Effect of molecular weight of hypromellose on mucin diffusion and oral absorption behavior of fenofibrate nanocrystal

被引:16
作者
Ueda, Keisuke [1 ]
Iwai, Takaaki [1 ]
Sunazuka, Yushi [1 ]
Chen, Ziqiao [1 ]
Kato, Nao [1 ]
Higashi, Kenjirou [1 ]
Moribe, Kunikazu [1 ]
机构
[1] Chiba Univ, Grad Sch Pharmaceut Sci, Chuo Ku, 1-8-1 Inohana, Chiba 2608675, Japan
关键词
Drug nanocrystal; Poorly water-soluble drug; Hypromellose; Mucin; Unstirred water layer; Oral absorption; AMORPHOUS SOLID DISPERSIONS; UNSTIRRED WATER LAYER; DRUG-DELIVERY; SOLUBLE DRUGS; GASTROINTESTINAL MUCUS; CYCLOSPORINE-A; PARTICLE-SIZE; NANOPARTICLES; DISSOLUTION; FORMULATION;
D O I
10.1016/j.ijpharm.2019.04.033
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
We investigated the effect of variation in the molecular weight of hypromellose (HPMC) on the oral absorption of fenofibrate (FFB) nanocrystal. Four types of HPMC with different molecular weights and sodium dodecyl sulfate (SDS) were used as dispersion stabilizers for FFB nanocrystal suspension. Wet-milling of FFB crystal with HPMC and SDS formed diamond-shaped FFB nanocrystals with approximately 150 nm diameter. HPMC was strongly adsorbed onto the FFB nanocrystal interface, and the amount of HPMC adsorbed was not dependent on the molecular weight of HPMC. However, the decrease in the molecular weight of adsorbed HPMC led to an improvement in the permeability of FFB nanocrystal through the mucin layer. The decrease in molecular weight of HPMC enhanced the flexibility of FFB nanocrystal interface and effectively inhibited its interaction with mucin. This led to faster diffusion of FFB nanocrystal through mucin. In vivo oral absorption studies showed rapid FFB absorption from FFB nanocrystal formulations using HPMC of low molecular weights. The present study revealed that the molecular weight of the dispersion stabilizer for drug nanocrystal formulation should be taken into consideration to achieve improved absorption of poorly water-soluble drugs after oral administration.
引用
收藏
页码:39 / 47
页数:9
相关论文
共 54 条
[1]   Polymeric Amorphous Solid Dispersions: A Review of Amorphization, Crystallization, Stabilization, Solid-State Characterization, and Aqueous Solubilization of Biopharmaceutical Classification System Class II Drugs [J].
Baghel, Shrawan ;
Cathcart, Helen ;
O'Reilly, Niall J. .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2016, 105 (09) :2527-2544
[2]   Pharmaceutical cocrystals, salts and multicomponent systems; intermolecular interactions and property based design [J].
Berry, David J. ;
Steed, Jonathan W. .
ADVANCED DRUG DELIVERY REVIEWS, 2017, 117 :3-24
[3]   Recovery of BCS Class II drugs during aqueous redispersion of core-shell type nanocomposite particles produced via fluidized bed coating [J].
Bhakay, Anagha ;
Dave, Rajesh ;
Bilgili, Ecevit .
POWDER TECHNOLOGY, 2013, 236 :221-234
[4]   Comparative study of Pluronic® F127-modified liposomes and chitosan-modified liposomes for mucus penetration and oral absorption of cyclosporine A in rats [J].
Chen, Dan ;
Xia, Dengning ;
Li, Xiuying ;
Zhu, Quanlei ;
Yu, Hongzhen ;
Zhu, Chunliu ;
Gan, Yong .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2013, 449 (1-2) :1-9
[5]   Preparation of cyclosporine A nanoparticles by evaporative precipitation into aqueous solution [J].
Chen, XX ;
Young, TJ ;
Sarkari, M ;
Williams, RO ;
Johnston, KP .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2002, 242 (1-2) :3-14
[6]   Effect of polymer molecular weight on nanocomminution of poorly soluble drug [J].
Choi, Ji-Yeun ;
Park, Chul Ho ;
Lee, Jonghwi .
DRUG DELIVERY, 2008, 15 (05) :347-353
[7]   Preparation and characterization of spironolactone nanoparticles by antisolvent precipitation [J].
Dong, Yuancai ;
Ng, Wai Kiong ;
Shen, Shoucang ;
Kim, Sanggu ;
Tan, Reginald B. H. .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2009, 375 (1-2) :84-88
[8]   Stable carbamazepine colloidal systems using the cosolvent technique [J].
Douroumis, D. ;
Fahr, A. .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2007, 30 (05) :367-374
[9]   Oral drug delivery with polymeric nanoparticles: The gastrointestinal mucus barriers [J].
Ensign, Laura M. ;
Cone, Richard ;
Hanes, Justin .
ADVANCED DRUG DELIVERY REVIEWS, 2012, 64 (06) :557-570
[10]   EXPERIMENTAL ESTIMATION OF THE EFFECTIVE UNSTIRRED WATER LAYER THICKNESS IN THE HUMAN JEJUNUM, AND ITS IMPORTANCE IN ORAL-DRUG ABSORPTION [J].
FAGERHOLM, U ;
LENNERNAS, H .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 1995, 3 (05) :247-253