Department of Pharmacology, Faculty of Veterinary Medicine, Beni-Suef University, Beni-Suef, 62511, Egypt.
Department of Veterinary Medicine, Faculty of Veterinary Medicine, Beni-Suef University, Beni-Suef, 62511, Egypt.
AAPS PharmSciTech. 2020 Nov 18;21(8):326. doi: 10.1208/s12249-020-01833-7.
Brucellosis is a common zoonotic infection, particularly in the developing world. The recommended treatment regimens for brucellosis involve the use of two medications such as doxycycline and curcumin in order to avoid relapses and prolonged use of these drugs. Doxycycline has excellent activity in the acidic phagolysosomal environment, while curcumin modulates the immune system function and macrophage activity. Due to the intracellular existence of Brucellae and the different anti-immune mechanisms of Brucella, the treatment of Brucella infection faces many limitations. The design of nanosystems is a promising treatment approach for brucellosis. The objective of this study was to design and evaluate the efficacy of in situ pH-responsive curcumin-loaded niosome hydrogel and doxycycline-loaded chitosan-sodium alginate nanoparticles as chemotherapeutic agents against brucellosis. The prepared formulae showed a spherical nano shape with a slow drug release pattern and small particle size. The prepared formulae were evaluated in vivo using Guinea pigs experimentally infected with Brucella melitensis biovar3. The prepared formula combination gave a significant high reduction rate of Brucella spleen viable count compared with that of untreated controls at p < 0.05. The results showed that the treatment schemes were not fully successful in eliminating Brucella infection in Guinea pigs; however, they significantly (p < 0.05) reduced the viable Brucella count in a shorter time and sub-therapeutic doses. Collectively the novel prepared formulae could be a successful therapy for the effective treatment of brucellosis infection at the recommended therapeutic doses. Graphical abstract.
布鲁氏菌病是一种常见的人畜共患病,尤其在发展中国家较为多见。布鲁氏菌病的推荐治疗方案包括使用两种药物,如强力霉素和姜黄素,以避免复发和长期使用这些药物。强力霉素在酸性吞噬溶酶体环境中具有良好的活性,而姜黄素调节免疫系统功能和巨噬细胞活性。由于布鲁氏菌在细胞内的存在以及布鲁氏菌不同的免疫机制,布鲁氏菌感染的治疗面临许多限制。纳米系统的设计是治疗布鲁氏菌病的一种有前途的方法。本研究旨在设计和评估原位 pH 响应姜黄素载药尼森囊水凝胶和载药壳聚糖-海藻酸钠纳米粒作为抗布鲁氏菌病化疗药物的疗效。所制备的配方表现出球形纳米形状,具有缓慢的药物释放模式和较小的粒径。所制备的配方在感染布鲁氏菌 melitensis biovar3 的豚鼠体内进行了体内评估。与未治疗的对照组相比,该配方组合对布鲁氏菌脾脏活菌计数的降低率显著更高(p<0.05)。结果表明,这些治疗方案未能完全成功地消除豚鼠中的布鲁氏菌感染;然而,它们在更短的时间内显著(p<0.05)降低了活菌布鲁氏菌的数量,并且使用的是亚治疗剂量。总的来说,这些新的配方可以成为有效治疗布鲁氏菌感染的成功疗法,使用推荐的治疗剂量。