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Ziyi Lin, Jianjun Wu, Guanfeng Xu, Jiaqi Zhu, Haitong Wan, Yu He. Biomedical Applications of Medicinal Plant Extracellular Vesicles: Recent Advancements and Prospects[J]. Journal of Pharmaceutical Analysis. doi: 10.1016/j.jpha.2026.101616
Citation: Ziyi Lin, Jianjun Wu, Guanfeng Xu, Jiaqi Zhu, Haitong Wan, Yu He. Biomedical Applications of Medicinal Plant Extracellular Vesicles: Recent Advancements and Prospects[J]. Journal of Pharmaceutical Analysis. doi: 10.1016/j.jpha.2026.101616

Biomedical Applications of Medicinal Plant Extracellular Vesicles: Recent Advancements and Prospects

doi: 10.1016/j.jpha.2026.101616
Funds:

This work was supported by "Pioneer" and "Leading Goose" R&

D Program of Zhejiang (Program No.: 2025C02192).

  • Received Date: Apr. 29, 2025
  • Accepted Date: Mar. 26, 2026
  • Rev Recd Date: Mar. 25, 2026
  • Available Online: Mar. 28, 2026
  • Medicinal plant extracellular vesicles (MPEVs) are a class of nano-scale membrane vesicles derived from medicinal plants. As an important mediator of intracellular and intercellular communication, they are essential for both plant metabolism and immune defense. Furthermore, they also transport bioactive components to target cells through endocytosis and plasma membrane invagination, thereby achieving cross-border regulation of physiological activities in fungi and animal cells. Numerous preclinical investigations have confirmed that MPEVs have been extracted from dozens of medicinal plants such as Ginger and Ginseng, and they have the potential to target and penetrate biological barriers. Besides, MPEVs have the advantages of wide source, high yield, low immunogenicity, excellent biocompatibility, and strong modifiability, positioning them as a scalable and sustainable alternative to mammalian-derived extracellular vesicles. Nevertheless, there remains a knowledge gap regarding the standardization of isolation and characterization techniques for MPEVs from various medicinal plants, and clinical research and application are still lacking. Whereupon this paper systematically reviews the research on the formation, classification, isolation and identification methods, biological activities and potential applications as carriers of bioactive substances of MPEVs, with the aim of promoting the establishment of research standards for MPEVs, and providing a theoretical reference for advancing the study and application of MPEVs as novel active ingredients.
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  • [1]
    J. Seras-Franzoso, Z.V. Diaz-Riascos, J.L. Corchero, et al., Extracellular vesicles from recombinant cell factories improve the activity and efficacy of enzymes defective in lysosomal storage disorders, J. Extracell. Vesicles 10 (2021), e12058.
    [2]
    E.M. Kramer-Albers, A.F. Hill, Extracellular vesicles: Interneural shuttles of complex messages, Curr. Opin. Neurobiol. 39 (2016) 101-107.
    [3]
    L. Cheng, A.F. Hill, Therapeutically harnessing extracellular vesicles, Nat. Rev. Drug Discov. 21 (2022) 379-399.
    [4]
    I.K. Herrmann, M.J.A. Wood, G. Fuhrmann, Extracellular vesicles as a next-generation drug delivery platform, Nat. Nanotechnol. 16 (2021) 748-759.
    [5]
    W. Halperin, W.A. Jensen, Ultrastructural changes during growth and embryogenesis in carrot cell cultures, J. Ultrastruct. Res. 18 (1967) 428-443.
    [6]
    Y. Cui, J. Gao, Y. He, et al., Plant extracellular vesicles, Protoplasma 257 (2020) 3-12.
    [7]
    H.A. Dad, T. Gu, A. Zhu, et al., Plant exosome-like nanovesicles: Emerging therapeutics and drug delivery nanoplatforms, Mol. Ther. 29 (2021) 13-31.
    [8]
    Q. Cai, L. Qiao, M. Wang, et al., Plants send small RNAs in extracellular vesicles to fungal pathogen to silence virulence genes, Science 360 (2018) 1126-1129.
    [9]
    B. Kurtosi, A. Kazsoki, R. Zelko, A systematic review on plant-derived extracellular vesicles as drug delivery systems, Int. J. Mol. Sci. 25 (2024), 7559.
