A platform direct compression formulation for low dose sustained-release tablets enabled by a dual particle engineering approach

被引:9
|
作者
Sun, Wei-Jhe [1 ]
Chen, Hongbo [1 ]
Aburub, Aktham [2 ]
Sun, Changquan Calvin [1 ]
机构
[1] Univ Minnesota, Dept Pharmaceut, Coll Pharm, Pharmaceut Mat Sci & Engn Lab, 9-127B Weaver Densford Hall,308 Harvard St SE, Minneapolis, MN 55455 USA
[2] Eli Lilly & Co, Lilly Res Labs, Small Mol Design & Dev, Indianapolis, IN 46285 USA
关键词
Sustained release; Particle engineering; Direct compression; Nanocoating; Acetaminophen; Celecoxib; Nicotinamide; Tableting; FLOW PROPERTIES; MICROCRYSTALLINE CELLULOSE; EXPEDITED DEVELOPMENT; SYSTEMS;
D O I
10.1016/j.powtec.2018.10.054
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Content uniformity (CU) is a well-recognized challenge for low-dose direct compression (DC) tablet formulations. Using a dual particle engineering approach that involves a) forming a segregation-resistant drug-carrier composite to improve CU and b) nanocoating HPMC to enhance flowability, we have developed a platform DC formulation for preparing low-dose drug sustained-release (SR) tablets with excellent CU. In addition to demonstrated robustness in manufacturability, this platform formulation has the flexibility for modifying drug release rate. Thus, it is useful for expedited and material-sparing development of low dose SR tablets using the economical DC process. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:856 / 863
页数:8
相关论文
共 11 条
  • [1] Particle Engineering for Enabling a Formulation Platform Suitable for Manufacturing Low-Dose Tablets by Direct Compression
    Sun, Wei-Jhe
    Aburub, Aktham
    Sun, Changquan Calvin
    JOURNAL OF PHARMACEUTICAL SCIENCES, 2017, 106 (07) : 1772 - 1777
  • [2] SUSTAINED-RELEASE NITROFURANTOIN TABLETS BY DIRECT COMPRESSION
    CONTE, U
    COLOMBO, P
    CARAMELLA, C
    LAMANNA, A
    FARMACO-EDIZIONE PRATICA, 1979, 34 (07): : 306 - 316
  • [3] Continuous direct compression as manufacturing platform for sustained release tablets
    Van Snick, B.
    Holman, J.
    Cunningham, C.
    Kumar, A.
    Vercruysse, J.
    De Beer, T.
    Remon, J. P.
    Vervaet, C.
    INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2017, 519 (1-2) : 390 - 407
  • [4] Direct compression of sustained-release matrix tablets of enteric cellulose esters
    Guo, HX
    Heinämäki, J
    Antikainen, O
    Yliruusi, J
    STP PHARMA SCIENCES, 2002, 12 (05): : 287 - 292
  • [5] Sustained release theophylline tablets by direct compression Part 1: formulation and in vitro testing
    Pather, SI
    Russell, I
    Syce, JA
    Neau, SH
    INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1998, 164 (1-2) : 1 - 10
  • [6] SUSTAINED-RELEASE SALBUTAMOL TABLETS - FORMULATION ENGINEERING AND EVALUATION USE OF FAT AND WAX MATRIX .2A.
    LALLA, JK
    KAPADNEKAR, KSG
    RESEARCH AND INDUSTRY, 1985, 30 (03): : 189 - 191
  • [7] Further enhancement of the sustained-release properties and stability of direct compression gel matrix bilayer tablets by controlling the particle size of HPMC and drug microencapsulation
    Liu, Tong
    Wang, Jiahui
    Feng, Yupeng
    Wang, Haoran
    Xu, Yunlong
    Yin, Tian
    Zhang, Yu
    He, Haibing
    Gou, Jingxin
    Tang, Xing
    POWDER TECHNOLOGY, 2024, 448
  • [8] Effect of polysulfonate resins and direct compression fillers on multiple-unit sustained-release dextromethorphan resinate tablets
    Pongjanyakul, T
    Priprem, A
    Chitropas, P
    Puttipipatkhachorn, S
    AAPS PHARMSCITECH, 2005, 6 (02):
  • [9] Effect of polysulfonate resins and direct compression fillers on multiple-unit sustained-release dextromethorphan resinate tablets
    Pongjanyakul T.
    Priprem A.
    Chitropas P.
    Puttipipatkhachorn S.
    AAPS PharmSciTech, 6 (2) : E190 - E197
  • [10] A formulation approach for development of HPMC-based sustained release tablets for tolterodine tartrate with a low release variation
    Cao, Qing-Ri
    Choi, Jae-Seung
    Liu, Yan
    Xu, Wei-Juan
    Yang, Mingshi
    Lee, Beom-Jin
    Cui, Jing-Hao
    DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2013, 39 (11) : 1720 - 1730