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Evaluation of the Storage Stability of Extracellular Vesicles
Published on: May 22, 2019
Stability Challenges and Engineering Strategies of Plant-Derived Extracellular Vesicle-Like Particles: A
Hengyi Li1, Yuxiang Yan1,2, Meifang Lin1,2
1Fujian Key Laboratory of Oral Diseases, School and Hospital of Stomatology, Fujian Medical University, Fuzhou, People's Republic of China.
Plant-derived extracellular vesicle-like particles (PD-EVLPs) show therapeutic promise but face stability challenges during isolation, storage, and administration. This review addresses these issues to guide standardization and clinical translation.
Area of Science:
- Biotechnology and Nanomedicine
- Plant-derived nanocarriers
- Therapeutic agent development
Background:
- Plant-derived extracellular vesicle-like particles (PD-EVLPs) are biocompatible nanocarriers with therapeutic potential, including anti-inflammatory and wound healing properties.
- Clinical translation of PD-EVLPs is hindered by stability issues during preparation, storage, and in vivo administration.
- Current isolation and preservation methods compromise PD-EVLP integrity, dispersity, and purity, impacting their ex vivo stability.
Purpose of the Study:
- To comprehensively review the PD-EVLP pipeline from preparation to application.
- To identify and analyze stability challenges at each stage of PD-EVLP handling.
- To explore engineering strategies for enhancing PD-EVLP stability and guide preclinical study design.
Main Methods:
- Literature review of PD-EVLP preparation, stability, and engineering strategies.
- Analysis of challenges in isolation, storage, and administration routes.
- Evaluation of potential risks associated with stability modifications.
Main Results:
- Non-standardized isolation protocols, freeze-thaw cycles, and lyophilization negatively impact PD-EVLP stability.
- Gastric/intestinal fluids and rapid immune clearance challenge in vivo bioavailability.
- Engineering strategies can enhance PD-EVLP stability but require careful risk assessment.
Conclusions:
- Standardizing PD-EVLP preparation protocols is crucial for consistent yield, purity, and structural integrity.
- Addressing ex vivo and in vivo stability concerns is essential for effective therapeutic application.
- A comprehensive framework is needed to guide the development and clinical translation of PD-EVLPs.
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