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载有盐酸小檗碱和双醋瑞因的双传递脂质体:采用Box-Behnken设计的制剂与优化

Berberine HCl and diacerein loaded dual delivery transferosomes: Formulation and optimization using Box-Behnken design.

作者信息

Singh Siddharth, Awasthi Rajendra

机构信息

Department of Pharmaceutical Sciences, School of Health Sciences & Technology, UPES, Dehradun, Uttarakhand, India.

出版信息

ADMET DMPK. 2024 Apr 29;12(3):553-580. doi: 10.5599/admet.2268. eCollection 2024.

Abstract

INTRODUCTION

Berberine is a poorly water-soluble alkaloid compound showing significant anti-inflammatory characteristics. It reduces the levels of pro-inflammatory and inflammatory cytokines, including tumour necrosis factor (TNF-α, IFN-γ) and interleukin (IL-23, IL-12, and IL-23). Diacerein significantly reduces the splenomegaly associated with psoriasis. It downregulates the production of TNF-α and IL-12.

METHOD

This study reported the development of transferosomes containing berberine HCl and diacerein using a film hydration method followed by optimization using a Box-Behnken design. Sodium deoxycholate was used as an edge activator. The impact of independent variables (amount of phosphatidylcholine, amount of edge activator, and sonication cycles) on dependent variables (particle size and entrapment efficiency) was examined. The optimized formulation was characterized for polydispersity index, vesicle size, entrapment efficiency, ζ potential, spectral analysis like Fourier transform infrared, thermal analysis, X-ray diffraction, deformability, transmission electron microscopy, antioxidant assay, release, and skin permeation studies.

RESULTS

The optimized formulation had a particle size of 110.90±2.8 nm with high entrapment efficiency (89.50±1.5 of berberine HCl and 91.23±1.8 of diacerein). Deformability, polydispersity index, ζ potential, and antioxidant activity of the optimized formulation were 2.44, 0.296, -13.3, and 38.36 %, respectively. Optimized transferosomes exhibited 82.093±0.81 % and 85.02±3.81 % release of berberine HCl and diacerein after 24 h of dissolution study. The transdermal flux of optimized formulation was 0.0224 μg cm h (2.24 cm h permeation coefficient) and 0.0462 μg cm h (4.62 cm h permeation coefficient), respectively, for berberine HCl and diacerein. Raman analysis of treated pig skin confirmed that the transferosomes can permeate the skin. No change in the skin condition or irritation was observed in BALB/c mice. Formulation stored at 4 and 25±2 °C / 60±5 % relative humidity was stable for 3 months.

CONCLUSIONS

Thus, the results demonstrated successful optimization of the transferosomes for the efficient topical delivery of berberine HCl and diacerein in the effective management of psoriasis.

摘要

引言

黄连素是一种水溶性较差的生物碱化合物,具有显著的抗炎特性。它可降低促炎和炎性细胞因子的水平,包括肿瘤坏死因子(TNF-α、IFN-γ)和白细胞介素(IL-23、IL-12和IL-23)。双醋瑞因可显著减轻与银屑病相关的脾肿大。它下调TNF-α和IL-12的产生。

方法

本研究报道了采用薄膜水化法制备含盐酸小檗碱和双醋瑞因的传递体,随后使用Box-Behnken设计进行优化。脱氧胆酸钠用作边缘活化剂。研究了自变量(磷脂酰胆碱的量、边缘活化剂的量和超声处理次数)对因变量(粒径和包封率)的影响。对优化后的制剂进行了多分散指数、囊泡大小、包封率、ζ电位、傅里叶变换红外光谱分析、热分析、X射线衍射、变形性、透射电子显微镜、抗氧化测定、释放和皮肤渗透研究等表征。

结果

优化后的制剂粒径为110.90±2.8 nm,包封率高(盐酸小檗碱为89.50±1.5%,双醋瑞因为91.23±1.8%)。优化后的制剂的变形性、多分散指数、ζ电位和抗氧化活性分别为2.44、0.296、-13.3和38.36%。在溶出度研究24小时后,优化后的传递体对盐酸小檗碱和双醋瑞因的释放率分别为82.093±0.81%和85.02±3.81%。优化后制剂的透皮通量分别为盐酸小檗碱0.0224 μg/cm²·h(渗透系数为2.24 cm/h)和双醋瑞因0.0462 μg/cm²·h(渗透系数为4.62 cm/h)。对处理过的猪皮肤进行拉曼分析证实传递体可渗透皮肤。在BALB/c小鼠中未观察到皮肤状况改变或刺激。在4℃和25±2℃/相对湿度60±5%下储存的制剂3个月内稳定。

结论

因此,结果表明成功优化了传递体,可有效局部递送盐酸小檗碱和双醋瑞因,用于银屑病的有效治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aef5/11289510/664955285744/ADMET-12-2268-g001.jpg

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