The Binary System of Ibuprofen-Nicotinamide Under Nanoscale Confinement: From Cocrystal to Coamorphous State

被引:27
作者
Bi, Yanping [1 ]
Xiao, Deli [2 ]
Ren, Shuai [3 ]
Bi, Shuyan [4 ]
Wang, Jianzhu [1 ]
Li, Fei [1 ]
机构
[1] Taishan Med Univ, Sch Pharmaceut Sci, 619 Changcheng Rd, Tai An 271016, Shandong, Peoples R China
[2] China Pharmaceut Univ, Key Lab Drug Qual Control & Pharmacovigilance, Minist Educ, Nanjing 210009, Jiangsu, Peoples R China
[3] Taishan Med Univ, Grad Sch, 619 Changcheng Rd, Tai An 271016, Shandong, Peoples R China
[4] PKU Healthcare Ind Grp, Zibo Hosp, Dept Ultrasound, 2 Xishanwu St, Zibo 255069, Peoples R China
基金
中国国家自然科学基金;
关键词
amorphous; cocrystals; dissolution rate; microspheres; nanotechnology; porosity; silica; AMORPHOUS SOLID DISPERSIONS; DRUG FORMULATIONS; DISSOLUTION;
D O I
10.1016/j.xphs.2017.06.005
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Coamorphous systems have gained success in stabilizing amorphous drugs and improving their solubility and dissolution. Here we proposed to confine a binary mixture of drug and coformer (CF) within nanopores to obtain a nanoconfined coamorphous (NCA) system. For proving feasibility of this proposal, a poorly water-soluble drug (ibuprofen) and a frequently used pharmaceutical CF (nicotinamide) were loaded into nanopores of mesoporous silica microspheres. The solid state of NCA system was characterized by differential scanning calorimetry, X-ray powder diffraction, infrared spectrum, and solid-state nuclear magnetic resonance. With large numbers of nanopores, mesoporous silica microspheres appear to be a feasible carrier to transform a cocrystal system into coamorphism by nanoscale confinement. Benefiting from both nanoscale confinement and CF, the NCA system of ibuprofen achieved synchronic increase in dissolution properties and physical stability. Consequently, the NCA strategy is effective in achieving coamorphous state and offers a promising alternative for formulating poorly water-soluble drugs. (C) 2017 American Pharmacists Association (R). Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:3150 / 3155
页数:6
相关论文
共 16 条
[11]   Solid-state properties and dissolution behaviour of tablets containing co-amorphous indomethacin-arginine [J].
Lenz, Elisabeth ;
Jensen, Katrine Tarp ;
Blaabjerg, Lasse Ingerslev ;
Knop, Klaus ;
Grohganz, Holger ;
Lobmann, Korbinian ;
Rades, Thomas ;
Kleinebudde, Peter .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2015, 96 :44-52
[12]   Mesoporous silica formulation strategies for drug dissolution enhancement: a review [J].
McCarthy, Carol A. ;
Ahern, Robert J. ;
Dontireddy, Rakesh ;
Ryan, Katie B. ;
Crean, Abina M. .
EXPERT OPINION ON DRUG DELIVERY, 2016, 13 (01) :93-108
[13]   Determination of the Physical State of Drug Molecules in Mesoporous Silicon with Different Surface Chemistries [J].
Riikonen, Joakim ;
Makila, Ermei ;
Salonen, Jarno ;
Lehto, Vesa-Pekka .
LANGMUIR, 2009, 25 (11) :6137-6142
[14]   Coamorphous Atorvastatin Calcium to Improve its Physicochemical and Pharmacokinetic Properties [J].
Shayanfar, Ali ;
Ghavimi, Hamed ;
Hamishehkar, Hamed ;
Jouyban, Abolghasem .
JOURNAL OF PHARMACY AND PHARMACEUTICAL SCIENCES, 2013, 16 (04) :577-587
[15]   Non-Covalent Derivatives: Cocrystals and Eutectics [J].
Stoler, Emily ;
Warner, John C. .
MOLECULES, 2015, 20 (08) :14833-14848
[16]   Probing the mechanisms of drug release from amorphous solid dispersions in medium-soluble and medium-insoluble carriers [J].
Sun, Dajun D. ;
Lee, Ping I. .
JOURNAL OF CONTROLLED RELEASE, 2015, 211 :85-93