Perissutti Beatrice, Newton John Michael, Podczeck Fridrun, Rubessa Fulvio
Department of Pharmaceutical Sciences, University of Trieste, Piazzale Europa 1, 34127 Trieste, Italy.
Eur J Pharm Biopharm. 2002 Jan;53(1):125-32. doi: 10.1016/s0939-6411(01)00209-0.
The aim of this research was to use a ram extruder to prepare directly a fast release dosage form with uniform shape and density, containing carbamazepine (C) as a water-insoluble drug and polyethylene glycol 4000 (PEG) as a low melting binder. The potential inclusion of lactose (L) as a hydrophilic filler was also considered. The temperature suitable to ensure a successful extrusion process of several formulations containing PEG in different percentages was found to be below the melting point of the PEG. The influence of composition on the extrusion process of different ram speeds was checked by measuring the pressure at the steady state, the apparent shear rate and the apparent shear stress of a range of mixtures of drug, lactose and PEG. The physical-mechanical properties of extrudates, including tensile strength and Young's modulus, prepared with different ram velocities were also determined. The solid-state physical structure by differential scanning calorimetry (DSC) and X-ray powder diffraction (XRD) was established. The dissolution of the extrudates and their corresponding physical mixtures were compared. The mixtures were found to be shear thinning when extruded; the tensile strength of extrudates was dependent on the composition but not the extrusion rate, while the value of Young's modulus was strongly influenced by the rate of extrusion, but less affected by the composition of the extrudates. The results of DSC and XRD indicated that the solid structure of the extrudates corresponded to that of a physical mixture of the components, hence there had been no change in the physical form of the drug induced by extrusion. In terms of dissolution, the rate of the extrusion process did not influence the performance of the products, whereas the composition did. The extruded mixtures of an equivalent composition exhibited a more rapid release than a simple physical mixture. The addition of lactose reduced the dissolution rate.
本研究的目的是使用柱塞式挤出机直接制备形状和密度均匀的速释剂型,其中含有水不溶性药物卡马西平(C)和低熔点粘合剂聚乙二醇4000(PEG)。还考虑了潜在地加入乳糖(L)作为亲水性填充剂。发现适合确保几种不同百分比PEG配方成功挤出过程的温度低于PEG的熔点。通过测量一系列药物、乳糖和PEG混合物在稳态下的压力、表观剪切速率和表观剪切应力,检查了组成对不同柱塞速度挤出过程的影响。还测定了用不同柱塞速度制备的挤出物的物理机械性能,包括拉伸强度和杨氏模量。通过差示扫描量热法(DSC)和X射线粉末衍射(XRD)确定了固态物理结构。比较了挤出物及其相应物理混合物的溶出度。发现混合物在挤出时表现出剪切变稀;挤出物的拉伸强度取决于组成而不是挤出速率,而杨氏模量的值受挤出速率的强烈影响,但受挤出物组成的影响较小。DSC和XRD结果表明,挤出物的固体结构与各组分物理混合物的结构相对应,因此挤出过程未引起药物物理形态的变化。在溶出方面,挤出过程的速率不影响产品性能,而组成则有影响。同等组成的挤出混合物比简单物理混合物表现出更快的释放。乳糖的加入降低了溶出速率。