探索局部阿托伐他汀透明质体凝胶作为减少全身皮质类固醇剂量的辅助:一项针对严重口腔扁平苔藓患者的随机临床试验。

IF 5.5 3区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Mahitab Elsayed, Aya Essawy, Radwa M Ismail, Yasmine Gamil, Mohamed G Hamed, Dalia Elsabaawy, Eman Abdelhakeem, Doaa Hegazy, Radwa M A Abd-Elal
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引用次数: 0

摘要

口腔扁平苔藓(OLP)是一种慢性炎症性疾病,局部治疗选择有限,长期依赖皮质类固醇。本研究研究了一种新型负载阿托伐他汀的透明质体凝胶(ATV-Hyalugel)作为局部佐剂,以减少严重OLP患者全身皮质类固醇的使用。本研究的目的是开发、优化、表征ATV-Hyalugel,并通过随机对照临床试验评价其临床疗效。通过薄膜水合法制备atv负载的透明质体(ATV-HAs),并采用i -最优混合设计(自变量:磷脂、Tween 80和透明质酸;响应:包封效率(EE%)、粒径(PS)和ζ电位(ZP))进行优化。将最佳配方掺入壳聚糖凝胶中,对其pH、流变学行为和体外释药性能进行了表征。为期四周的随机对照试验(n = 90)比较:第一组接受标准强的松龙(40 mg/天),而第二组接受半剂量强的松龙(20 mg/天)联合ATV-Hyalugel(局部,每日3次)。每周记录疼痛和溃疡评分。采用Mann-Whitney U检验(非参数;α = 0.05)进行组间比较,采用Kruskal-Wallis检验评估从基线到第4周的组内改善情况。优化后的ATV-HAs具有较高的EE%(79.1±0.4%),均匀的PS(221.2±5.1 nm)和稳定的ZP(-31.6±0.2 mV)。atv -透明凝胶具有与粘膜相容的pH值(6.48±0.2)、假塑性流变学和以扩散驱动动力学为主的缓释特性。临床方面,尽管两组的皮质类固醇用量减少了50%,但到第2周时,两组的治疗效果达到了等效(p < 0.05)。从基线到第4周,两组症状均显著减轻(p
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Exploring topical atorvastatin hyalurosomal gel as an adjuvant for reducing systemic corticosteroid dosage: a randomized clinical trial in severe oral lichen planus patients.

Oral lichen planus (OLP) is a chronic inflammatory disorder with limited topical treatment options and long-term corticosteroid dependency. This study investigates a novel atorvastatin-loaded hyalurosomal gel (ATV-Hyalugel) as a topical adjuvant to reduce systemic corticosteroid use in severe OLP. The objective of the study is to develop, optimize, characterize ATV-Hyalugel and evaluate its clinical efficacy in a randomized controlled clinical trial. ATV-loaded hyalurosomes (ATV-HAs) were prepared via thin-film hydration and optimized using an I-optimal mixture design (independent variables: phospholipid, Tween 80, and hyaluronic acid; responses: entrapment efficiency (EE%), particle size (PS), and zeta potential (ZP). The optimal formulation was incorporated into a chitosan gel, which was characterized for its pH, rheological behavior, and in-vitro drug release. Four weeks randomized controlled trial (n = 90) compared: group one received standard prednisolone (40 mg/day) while group two received half-dose prednisolone (20 mg/day) in combination with ATV-Hyalugel (topically, three times daily). Pain and ulcer scores were recorded weekly. Between-group comparisons were performed using the Mann-Whitney U test (non-parametric; α = 0.05), and within-group improvement from baseline to Week 4 was assessed using the Kruskal-Wallis test. Optimized ATV-HAs demonstrated high EE% (79.1 ± 0.4%), uniform PS (221.2 ± 5.1 nm), and stable ZP (-31.6 ± 0.2 mV). ATV-Hyalugel exhibited mucosa-compatible pH (6.48 ± 0.2), pseudoplastic rheology, and a sustained release profile dominated by diffusion-driven kinetics. Clinically, group two achieved therapeutic equivalence to group one by Week 2 (p > 0.05), despite receiving 50% less corticosteroid. Both groups showed significant symptom reduction from baseline to Week four (p < 0.0001, Kruskal-Wallis). No adverse events were reported with ATV-Hyalugel. ATV-Hyalugel enables a 50% corticosteroid dose reduction while maintaining clinical efficacy. Its favorable release kinetics and safety profile support its use as an innovative adjuvant therapy for severe OLP.

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来源期刊
Drug Delivery and Translational Research
Drug Delivery and Translational Research MEDICINE, RESEARCH & EXPERIMENTALPHARMACOL-PHARMACOLOGY & PHARMACY
CiteScore
11.70
自引率
1.90%
发文量
160
期刊介绍: The journal provides a unique forum for scientific publication of high-quality research that is exclusively focused on translational aspects of drug delivery. Rationally developed, effective delivery systems can potentially affect clinical outcome in different disease conditions. Research focused on the following areas of translational drug delivery research will be considered for publication in the journal. Designing and developing novel drug delivery systems, with a focus on their application to disease conditions; Preclinical and clinical data related to drug delivery systems; Drug distribution, pharmacokinetics, clearance, with drug delivery systems as compared to traditional dosing to demonstrate beneficial outcomes Short-term and long-term biocompatibility of drug delivery systems, host response; Biomaterials with growth factors for stem-cell differentiation in regenerative medicine and tissue engineering; Image-guided drug therapy, Nanomedicine; Devices for drug delivery and drug/device combination products. In addition to original full-length papers, communications, and reviews, the journal includes editorials, reports of future meetings, research highlights, and announcements pertaining to the activities of the Controlled Release Society.
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