    [10]
    E. Chargaff, R. West, The biological significance of the thromboplastic protein of blood, The Journal of biological chemistry 166 (1946) 189-197.
    [11]
    P. Wolf, The nature and significance of platelet products in human plasma, Br. J. Haematol. 13 (1967) 269-288.
    [12]
    W.A. Jensen, The ultrastructure and composition of the egg and central cell of cotton, American Journal of Botany 52 (1965) 781-797.
    [13]
    B.T. Pan, R.M. Johnstone, Fate of the transferrin receptor during maturation of sheep reticulocytes in vitro: Selective externalization of the receptor, Cell 33 (1983) 967-978.
    [14]
    S. Ju, J. Mu, T. Dokland, et al., Grape exosome-like nanoparticles induce intestinal stem cells and protect mice from DSS-induced colitis, Mol. Ther. 21 (2013) 1345-1357.
    [15]
    G. Pocsfalvi, L. Turiak, A. Ambrosone, et al., Protein biocargo of Citrus fruit-derived vesicles reveals heterogeneous transport and extracellular vesicle populations, J. Plant Physiol. 229 (2018) 111-121.
    [16]
    A.C. Dixson, T.R. Dawson, D. Di Vizio, et al., Context-specific regulation of extracellular vesicle biogenesis and cargo selection, Nat. Rev. Mol. Cell Biol. 24 (2023) 454-476.
    [17]
    E.I. Buzas, The roles of extracellular vesicles in the immune system, Nat. Rev. Immunol. 23 (2023) 236-250.
    [18]
    R. Kalluri, V.S. LeBleu, The biology, function, and biomedical applications of exosomes, Science 367 (2020), eaau6977.
    [19]
    G. van Niel, G. D’Angelo, G. Raposo, Shedding light on the cell biology of extracellular vesicles, Nat. Rev. Mol. Cell Biol. 19 (2018) 213-228.
    [20]
    A. Bano, R. Vats, P. Yadav, et al., Exosomics in oral cancer diagnosis, prognosis, and therapeutics - An emergent and imperative non-invasive natural nanoparticle-based approach, Crit. Rev. Oncol. Hematol. 178 (2022), 103799.
    [21]
    D.K. Jeppesen, A.M. Fenix, J.L. Franklin, et al., Reassessment of exosome composition, Cell 177 (2019) 428-445.e18.
    [22]
    Q. Chen, M. Zu, H. Gong, et al., Tea leaf-derived exosome-like nanotherapeutics retard breast tumor growth by pro-apoptosis and microbiota modulation, J. Nanobiotechnology 21 (2023), 6.
    [23]
    D.G. Meckes Jr, N. Raab-Traub, Microvesicles and viral infection, J. Virol. 85 (2011) 12844-12854.
    [24]
    M.A. Antonyak, B. Li, L.K. Boroughs, et al., Cancer cell-derived microvesicles induce transformation by transferring tissue transglutaminase and fibronectin to recipient cells, Proc. Natl. Acad. Sci. USA 108 (2011) 4852-4857.
    [25]
    S.C. Abreu, D.J. Weiss, P.R.M. Rocco, Extracellular vesicles derived from mesenchymal stromal cells: A therapeutic option in respiratory diseases? Stem Cell Res. Ther. 7 (2016), 53.
    [26]
    C. Thery, M. Ostrowski, E. Segura, Membrane vesicles as conveyors of immune responses, Nat. Rev. Immunol. 9 (2009) 581-593.
    [27]
    J. Wolfers, A. Lozier, G. Raposo, et al., Tumor-derived exosomes are a source of shared tumor rejection antigens for CTL cross-priming, Nat. Med. 7 (2001) 297-303.
    [28]
    M. Potesta, V. Roglia, M. Fanelli, et al., Effect of microvesicles from Moringa oleifera containing miRNA on proliferation and apoptosis in tumor cell lines, Cell Death Discov. 6 (2020), 43.
    [29]
    G.K. Atkin-Smith, R. Tixeira, S. Paone, et al., A novel mechanism of generating extracellular vesicles during apoptosis via a beads-on-a-string membrane structure, Nat. Commun. 6 (2015), 7439.
