
微通道反应器内纳米头孢呋辛酯制备工艺优化
张乾霞; 娄金婷; 周月; 段永鸿; 王洁欣*
北京化工大学学报(自然科学版) ›› 2011, Vol. 38 ›› Issue (1) : 15-20.
微通道反应器内纳米头孢呋辛酯制备工艺优化
Optimization of the preparation of cefuroxime axetil nanoparticles in a microchannel by orthogonal tests
[1]平其能. 纳米药物和纳米载体系统[J]. 中国新药杂志, 2002, 11(1): 42-46.
Ping Q N. Nano-medicines and nano-carrier system[J]. Chinese Journal of New
Drugs, 2002, 11(1): 42-46. (in Chinese)
[2]Won D, Kim M, Lee S, et al. Improved physicochemical characteristics of felodipine solid dispersion particles by supercritical antisolvent precipitation process[J]. International Journal of Pharmaceutics,2005, 301(1/2): 199-208.[3]ZhongJ, Shen Z G, Yang Y, et al. Preparation and characterization of uniform nanosized cephradine by combination of reactive precipitation and liquid anti-solvent precipitation under high gravity environment[J]. International Journal of Pharmaceutics, 2005, 301(1/2): 286-293.
[4]Kim J, Kim M, Park H, et al. Physicochemical properties and oral bioa
vailability of amorphous atorvastatin hemi-calcium using spray-drying and SAS
process[J]. International Journal of Pharmaceutics, 2008, 359(1/2): 211-219.[5]WangZ, Chen J F, Le Y, et al. Preparation of ultrafine beclomethasone dipropionate drug powder by antisolvent precipitation[J]. Industrial & Engineering Chemistry Research, 2007, 46(14): 4839-4845.
[6]Wagner J, Khler J M. Continuous synthesis of gold nanoparticles in a microreactor[J]. Nano Letters, 2005, 4(5): 685-691.
[7]国家药典委员会. 中华人民共和国药典(二部)[M]. 北京: 化学工业出版社, 2005: 291. Chinese Pharmacopoeia Commission. Pharmacopoeia of the People’s Republic of China: Chemical Industry Press, 2005: 291. (in Chinese)
[8]ZhangJ Y, Shen Z G, Zhong J, et al. Preparation of amorphous cefuroxime axetil nanoparticles by controlled nanoprecipitation method without surfacta
nts[J]. International Journal of Pharmaceutics, 2006, 323(1): 153-160.
[9]ViolantoM R, Fishcher H W. Method formaking uniformly sized particles from water-insoluble organic compounds: US, 4826689[P]. 1989-05-02.
[10]马静, 王玉红, 王丹梅, 等. 旋转填充床中反溶剂重结晶法制备超细硫酸沙丁胺醇实验研究[J]. 材料科学与工程学报, 2004, 22(1): 74-77.
Ma J, Wang Y H, Wang D M, et al. Preparation of particles of ultra-fine salbuta
mol sulfate by anti-solvent re-crystallization in a rotating packed bed[J].
Journal of Matererial Science Engineering, 2004, 22(1): 74-77. (in Chinese)
[11]ZhaoH, Wang J X, Wang Q A, et al. Controlled liquid antisolvent precipitation of hydrophobic pharmaceutical nanoparticles in a microchannel reactor[J]. Industrial & Engineering Chemistry Research, 2007, 46(24): 8229-8235.
[12]KarnikR, Gu F, Basto P, et al. Microfluidic platform for controlled synthesis of polymeric nanoparticles[J]. Nano Letters, 2008, 8(9): 2906-2912.
[13]Kim M, Jin S, Kim J, et al. Preparation, characterization and in vivo evaluation of amorphous atorvastatin calcium nanoparticles using supercritical
antisolvent (SAS) process[J]. European Journal of Pharmaceutics and Biopharm
aceutics, 2008, 69(2): 454-465.
[14]龙涛, 田熙科, 杨超, 等. 超细阿奇霉素的制备及表征[J]. 化工进展, 2005, 24(7): 763-766.
Long T, Tian X K, Yang C, et al. Preparation and characterization of ultra-fine
Azihromycin[J]. Chemical Industry and Engineering Progress, 2005, 24(7): 763-766. (in Chinese)
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