Costa Salvana, Barreto Ighor Costa, Gama Nataly, Santos Kathylen, Oliveira Cleomárcio Miguel de, Costa Isabela Silva, Vila Nova Monique, Santos Ruane, Borges Arthur, de Alencar Filho José Marcos Teixeira, do Nascimento Ticiano Gomes
Institute of Pharmaceutical Science, Federal University of Alagoas, Maceio 57072-970, Alagoas, Brazil.
Superintendency of Environment and Infrastructure, Federal University of Bahia, Salvador 40170-110, Bahia, Brazil.
Pharmaceutics. 2025 Jul 11;17(7):898. doi: 10.3390/pharmaceutics17070898.
Propolis, known for its medicinal properties, faces challenges in pharmaceutical applications due to its low aqueous solubility, attributed to its resinous and hydrophobic nature. This limits oral administration, reducing its bioavailability and pharmacological activities. To overcome these barriers, cyclodextrins (CDs), cyclic oligosaccharides, are widely studied as carrier systems that enhance the solubility and bioavailability of propolis and other nonpolar compounds. This study aimed to review patents that developed innovative therapeutic approaches to improve the physicochemical and biological properties of propolis through complexation with CDs. Active and application patents registered over the last 17 years were searched across multiple databases, resulting in the selection of eight inventions for detailed analysis. These patents highlight therapeutic applications of propolis-CD systems for conditions such as diabetes and skin and gastrointestinal cancers, as well as antimicrobial, immunostimulant, and antioxidant effects. Additionally, novel extraction processes free of organic solvents, including nanometric-scale powder extracts, are described. Findings from scientific articles support the patent data, demonstrating that CD complexation significantly enhances the solubility and therapeutic efficacy of propolis. Thus, these patents present an innovative and promising strategy for developing propolis-based pharmaceutical products.
蜂胶因其药用特性而闻名,但由于其树脂状和疏水性,在制药应用中面临挑战,这导致其水溶解度较低。这限制了口服给药,降低了其生物利用度和药理活性。为了克服这些障碍,环糊精(CDs),即环状寡糖,作为提高蜂胶和其他非极性化合物溶解度和生物利用度的载体系统被广泛研究。本研究旨在综述通过与CDs络合来改善蜂胶理化和生物学性质的创新治疗方法的专利。在多个数据库中搜索了过去17年注册的活性和应用专利,最终选择了八项发明进行详细分析。这些专利强调了蜂胶-CD系统在糖尿病、皮肤癌和胃肠道癌等病症中的治疗应用,以及抗菌、免疫刺激和抗氧化作用。此外,还描述了不含有机溶剂的新型提取工艺,包括纳米级粉末提取物。科学文章的研究结果支持了专利数据,表明CD络合显著提高了蜂胶的溶解度和治疗效果。因此,这些专利为开发基于蜂胶的药品提供了一种创新且有前景的策略。