    [30]
    D. Liu, X. Kou, C. Chen, et al., Circulating apoptotic bodies maintain mesenchymal stem cell homeostasis and ameliorate osteopenia via transferring multiple cellular factors, Cell Res. 28 (2018) 918-933.
    [31]
    L. Corredor, G.A. Vergou, V. Skalicky, et al., Apoptotic bodies in phytoplankton suggest evolutionary conservation of cell death mechanisms, Nat. Commun. 16 (2025), 8427.
    [32]
    Y. Wang, J. Pang, Q. Wang, et al., Delivering antisense oligonucleotides across the blood-brain barrier by tumor cell-derived small apoptotic bodies, Adv. Sci. 8 (2021), 2004929.
    [33]
    Q. Ma, M. Liang, Y. Wu, et al., Osteoclast-derived apoptotic bodies couple bone resorption and formation in bone remodeling, Bone Res. 9 (2021), 5.
    [34]
    C. Zheng, B. Sui, X. Zhang, et al., Apoptotic vesicles restore liver macrophage homeostasis to counteract type 2 diabetes, J. Extracell. Vesicles 10 (2021), e12109.
    [35]
    L. Bao, G. Dou, R. Tian, et al., Engineered neutrophil apoptotic bodies ameliorate myocardial infarction by promoting macrophage efferocytosis and inflammation resolution, Bioact. Mater. 9 (2022) 183-197.
    [36]
    L. Yu, Migrasomes: The knowns, the known unknowns and the unknown unknowns: A personal perspective, Sci. China Life Sci. 64 (2021) 162-166.
    [37]
    M. Zhu, Q. Zou, R. Huang, et al., Lateral transfer of mRNA and protein by migrasomes modifies the recipient cells, Cell Res. 31 (2021) 237-240.
    [38]
    Y. Zhang, J. Wang, Y. Ding, et al., Migrasome and tetraspanins in vascular homeostasis: Concept, present, and future, Front. Cell Dev. Biol. 8 (2020), 438.
    [39]
    D. Jiang, Z. Jiang, D. Lu, et al., Migrasomes provide regional cues for organ morphogenesis during zebrafish gastrulation, Nat. Cell Biol. 21 (2019) 966-977.
    [40]
    W. Xu, L. Jia, W. Shi, et al., Abscisic acid accumulation modulates auxin transport in the root tip to enhance proton secretion for maintaining root growth under moderate water stress, New Phytol. 197 (2013) 139-150.
    [41]
    J.A. Welsh, D.C.I. Goberdhan, L. O’Driscoll, et al., Minimal information for studies of extracellular vesicles (MISEV2023): From basic to advanced approaches, J. Extracell. Vesicles 13 (2024), e12404.
    [42]
    M. Regente, G. Corti-Monzon, A.M. Maldonado, et al., Vesicular fractions of sunflower apoplastic fluids are associated with potential exosome marker proteins, FEBS Lett. 583 (2009) 3363-3366.
    [43]
    K. Iwai, S. Yamamoto, M. Yoshida, et al., Isolation of extracellular vesicles in saliva using density gradient ultracentrifugation, Methods Mol. Biol. 1660 (2017) 343-350.
    [44]
    Q. Zhao, T. Wang, H. Wang, et al., Consensus statement on research and application of Chinese herbal medicine derived extracellular vesicles-like particles (2023 edition), Chin. Herb. Med. 16 (2024) 3-12.
    [45]
    M. Zhang, E. Viennois, M. Prasad, et al., Edible ginger-derived nanoparticles: A novel therapeutic approach for the prevention and treatment of inflammatory bowel disease and colitis-associated cancer, Biomaterials 101 (2016) 321-340.
    [46]
    W. Zhang, Q. Song, X. Bi, et al., Preparation of pueraria Lobata root-derived exosome-like nanovesicles and evaluation of their effects on mitigating alcoholic intoxication and promoting alcohol metabolism in mice, Int. J. Nanomedicine 19 (2024) 4907-4921.
    [47]
    B. He, Q. Cai, L. Qiao, et al., RNA-binding proteins contribute to small RNA loading in plant extracellular vesicles, Nat. Plants 7 (2021) 342-352.
    [48]
    A.P. Suresh, S.P. Kalarikkal, B. Pullareddy, et al., Low pH-based method to increase the yield of plant-derived nanoparticles from fresh ginger rhizomes, ACS Omega 6 (2021) 17635-17641.
