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

IF 3.4 Q2 CHEMISTRY, MEDICINAL ADMET and DMPK Pub Date : 2024-04-29 eCollection Date: 2024-01-01 DOI:10.5599/admet.2268
Siddharth Singh, Rajendra Awasthi
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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, in-vitro release, and ex-vivo 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-2 h-1 (2.24 cm h-1 permeation coefficient) and 0.0462 μg cm-2 h-1 (4.62 cm h-1 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.

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盐酸小檗碱和地卡西林负载型双给药转运体:采用方框-贝肯设计进行配制和优化。
简介小檗碱是一种水溶性较差的生物碱化合物,具有显著的抗炎特性。它能降低促炎和炎症细胞因子的水平,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)。银屑病患者的脾脏肿大程度会明显减轻。它能下调 TNF-α 和 IL-12 的产生:本研究报告采用薄膜水合法开发了含有盐酸小檗碱和双醋瑞因的转运体,然后采用方框-贝肯设计法进行了优化。脱氧胆酸钠被用作边缘活化剂。研究了自变量(磷脂酰胆碱的用量、边缘活化剂的用量和超声周期)对因变量(粒度和包埋效率)的影响。对优化配方进行了多分散指数、囊泡大小、夹带效率、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、抗氧化检测、体外释放和体外皮肤渗透研究:优化配方的粒径为 110.90±2.8 nm,具有较高的包封效率(盐酸小檗碱的包封效率为 89.50±1.5,二醋瑞因的包封效率为 91.23±1.8)。优化配方的变形率、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%。经过 24 小时的溶出研究,优化后的转移体盐酸小檗碱和迪卡西林的释放率分别为 82.093±0.81 % 和 85.02±3.81%。优化制剂的透皮通量分别为 0.0224 μg cm-2 h-1 (渗透系数为 2.24 cm h-1)和 0.0462 μg cm-2 h-1 (渗透系数为 4.62 cm h-1)。对处理过的猪皮肤进行的拉曼分析证实,转移体可以渗透皮肤。BALB/c 小鼠的皮肤状况和刺激性均未发生变化。配方在 4 和 25±2 °C / 60±5 % 相对湿度条件下储存 3 个月保持稳定:因此,研究结果表明成功优化了转运体,使盐酸小檗碱和地卡西林能有效地局部给药,从而有效治疗银屑病。
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来源期刊
ADMET and DMPK
ADMET and DMPK Multiple-
CiteScore
4.40
自引率
0.00%
发文量
22
审稿时长
4 weeks
期刊介绍: ADMET and DMPK is an open access journal devoted to the rapid dissemination of new and original scientific results in all areas of absorption, distribution, metabolism, excretion, toxicology and pharmacokinetics of drugs. ADMET and DMPK publishes the following types of contributions: - Original research papers - Feature articles - Review articles - Short communications and Notes - Letters to Editors - Book reviews The scope of the Journal involves, but is not limited to, the following areas: - physico-chemical properties of drugs and methods of their determination - drug permeabilities - drug absorption - drug-drug, drug-protein, drug-membrane and drug-DNA interactions - chemical stability and degradations of drugs - instrumental methods in ADMET - drug metablic processes - routes of administration and excretion of drug - pharmacokinetic/pharmacodynamic study - quantitative structure activity/property relationship - ADME/PK modelling - Toxicology screening - Transporter identification and study
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