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离子对载匹鲁卡品胶束作为治疗近视的眼部给药系统。

Ion-paired pirenzepine-loaded micelles as an ophthalmic delivery system for the treatment of myopia.

机构信息

State Key Laboratory of Natural Medicines, Department of Pharmaceutics, China Pharmaceutical University, Nanjing, China.

Children's Hospital of Nanjing Medical University, Nanjing, China.

出版信息

Nanomedicine. 2017 Aug;13(6):2079-2089. doi: 10.1016/j.nano.2017.05.001. Epub 2017 May 21.

Abstract

Myopia is one of the most common ocular disorders for which standard treatments, such as refractive surgery, often involve invasive procedures. Pirenzepine (PRZ), a muscarinic receptor antagonist, has been recognized as a promising candidate for the treatment of myopia, but possesses poor ocular bioavailability. The overall objective of this study was to prepare PRZ-sorbic acid complexes suitable to be encapsulated into micelles with high efficiency for optimal ophthalmic delivery. The results demonstrated that sorbic acid, used as the counter ion, had the most significant effects in increasing the octanol-water distribution coefficient of PRZ as well as improving its corneal permeability in vitro among various counter ions tested. In vivo absorption results showed that a 1.5 times higher bioavailability was achieved by the addition of sorbic acid at a 1:1 ratio. Cytotoxicity studies in vitro and biocompatibility studies in vivo indicated that the micelles did not cause significant toxicities to the eyes.

摘要

近视是最常见的眼部疾病之一,标准治疗方法,如屈光手术,通常涉及侵入性手术。匹鲁卡品(PRZ),一种毒蕈碱受体拮抗剂,已被认为是治疗近视的有前途的候选药物,但眼部生物利用度差。本研究的总体目标是制备适合封装到胶束中的 PRZ-山梨酸复合物,以实现最佳的眼部传递。结果表明,山梨酸作为抗衡离子,在增加 PRZ 的辛醇-水分配系数以及提高其体外角膜透过性方面,比测试的各种抗衡离子具有更显著的效果。体内吸收结果表明,添加山梨酸以 1:1 的比例可使生物利用度提高 1.5 倍。体外细胞毒性研究和体内生物相容性研究表明,胶束对眼睛没有明显的毒性。

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