    [49]
    R. Lee, H.J. Ko, K. Kim, et al., Anti-melanogenic effects of extracellular vesicles derived from plant leaves and stems in mouse melanoma cells and human healthy skin, J. Extracell. Vesicles 9 (2020), 1703480.
    [50]
    M. Wu, Y. Ouyang, Z. Wang, et al., Isolation of exosomes from whole blood by integrating acoustics and microfluidics, Proc. Natl. Acad. Sci. USA 114 (2017) 10584-10589.
    [51]
    A. Gamez-Valero, M. Monguio-Tortajada, L. Carreras-Planella, et al., Size-exclusion chromatography-based isolation minimally alters extracellular vesicles‘ characteristics compared to precipitating agents, Sci. Rep. 6 (2016), 33641.
    [52]
    M. Yang, Q. Luo, X. Chen, et al., Bitter melon derived extracellular vesicles enhance the therapeutic effects and reduce the drug resistance of 5-fluorouracil on oral squamous cell carcinoma, J. Nanobiotechnology 19 (2021), 259.
    [53]
    Y. Zhang, B. Zhao, J. Wang, et al., Novel exosome-like vesicles from Dendrobium officinale: Unraveling a pioneering extraction protocol and their skin anti-aging potentials, Extracell. Vesicle 6 (2025), 100090.
    [54]
    Y. Huang, S. Wang, Q. Cai, et al., Effective methods for isolation and purification of extracellular vesicles from plants, J. Integr. Plant Biol. 63 (2021) 2020-2030.
    [55]
    X. Chen, Y. Zhou, J. Yu, Exosome-like nanoparticles from ginger rhizomes inhibited NLRP3 inflammasome activation, Mol. Pharm. 16 (2019) 2690-2699.
    [56]
    H. Shao, H. Im, C.M. Castro, et al., New technologies for analysis of extracellular vesicles, Chem. Rev. 118 (2018) 1917-1950.
    [57]
    M. De Palma, A. Ambrosone, A. Leone, et al., Plant roots release small extracellular vesicles with antifungal activity, Plants (Basel) 9 (2020), 1777.
    [58]
    M. Zu, D. Xie, B.S.B. Canup, et al., ‘Green’ nanotherapeutics from tea leaves for orally targeted prevention and alleviation of colon diseases, Biomaterials 279 (2021), 121178.
    [59]
    J.Y. You, S. Kang, W.J. Rhee, Isolation of cabbage exosome-like nanovesicles and investigation of their biological activities in human cells, Bioact. Mater. 6 (2021) 4321-4332.
    [60]
    S. Li, R. Zhang, A. Wang, et al., Panax notoginseng: Derived exosome-like nanoparticles attenuate ischemia reperfusion injury via altering microglia polarization, J. Nanobiotechnology 21 (2023), 416.
    [61]
    Z. Zhao, M. Li, H. Zhang, et al., Comparative proteomic analysis of plasma membrane proteins in rice leaves reveals a vesicle trafficking network in plant immunity that is provoked by blast fungi, Front. Plant Sci. 13 (2022), 853195.
    [62]
    R. Aebersold, M. Mann, Mass-spectrometric exploration of proteome structure and function, Nature 537 (2016) 347-355.
    [63]
    G. Ekanayake, J. Piibor, G. Midekessa, et al., Systematic characterization of extracellular vesicles from potato (Solanum tuberosum cv. Laura) roots and peels: Biophysical properties and proteomic profiling, Front. Plant Sci. 15 (2024), 1477614.
    [64]
    N. Liu, N. Wang, J. Bao, et al., Lipidomic analysis reveals the importance of GIPCs in Arabidopsis Leaf extracellular vesicles, Mol. Plant 13 (2020) 1523-1532.
    [65]
    M. Yang, J. Guo, J. Li, et al., Platycodon grandiflorum-derived extracellular vesicles suppress triple-negative breast cancer growth by reversing the immunosuppressive tumor microenvironment and modulating the gut microbiota, J. Nanobiotechnology 23 (2025), 92.
    [66]
    G. Yan, Q. Xiao, J. Zhao, et al., Brucea javanica derived exosome-like nanovesicles deliver miRNAs for cancer therapy, J. Control. Release 367 (2024) 425-440.
