Parametric Study of Acoustic Excitation-Based Glycerol-Water Microsphere Fabrication in Single Nozzle Jetting

被引:11
作者
Herran, C. Leigh [1 ]
Wang, Wei [1 ]
Huang, Yong [1 ]
Mironov, Vladimir [2 ]
Markwald, Roger [2 ]
机构
[1] Clemson Univ, Dept Mech Engn, Clemson, SC 29634 USA
[2] Med Univ S Carolina, Dept Regenerat Med & Cell Biol, Charleston, SC 29425 USA
来源
JOURNAL OF MANUFACTURING SCIENCE AND ENGINEERING-TRANSACTIONS OF THE ASME | 2010年 / 132卷 / 05期
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
DROP FORMATION; DRUG-RELEASE; POLYMER MICROSPHERES; SIZE; DYNAMICS; DEFORMATION; BREAKUP;
D O I
10.1115/1.4002187
中图分类号
T [工业技术];
学科分类号
120111 [工业工程];
摘要
Microspheres or droplets are increasingly finding various biomedical applications as drug microspheres and multicellular spheroids. Single nozzle-based continuous jetting with the help of acoustic excitation and/or carrier stream is a basic process for mono-disperse microsphere fabrication. Precise control of microsphere size and size distribution in single nozzle jetting is still of great manufacturing interest. The objective of this study is to numerically model a glycerol-water microsphere fabrication process during acoustic excitation-based single nozzle continuous jetting. Using a volume of fluid method, this study has investigated the effects of material properties and fabrication conditions such as the acoustic excitation frequency and amplitude and the carrier stream velocity on the size of microspheres fabricated. (1) The microsphere diameter decreases as the glycerol volume percentage increases. (2) The excitation frequency and pressure have a pronounced effect on the microsphere size. The microsphere diameter decreases as the excitation frequency increases, and the microsphere diameter increases with the excitation pressure amplitude. (3) The microsphere size decreases as the carrier stream velocity increases. [DOI:10.1115/1.4002187]
引用
收藏
页数:7
相关论文
共 34 条
[1]
Drop formation from a capillary tube: Comparison of one-dimensional and two-dimensional analyses and occurrence of satellite drops [J].
Ambravaneswaran, B ;
Wilkes, ED ;
Basaran, OA .
PHYSICS OF FLUIDS, 2002, 14 (08) :2606-2621
[2]
The production of uniformly sized polymer microspheres [J].
Amsden, B .
PHARMACEUTICAL RESEARCH, 1999, 16 (07) :1140-1143
[3]
[Anonymous], 2006, HDB CHEM PHYS 2006 2
[4]
[Anonymous], 2006, US GUID
[5]
Use of microsphere technology for targeted delivery of rifampin to Mycobacterium tuberculosis-infected macrophages [J].
Barrow, ELW ;
Winchester, GA ;
Staas, JK ;
Quenelle, DC ;
Barrow, WW .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1998, 42 (10) :2682-2689
[6]
Uniform double-walled polymer microspheres of controllable shell thickness [J].
Berkland, C ;
Pollauf, E ;
Pack, DW ;
Kim, K .
JOURNAL OF CONTROLLED RELEASE, 2004, 96 (01) :101-111
[7]
Microsphere size, precipitation kinetics and drug distribution control drug release from biodegradable polyanhydride microspheres [J].
Berkland, C ;
Kipper, MJ ;
Narasimhan, B ;
Kim, KK ;
Pack, DW .
JOURNAL OF CONTROLLED RELEASE, 2004, 94 (01) :129-141
[8]
PLG microsphere size controls drug release rate through several competing factors [J].
Berkland, C ;
Kim, K ;
Pack, DW .
PHARMACEUTICAL RESEARCH, 2003, 20 (07) :1055-1062
[9]
Precise control of PLG microsphere size provides enhanced control of drug release rate [J].
Berkland, C ;
King, M ;
Cox, A ;
Kim, K ;
Pack, DW .
JOURNAL OF CONTROLLED RELEASE, 2002, 82 (01) :137-147
[10]
Fabrication of PLG microspheres with precisely controlled and monodisperse size distributions [J].
Berkland, C ;
Kim, KK ;
Pack, DW .
JOURNAL OF CONTROLLED RELEASE, 2001, 73 (01) :59-74