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Virgin Coconut Oil Containing Injectable Vehicles for Ibuprofen Sustainable Release

机译:含有石油可持续释放的植维椰子油的可注射车辆

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Virgin coconut oil (VCO) has been utilized as traditional medicine and herbal vehicle especially in tropical countries. The wax formation dispersed in this oil during storage at cool environment makes it not homogenous and opaque. The utilization of this oil is limited for the cool climate countries and also this is difficult for using it as injectable oil vehicle in pharmaceuticals. Therefore the decrease of wax formation temperature will possibly diminish this problematic behavior. The purpose of this study is to investigate the wax inhibitor capability of other injectable vehicles and controlled drug release characteristic of VCO without or containing these vehicles. Ibuprofen (IB) which is non steroidal anti-inflammatory drugs (NSAIDs) was used as a model drug because it can be soluble in VCO. N-methyl-2-pyrrolidone (NMP), benzyl benzoate (BB), benzyl alcohol (BA), isopropyl myristate (IM) and ethyl oleate (EO) were employed as injectable vehicles. Viscosity, pour point, cloud point and polarized light microscope examinations were conducted to characterize the change of VCO physical properties. In vitro drug release experiment was performed using dialysis method at 50 rpm and 37°C, in phosphate buffer pH 7.4. Then least square fitting in vitro release data to the different mathematical expressions (power law, first order, Higuchi's and zero order) was carried out using Scientist 2.1 Programme. Because injectable vehicles decreased viscosity of VCO, they improved the efficiency for measuring the VCO viscosity at lower temperature. BB and NMP were chosen as representative of the injectable vehicles because they showed many proper properties for injectable formula. Both pour point and cloud point were apparently reduced by BB greater than NMP, because BB could disturb the wax crystal formation as seen under polarized light microscope. The release rates of IB without or containing injectable vehicles were not different. From curve fitting, drug release profiles were first order kinetic therefore the drug release depended on the drug concentration in dialysis tube. From the results indicated that the injectable vehicles especially, BB and NMP could inhibit the VCO wax formation but not affected the drug release kinetic from VCO.
机译:处女椰子油(VCO)已被用作传统医学和草药,特别是在热带国家。在凉爽的环境中储存期间,在该油中分散在该油中的蜡形成使其不均匀和不透明。这种油的利用对于凉爽的气候国家有限,而且这难以将其用作药物中的注射油车辆。因此,蜡形成温度的降低可能会减少这种有问题的行为。本研究的目的是探讨其他可注射车辆的蜡抑制剂和VCO的控制药物释放特性,没有或含有这些车辆。是非甾体抗炎药(NSAID)的布洛芬(IB)用作模型药物,因为它可以溶于VCO。使用N-甲基-2-吡咯烷酮(NMP),苯甲酸苄酯(BB),苄醇(BA),异丙基肌酐(IM)和乙酸盐(EO)作为注射载体。进行粘度,倾点,浊点和偏振光显微镜检查,以表征VCO物理性质的变化。在体外药物释放实验中使用透析方法在50rpm和37℃下在磷酸盐缓冲液pH 7.4中进行。然后,使用科学家2.1程序进行最小二乘释放数据以不同的数学表达式(电力法,第一顺序,HIGUCHI和零阶)进行。因为可注射车辆降低了VCO的粘度,所以它们改善了测量在较低温度下测量VCO粘度的效率。选择Bb和NMP作为可注射车辆的代表性,因为它们显示出可注射配方的许多适当的性质。倾点和浊点都明显减少了大于NMP的BB,因为BB可以在偏振光显微镜下看到蜡晶体形成。 IB的释放速率没有或含有可注射车辆的释放速率没有不同。从曲线配件,药物释放型材是第一阶动力学,因此药物释放依赖于透析管中的药物浓度。从结果表明,注射型车辆尤其是BB和NMP可以抑制VCO蜡形成,但不影响来自VCO的药物释放动力学。

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