critical factors which could impact the quality attributes of the CIP IR tablets. In summary, we demonstrated the ability of near-infrared spectroscopy coupled with chemometrics as a powerful tool to monitor critical quality attributes (CQA) identified during formulation development.

摘要

本研究的目的是使用近红外光谱(NIRS)结合多元化学计量模型,在盐酸环丙沙星(CIP)速释片的制剂开发和生产过程中监测颗粒和片剂的质量属性。对从我们早期研究中确定的关键滚压工艺参数、压缩力(CFt)和制剂变量进行了更详细的评估。在开发阶段建立了多元主成分分析(PCA)和偏最小二乘(PLS)模型,并将其用作预测颗粒和片剂质量的控制工具。经过验证的模型用于监测和控制在不同地点生产的批次,以评估其对变化的稳健性。结果表明,在所测试的范围内,滚压压力(RP)和CFt对颗粒和成品的质量起着关键作用。更换粘合剂来源对颗粒和片剂的质量属性没有统计学影响。然而,润滑剂类型对颗粒大小有显著影响。使用经过验证的PLS回归模型预测了制造过程中的混合均匀性、压碎力、崩解时间,预测标准误差(SEP)值可接受,而对于从不同生产地点获得的批次,模型的SEP较高。通过这项研究,我们能够确定可能影响CIP速释片质量属性的关键因素。总之,我们证明了近红外光谱结合化学计量学作为一种强大工具来监测制剂开发过程中确定的关键质量属性(CQA)的能力。