    [67]
    Y. Li, S. Shao, Y. Zhou, et al., Oral administration of Folium Artemisiae Argyi-derived exosome-like nanovesicles can improve ulcerative colitis by regulating intestinal microorganisms, Phytomedicine 137 (2025), 156376.
    [68]
    Y. Zhang, X. Zhang, T. Kai, et al., Lycium ruthenicum Murray derived exosome-like nanovesicles inhibit Aβ-induced apoptosis in PC12 cells via MAPK and PI3K/AKT signaling pathways, Int. J. Biol. Macromol. 277 (2024), 134309.
    [69]
    C. Thery, L. Zitvogel, S. Amigorena, Exosomes: Composition, biogenesis and function, Nat. Rev. Immunol. 2 (2002) 569-579.
    [70]
    F. Wang, L. Li, J. Deng, et al., Lipidomic analysis of plant-derived extracellular vesicles for guidance of potential anti-cancer therapy, Bioact. Mater. 46 (2025) 82-96.
    [71]
    L. Zeng, H. Wang, W. Shi, et al., Aloe derived nanovesicle as a functional carrier for indocyanine green encapsulation and phototherapy, J. Nanobiotechnology 19 (2021), 439.
    [72]
    J. Xiao, S. Feng, X. Wang, et al., Identification of exosome-like nanoparticle-derived microRNAs from 11 edible fruits and vegetables, PeerJ 6 (2018), e5186.
    [73]
    X. Li, N.G.F. Cooper, T.E. O'Toole, et al., Choice of library size normalization and statistical methods for differential gene expression analysis in balanced two-group comparisons for RNA-seq studies, BMC Genomics 21 (2020), 75.
    [74]
    Z. Zhao, S. Yu, M. Li, et al., Isolation of exosome-like nanoparticles and analysis of microRNAs derived from coconut water based on small RNA high-throughput sequencing, J. Agric. Food Chem. 66 (2018) 2749-2757.
    [75]
    E.A. Astakhova, A.S. Gubaeva, D.A. Naumova, et al., Spectral flow cytometry: The current state and future of the technology, Int. J. Mol. Sci. 26 (2025), 5911.
    [76]
    H. Liu, Y. Tian, C. Xue, et al., Analysis of extracellular vesicle DNA at the single-vesicle level by nano-flow cytometry, J. Extracell. Vesicles 11 (2022), e12206.
    [77]
    W. Li, B. Shao, C. Liu, et al., Noninvasive diagnosis and molecular phenotyping of breast cancer through microbead-assisted flow cytometry detection of tumor-derived extracellular vesicles, Small Meth. 2 (2018), 1800122.
    [78]
    S. Saroj, P. Us, S. Patil, et al., Herb extracellular vesicle-chitosan-PEGylated graphene oxide conjugate delivers estrogen receptor α targeting siRNA to breast cancer cells, ACS Appl. Bio Mater. 7 (2024) 2741-2751.
    [79]
    G. Bordanaba-Florit, F. Royo, S.G. Kruglik, et al., Using single-vesicle technologies to unravel the heterogeneity of extracellular vesicles, Nat. Protoc. 16 (2021) 3163-3185.
    [80]
    A. Enciso-Martinez, E. Van Der Pol, C.M. Hau, et al., Label-free identification and chemical characterisation of single extracellular vesicles and lipoproteins by synchronous Rayleigh and Raman scattering, J. Extracell. Vesicles 9 (2020), 1730134.
    [81]
    E.G. Cho, S.Y. Choi, H. Kim, et al., Panax ginseng-derived extracellular vesicles facilitate anti-senescence effects in human skin cells: An eco-friendly and sustainable way to use ginseng substances, Cells 10 (2021), 486.
    [82]
    M. Cao, H. Yan, X. Han, et al., Ginseng-derived nanoparticles alter macrophage polarization to inhibit melanoma growth, J. Immunother. Cancer 7 (2019), 326.
    [83]
    L. Yang, W. Jin, X. Tang, et al., Ginseng-derived nanoparticles inhibit lung cancer cell epithelial mesenchymal transition by repressing pentose phosphate pathway activity, Front. Oncol. 12 (2022), 942020.
