Zaman Mustafa A, Martin Gary P, Rees Gareth D
King's College London, Phamaceutical Science Division, Franklin-Wilkins Building, 150 Stamford Street, London SE1 9NH, UK.
J Dent. 2008 May;36(5):351-9. doi: 10.1016/j.jdent.2008.01.014. Epub 2008 Mar 14.
Effective delivery of oral care actives from conventional hydrogel formulations is often compromised by poor retention associated with shear forces present in the mouth, salivary washout and over-hydration of the gel which can lead to structural breakdown and adhesive failure. Non-aqueous gels offer the opportunity to formulate rheologically acceptable vehicles with higher concentrations of bioadhesive polymer than is possible using water as the primary solvent. Accordingly, this study describes the formulation and characterisation of the rheology, hydration and bioadhesive properties of a range of non-aqueous delivery systems (NADS).
The formulations were composed principally of glycerol, with varying amounts of polyethylene glycol (PEG) 400 and Carbopol 974P being incorporated in the ranges 0-31.34% and 0-4% (w/w). Work of adhesion (WOA) and maximum force of detachment (Fmax) were determined using a Dartec tensile tester after application of a normal force. Rheology was assessed using a Bohlin CS CVO rheometer.
WOA and Fmax increased with increasing compression time and Carbopol concentration. Addition of 30% (w/w) PEG 400 to the formulation containing 2% Carbopol in glycerol improved bioadhesive function. Formulation rheology was largely controlled by the Carbopol concentration, and to a lesser extent by the concentration of PEG 400 and these, in turn, largely determined the bioadhesion parameters and rates of hydration.
The results of this in vitro study suggest that bioadhesion, and consequently potential drug bioavailability, would be enhanced by use of a water miscible non-aqueous delivery vehicle such as glycerol containing a bioadhesive polymer such as Carbopol with the addition of controlled amounts of PEG as plasticiser.
传统水凝胶制剂中口腔护理活性成分的有效递送常常受到损害,这是由于与口腔中存在的剪切力、唾液冲刷以及凝胶过度水合相关的保留性差所导致的,而这可能会导致结构破坏和粘附失效。非水凝胶提供了配制流变学上可接受的载体的机会,其生物粘附聚合物的浓度高于以水为主要溶剂时的浓度。因此,本研究描述了一系列非水递送系统(NADS)的流变学、水合作用和生物粘附特性的配方及表征。
制剂主要由甘油组成,不同量的聚乙二醇(PEG)400和卡波姆974P的加入量范围分别为0 - 31.34%和0 - 4%(w/w)。在施加法向力后,使用Dartec拉伸测试仪测定粘附功(WOA)和最大分离力(Fmax)。使用Bohlin CS CVO流变仪评估流变学。
WOA和Fmax随着压缩时间和卡波姆浓度的增加而增加。向含有2%卡波姆的甘油制剂中添加30%(w/w)PEG 400可改善生物粘附功能。制剂流变学在很大程度上受卡波姆浓度控制,在较小程度上受PEG 400浓度控制,而这些又在很大程度上决定了生物粘附参数和水合速率。
这项体外研究的结果表明,使用与水混溶的非水递送载体(如含有生物粘附聚合物(如卡波姆)的甘油)并添加适量的PEG作为增塑剂,可增强生物粘附性,从而提高潜在的药物生物利用度。