Insights to the action of additives for stabilization of ultrafine particles of Fenofibrate in aqueous suspensions produced by Sonoprecipitation

被引:12
作者
Pandey, Komal U. [1 ]
Poornachary, Sendhil K. [2 ]
Dalvi, Sameer, V [1 ]
机构
[1] Indian Inst Technol Gandhinagar, Chem Engn, Gandhinagar 382355, Gujarat, India
[2] ASTAR, Inst Chem & Engn Sci, Pesek Rd, Jurong Isl 627833, Singapore
关键词
Liquid antisolvent precipitation; Fenofibrate; Additives; Nucleation; Ultrasound; Single crystals; Molecular simulation; Interaction; Dissolution rate; SALBUTAMOL SULFATE; DRUG NANOCRYSTALS; PRECIPITATION; CRYSTAL; MICRONIZATION; ENHANCEMENT; DISSOLUTION; SIMULATION; BEHAVIOR; GROWTH;
D O I
10.1016/j.powtec.2019.12.059
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Sonoprecipitation of Fenofibrate (FNB) was carried out in the presence of polymeric additives and surfactants. The particle size and morphology was found to be significantly affected by the mixing conditions and the type of additives used. In order to understand the mechanism by which the additives affect FNB particle growth and morphology, intermolecular interactions between the additive and FNB crystal surfaces were modeled. Among the additives used, Tween 80 was found to be a great habit modifier. Hydrogen bonding interactions between Tween 80 and FNB molecules exposed on the (010) face of FNB particles leads to a needle-like morphology. The experimental and modelling studies indicate that hydroxyl propyl methyl cellulose (HPMC) and bovine serum albumin (BSA) show stronger crystal growth inhibition effect and provide better stabilization compared to polyvinyl pyrolidone (PVP) and Tween 80. FNB particles precipitated with ultrasound and additives were found to exhibit faster drug release profiles compared to the particles precipitated without ultrasound but in the presence of additives. (c) 2020 Elsevier B.V. All rights reserved.
引用
收藏
页码:310 / 325
页数:16
相关论文
共 34 条
[1]  
[Anonymous], 2015, J BIOANAL BIOMED
[2]  
Azad M.A., 2013, DRUG DEV IND PHARM, V40, P1
[3]   Precipitation and stabilization of ultrafine particles of Fenofibrate in aqueous suspensions by RESOLV [J].
Dalvi, Sameer V. ;
Azad, Mohammad A. ;
Dave, Rajesh .
POWDER TECHNOLOGY, 2013, 236 :75-84
[4]   Controlling Particle Size of a Poorly Water-Soluble Drug Using Ultrasound and Stabilizers in Antisolvent Precipitation [J].
Dalvi, Sameer V. ;
Dave, Rajesh N. .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2009, 48 (16) :7581-7593
[5]   A novel bottom-up process to produce drug nanocrystals: Controlled crystallization during freeze-drying [J].
de Waard, H. ;
Hinrichs, W. L. J. ;
Frijlink, H. W. .
JOURNAL OF CONTROLLED RELEASE, 2008, 128 (02) :179-183
[6]   Atomistic Simulation To Understand Anisotropic Growth Behavior of Naproxen Crystal in the Presence of Polymeric Additives [J].
Gupta, Krishna M. ;
Yani, Yin ;
Poornachary, Sendhil K. ;
Chow, Pui Shan .
CRYSTAL GROWTH & DESIGN, 2019, 19 (07) :3768-3776
[7]   Understanding the solid-state forms of fenofibrate - A spectroscopic and computational study [J].
Heinz, Andrea ;
Gordon, Keith C. ;
McGoverin, Cushla M. ;
Rades, Thomas ;
Strachan, Clare J. .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2009, 71 (01) :100-108
[8]   Continuous and scalable process for water-redispersible nanoformulation of poorly aqueous soluble APIs by antisolvent precipitation and spray-drying [J].
Hu, Jun ;
Ng, Wai Kiong ;
Dong, Yuancai ;
Shen, Shoucang ;
Tan, Reginald B. H. .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2011, 404 (1-2) :198-204
[9]   Preparation of ultrafine fenofibrate powder by solidification process from emulsion [J].
Huang, Qiao-Ping ;
Wang, Jie-Xin ;
Zhang, Zhi-Bing ;
Shen, Zhi-Gang ;
Chen, Jian-Feng ;
Yun, Jimmy .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2009, 368 (1-2) :160-164
[10]   Micronization of drugs using supercritical carbon dioxide [J].
Kerc, J ;
Srcic, S ;
Knez, Z ;
Sencar-Bozic, P .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1999, 182 (01) :33-39