利用 Novasome 纳米载体优化透皮给药:质量源于设计(QbD)框架。

Prabhjot Kaur, Priyanka Kriplani
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引用次数: 0

摘要

一种革命性的基于胶囊的药物输送技术,称为novasome技术,在有效性和效率方面优于传统的脂质体系统。它由游离脂肪酸,胆固醇和表面活性剂组成,它们结合在一起产生更好的囊泡特性,用于药物管理。许多研究努力已经检验了表面活性剂类型、游离脂肪酸及其比例的理想混合物,以及可能对囊泡特性产生重大影响的配方元素。研究表明,novasome技术可用于输送各种药物,如疫苗、尼氟酸、唑米曲坦和terconazole。为了开发具有显著药物负荷和纳米形态的最有效的novasomal制剂,重要的是找到核心成分之间的适当比例以及关键的制造工艺决定因素。理解这些因素之间的相互作用需要将设计质量(QBD)与实验设计(DoE)相结合。这些可以应用于放大和实验室规模的应用。这篇文章包括novasome和QBD参与的详细观点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Optimizing Transdermal Drug Delivery with Novasome Nanocarriers: A Quality by Design (QbD) Framework.

A revolutionary encapsulation-based drug delivery technique called novasome technology outperforms conventional liposome systems in terms of effectiveness and efficiency. It is comprised of free fatty acid, cholesterol, and surfactant, which combine to yield better vesicle properties for medication administration. Numerous research endeavors have examined the ideal blend of surfactant types, free fatty acids, and their proportions, along with the formulation elements that might substantially impact the vesicle properties. It has been shown that novasome technology may be used to deliver various drugs, such as vaccines, niflumic acid, zolmitriptan, and terconazole. To develop the most effective novasomal formulations with significant drug loading and nano-metric form, it is important to find the appropriate ratio between core components along with critical manufacturing process determinants. Understanding the interplay between these factors requires applying Quality by Design (QBD) in combination with Design of Experiments (DoE). These may be applied for both scale-up and lab-scale applications. This manuscript includes a detailed view of novasomes and the involvement of QBD.

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