Mendes Ana I, Rebelo Rita, Aroso Ivo, Correlo Vitor M, Fraga Alexandra G, Pedrosa Jorge, Marques Alexandra P
Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Campus de Gualtar, 4710-057 Braga, Portugal; ICVS/3B's-PT Government Associate Laboratory, Braga/Guimarães, Portugal.
ICVS/3B's-PT Government Associate Laboratory, Braga/Guimarães, Portugal; 3B's Research Group, I3Bs - Research Institute on Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark, Zona Industrial da Gandra, 4805-017 Barco, Guimarães, Portugal.
Int J Pharm. 2022 Jul 25;623:121954. doi: 10.1016/j.ijpharm.2022.121954. Epub 2022 Jun 24.
Skin infection by Mycobacterium ulcerans causes Buruli ulcer (BU) disease, a serious condition that significantly impact patient' health and quality of life and can be very difficult to treat. Treatment of BU is based on daily systemic administration of antibiotics for at least 8 weeks and presents drawbacks associated with the mode and duration of drug administration and potential side effects. Thus, new therapeutic strategies are needed to improve the efficacy and modality of BU therapeutics, resulting in a more convenient and safer antibiotic regimen. Hence, we developed a dual delivery system based on poly(hydroxybutyrate-co-hydroxyvalerate) (PHBV) microparticles and a gellan gum (GG) hydrogel for delivery of rifampicin (RIF) and streptomycin (STR), two antibiotics used for BU treatment. RIF was successfully loaded into PHBV microparticles, with an encapsulation efficiency of 43%, that also revealed a mean size of 10 µm, spherical form and rough topography. These microparticles were further embedded in a GG hydrogel containing STR. The resultant hydrogel showed a porous microstructure that conferred a high water retention capability (superior to 2000%) and a controlled release of both antibiotics. Also, biological studies revealed antibacterial activity against M. ulcerans, and a good cytocompatibility in a fibroblast cell line. Thus, the proposed drug delivery system can constitute a potential topical approach for treatment of skin ulcers caused by BU disease.
溃疡分枝杆菌引起的皮肤感染会导致布氏溃疡(BU)病,这是一种严重疾病,会对患者的健康和生活质量产生重大影响,且治疗难度很大。布氏溃疡的治疗基于每日全身使用抗生素至少8周,存在与给药方式和持续时间以及潜在副作用相关的缺点。因此,需要新的治疗策略来提高布氏溃疡治疗的疗效和方式,从而形成更方便、更安全的抗生素治疗方案。因此,我们开发了一种基于聚(3-羟基丁酸酯-共-3-羟基戊酸酯)(PHBV)微粒和结冷胶(GG)水凝胶的双递送系统,用于递送利福平(RIF)和链霉素(STR),这两种用于治疗布氏溃疡的抗生素。利福平成功负载到PHBV微粒中,包封率为43%,其平均粒径为10μm,呈球形且表面粗糙。这些微粒进一步包埋在含有链霉素的结冷胶水凝胶中。所得水凝胶呈现出多孔微观结构,具有高保水能力(超过2000%),且两种抗生素均能实现控释。此外,生物学研究表明该系统对溃疡分枝杆菌具有抗菌活性,并且在成纤维细胞系中具有良好的细胞相容性。因此,所提出的药物递送系统可构成一种治疗布氏溃疡病引起的皮肤溃疡的潜在局部治疗方法。