Microwave processed solid dispersions for enhanced dissolution of gemfibrozil using non-ordered mesoporous silica

被引:28
作者
Hussain, Talib [1 ]
Waters, Laura J. [1 ]
Parkes, Gareth M. B. [2 ]
Shahzad, Yasser [1 ,3 ]
机构
[1] Univ Huddersfield, Dept Pharm, Huddersfield, W Yorkshire, England
[2] Univ Huddersfield, Dept Chem, Huddersfield, W Yorkshire, England
[3] Univ Cent Punjab, Fac Pharm, Lahore, Pakistan
关键词
Amorphous; Dissolution enhancement; Gemfibrozil; Microwave heating; Silica; Solid dispersion; DRUG-DELIVERY SYSTEMS; POORLY SOLUBLE DRUGS; ORAL BIOAVAILABILITY; FORMULATION; FENOFIBRATE; IMPROVEMENT; SOLUBILITY; PARTICLES; IBUPROFEN; BEHAVIOR;
D O I
10.1016/j.colsurfa.2017.02.007
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
This study describes the application of three non-ordered mesoporous silicas (Syloid AL(-1), Syloid 72 and Syloid 244) in improving the dissolution rate of a poorly aqueous soluble drug, namely gemfibrozil. For this purpose, solid dispersions were formulated using a robust and controlled microwave heating method. Prepared formulations were subjected to solid state characterisation and dissolution behaviour. Differential scanning calorimetry (DSC) and X-ray diffraction (XRD) results confirmed that microwave heating method incorporated gemfibrozil in an amorphous form in Syloid 72 and Syloid 244. This was attributed to a large pore volume and diameter compared with Syloid AL(-1) which has a small pore volume. Presence of more crystalline drug in the case of Syloid AL(-1) based formulations was attributed to larger surface area where drug was adsorbed in layers as confirmed by the scanning electron microscopy. DSC and XRD results also confirmed stability of formulations when stored for 3 months under stressed conditions (40 degrees C and 75% RH). FT-IR results show lack of interaction between silica and the drug in all cases. It was also noted that all three silica types improved the dissolution behaviour of gemfibrozil when compared with dissolution properties of pure drug. The surface properties of Syloid 72 were found optimum as it enhanced the rate of dissolution of gemfibrozil from microwave processed formulation far better than physically mixed formulations and those prepared with Syloid AL(-1) and Syloid 244. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:428 / 435
页数:8
相关论文
共 35 条
[1]  
Bastami Z., 2015, ASIAN J PHARM, V19
[2]   Solid dispersions, Part I: recent evolutions and future opportunities in manufacturing methods for dissolution rate enhancement of poorly water-soluble drugs [J].
Bikiaris, Dimitrios N. .
EXPERT OPINION ON DRUG DELIVERY, 2011, 8 (11) :1501-1519
[3]   Supersaturating Drug Delivery Systems: The Answer to Solubility-Limited Oral Bioavailability? [J].
Brouwers, Joachim ;
Brewster, Marcus E. ;
Augustijns, Patrick .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2009, 98 (08) :2549-2572
[4]   Core/shell structured silica spheres with controllable thickness of mesoporous shell and its adsorption, drug storage and release properties [J].
Chen, Xuecheng .
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 2013, 428 :79-85
[5]  
Chuang IS, 1996, J AM CHEM SOC, V118, P401
[6]   THE STABILITY OF DRUG ADSORBATES ON SILICA [J].
DANIELS, R ;
KERSTIENS, B ;
TISCHINGERWAGNER, H ;
RUPPRECHT, H .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1986, 12 (11-13) :2127-2156
[7]   Hydrogen bonding with adsorbent during storage governs drug dissolution from solid-dispersion granules [J].
Gupta, MK ;
Tseng, YC ;
Goldman, D ;
Bogner, RH .
PHARMACEUTICAL RESEARCH, 2002, 19 (11) :1663-1672
[8]   High drug load, stable, manufacturable and bioavailable fenofibrate formulations in mesoporous silica: a comparison of spray drying versus solvent impregnation methods [J].
Hong, Shiqi ;
Shen, Shoucang ;
Tan, David Cheng Thiam ;
Ng, Wai Kiong ;
Liu, Xueming ;
Chia, Leonard S. O. ;
Irwan, Anastasia W. ;
Tan, Reginald ;
Nowak, Steven A. ;
Marsh, Kennan ;
Gokhale, Rajeev .
DRUG DELIVERY, 2016, 23 (01) :316-327
[9]  
Hussain T., 2014, APPL MICROWAVE FORMU
[10]   Comparison of mesoporous silicon and non-ordered mesoporous silica materials as drug carriers for itraconazole [J].
Kinnari, Paivi ;
Makila, Ermei ;
Heikkila, Teemu ;
Salonen, Jarno ;
Hirvonen, Jouni ;
Santos, Helder A. .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2011, 414 (1-2) :148-156