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Development of Ketoprofen Microemulsion for Transdermal Drug Delivery

机译:酮洛芬微乳液进行透皮药物递送的研制

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The aim of this study was to prepare microemulsion for transdermal drug delivery of ketoprofen (KP). The physicochemical and chemical properties of microemulsion were evaluated. The microemulsion were composed of isopropyl myristate (IPM) as oil phase, water, PEG40-hydrogenated castor oil (Cremophore RH40) as surfactant and PEG400 as co-surfactant, and the surfactant: co-surfactant ratio used was 1:1. The viscosity, droplet size, pH, conductivity of microemulsion and skin permeation of KP through shed snake skin were evaluated. The particle size, viscosity and conductivity of microemulsions were in the range of 172-468 nm, 234.82-1067.35 cP and 6.80-20.87μS/cm, respectively. The ratio of IPM and surfactant mixture played an important role on KP loading capacity of microemulsions formulation and skin permeation of KP. While amount of surfactant increased, the loading capacity of KP increased, but the skin permeation of KP decreased. The results suggested that the novel microemulsion system composed of IPM, water, Cremophore RH40: PEG400 (ratio 1:1) can be applied for using as a transdermal drug delivery carrier.
机译:本研究的目的是制备酮丙烯(KP)的透皮药物递送微乳液。评价微乳液的物理化学和化学性质。将微乳液由异丙基肌号(IPM)作为油相,水,PEG40-氢化蓖麻油(CREMophore RH40)作为表面活性剂和PEG400作为辅助表面活性剂组成,并且表面活性剂:使用的共表面活性剂比为1:1。评价粘度,液滴尺寸,pH,微乳液和KP皮肤渗透的PH,通过梭蛇皮肤渗透。粒径,粘度和微乳液的电导率均分别172-468纳米,234.82-1067.35厘泊和6.80-20.87μS/厘米的范围内,。 IPM和表面活性剂混合物的比例在微乳液配方和KP皮肤渗透的KP负载能力上发挥了重要作用。虽然表面活性剂的量增加,但KP的负载能力增加,但KP的皮肤渗透率下降。结果表明,由IPM,水,CREMophore RH40:PEG400(比率1:1)组成的新型微乳液系统可以用作透皮药物递送载体。

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