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含卡波姆971P的牙科水凝胶处方中的干燥植物提取物

[Dry plant extracts in the prescription of dental hydrogels with Carbopol 971P].

作者信息

Kołodziejska Justyna, Berner-Strzelczyk Aneta, Piechota-Urbańska Magdalena

机构信息

Katedra Farmacji Stosowanej, Uniwersytet Medyczny w Łodzi.

出版信息

Polim Med. 2009;39(3):27-35.

Abstract

The study assumption was to work out a prescription for dental anti-inflammatory hydrogel on Carbopol 971P base. Dry plant extracts (sage, horsetail) and nonsteroidal anti-inflammatory drug (sodium ibuprofen) were introduced into the prescription of a model hydrogel. The aim of the study was to estimate pharmaceutical availability of the applied therapeutic agents and to test their effect on physicochemical properties of the produced form of a drug. The physicochemical parameters of the produced preparation were tested. Viscosity tests were performed using cone-plate digital rheometer. Extensometric method was used to test extensibility. pH measurements were performed by direct immersing the electrode connected with pH-meter into the hydrogel samples of uniform mass. Pharmaceutical availability of therapeutic agents contained in hydrogel (active components of plant extracts, sodium ibuprofen) was estimated. The rate of the process of mass exchange was tested by spectrophotometric method determining the quantity of therapeutic agents diffusing into acceptor fluid at the same time intervals. Sodium ibuprofen is better released from the hydrogel containing horsetail extract (815.5 c.u.) than from the hydrogel of parallel prescription containing sage extract (640.8 c.u.). Hydrogels containing dry extract from horsetail have greater extensibility and lower structural viscosity as well as the value of yield stress than equivalent hydrogels containing sage extract. Introduction of sodium ibuprofen into the prescription of hydrogels with plant extracts modifies rheological parameters (greater extensibility, lower viscosity of the preparation). The tests of the kinetics of therapeutic agents release demonstrated that the presence of sodium ibuprofen in the prescription of hydrogels exerts an influence on the decrease of the effectiveness of the release of active substances contained in these extracts.

摘要

本研究的假设是研发一种以卡波姆971P为基质的牙科消炎水凝胶处方。将干燥植物提取物(鼠尾草、木贼)和非甾体抗炎药(布洛芬钠)引入模型水凝胶的处方中。本研究的目的是评估所用治疗剂的药物可用性,并测试它们对所制备药物剂型物理化学性质的影响。对所制备制剂的物理化学参数进行了测试。使用锥板数字流变仪进行粘度测试。采用引伸计法测试延展性。通过将与pH计相连的电极直接浸入质量均匀的水凝胶样品中来进行pH测量。评估了水凝胶中所含治疗剂(植物提取物的活性成分、布洛芬钠)的药物可用性。通过分光光度法测定在相同时间间隔内扩散到接受液中的治疗剂数量,测试了质量交换过程的速率。布洛芬钠从含有木贼提取物的水凝胶(815.5个单位)中的释放效果比从含有鼠尾草提取物的平行处方水凝胶(640.8个单位)中更好。与含有鼠尾草提取物的等效水凝胶相比,含有木贼干燥提取物的水凝胶具有更大的延展性、更低的结构粘度以及屈服应力值。将布洛芬钠引入含有植物提取物的水凝胶处方中会改变流变学参数(更大的延展性、制剂更低的粘度)。治疗剂释放动力学测试表明,水凝胶处方中布洛芬钠的存在会对这些提取物中所含活性物质的释放效果降低产生影响。

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