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聚氧乙烯脂肪酸酯作为盐酸吗啡和硫酸吗啡透皮吸收的潜在促进剂。

Polyoxyethylene fatty acid esters as potential promotors of transdermal absorption for morphine hydrochloride and sulphate.

作者信息

Samczewska Grazyna, Piechota-Urbańska Magdalena, Kołodziejska Justyna

机构信息

Katedra Farmacji Stosowanej, Uniwersytetu Medycznego w Lodzi.

出版信息

Polim Med. 2006;36(2):17-32.

Abstract

The presence of opioid receptors mu in pathologically changed skin and mucosa justifies application of preparations with morphine salts to obtain topical analgesic activity. Numerous factors associated with the vehicle and therapeutic agent physiochemical properties affect the capability and rate of penetration of a therapeutic substance in the form of a drug into dermis. Promotors of transcutaneous absorption, which weaken the integrity of epidermal corneal layer and thus, increase therapeutic substance penetration play more and more important role. In this study non-ionic macromolecular surface active compounds from Rokacets group were suggested as potential promotors of transdermal absorption for morphine sulphate and hydrochloride. The aim of the study was to work out prescription composition of ointment with morphine salts of optimal rheological and morphological parameters and high pharmaceutical availability of the therapeutic agent (morphine sulphate, hydrochloride). Three model emulsive ointment vehicles were prepared and selected promoters of transdermal absorption were introduced into them. On the basis of the formed vehicles ointments were made with morphine sulphate and hydrochloride. The obtained vehicles and ointment preparations were subjected to rheological tests. Spreadness was determined by extensometric method and viscosity with digital cone-plate rheometer. Morphological parameters of the vehicles and ointments, such as: pH and pharmacopeal density were estimated. Carrying out direct diffusion from the surface of the preparation to acceptor fluid (to water), the amount of the released therapeutic substance in time function was determined by spectrophotometric method. The performed tests demonstrated that the investigated vehicles and ointments are non-Newtonian systems, viscoelastic and highly thixotropic. The kind of morphine salt affects the spreadness and viscosity of model ointments. Preparations with morphine hydrochloride have higher spreadness than viscosity and more alkaline pH. From among the investigated non-ionic surface active compounds Rokacet R-40 appeared to be the most beneficial promotor of transdermal absorption for both pharmacopeal morphine salts. Pharmaceutical availability of morphine sulphate and hydrochloride is the highest from ointments with its content in the vehicle prescription.

摘要

病理改变的皮肤和黏膜中存在μ阿片受体,这证明使用含吗啡盐的制剂以获得局部镇痛活性是合理的。许多与载体和治疗剂物理化学性质相关的因素会影响药物形式的治疗物质渗透到真皮中的能力和速率。经皮吸收促进剂通过削弱表皮角质层的完整性从而增加治疗物质的渗透,其作用越来越重要。在本研究中,Rokacets组的非离子大分子表面活性化合物被认为是硫酸吗啡和盐酸吗啡经皮吸收的潜在促进剂。该研究的目的是确定具有最佳流变学和形态学参数以及治疗剂(硫酸吗啡、盐酸吗啡)高药物可用性的含吗啡盐软膏的处方组成。制备了三种模型乳化软膏载体,并将选定的经皮吸收促进剂引入其中。基于形成的载体,制备了含硫酸吗啡和盐酸吗啡的软膏。对所得载体和软膏制剂进行流变学测试。通过引伸计法测定铺展性,用数字锥板流变仪测定粘度。评估了载体和软膏的形态学参数,如pH值和药典密度。通过从制剂表面直接扩散到接受液(水)中,用分光光度法测定随时间释放的治疗物质的量。所进行的测试表明,所研究的载体和软膏是非牛顿体系,具有粘弹性和高触变性。吗啡盐的种类会影响模型软膏的铺展性和粘度。含盐酸吗啡的制剂铺展性高于粘度,pH值更偏碱性。在所研究的非离子表面活性化合物中,Rokacet R - 40似乎是两种药典吗啡盐经皮吸收最有益的促进剂。硫酸吗啡和盐酸吗啡在载体处方中含量最高的软膏中药物可用性最高。

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