    [84]
    J. Kim, Y. Zhu, S. Chen, et al., Anti-glioma effect of ginseng-derived exosomes-like nanoparticles by active blood-brain-barrier penetration and tumor microenvironment modulation, J. Nanobiotechnology 21 (2023), 253.
    [85]
    S. Yang, S. Lu, L. Ren, et al., Ginseng-derived nanoparticles induce skin cell proliferation and promote wound healing, J. Ginseng Res. 47 (2023) 133-143.
    [86]
    A. Kumar, K. Sundaram, Y. Teng, et al., Ginger nanoparticles mediated induction of Foxa2 prevents high-fat diet-induced insulin resistance, Theranostics 12 (2022) 1388-1403.
    [87]
    K. Sundaram, D.P. Miller, A. Kumar, et al., Plant-derived exosomal nanoparticles inhibit pathogenicity of Porphyromonas gingivalis, iScience 21 (2019) 308-327.
    [88]
    W.M. Abd El Wahab, A.A. El-Badry, S.S. Mahmoud, et al., Ginger (Zingiber Officinale)-derived nanoparticles in Schistosoma mansoni infected mice: Hepatoprotective and enhancer of etiological treatment, PLoS Negl. Trop. Dis. 15 (2021), e0009423.
    [89]
    X. Zhuang, Z. Deng, J. Mu, et al., Ginger-derived nanoparticles protect against alcohol-induced liver damage, J. Extracell. Vesicles 4 (2015), 28713.
    [90]
    M.K. Kim, Y.C. Choi, S.H. Cho, et al., The antioxidant effect of small extracellular vesicles derived from Aloe vera peels for wound healing, Tissue Eng. Regen. Med. 18 (2021) 561-571.
    [91]
    J. Wu, X. Ma, Y. Lu, et al., Edible pueraria Lobata-derived exosomes promote M2 macrophage polarization, Molecules 27 (2022), 8184.
    [92]
    X. Zhang, Z. Pan, Y. Wang, et al., Taraxacum officinale-derived exosome-like nanovesicles modulate gut metabolites to prevent intermittent hypoxia-induced hypertension, Biomed. Pharmacother. 161 (2023), 114572.
    [93]
    S. Tan, Z. Liu, M. Cong, et al., Dandelion-derived vesicles-laden hydrogel dressings capable of neutralizing Staphylococcus aureus exotoxins for the care of invasive wounds, J. Control. Release 368 (2024) 355-371.
    [94]
    X. Chen, L. Huang, M. Zhang, et al., Comparison of nanovesicles derived from Panax notoginseng at different size: Physical properties, composition, and bioactivity, Front. Pharmacol. 15 (2024), 1423115.
    [95]
    H. Zhu, M. Chang, Q. Wang, et al., Identifying the potential of miRNAs in Houttuynia cordata-derived exosome-like nanoparticles against respiratory RNA viruses, Int. J. Nanomedicine 18 (2023) 5983-6000.
    [96]
    Y. Chi, L. Shi, S. Lu, et al., Inhibitory effect of Lonicera japonica-derived exosomal miR2911 on human Papilloma virus, J. Ethnopharmacol. 318 (2024), 116969.
    [97]
    M. Zhu, H. Xu, Y. Liang, et al., Edible exosome-like nanoparticles from Portulaca oleracea L mitigate DSS-induced colitis via facilitating double-positive CD4+CD8+T cells expansion, J. Nanobiotechnology 21 (2023), 309.
    [98]
    Y. Song, F. Wang, J. Xia, et al., Bioactivity and multi-omics profiling of purslane-derived nanovesicles with therapeutic implications in diabetic wounds, J. Adv. Res. (2025).
    [99]
    M. Zhang, X. Xu, L. Su, et al., Oral administration of Sophora Flavescens-derived exosomes-like nanovesicles carrying CX5461 ameliorates DSS-induced colitis in mice, J. Nanobiotechnology 22 (2024), 607.
    [100]
    C. Gao, Y. Zhou, Z. Chen, et al., Turmeric-derived nanovesicles as novel nanobiologics for targeted therapy of ulcerative colitis, Theranostics 12 (2022) 5596-5614.
    [101]
    M.K. Sriwastva, Z. Deng, B. Wang, et al., Exosome-like nanoparticles from Mulberry bark prevent DSS-induced colitis via the AhR/COPS8 pathway, EMBO Rep. 23 (2022), e53365.
