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微晶纤维素流动性的表征及其性能参数相关性的可视化 被引量:13

Characterizing flowability of microcrystalline cellulose and its visualizing the correlation of the performance parameters
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摘要 本文通过多元分析方法评价不同型号微晶纤维素的流动性差异,并利用R语言可视化功能初步探索了微晶纤维素性能参数之间的内在联系。为验证多元分析方法的可操作性,与常规方法如休止角法、Hausner比值、Carr’s指数、川北方程参数a等方法进行对比分析。通过川北方程参数1/b和压力-抗张强度曲线法分别测定微晶纤维素的填充性和可压性,利用R语言可视化分析表征流动性、填充性和可压性的参数的相关性。微晶纤维素WJ(MCCWJ)系列总体流动性稍差于微晶纤维素PH(MCCPH)系列,MCCPH-302的可压性最佳,流动性与填充性最优者为MCCPH-102,常规方法测定的结果与多元分析方法结果基本一致。通过可视化相关系数图分析得出微晶纤维素的流动性与填充性呈正相关,与可压性呈负相关,且具有统计学意义(P<0.01)。结果表明,使用多元分析方法对粉体的流动性是科学可行的,相对于传统表征流动性的方法有较客观的标准。通过R语言可视化功能对粉体的性能参数相关性可视化,为制剂辅料的筛选提供了方便。 In this study, multivariate statistical analysis was applied to characterize the flowability of different types of microcrystalline cellulose(MCC), and the visualization of R language was used to explore the intrinsic correlation on its performances. To verify the operability of multivariate statistical analysis, we compared the results of the conventional methods such as repose angle method, Hausner ratio method, Carr’s index method and the parameter a of Kawakita equation to determine whether there are significant differences between the conventional ones and multivariate statistical analysis. Moreover, the fillibility and compressibility were characterized by parameters 1/b of Kawakita equation and the means of pressure-tensile strength and compressibility curve method, respectively. The data was analyzed through R language for visualizing the correlation among the performance parameters of MCC. The flowability of the series of microcrystalline cellulose PH(MCCPH) were superior to the series of microcrystalline cellulose WJ(MCCWJ), the compressibility of MCCPH-302 was optimum, and the flowability and fallibility of MCCPH-102 were better than others. The results of conventional methods were consistent with multivariate statistical analysis. The fillibility was positively correlated with flowability, both negatively correlated with compressibility by analyzing correlation coefficient diagram, which was statistically significant(P 〈 0.01). It is reasonable that adopting multivariate statistical analysis to character the flowability of powders, which is more objective than the traditional approach. The correlation visualization of performance parameters of powders provides convenience for screening preparation material via the visualization of R language.
作者 余玲飞 胡容峰 苏丹 方文悠 王斌 高松 YU Ling-fei;HU Rong-feng;SU Dan;FANG Wen-you;WANG Bin;GAO Song(Key Laboratory of Xin 'an Medical, Ministry of Education;Anhui "115" Xin'an Pharmaceutical R&D Innovation Team;Key Laboratory of Anhui Provincial TCM Research and Development, Anhui University of Chinese Medicine, Hefei 230038, China;Provincial Hospital of Anhui Medical University, Hefei 230001, China)
出处 《药学学报》 CAS CSCD 北大核心 2018年第5期806-811,共6页 Acta Pharmaceutica Sinica
基金 国家自然科学基金资助项目(81573615,81274100) 安徽省学术和技术带头人及后备人选学术科研活动经费资助项目(皖人社秘2011-381号-26) 安徽中医药大学校级科学研究基金项目(2016zr009) 安徽省"115"新安医药研究与开发创新团队.
关键词 微晶纤维素 流动性 多元分析法 主成分分析 可视化分析 microcrystalline cellulose flowability multivariate statistical analysis principal component analysis visualization analysis
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  • 1聂淑芳,潘卫三,杨星钢,刘宏飞,刘志东.对大鼠在体肠单向灌流技术中重量法的评价[J].中国新药杂志,2005,14(10):1176-1179. 被引量:90
  • 2郑宇,涂家生,庞卉,银春.药用粉末可压性研究概况[J].药学进展,2006,30(3):114-118. 被引量:6
  • 3高春生,王玮,黄健,周翠萍,单利,梅兴国.直接压片辅料-Cellactose~80的粉体学性能评价[J].中国药学杂志,2007,42(2):128-131. 被引量:26
  • 4蒋且英,廖正根,赵国巍,黄海静.吸湿原理及中药制剂防潮方法研究概况[J].中国药房,2007,18(33):2626-2628. 被引量:44
  • 5SHIVANAND P, SPROCKEL OL. Compaction behavior of cellu- lose polymers[J]. Powder Technol, 1992, 69(2) : 177 -184.
  • 6KHAN KA, RHODES CT. Production of tablets by direct com- pression[J]. JPharmSei, 1973, 8(1): 1-5.
  • 7AUGSBURGER L, STEPHEN HW. Pharmaceutical dosage forms: Tablets [M]. New York: Marcel Dekker Inc, 1990:195 -196.
  • 8SHANGRAW RF, DEMAREST DA. A sur,ley of current indus- trial practices in the formulation and manufacture of tablets and capsules[J]. Pharm Technol, 1993, 17(1): 32.
  • 9GONNISSEN Y, VERHOEVEN E, PEETERS E, et al. Copro- cessing via spray drying as a formulation platform to improve the compactability of various drugs [ J]. Eur J Pharm Biopharm, 2008, 69(1) : 320 -334.
  • 10BACHER C, OLSEN PM, BERTELSEN P, et al. Compressibili- ty and compactibility of granules produced by wet and dry granu- lation[J], lnt JPharm, 2008, 358(1-2): 69-74.

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