Fusion Method for Solubility and Dissolution Rate Enhancement of Ibuprofen Using Block Copolymer Poloxamer 407

被引:43
|
作者
Dugar, Rohit P. [1 ]
Gajera, Bhavin Y. [1 ]
Dave, Rutesh H. [1 ]
机构
[1] Long Isl Univ, Div Pharmaceut Sci, Arnold & Marie Schwartz Coll Pharm & Hlth Sci, Brooklyn, NY 11201 USA
来源
AAPS PHARMSCITECH | 2016年 / 17卷 / 06期
关键词
dissolution rate enhancement; fusion method; ibuprofen; poloxamer; solubility enhancement; SOLID DISPERSIONS; RELEASE CHARACTERISTICS; PROCESS PARAMETERS; SOLUBLE DRUGS; GRANULATION; BIOAVAILABILITY; DELIVERY; CYCLODEXTRIN; COMPLEXATION; FORMULATIONS;
D O I
10.1208/s12249-016-0482-6
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Aim of current research was to prepare ibuprofen-poloxamer 407 binary mixtures using fusion method and characterize them for their physicochemical and performance properties. Binary mixtures of ibuprofen and poloxamer were prepared in three different ratios (1:0.25, 1:0.5, and 1:0.75, respectively) using a water-jacketed high shear mixer. In vitro dissolution and saturation solubility studies were carried out for the drug, physical mixtures, and formulations for all ratios in de-ionized water, 0.1 N HCl (pH = 1.2), and phosphate buffer (pH = 7.2). Thermal and physical characterization of samples was done using modulated differential scanning calorimetry (mDSC), X-ray powder diffraction (XRD), and infrared spectroscopy (FTIR). Flow properties were evaluated using a powder rheometer. Maximum solubility enhancement was seen in acidic media for fused formulations where the ratio 1: 0.75 had 18-fold increase. In vitro dissolution studies showed dissolution rate enhancement for physical mixtures and the formulations in all three media. The most pronounced effect was seen for formulation (1: 0.75) in acidic media where the cumulative drug release was 58.27% while for drug, it was 3.67%. Model independent statistical methods and ANOVA based methods were used to check the significance of difference in the dissolution profiles. Thermograms from mDSC showed a characteristic peak for all formulations with T-peak of around 45 degrees C which suggested formation of a eutectic mixture. XRD data displayed that crystalline nature of ibuprofen was intact in the formulations. This work shows the effect of eutectic formation and micellar solubilization between ibuprofen and poloxamer at the given ratios on its solubility and dissolution rate enhancement.
引用
收藏
页码:1428 / 1440
页数:13
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