Fixed Dose Combination Formulations: Multilayered Platforms Designed for the Management of Cardiovascular Disease

被引:18
作者
Andrews, G. P. [1 ]
Li, S. [1 ]
Almajaan, A. [1 ]
Yu, T. [1 ]
Martini, L. [3 ]
Healy, A. [2 ]
Jones, D. S. [1 ]
机构
[1] Queens Univ, Sch Pharm, Pharmaceut Engn Grp, Belfast BT9, Antrim, North Ireland
[2] Trinity Coll Dublin, Sch Pharm & Pharmaceut Sci, Panoz Inst, Dublin 2, Ireland
[3] Royal Pharmaceut Soc, London E1W 1AW, England
基金
爱尔兰科学基金会;
关键词
fixed dose combination; hot-melt coextrusion; multilayer drug delivery; biphasic drug release; simvastatin; enhanced bioavailability; HOT-MELT EXTRUSION; DISPERSIONS;
D O I
10.1021/acs.molpharmaceut.8b01068
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
100103 [病原生物学]; 100218 [急诊医学];
摘要
Hyperlipidaemia is considered as one of the main risk factors associated with cardiovascular diseases (CVDs). Among different lipidlowering agents used to manage hyperlipidaemia, statins are highly prescribed for management of hyperlipidaemia with simvastatin being one of the most common. Simvastatin is susceptible to extensive metabolism by CYP450 3A4 and 3A5, which are expressed both in the liver and the gastrointestinal tract. Nevertheless, the localization of these enzymes is site-dependent with lower concentration at the distal/proximal regions of the small intestine/colon. In addition to statins, medications such as antihypertensive agents and anticoagulants are introduced as adjuvants, for the treatment of cardiovascular disease. The aim of this study was to design a bilayer delivery system capable of delivering biphasic release of simvastatin and aspirin, within a fixed dose combination. A delayed release platform based on a combination of anionic polymers prepared using hot-melt extrusion was developed to delay the release of simvastatin. An optimized formulation tested for dissolution performance clearly demonstrated an ability to delay the release of simvastatin. In addition, an immediate release layer based on Kollidon VA64 was successfully developed to deliver aspirin. Both formulations were then manufactured as a bilayer drug delivery system (tablets and coextrudates), and the release performance was examined. On the basis of the obtained results, these formulations may be used as a platform for delivering a wide range of medications in a biphasic manner.
引用
收藏
页码:1827 / 1838
页数:12
相关论文
共 26 条
[1]
[Anonymous], CARD DIS CVDS
[2]
[Anonymous], 2014, Lippincott Illustrated Reviews: Pharmacology
[3]
STABILITY OF ASPIRIN IN DIFFERENT MEDIA [J].
BAKAR, SK ;
NIAZI, S .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1983, 72 (09) :1024-1026
[4]
The epidemiology of cardiovascular disease in the UK 2014 [J].
Bhatnagar, Prachi ;
Wickramasinghe, Kremlin ;
Williams, Julianne ;
Rayner, Mike ;
Townsend, Nick .
HEART, 2015, 101 (15) :1182-1189
[5]
Co-extruded solid solutions as immediate release fixed-dose combinations [J].
Dierickx, L. ;
Van Snick, B. ;
Monteyne, T. ;
De Beer, T. ;
Remon, J. P. ;
Vervaet, C. .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2014, 88 (02) :502-509
[6]
Dressman J., 2005, Pharmaceutical dissolution testing
[7]
COMPARISON OF CANINE AND HUMAN GASTROINTESTINAL PHYSIOLOGY [J].
DRESSMAN, JB .
PHARMACEUTICAL RESEARCH, 1986, 3 (03) :123-131
[8]
MEASUREMENT OF GASTROINTESTINAL PH PROFILES IN NORMAL AMBULANT HUMAN-SUBJECTS [J].
EVANS, DF ;
PYE, G ;
BRAMLEY, R ;
CLARK, AG ;
DYSON, TJ ;
HARDCASTLE, JD .
GUT, 1988, 29 (08) :1035-1041
[9]
Hydroxypropyl Methylcellulose Acetate Succinate-Based Spray-Dried Dispersions: An Overview [J].
Friesen, Dwayne T. ;
Shanker, Ravi ;
Crew, Marshall ;
Smithey, Daniel T. ;
Curatolo, W. J. ;
Nightingale, J. A. S. .
MOLECULAR PHARMACEUTICS, 2008, 5 (06) :1003-1019
[10]
Enhanced dissolution rate and oral bioavailability of simvastatin nanocrystal prepared by sonoprecipitation [J].
Jiang, Tongying ;
Han, Ning ;
Zhao, Buwen ;
Xie, Yuling ;
Wang, Siling .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2012, 38 (10) :1230-1239