Preparation and characterization of pH-independent sustained release tablet containing solid dispersion granules of a poorly water-soluble drug

被引:33
|
作者
Huyen Thi Thanh Tran [1 ]
Park, Jun Bom [1 ]
Hong, Ki-Hyuk [1 ]
Choi, Han-Gon [2 ]
Han, Hyo-Kyung [3 ]
Lee, Jaehwi [4 ]
Oh, Kyung Taek [4 ]
Lee, Beom-Jin [1 ]
机构
[1] Kangwon Natl Univ, Bioavailabil Control Lab, Coll Pharm, Chunchon 200701, South Korea
[2] Hanyang Univ, Coll Pharm, Ansan 426791, South Korea
[3] Dongguk Univ, Coll Pharm, Seoul 100715, South Korea
[4] Chung Ang Univ, Coll Pharm, Seoul 155756, South Korea
关键词
Solid dispersion granules; Surface adsorption; Sustained release tablet; pH-independent release; EDS imaging; POLYETHYLENE OXIDES PEOS; MATRIX TABLETS; LOSARTAN POTASSIUM; DISSOLUTION; FORMULATION; BEHAVIOR; POLYMER;
D O I
10.1016/j.ijpharm.2011.05.052
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Sustained release (SR) tablets containing solid dispersions (SD) granules of a poorly water-soluble drug were prepared to investigate the controlled pH-independent release of the drug. Losartan potassium (LST), an anti-hypertensive agent was chosen as a model drug because of its pH-dependent solubility and short elimination half-life. Poloxamer 188 was used as an SD carrier. A free-flowing SD granule was prepared by adsorbing the melt of the drug and poloxamer 188 onto the surface of an adsorbent. Aerosil 300 (fumed silicon dioxide), followed by direct compression with polyethylene oxide (PEO, 5 x 10(6)) to obtain an SD-loaded SR (SD-SR) matrix tablet. Differential scanning calorimetry (DSC) and powder Xray diffraction (PXRD) revealed partially amorphous structures of the drug in the SD granules. Scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDS) images indicated adsorption of SD granules onto the surface of the adsorbent. The SD granules dissolved completely within 10 min, a dissolution rate much higher than that of pure LST. Moreover, pH-independent sustained release of LST from the SD-SR tablet was achieved for 2 h in gastric fluid (pH 1.2) and for 10 h in intestinal fluid (pH 6.8). A combination of SD techniques using surface adsorption and SR concepts is a promising approach to control the release rate of poorly water-soluble drugs in a pH-independent manner. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:83 / 88
页数:6
相关论文
共 50 条
  • [21] Preparation and Characterization of Water-soluble Microcapsule for Sustained Drug Release Using Eudragit RS 100
    Park, Jeong-Min
    Park, Soo-Jin
    MACROMOLECULAR RESEARCH, 2010, 18 (12) : 1191 - 1194
  • [22] Dissolution mechanism of poorly water-soluble drug from extended release solid dispersion system with ethylcellulose and hydroxypropylmethylcellulose
    Ohara, T
    Kitamura, S
    Kitagawa, T
    Terada, K
    INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2005, 302 (1-2) : 95 - 102
  • [23] Encapsulatton of Solid Dispersion in Solid Lipid Particles for Dissolution Enhancement of Poorly Water-soluble Drug
    Khanh Thi My Tran
    Toi Van Vo
    Lee, Beom-Jin
    Duan, Wei
    Phuong Ha-Lien Tran
    Thao Truong-Dinh Tran
    CURRENT DRUG DELIVERY, 2018, 15 (04) : 576 - 584
  • [24] Improved Bioavailability of Poorly Water-Soluble Drug Curcumin in Cellulose Acetate Solid Dispersion
    Wan, Shuxin
    Sun, Yingqian
    Qi, Xiuxiang
    Tan, Fengping
    AAPS PHARMSCITECH, 2012, 13 (01): : 159 - 166
  • [25] Improved Bioavailability of Poorly Water-Soluble Drug Curcumin in Cellulose Acetate Solid Dispersion
    Shuxin Wan
    Yingqian Sun
    Xiuxiang Qi
    Fengping Tan
    AAPS PharmSciTech, 2012, 13 : 159 - 166
  • [26] Factorial Design Assisted pH-independent Delivery System of Poorly Soluble Drug Cinnarizine
    Mehta, Dharmik M.
    Parejiya, Punit B.
    Patel, Hetal K.
    Trivedi, Palak J.
    Suthar, Disha D.
    Shelat, Pragna K.
    ASIAN JOURNAL OF PHARMACEUTICS, 2016, 10 (03) : 160 - 167
  • [27] Process optimization and characterization of poloxamer solid dispersions of a poorly water-soluble drug
    Shah, Tejal J.
    Amin, Avani F.
    Parikh, Jolly R.
    Parikh, Rajesh H.
    AAPS PHARMSCITECH, 2007, 8 (02)
  • [28] Process optimization and characterization of poloxamer solid dispersions of a poorly water-soluble drug
    Tejal J. Shah
    Avani F. Amin
    Jolly R. Parikh
    Rajesh H. Parikh
    AAPS PharmSciTech, 8
  • [29] Modulation of drug release by utilizing pH-independent matrix system comprising water soluble drug verapamil hydrochloride
    Baviskar, Dheeraj
    Sharma, Rajesh
    Jain, Dinesh
    PAKISTAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2013, 26 (01) : 137 - 144
  • [30] Dissolution-modulating mechanism of alkalizers and polymers in a nanoemulsifying solid dispersion containing ionizable and poorly water-soluble drug
    Tran, Thao Truong-Dinh
    Tran, Phuong Ha-Lien
    Lee, Beom-Jin
    EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2009, 72 (01) : 83 - 90