乳化剂和分散介质的组成对半固体制剂碱性质的影响

Q3 Pharmacology, Toxicology and Pharmaceutics
N. Lyapunov, E. Bezuglaya, A. Liapunova, I. Zinchenko, Oleksii Liapunov, Oleksii Lysokobylka, Yu. M. Stolper
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引用次数: 2

摘要

的目标。研究cetostearyl alcohol (CSA)对不同分散介质下碱的流变性能、丙二醇(PG)的释放以及碱的吸水性能的影响。材料和方法。研究了一种非离子表面活性剂及其聚集体在以水为主的混合溶剂、混合溶剂PG -巨醇400 (M400)和不同分散介质的亲水性碱载体中的胶束结构。采用模拟阳离子表面活性剂的自旋探针法和旋转粘度法进行了研究。用光学显微镜研究了碱的微观结构。采用垂直扩散室进行PG和M400的体外释放试验,研究PG和M400在溶液和基质中的释放情况。采用气相色谱法测定透析液中PG和M400的含量。溶液和碱对水的吸收是通过膜透析来测定的。结果。CSA作为碱基与表面活性剂按一定比例结合的一部分,是提高其流变学参数、降低体外释放试验中PG释放参数、降低吸水率的重要因素。对分散介质结构不同的碱类,其影响机理也不同。在以水结构为主的碱基中,表面活性剂和CSA的超分子结构发生了侧向相分离,形成了表面活性剂的液体畴和CSA的固体畴,从而促进了混凝结构的形成。在非水混合溶剂PG - M400中,未形成表面活性剂胶束,未形成表面活性剂与CSA分子的混合聚集体;在25℃时,表面活性剂和CSA分别成为悬浮液的分散相,形成凝胶。将CSA加入到由poloxam338、PG、M400和阳离子表面活性剂组成的水溶液中,改变了CSA的流动行为,流变学参数增加,导致CSA对PG和M400的释放速率降低,释放时间延长,吸水能力增强。与M400相比,PG从溶液中释放的速度和程度更大。结论。CSA与表面活性剂联合添加到半固体制备的碱中是改变其流变参数、PG释放动力学和体外实验吸水率的重要因素。这种效果的机理是不同的,取决于碱的分散介质的组成和结构
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of the composition of emulsifiers and the dispersion medium on the properties of bases for semi-solid preparations
The aim. To study the effect of cetostearyl alcohol (CSA) on the rheological properties of bases with different dispersion media, the release of propylene glycol (PG) from them, and the ability of these bases to absorb water. Materials and methods. Micelles of a non-ionic surfactant and its aggregates with CSA in a mixed solvent where the structure of water prevails, mixed solvent PG – macrogol 400 (M400) and hydrophilic bases-vehicles with different dispersion media were studied. The research was carried out by the spin probe method using a probe simulating a cationic surfactant and by rotational viscometry. The microstructure of the bases was studied by optical microscopy. The in vitro release test to study the release of PG and M400 from solutions and bases was performed using vertical diffusion chambers. The content of PG and M400 in the dialysate was determined by gas chromatography according to the validated analytical procedures. The absorption of water by solutions and bases was determined by dialysis through the membrane. Results. CSA, which was the part of the bases together with surfactants in certain ratios, was a significant factor in increasing their rheological parameters, reducing the parameters of PG release during in vitro release tests, as well as reducing water absorption. The mechanisms of such influence are different for bases with different structures of the dispersion medium. In the bases, where the structure of water prevailed, lateral phase separation occurred in the supramolecular structures of surfactant and CSA with the formation of liquid domains of surfactant and solid domains of CSA, which contributed to the formation of coagulation structures. In the mixed non-aqueous solvent PG – M400, surfactant micelles and mixed aggregates of surfactant and CSA molecules were not formed; at 25 oC, surfactants and CSA became separate dispersed phases of suspensions, which contributed to the formation of gels. When CSA was added into an aqueous solution of poloxamer 338, PG, M400 and cationic surfactant, the flow behaviour changed, and the rheological parameters increased, which led to a decrease in the release rate and extended for PG and M400 as well as in the ability to absorb water. The rate and extent of PG release from the solution were greater compared to the M400 release. Conclusions. The addition of CSA in combination with surfactants into the bases for semi-solid preparations is a significant factor for modifying their rheological parameters, the kinetics of PG release from them, and water absorption during experiments in vitro. The mechanisms of such an effect are different and depend on the composition and structure of the dispersion medium of the base
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来源期刊
ScienceRise: Pharmaceutical Science
ScienceRise: Pharmaceutical Science Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
1.70
自引率
0.00%
发文量
39
审稿时长
6 weeks
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