Pham Duy Toan, Nguyen Ngoc Nha Thao
Can Tho University of Medicine and Pharmacy, Faculty of Pharmacy, Department of Pharmaceutical Technology, Can Tho, Vietnam.
Turk J Pharm Sci. 2018 Aug;15(2):171-177. doi: 10.4274/tjps.91885. Epub 2018 Jul 17.
In this study, we aimed to develop and optimize an anti-allergic cream containing dexamethasone and chlorpheniramine using the design of experiments (DoE) method. The optimized product was investigated for its physicochemical properties and therapeutic effects in rabbits.
The creams were formulated using the simple mixing process, which was optimized by the Design Expert software. The products were then evaluated the properties such as pH, skin diffusion profile, short-term stability, qualitative, and assay, using the newly validated UV-Vis spectrophotoscopy quantitative method. efficacy tests in rabbits of the best products were compared with the marketed Phenergan (promethazine 2%).
The UV-Vis method used to simultaneously determine the amount of both dexamethasone and chlorpheniramine was successfully developed and validated. Using the DoE method, it was clear that the release profile of dexamethasone depended on the amount of sodium lauryl sulfate, propylene glycol, and DMSO. In contrast, only DMSO affected the release pattern of chlorpheniramine. The best formulation was optimized by the software. The product showed acceptable parameters in pH (5.7±0.1), short-term stability over 10 days, and skin diffusion profiles of 20.47±1.25% and 4.92±0.42% after 40 min for dexamethasone and chlorpheniramine, respectively. In addition, the product demonstrated no observable inflammatory response in the experimental animals. Also, it illustrated 2-fold better anti-allergic efficacy than the marketed product (i.e., 27.2 compared with 43.4 min in the recovery time).
We were successful in developing and optimizing an anti-allergic cream containing dexamethasone and chlorpheniramine. The best product satisfied all required parameters. Interestingly, our product showed higher efficacy than Phenergan. These results can be a background for further clinical trials.
在本研究中,我们旨在运用实验设计(DoE)方法开发并优化一种含有地塞米松和氯苯那敏的抗过敏乳膏。对优化后的产品进行了理化性质研究及在兔身上的治疗效果研究。
采用简单混合工艺制备乳膏,并通过Design Expert软件进行优化。然后使用新验证的紫外可见分光光度法定量方法对产品的pH值、皮肤扩散情况、短期稳定性、定性及含量测定等性质进行评估。将最佳产品在兔身上的功效测试结果与市售的非那根(异丙嗪2%)进行比较。
成功开发并验证了用于同时测定地塞米松和氯苯那敏含量的紫外可见方法。运用DoE方法可知,地塞米松的释放情况取决于月桂醇硫酸酯钠、丙二醇和二甲基亚砜的用量。相比之下,只有二甲基亚砜影响氯苯那敏的释放模式。通过软件优化出了最佳配方。该产品在pH值(5.7±0.1)方面参数可接受,在10天内具有短期稳定性,地塞米松和氯苯那敏在40分钟后的皮肤扩散率分别为20.47±1.25%和4.92±0.42%。此外,该产品在实验动物中未观察到明显的炎症反应。而且,其抗过敏功效比市售产品高出两倍(即恢复时间分别为27.2分钟和43.4分钟)。
我们成功开发并优化了一种含有地塞米松和氯苯那敏的抗过敏乳膏。最佳产品满足所有要求参数。有趣的是,我们的产品显示出比非那根更高的疗效。这些结果可为进一步的临床试验提供依据。