Exploring the Physicochemical Compatibility of Minoxidil in Combination with Different Active Pharmaceutical Ingredients in Ready-to-use Vehicles for Alopecia Treatment.

Bruna Marianni, Savvas Koulouridas, Hudson Caetano Polonini
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Abstract

Background: Alopecia is globally known as a distressing medical disorder that affects men and women, and current commercially available minoxidil solutions are formulated with irritant vehicles with frequent complaints of dermatologic adverse effects.

Objectives: This study aimed to investigate further the compatibility of ready-to-use vehicles for the preparation of tailored formulations for alopecia treatment, namely TrichoSol™ (a ready-to-use vehicle for personalized hair solutions) and TrichoFoam™ (a ready-to-use vehicle for personalized foam formulations), in combination with minoxidil and other active pharmaceutical ingredients (APIs), to establish adequate beyond-use dates (BUD) for the given formulations.

Methods: Products under evaluation were compounded using TrichoSol™ or TrichoFoam™, with direct incorporation of the APIs into these vehicles. Samples were then stored at controlled room temperature for up to 180 days. High-performance liquid chromatography (HPLC) methods were developed and validated, and then utilized to evaluate the compatibility of the APIs in TrichoSol™ and TrichoFoam™. Forced degradation studies were conducted to assess API stability under various stress conditions, and Antimicrobial Effectiveness Testing (AET) was performed at 0 and 180 days after compounding.

Results: According to our results, BUDs of up to 90-180 days were obtained for the examined formulations stored at room temperature, considering a degradation of maximum 10% of the nominal concentration of the APIs within them. The formulations exhibited no discernible physical alterations throughout this period and maintained chemical stability within acceptable limits. Microbiological evaluations confirmed the efficacy of the preservative system.

Conclusion: Products compounded with TrichoSol™ and TrichoFoam™ showed suitable stability to be used as personalized treatments for alopecia. We can then suggest that the vehicles TrichoSol™ and TrichoFoam™ present effective solutions for compounding personalized hair care treatments.

探索米诺地尔与不同活性药物成分联合用于治疗脱发的即食载体的理化相容性。
背景:脱发在全球范围内被认为是一种影响男性和女性的令人痛苦的医学疾病,目前市售的米诺地尔溶液是用刺激性载体配制的,经常出现皮肤不良反应。目的:本研究旨在进一步研究制备用于治疗脱发的定制配方的即用型载体,即TrichoSol™(用于个性化头发溶液的即用型载体)和TrichoFoam™(用于个性化泡沫配方的即用型载体)与米诺地尔和其他活性药物成分(api)的相容性,以确定给定配方的足够的使用期限(BUD)。方法:使用TrichoSol™或TrichoFoam™复配被评价产品,将原料药直接掺入这些载体中。然后将样品在室温下保存180天。建立并验证了高效液相色谱(HPLC)方法,并利用高效液相色谱(HPLC)评价原料药在TrichoSol™和TrichoFoam™中的相容性。进行强制降解研究,以评估各种应激条件下原料药的稳定性,并在配制后0和180天进行抗菌有效性测试(AET)。结果:根据我们的结果,考虑到其中原料药的标称浓度的最大10%的降解,在室温下储存的所检查的配方获得了长达90-180天的芽。在此期间,配方没有表现出明显的物理变化,并在可接受的限度内保持化学稳定性。微生物学评价证实了防腐体系的有效性。结论:与TrichoSol™和TrichoFoam™复配的产品具有良好的稳定性,可用于个性化治疗脱发。然后,我们可以建议TrichoSol™和TrichoFoam™为复合个性化护发护理提供有效的解决方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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