Production of dosage forms for oral drug delivery by laminar extrusion of wet masses

被引:4
作者
Muellers, Katrin C. [1 ,2 ]
Wahl, Martin A. [2 ]
Pinto, Joao F. [1 ]
机构
[1] Univ Lisbon, Dept Farm Galen & Tecnol Farmaceut, Fac Farm, P-1649003 Lisbon, Portugal
[2] Univ Tubingen, Inst Pharmazeut, Tubingen, Germany
关键词
Dosage form; Drug delivery; Hydroxypropyl methylcellulose; Laminar extrusion; Wet mass extrusion; HOT-MELT EXTRUSION; MICROCRYSTALLINE CELLULOSE PASTES; LIQUID-PHASE MIGRATION; SPHERONIZATION PROCESS; POWDER MASSES; PELLETS; RELEASE; TABLETS; SPHERONISATION; STRENGTH;
D O I
10.1016/j.ejpb.2013.01.004
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Laminar extrusion of wet masses was studied as a novel technology for the production of dosage forms for oral drug delivery. Extrusion was carried out with a ram extruder. Formulations contained either microcrystalline cellulose (MCC) or dicalcium phosphate (DCP) as diluent, hydroxypropyl methylcellulose (HPMC), lactose, and water. Extrudates were characterized for their tensile strength, Young's modulus of elasticity, water absorption, gel forming capacity, and release of two model drugs, coumarin (COU) and propranolol hydrochloride (PRO). Cohesive extrudates could be produced with both filling materials (MCC and DCP) when HPMC was included as a binder at low amounts (3.3-4.5% w/w dry weight). Employing more HPMC, the elasticity of the wet masses increased which resulted in distinct surface defects. For MCC, the maximum HPMC amount that could be included in the formulations (15% w/w dry weight) did not affect the mechanical properties or decrease the drug release significantly. For DCP extrudates, the maximally effective HPMC amount was 30% (w/w dry weight) with influence on both the mechanical properties and drug release. This study suggests that laminar extrusion of wet masses is a feasible technique for the production of dosage forms for oral drug delivery. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:626 / 632
页数:7
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