PNExo™ Exosome-Cucumber(PNE-VC04)
| Name | PNExo™ Exosome-Cucumber |
| Cat No. | PNE-VC04 |
| Source | Exosome derived from Cucumber |
| Product Overview | Plant exosomes are nanosized (30-150 nm) membrane vesicles that contain biomolecules. Plant-derived exosomes refer to naturally occurring nanoparticles derived from plants that contain bioactive molecules and proteins. These exosomes have been shown to have multiple benefits in a variety of applications, such as skincare, drug delivery, and biomedicine. Plant-derived exosomes have been found to possess antioxidant, anti-inflammatory, and anti-aging properties, making them an attractive option for the development of new and innovative therapies. Plant-derived natural substances are widely used as cosmeceutical materials because they exert beneficial effects on the human skin, such as antiaging, moisturizing, whitening, regeneration, and nutritional supply. Besides, they could delivery therapeutic compounds to target cells, potentially revolutionizing the way in which drugs are administered. Overall, plant-derived exosomes hold great promise for a wide range of applications in the fields of medicine and biotechnology. PNExo™ is focused on the production and delivery of high quality plant-derived exosomes products. Exosomes are important tools of intercellular communication with a variety of biological functions, including cell regeneration and immune regulation. PNExo™ products undergo a rigorous screening and purification process that guarantees their high purity and activity. Lyophilization is useful for a long-term storage at 4°C, and frozen liquid should be kept at -20°C to -80°C. Ultracentrifugation and precipitation techniques are mainly used in exosome Isolation. It had been reported that both methods yielded extracellular vesicles in the size range of exosomes and included apoproteins, which can be used in downstream analyses. Creative Biostructure PNExo™ exosome products guarantee higher purity and quality to meet our customer research. |
| Form | Lyophilized powder |
| Concentration | > 1x10^6 particles |
| Storage | Lyophilized powder store at 4 °C. Frozen liquid store at -20°C to -80°C. Recommended to avoid repeated freeze-and-thaw cycles. |
| Reconstitution | Reconstitute lyophilized exosome by adding deionized water for a desired final concentration. Centrifuge before opening to ensure exosomes are at bottom, resuspend exosomes by pipetting and/or vortex, please avoid bubbles. Centrifuge again and mix well for using. |
At Creative Biostructure, we offer comprehensive solutions beyond standard exosome products. For researchers and developers working with plant-derived exosomes like PNExo™ Exosome-Cucumber, we provide customized services covering exosome isolation, purification, characterization, and analytical support. Our capabilities also include GMP-compliant exosome manufacturing and full-process CDMO services, tailored to support both early-stage research and large-scale production. Whether you're exploring new applications or scaling up for commercialization, our team is ready to support your project with scientific precision and manufacturing expertise.
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Characterization of cucumber sarcocarp-derived nanovesicles (CsDNVs) and cucumber pericarp-derived nanovesicles (CpDNVs) isolated under varying centrifugal forces. (A-B) TEM images of CsDNVs isolated at 100,000 × g for 60 and 30 min. (C-D) TEM images of CpDNVs isolated at the same conditions. (E-F) Particle size distributions of CsDNVs and CpDNVs at different centrifugation speeds. (G-H) TEM images of CsDNVs and CpDNVs isolated at 30,000 × g for 30 min. Scale bars: 200 nm. (Chen T, et al., 2022)
Figure 1. In vitro anticancer activity of cucumber sarcocarp-derived nanovesicles (CsDNVs) and cucumber pericarp-derived nanovesicles (CpDNVs). (A) Confocal microscopy showing uptake of DiO-labeled CsDNVs by A549 cells; nuclei (Hoechst), membranes (DiI), and nanovesicles (DiO) are visualized. Scale bar: 25 μm. (B) Quantification of CsDNV uptake over time. (C) MTT assay assessing cytotoxicity of CuB, CsDNVs, and CpDNVs. (D) Flow cytometry analysis of apoptosis in A549 cells treated with free CuB, CsDNVs, or CpDNVs. (E) Apoptosis rate comparison among treatment groups.
Figure 2. In vivo anticancer effects of CsDNVs in a nude mouse tumor model. (A) Treatment schedule of CsDNVs and CuB in nude mice. (B) Tumor volume monitored over time following intravenous administration of PBS, CuB, or CsDNVs. (C) Body weight changes during treatment. (D) Final tumor weight after 14 days of treatment. (E) Representative images of tumors collected from each treatment group. (F) H&E staining of tumor tissues from PBS, CuB, and CsDNVs groups. Scale bar: 100 μm.
Figure 1. Evaluation of DiI dermal penetration via different cucumber-derived formulations. (A) Representative inverted epifluorescence microscopy images showing DiI distribution in skin sections. All images were acquired under identical imaging conditions (200× magnification, 50 ms exposure, scale bar = 50 µm). (B) Quantitative analysis of penetration metrics, including relative stratum corneum thickness (R-SCT), relative penetrated amount (R-APA), and mean penetration depth (R-MPD). Results indicate enhanced dermal delivery with PEVs, especially when DiI was preloaded before high-pressure homogenization (HPH). Data support the role of cucumber-derived PEVs as effective nanocarriers for topical drug delivery.