4.7 Article

PEG Conjugated Zein Nanoparticles for In Vivo Use

期刊

PHARMACEUTICS
卷 14, 期 9, 页码 -

出版社

MDPI
DOI: 10.3390/pharmaceutics14091831

关键词

polyethene glycol; nanoparticles; Zein; protein-based drug delivery systems; nanomedicine; microfluidics

资金

  1. Canadian Graduate Scholarships-Doctoral Program Canadian Institutes of Health Research (CGS-D CIHR) [21R04868]
  2. NMIN [10901]
  3. University of British Columbia Four Year Doctoral Graduate Fellowship [6569]
  4. CGS-D CIHR [21R04868]
  5. BC Cancer Research Sustainment - BC Cancer Foundation

向作者/读者索取更多资源

The research discovered that Zein nanoparticles modified with pre-functionalized PEG can maintain stability and have good cellular uptake capability in physiologically relevant conditions. These Zein:PEG-Zein nanoparticles also exhibit a long circulation half-life and suitability for single-use administration.
Zein can be utilized to form nanoscale particles for drug delivery applications. Despite the ease of synthesis, these particles often aggregate when exposed to physiologically relevant conditions (e.g., pH and salt concentrations). This instability has prevented their further development in applications requiring intravenous administration. To mitigate this colloidal instability, this research explored Zein nanoparticles (NP)s that were modified with polyethylene glycol (PEG) either through functionalized PEG pre- or post-NP formation. The results suggest that the pre-functionalization of the Zein using N-hydroxysuccinimide ester terminated PEG is the method of choice for synthesizing Zein NPs with conjugated PEG (Zein:PEG-Zein NPs). Zein:PEG-Zein NPs formed using this method displayed excellent stability in physiologically relevant conditions over 72 h and were stable at 4 degrees C for at least 3 months. When the NPs were cultured with cells for 72 h, no cytotoxicity or early signs of apoptosis were identified. Cellular uptake of the Zein:PEG-Zein NPs did not seem to be impacted by the amount of PEG incorporated in the NP but were concentration-, time-, and temperature-dependent. The lowest percent, stable Zein:PEG-Zein NP formulation (80% unmodified Zein and 20% PEG-modified Zein) induced no observable toxicity over 14 days in CD-1 mice dosed at 70 mg/kg via the tail vein. However, repeat dose pharmacokinetic (PK) studies demonstrated that following the first dose, the second dose caused health issues that required euthanasia shortly after administration. For those animals that survived, there was faster plasma elimination of the Zein:PEG-Zein NPs. Despite this, the Zein:PEG-Zein NPs represent a significantly improved formulation approach, one that displays a long circulation half-life and is suitable for single-use administration. Repeat dose applications will require additional methods to silence the immune response that is generated when using these NPs intravenously.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据