相关实验视频
Updated: Jul 26, 2026

08:28
Development of an In Vitro Ocular Platform to Test Contact Lenses
Published on: April 6, 2016
11.2K
新型稳定菌根配方用于nepafenac的眼部输送:优化,表征和体外评估
Ronak Vashi1,2, Kishorkumar Sorathia1
1Faculty of Pharmacy, Dharmsinh Desai University, College road, Nadiad, Gujarat, India 387003.
Drug development and industrial pharmacy
|January 10, 2026
概括
研究人员开发了一种稳定,清晰的眼科纳米细胞配方Nepafenac. 这种新配方提供了一种潜在的优越替代方案,以目前的悬浮基治疗术后的脑膜炎.
科学领域:
- 眼科医生 眼科 眼科
- 纳米技术 纳米技术
- 制药科学 制药科学
背景情况:
- 目前用于手术后卵巢炎的尼帕菲纳克悬浮配方存在制造方面的挑战和患者合规问题.
- 高粘度,流和异物感觉限制了患者对现有治疗的坚持.
研究的目的:
- 开发一种稳定,清晰的眼科纳米细胞配方Nepafenac.
- 创建一个更为患者友好和更具成本效益的替代方案,以目前的尼帕菲纳克悬浮剂.
主要方法:
- 利用预配方研究来确定必要的辅助成分.
- 使用Box-Behnken方法优化表面活性剂和晶体抑制剂度.
- 评估了优化配方的物理化学特性,体外安全性和稳定性.
主要成果:
- 优化的纳米分子配方的平均颗粒大小为10-20nm,动态粘度为43.5mPas,pH为7.4.
- 通过MTT细胞活力和HET-CAM测试证明了体外安全性.
- 在实时储存条件下表现出长达6个月的物理化学稳定性.
结论:
- 开发的纳米状Nepafenac配方是眼科药物输送的有希望的替代方案.
- 这种配方解决了与当前基于悬浮的尼帕菲纳克产品相关的局限性.
相关概念视频
Modified-Release Drug Delivery Systems: Bioavailability
Modified-release (MR) dosage forms are designed to extend drug release over time, thereby maintaining stable plasma concentrations and reducing dosing frequency. However, their bioavailability is typically below 100% due to incomplete drug release and presystemic metabolism, and limitations in drug permeability across the gastrointestinal epithelium, all of which can restrict the fraction of the drug reaching systemic circulation. Consequently, studying the in vivo bioavailability of MR...
Modified-Release Drug Delivery Systems: Site-Targeted
Site-targeted drug delivery systems enhance therapeutic efficacy while minimizing systemic toxicity and treatment costs. Unlike conventional methods, these systems ensure precise drug delivery, improving bioavailability and reducing side effects. Targeted drug delivery is classified into three levels. First-order targeting directs drugs to the capillary beds of specific organs or tissues. Second-order targets specific cell types, such as tumor cells, using receptor-mediated interactions.
Ophthalmic Drug Delivery Systems
Ophthalmic drug delivery faces major limitations due to poor absorption across the corneal membrane. This process is primarily driven by diffusion and is influenced by two main factors: the physicochemical properties of the drug and tear drainage. Most ophthalmic drugs, such as pilocarpine, epinephrine, atropine, and local anesthetics, are weak bases. They are typically formulated at an acidic pH to enhance chemical stability. However, this leads to high ionization, reducing their ability to...