    [102]
    D.C. Xie, Oral Treatment of Dendrobium officinale-derived nanovesicles in the application of ulcerative colitis [dissertation], Chongqing: Southwest University, 2022.
    [103]
    L. Xiao, J. Wang, M. Yu, et al., Emerging nutritional potential of edible-medicinal homologous coix lacryma-jobi seed-derived exosomes for treatment of ulcerative colitis, Int. J. Biol. Macromol. 332 (2025), 148799.
    [104]
    Q. Lv, H. Yang, Y. Xie, et al., Prunus mume derived extracellular vesicle-like particles alleviate experimental colitis via disrupting NEK7-NLRP3 interaction and inflammasome activation, J. Nanobiotechnology 23 (2025), 532.
    [105]
    F. Qiu, J. Wang, M. Guo, et al., Rgl-exomiR-7972, a novel plant exosomal microRNA derived from fresh Rehmanniae Radix, ameliorated lipopolysaccharide-induced acute lung injury and gut dysbiosis, Biomed. Pharmacother. 165 (2023), 115007.
    [106]
    Q.B. Chen, The Study of Tea Flower-derived nanovesicles in the treatment of breast cancer [dissertation], Chongqing: Southwest University, 2019.
    [107]
    D. Sasaki, H. Suzuki, K. Kusamori, et al., Development of rice bran-derived nanoparticles with excellent anti-cancer activity and their application for peritoneal dissemination, J. Nanobiotechnology 22 (2024), 114.
    [108]
    L. Zhang, F. He, L. Gao, et al., Engineering exosome-like nanovesicles derived from Asparagus cochinchinensis can inhibit the proliferation of hepatocellular carcinoma cells with better safety profile, Int. J. Nanomedicine 16 (2021) 1575-1586.
    [109]
    Q. Gao, N. Chen, B. Li, et al., Natural lipid nanoparticles extracted from Morus nigra L. leaves for targeted treatment of hepatocellular carcinoma via the oral route, J. Nanobiotechnology 22 (2024), 4.
    [110]
    D. Wang, H. Zhang, X. Liao, et al., Oral administration of Robinia pseudoacacia L. flower exosome-like nanoparticles attenuates gastric and small intestinal mucosal ferroptosis caused by hypoxia through inhibiting HIF-1α- and HIF-2α-mediated lipid peroxidation, J. Nanobiotechnology 22 (2024), 479.
    [111]
    S. Zhang, J. Xia, Y. Zhu, et al., Establishing Salvia miltiorrhiza-derived exosome-like nanoparticles and elucidating their role in angiogenesis, Molecules 29 (2024), 1599.
    [112]
    F. Sahin, P. Kocak, M.Y. Gunes, et al., In vitro wound healing activity of wheat-derived nanovesicles, Appl. Biochem. Biotechnol. 188 (2019) 381-394.
    [113]
    Q. Zhao, J. Feng, F. Liu, et al., Rhizoma Drynariae-derived nanovesicles reverse osteoporosis by potentiating osteogenic differentiation of human bone marrow mesenchymal stem cells via targeting ERα signaling, Acta Pharm. Sin. B 14 (2024) 2210-2227.
    [114]
    J.H. Hwang, Y.S. Park, H.S. Kim, et al., Yam-derived exosome-like nanovesicles stimulate osteoblast formation and prevent osteoporosis in mice, J. Control. Release 355 (2023) 184-198.
    [115]
    X. Zhou, S. Xu, Z. Zhang, et al., Gouqi-derived nanovesicles (GqDNVs) inhibited dexamethasone-induced muscle atrophy associating with AMPK/SIRT1/PGC1α signaling pathway, J. Nanobiotechnology 22 (2024), 276.
    [116]
    J. Du, Z. Liang, J. Xu, et al., Plant-derived phosphocholine facilitates cellular uptake of anti-pulmonary fibrotic HJT-sRNA-m7, Sci. China Life Sci. 62 (2019) 309-320.
    [117]
    W. Gao, M. Hou, X. Chen, et al., Mechanism of astragali radix vesicle-like nanoparticles for reducing blood glucose in db/db diabetic mice by regulating gut microbiota, Chin. J. Exp. Tradit. Med. Formulae 27 (2021) 111-118.
