Tailor-made release triggering from hot-melt extruded complexes of basic polyelectrolyte and poorly water-soluble drugs

被引:28
|
作者
Kindermann, Christoph [1 ]
Matthee, Karin [1 ]
Strohmeyer, Jutta [2 ]
Sievert, Frank [2 ]
Breitkreutz, Joerg [1 ]
机构
[1] Univ Dusseldorf, Inst Pharmaceut & Biopharmaceut, D-40225 Dusseldorf, Germany
[2] Ratiopharm GmbH, Ulm, Germany
关键词
Polyelectrolyte complex; Hot-melt extrusion; Acid-base reaction; Electrolyte triggering; Tailor-made dissolution; HIGHLY AGGREGATING SYSTEMS; SOLID DOSAGE FORMS; RAMAN-SPECTROSCOPY; INTERPOLYELECTROLYTE COMPLEXES; SOLUBILITY PARAMETERS; DELIVERY TECHNOLOGY; EXTRUSION; MECHANISM; POLYMERS; SALT;
D O I
10.1016/j.ejpb.2011.05.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The aim of the study was the formulation of polyelectrolyte complexes composed of poorly water-soluble acid drugs and basic polymethacrylates by hot-melt extrusion enabling a tailor-made release pattern by the addition of inorganic salts. The influence of different electrolytes was analyzed at varying conditions in order to control drug delivery from the complexes. Poorly water-soluble model drugs naproxen and furosemide were applied in their non-ionic form. After hot-melt extrusion of the naproxen-polymethacrylate powder blend. XRPD and DSC measurements indicated the formation of a single-phase amorphous system. Milled extrudates were stable under storage at long-term and intermediate conditions. Polyelectrolyte complex formation by an acid-base reaction during hot-melt extrusion could be proven by the lack of vibrations of dimethylamino and carboxylic groups by FT-IR and Raman spectroscopy. The complexes did not dissolve in demineralized water. Drug release could be immediately induced by addition of neutral electrolytes. Tailor-made dissolution profiles were realized by controlled electrolyte triggering. Maximal effects were achieved by concentrations of 0.05-0.15 M NaCl. Different anions of alkali halogenides revealed variant magnitudes of the effect depending on the anion radius. Polyelectrolyte complex formation and dissolution principles were also confirmed for furosemide. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:372 / 381
页数:10
相关论文
共 23 条
  • [1] Controlled release of a poorly water-soluble drug from hot-melt extrudates containing acrylic polymers
    Zhu, YC
    Shah, NH
    Malick, AW
    Infeld, MH
    McGinity, JW
    [J]. DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2006, 32 (05) : 569 - 583
  • [2] An approach for pH-independent release of poorly soluble ionizable drugs using hot-melt extrusion
    Darwich, May
    Mohylyuk, Valentyn
    Kolter, Karl
    Bodmeier, Roland
    Dashevskiy, Andriy
    [J]. JOURNAL OF DRUG DELIVERY SCIENCE AND TECHNOLOGY, 2024, 100
  • [3] Development and Evaluation of Polymeric Mixed Micelles Prepared using Hot-Melt Extrusion for Extended Delivery of Poorly Water-Soluble Drugs
    Feng, Sheng
    Zhang, Ziru
    Almotairy, Ahmed
    Repka, Michael A.
    [J]. JOURNAL OF PHARMACEUTICAL SCIENCES, 2023, 112 (11) : 2869 - 2878
  • [4] Comparison of fluidized hot-melt granulation and conventional wet granulation on processing water-soluble or poorly water-soluble active pharmaceutical ingredient
    Zhai, H.
    Andrews, G.
    Jones, D.
    Walker, G.
    Cregan, R.
    [J]. JOURNAL OF PHARMACY AND PHARMACOLOGY, 2008, 60 : A47 - A48
  • [5] Dissolution enhancement of poorly water-soluble APIs processed by hot-melt extrusion using hydrophilic polymers
    Maniruzzaman, M.
    Rana, M. M.
    Boateng, J. S.
    Mitchell, J. C.
    Douroumis, D.
    [J]. DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2013, 39 (02) : 218 - 227
  • [6] Cyclodextrin controlled release of poorly water-soluble drugs from hydrogels
    Woldum, Henriette Sie
    Larsen, Kim Lambertsen
    Madsen, Flemming
    [J]. DRUG DELIVERY, 2008, 15 (01) : 69 - 80
  • [7] Application of Hot Melt Extrusion for Poorly Water-Soluble Drugs: Limitations, Advances and Future Prospects
    Lu, Ming
    Guo, Zhefei
    Li, Yongcheng
    Pang, Huishi
    Lin, Ling
    Liu, Xu
    Pan, Xin
    Wu, Chuanbin
    [J]. CURRENT PHARMACEUTICAL DESIGN, 2014, 20 (03) : 369 - 387
  • [8] Application of fluidized hot-melt granulation as a novel granulation technique for processing poorly water-soluble active pharmaceutical ingredients
    Zhai, H.
    Andrews, G.
    Jones, D.
    Walker, G.
    [J]. JOURNAL OF PHARMACY AND PHARMACOLOGY, 2008, 60 : A60 - A60
  • [9] Understanding your formulations: characterisation of phase separation and drug distribution across hot melt extruded solid dispersions containing poorly water-soluble drugs
    Qi, S.
    [J]. JOURNAL OF PHARMACY AND PHARMACOLOGY, 2009, 61 : A160 - A161
  • [10] Novel approaches to characterizing phase separation and drug distribution across hot-melt-extruded solid dispersions containing poorly water-soluble drugs
    Qi, S.
    Moffat, J.
    Gryczke, A.
    Nollenberger, K.
    Belton, P.
    Reading, M.
    Craig, D.
    [J]. JOURNAL OF PHARMACY AND PHARMACOLOGY, 2008, 60 : A14 - A14