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维甲酸微乳剂从卡波姆和黄原胶凝胶中的释放:体外与离体渗透研究

Release of Tretinoin Solubilized in Microemulsion from Carbopol and Xanthan Gel: In Vitro versus Ex Vivo Permeation Study.

作者信息

Špaglová Miroslava, Papadakos Martina, Čuchorová Mária, Matušová Desana

机构信息

Department of Galenic Pharmacy, Faculty of Pharmacy, Comenius University in Bratislava, Odbojárov 10, SK-832 32 Bratislava, Slovakia.

出版信息

Polymers (Basel). 2023 Jan 9;15(2):329. doi: 10.3390/polym15020329.

Abstract

BACKGROUND

Tretinoin (TRE) is, for its anti-comedogenic and comedolytic activity, widely used in the topical treatment of acne vulgaris. The effect lies in the regulation of sebum production and collagen synthesis. The study is devoted to the formulation of dermal gels containing TRE using microemulsion as the drug solubilizer.

METHODS

The aim was to evaluate the effect of the reference microemulsion (ME) and lecithin-containing microemulsion (ME) on the release of TRE through the synthetic membrane (in vitro) and the pig's ear skin (ex vivo) through the Franz cell diffusion method. Subsequently, after an ex vivo study, the amount of the drug in the skin influenced by the applied formulation was determined. In addition, the impact of ME on the microscopic structure, texture, and rheological properties of gels was evaluated.

RESULTS

On the basis of the analysis of texture, rheological properties, and drug release studies, Carbopol formulations appear to be more appropriate and stable. Considering the synthetic membrane as a , the Carbopol gel penetrated about 2.5-higher amounts of TRE compared to the Xanthan gel. In turn, ex vivo studies suggest that ME slows the drug transfer to the dissolution medium, simulating absorption into the blood, which is a desirable effect in local treatment. The drug retention study proved the highest amounts of TRE in the skin to which microemulsion-Carbopol formulations were applied.

CONCLUSION

The results confirm the benefit of TRE solubilization in ME due to its bioavailability from the tested dermal formulations.

摘要

背景

维甲酸(TRE)因其抗粉刺和溶解粉刺的活性,被广泛用于寻常痤疮的局部治疗。其作用在于调节皮脂分泌和胶原蛋白合成。本研究致力于以微乳作为药物增溶剂来制备含TRE的皮肤凝胶。

方法

目的是通过Franz细胞扩散法评估参比微乳(ME)和含卵磷脂微乳对TRE透过合成膜(体外)和猪耳皮肤(离体)释放的影响。随后,在离体研究后,测定所应用制剂对皮肤中药物含量的影响。此外,评估了微乳对凝胶微观结构、质地和流变学性质的影响。

结果

基于质地、流变学性质和药物释放研究的分析,卡波姆制剂似乎更合适且稳定。以合成膜为对照,与黄原胶凝胶相比,卡波姆凝胶中TRE的渗透量高出约2.5倍。反过来,离体研究表明微乳减缓了药物向溶解介质的转移,模拟了药物吸收进入血液的过程,这在局部治疗中是一种理想的效果。药物滞留研究证明,在应用了微乳-卡波姆制剂的皮肤中TRE的含量最高。

结论

结果证实了将TRE溶解在微乳中的益处,因为其在所测试的皮肤制剂中具有生物利用度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/004e/9862831/42bbe5f05f44/polymers-15-00329-g001.jpg

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