Yao-Yao Wei , Yang Zhang , Xue Lu , Jie Zhou , Huang-Wei Cheng , Yuan-Yuan Liu , Hua Zhang , Wen Chen
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引用次数: 0
摘要
痛风是一种由尿酸钠(MSU)晶体沉积在关节和组织中引起的疾病。秋水仙碱(COL)因其价格低廉、疗效显著,已成为治疗急性痛风的一线药物。然而,秋水仙碱具有高度的细胞毒性,口服容易对胃肠道、肝脏和肾脏造成严重的不良反应。因此,本研究旨在开发一种新的皮肤给药配方,以解决该药物的安全性问题。此外,为了提高脂质体的性能,研究人员对脂质体进行了筛选,确定每mL脂质体中加入1.0-1.5 mg的神经酰胺III (Cer3)作为修饰剂,可以显著增强脂质体的稳定性,成功构建了Cer3/ col -脂质体(CCE)。将CCE与膜片基质混合制成携带秋水仙碱的CCE膜片,显示了两种剂型——酶体和膜片的优势叠加效应。与传统的COL给药方式相比,这种外用制剂可以达到有效的血药水平而不引起血药水平波动,具有良好的疗效和更高的安全性,是治疗痛风的一种有吸引力的替代方案。
Novel colchicine ethosomes cataplasm for the treatment of acute gouty arthritis
Gout is a disease caused by the deposition of sodium urate (MSU) crystals in the joints and tissues. Colchicine (COL) has become the first-line drug for the treatment of acute gout due to its low price and efficacy. However, colchicine is highly cytotoxic and oral administration is prone to cause severe adverse effects on the gastrointestinal tract, liver and kidney. Therefore, this study aimed to develop a novel dermal delivery formulation for addressing the safety concerns of this drug. The researchers used ethosomes encapsulation technology to improve the skin permeability of COL. In addition, in order to improve the performance of the ethosomes, it was screened and determined that the addition of 1.0–1.5 mg of ceramide III (Cer3) per mL of ethosomes as a modifier could significantly enhance the stability of the ethosomes, Cer3/COL-ethosomes (CCE) were successfully constructed. The CCE was then mixed with a cataplasm matrix to produce a colchicine-carrying CCE cataplasm, which demonstrated the superimposed effect of the advantages of the two dosage forms, the ethosomes and the cataplasm. Compared with the traditional delivery method of COL, this topical formulation is an attractive alternative for the treatment of gout as it can achieve effective blood levels without causing fluctuations in blood levels, and has good efficacy and higher safety profile.
期刊介绍:
Colloids and Surfaces B: Biointerfaces is an international journal devoted to fundamental and applied research on colloid and interfacial phenomena in relation to systems of biological origin, having particular relevance to the medical, pharmaceutical, biotechnological, food and cosmetic fields.
Submissions that: (1) deal solely with biological phenomena and do not describe the physico-chemical or colloid-chemical background and/or mechanism of the phenomena, and (2) deal solely with colloid/interfacial phenomena and do not have appropriate biological content or relevance, are outside the scope of the journal and will not be considered for publication.
The journal publishes regular research papers, reviews, short communications and invited perspective articles, called BioInterface Perspectives. The BioInterface Perspective provide researchers the opportunity to review their own work, as well as provide insight into the work of others that inspired and influenced the author. Regular articles should have a maximum total length of 6,000 words. In addition, a (combined) maximum of 8 normal-sized figures and/or tables is allowed (so for instance 3 tables and 5 figures). For multiple-panel figures each set of two panels equates to one figure. Short communications should not exceed half of the above. It is required to give on the article cover page a short statistical summary of the article listing the total number of words and tables/figures.