Drug Delivery and Nanomedicines Research Group, Department of Pharmaceutics, University of Nigeria, Nsukka, Nigeria.
Drug Delivery and Nanomedicines Research Group, Department of Pharmaceutics, University of Nigeria, Nsukka, Nigeria.
J Control Release. 2021 Jun 10;334:224-236. doi: 10.1016/j.jconrel.2021.04.020. Epub 2021 Apr 22.
Early treatment with parenteral antimalarials is key in preventing deaths and complications associated with severe and cerebral malaria. This can be challenging in 'hard-to-reach' areas in Africa where transit time to hospitals with facilities to administer drugs parenterally can be more than 6 h. Consequently, the World Health Organization has recommended the use of artesunate (ATS) suppositories for emergency treatment of patients, however, this treatment is only for children under 6 years. The intranasal route (INR) can provide a safe and effective alternative to parenteral and rectal routes for patients of all ages; thus, reducing delays to the initiation of treatment. Hence, we designed ATS-loaded nanostructured lipid carriers (NLCs) for intranasal administration. ATS-NLCs were formulated using varying concentrations of lipid matrices made up of solidified reverse micellar solutions (SRMS) comprising a 1:2 ratio of Phospholipon ® 90H and lipids (Softisan ® 154 or Compritol ®). ATS-NLCs were spherical, and the small sizes of ATS-NLCs obtained for some formulations (76.56 ± 1.04 nm) is an indication that ATS-NLCs can pass through the nasal mucosa and reach the brain or systemic circulation. Encapsulation efficiency of ATS in NLCs was ≥70% for all formulations. ATS-NLCs achieved up to 40% in vitro drug release in 1 h, while ex vivo permeation studies revealed that formulating ATS as NLCs enhanced permeation through pig nasal mucosa better than drug solution. Most importantly, the activity and reduction in parasitaemia [in mice infected with Plasmodium berghei ANKA in a murine cerebral malaria model] by ATS-NLCs administered through the INR (54.70%, 33.28%) was comparable to intramuscular administration (58.80%, 42.18%), respectively. Therefore, intranasal administration of NLCs of ATS has great potentials to serve as a satisfactory alternative to parenteral administration for the treatment of severe and cerebral malaria in both adults and children in remote areas of sub-Saharan Africa.
早期使用注射用抗疟药是预防严重疟疾和脑型疟疾相关死亡和并发症的关键。在非洲偏远地区,由于前往有注射给药设施的医院的运输时间可能超过 6 小时,这可能具有挑战性。因此,世界卫生组织建议使用青蒿琥酯(ATS)栓剂紧急治疗患者,但这种治疗仅适用于 6 岁以下儿童。鼻内途径(INR)可为所有年龄段的患者提供一种替代注射和直肠途径的安全有效方法;从而减少开始治疗的延迟。因此,我们设计了用于鼻内给药的载青蒿琥酯纳米结构脂质载体(NLCs)。使用不同浓度的脂质基质来制备 ATS-NLCs,这些脂质基质由固态反向胶束溶液(SRMS)组成,其包含 1:2 比例的 Phospholipon ® 90H 和脂质(Softisan ® 154 或 Compritol ®)。ATS-NLCs 呈球形,一些制剂获得的 ATS-NLCs 粒径较小(76.56±1.04nm),表明 ATS-NLCs 可以穿过鼻黏膜并到达大脑或全身循环。所有制剂中 ATS-NLCs 的包封效率均≥70%。ATS-NLCs 在 1 小时内达到高达 40%的体外药物释放,而体外渗透研究表明,将 ATS 制成 NLCs 可增强药物通过猪鼻黏膜的渗透作用,优于药物溶液。最重要的是,通过 INR 给予 ATS-NLCs 在感染 Plasmodium berghei ANKA 的小鼠脑型疟疾模型中表现出与肌肉内给药相当的疗效和寄生虫血症减少(54.70%,33.28%)。因此,通过 INR 给予 NLCs 的 ATS 鼻内给药具有很大的潜力,可作为撒哈拉以南非洲偏远地区成人和儿童严重疟疾和脑型疟疾的替代注射给药方法。