Datta Deepanjan, Priyanka Bandi Sony, Colaco Viola, Dhas Namdev, Siva Reddy D V, Vora Lalitkumar K
Department of Pharmaceutics, Manipal College of Pharmaceutical Sciences, Manipal Academy of Higher Education, Manipal 576104, Karnataka State, India.
Loka Laboratories Private Limited, Technology Business Incubator, BITS Pilani Hyderabad Campus, Jawahar Nagar, Medchal 500078, Telangana, India.
Int J Pharm. 2024 Jun 10;658:124192. doi: 10.1016/j.ijpharm.2024.124192. Epub 2024 May 3.
Ocular delivery is the most challenging aspect in the field of pharmaceutical research. The major hurdle for the controlled delivery of drugs to the eye includes the physiological static barriers such as the complex layers of the cornea, sclera and retina which restrict the drug from permeating into the anterior and posterior segments of the eye. Recent years have witnessed inventions in the field of conventional and nanocarrier drug delivery which have shown considerable enhancement in delivering small to large molecules across the eye. The dynamic challenges associated with conventional systems include limited drug contact time and inadequate ocular bioavailability resulting from solution drainage, tear turnover, and dilution or lacrimation. To this end, various bioactive-based nanosized carriers including liposomes, ethosomes, niosomes, dendrimer, nanogel, nanofibers, contact lenses, nanoprobes, selenium nanobells, nanosponge, polymeric micelles, silver nanoparticles, and gold nanoparticles among others have been developed to circumvent the limitations associated with the conventional dosage forms. These nanocarriers have been shown to achieve enhanced drug permeation or retention and prolong drug release in the ocular tissue due to their better tissue adherence. The surface charge and the size of nanocarriers (10-1000 nm) are the important key factors to overcome ocular barriers. Various nanocarriers have been shown to deliver active therapeutic molecules including timolol maleate, ampicillin, natamycin, voriconazole, cyclosporine A, dexamethasone, moxifloxacin, and fluconazole among others for the treatment of anterior and posterior eye diseases. Taken together, in a nutshell, this extensive review provides a comprehensive perspective on the numerous facets of ocular drug delivery with a special focus on bioactive nanocarrier-based approaches, including the difficulties and constraints involved in the fabrication of nanocarriers. This also provides the detailed invention, applications, biodistribution and safety-toxicity of nanocarriers-based therapeutcis for the ophthalmic delivery.
眼部给药是药物研究领域中最具挑战性的方面。药物向眼部的控释面临的主要障碍包括生理静态屏障,如角膜、巩膜和视网膜的复杂层,这些屏障限制药物渗透到眼的前段和后段。近年来,传统和纳米载体药物递送领域有了诸多发明,在将小分子至大分子递送至眼部方面有了显著提升。与传统系统相关的动态挑战包括药物接触时间有限,以及因溶液引流、泪液更新、稀释或流泪导致的眼部生物利用度不足。为此,人们开发了各种基于生物活性的纳米级载体,包括脂质体、醇质体、非离子表面活性剂囊泡、树枝状大分子、纳米凝胶、纳米纤维、隐形眼镜、纳米探针、硒纳米钟、纳米海绵、聚合物胶束、银纳米颗粒和金纳米颗粒等,以克服与传统剂型相关的局限性。由于这些纳米载体具有更好的组织粘附性,已显示它们能实现增强的药物渗透或滞留,并在眼部组织中延长药物释放。纳米载体的表面电荷和尺寸(10 - 1000纳米)是克服眼部屏障的重要关键因素。各种纳米载体已被证明能递送活性治疗分子,包括马来酸噻吗洛尔、氨苄西林、那他霉素、伏立康唑、环孢素A、地塞米松、莫西沙星和氟康唑等,用于治疗眼前段和后段眼部疾病。总之,这篇全面的综述提供了关于眼部药物递送众多方面的综合观点,特别关注基于生物活性纳米载体的方法,包括纳米载体制造中涉及的困难和限制。这也提供了基于纳米载体的眼科治疗药物的详细发明、应用、生物分布和安全性 - 毒性情况。