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Minitab用于中心复合设计与数据处理 被引量:19

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作者 杨铭
出处 《药学服务与研究》 CAS CSCD 2007年第3期231-234,共4页 Pharmaceutical Care and Research
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  • 3[5]Do B, Robinet S, Pradeau D, et al. Application of central composite designs for optimization of the chromatographic separation of monomethylarsonate and dimethylarsinate and of selenomethionine and selenite by ion-pair chromatography coupled with plasma mass spectrometric detection[J]. Analyst, 2001, 126: 594.
  • 4Abu-Izza KA, Garcia-Contreras L, Lu DR. Preparation and evaluation of sustained release AZT-loaded microspheres: Optimization of the release characteristics using response surface methodology[J]. J Pharm Sci, 1996, 85:144.
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  • 6Molpeceres J, Guzman M, Aberturas MR, et al. Application of central composite designs to the preparation of poly caprolactone nanoparticles by solvent displacement [J]. J Pharm Sci, 1996, 85: 206.
  • 7Do B, Robinet S, Pradeau D, et al. Application of central composite designs for optimization of the chromatographic separation of monomethylarsonate and dimethylarsinate and of selenomethionine and selenite by ion-pair chromatography coupled with plasma m
  • 8Meade VM, Burton MA, Gray BN, et al. Distribution of different sized microspheres in experimental hepatic tumours [J]. Eur J Clin Oncol, 1987,23:37.
  • 9Bastian P, Bartkowski R, Kohler H, et al. Chemo-embolization of experimental liver metstases. Part Ⅰ: distribution of biodegrable microspheres of different sizes in an animal model for the locoregional therapy [J]. Eur J Pharm Biopharm, 1998, 46: 243.
  • 10Campbell AM, Bailey IH, Burton MA. Analysis of the distribution of intra-arterial microspheres in human liver following hepatic yttrium-90microsphere therapy [J]. Phys Med Biol, 2000, 45:1023.

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