Tofacitinib Citrate-loaded Nanoparticle Gel for the Treatment of Alopecia Areata: Response Surface Design, Formulation and In vitro-in Vivo Characterization.

Mounika Kuchukuntla, Venkatesan Palanivel, Ananthula Madhubabu
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Abstract

Objective: The purpose of this research was to optimize the design and construction of nanoparticle gel (TFN-NPs) loaded with tofacitinib citrate (TFN) using poly lactic co glycolic acid (PLGA).

Method: PLGA (A) as the polymer, polyvinyl alcohol (PVA) (B) as the stabilizer and stirring speed (C) as independent variables were used. TFN-NPs were prepared using single emulsion-solvent evaporation. Box Behnken Design (BBD) was used to determine the optimal component ratio of TFN-NPs based on point prediction.

Results: The entrapment efficiency, particle size, and cumulative drug release of the best-composed TFN-NPs were, respectively, 79.82±0.9%, 236.19±5.07 nm, and 82.31±1.23%; the PDI, zeta potential, and drug loading were, respectively, 0.297±0.21, -30.21±0.94mV, and 69.81±0.16%. Gel formulation employing Carbopol as a gelling polymer was then developed using the optimal TFN-NPs mixture. Gel characterization, drug release, permeation studies, irritation, and pharmacokinetic studies were also conducted. Further solid state and morphology were evaluated using FTIR, DSC, XRD, SEM, TEM, and AFM on the developed topical gel formulation (TFN-NPG) and TFN-NPs. The release and permeation investigations indicated that TFN was slowly released (38.42±2.87%) and had significantly enhanced penetration into the epidermal membrane of mice. The cumulative irritation score of 0.33 determined during testing suggested little discomfort. The generated nanogels are stable and have a high drug penetration profile over the skin, as shown by the findings. When compared to both pure TFN solutions, TFN-NPs and TFN-NPG demonstrated superior pharmacokinetic properties.

Conclusion: Based on the results, the NPs and NPG formulations were depicted to enhance the activity of TFN compared to the free drug solution. TFN could be a safe and effective treatment for Alopecia areata. The tofacitinib citrate NPG could be a clinically translatable, safer topical formulation for managing Alopecia areata.

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负载柠檬酸托法替尼的纳米凝胶治疗斑秃:响应面设计、配方和体内外表征。
目的:优化以聚乳酸共乙醇酸(PLGA)为原料,负载柠檬酸托法替尼(tofacitinib cit酸托法替尼,TFN)的纳米凝胶(TFN- nps)的设计与构建。方法:以聚乳酸(PLGA) (A)为聚合物,聚乙烯醇(PVA) (B)为稳定剂,搅拌速度(C)为自变量。采用单乳液-溶剂蒸发法制备TFN-NPs。采用Box Behnken Design (BBD),基于点预测确定TFN-NPs的最佳组成比例。结果:最佳组成的TFN-NPs包封效率为79.82±0.9%,粒径为236.19±5.07 nm,累积药物释放量为82.31±1.23%;PDI、zeta电位和载药量分别为0.297±0.21、-30.21±0.94mV和69.81±0.16%。然后使用最佳的TFN-NPs混合物开发了以卡波波尔为胶凝聚合物的凝胶配方。凝胶表征,药物释放,渗透研究,刺激和药代动力学研究也进行了。采用FTIR、DSC、XRD、SEM、TEM和AFM对制备的外用凝胶制剂(TFN-NPG)和TFN-NPs进行了进一步的固态和形貌评价。释放和渗透实验表明,TFN释放缓慢(38.42±2.87%),并能显著增强对小鼠表皮膜的渗透。在测试过程中测定的累计刺激得分为0.33,表明不舒服。正如研究结果所示,所生成的纳米凝胶是稳定的,并且在皮肤上具有很高的药物渗透性。与纯TFN溶液相比,TFN- nps和TFN- npg表现出优越的药代动力学特性。结论:与游离药物溶液相比,NPs和NPG制剂对TFN活性有增强作用。TFN是一种安全有效的治疗斑秃的方法。托法替尼柠檬酸NPG可能是一种临床可翻译的,更安全的局部配方治疗斑秃。
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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