    [118]
    Y. Liu, S. Tao, Z. Zhang, et al., Perilla frutescens leaf-derived extracellular vesicle-like particles carry pab-miR-396a-5p to alleviate psoriasis by modulating IL-17 signaling, Research (Wash D C) 8 (2025), 0675.
    [119]
    J. Xie, H. Lan, H. Ma, et al., Oral epimedium nanovesicles promote hematopoietic stem cell regeneration via gut-microbiota-bone marrow axis to mitigate chemotherapy-induced myelosuppression, Nano Research (2025).
    [120]
    L. de la Canal, M. Pinedo, Extracellular vesicles: A missing component in plant cell wall remodeling, J. Exp. Bot. 69 (2018) 4655-4658.
    [121]
    D.G. Chukhchin, K. Bolotova, I. Sinelnikov, et al., Exosomes in the phloem and xylem of woody plants, Planta 251 (2019), 12.
    [122]
    D. De Bellis, L. Kalmbach, P. Marhavy, et al., Extracellular vesiculo-tubular structures associated with suberin deposition in plant cell walls, Nat. Commun. 13 (2022), 1489.
    [123]
    M. Regente, M. Pinedo, H. San Clemente, et al., Plant extracellular vesicles are incorporated by a fungal pathogen and inhibit its growth, J. Exp. Bot. 68 (2017) 5485-5495.
    [124]
    D.K. Kim, W.J. Rhee, Antioxidative effects of carrot-derived nanovesicles in cardiomyoblast and neuroblastoma cells, Pharmaceutics 13 (2021), 1203.
    [125]
    M. Zhang, J.F. Collins, D. Merlin, Do ginger-derived nanoparticles represent an attractive treatment strategy for inflammatory bowel diseases? Nanomedicine 11 (2016) 3035-3037.
    [126]
    S. Rome, Biological properties of plant-derived extracellular vesicles, Food Funct. 10 (2019) 529-538.
    [127]
    B.D. Rutter, R.W. Innes, Extracellular vesicles isolated from the leaf apoplast carry stress-response proteins, Plant Physiol. 173 (2017) 728-741.
    [128]
    C. Li, Q. Tian, M.K.U. Rahman, et al., Effect of anti-fungal compound phytosphingosine in wheat root exudates on the rhizosphere soil microbial community of watermelon, Plant Soil 456 (2020) 223-240.
    [129]
    N. Hatsugai, S. Iwasaki, K. Tamura, et al., A novel membrane fusion-mediated plant immunity against bacterial pathogens, Genes Dev. 23 (2009) 2496-2506.
    [130]
    G. Gonorazky, A.M. Laxalt, H.L. Dekker, et al., Phosphatidylinositol 4-phosphate is associated to extracellular lipoproteic fractions and is detected in tomato apoplastic fluids, Plant Biol. (Stuttg) 14 (2012) 41-49.
    [131]
    Q. An, K. Ehlers, K.H. Kogel, et al., Multivesicular compartments proliferate in susceptible and resistant MLA12-barley leaves in response to infection by the biotrophic powdery mildew fungus, New Phytol. 172 (2006) 563-576.
    [132]
    T. Yang, B. Fogarty, B. LaForge, et al., Delivery of small interfering RNA to inhibit vascular endothelial growth factor in zebrafish using natural brain endothelia cell-secreted exosome nanovesicles for the treatment of brain cancer, Aaps j. 19 (2017) 475-486.
    [133]
    Y. Qi, L. Guo, Y. Jiang, et al., Brain delivery of quercetin-loaded exosomes improved cognitive function in AD mice by inhibiting phosphorylated tau-mediated neurofibrillary tangles, Drug Deliv. 27 (2020) 745-755.
    [134]
    H. Cai, L. Huang, R. Hong, et al., Momordica charantia exosome-like nanoparticles exert neuroprotective effects against ischemic brain injury via inhibiting matrix metalloproteinase 9 and activating the AKT/GSK3β signaling pathway, Front. Pharmacol. 13 (2022), 908830.
    [135]
    W. Xie, M.F. Melzig, The stability of medicinal plant microRNAs in the herb preparation process, Molecules 23 (2018), 919.
    [136]
    F. Man, C. Meng, Y. Liu, et al., Correction to: The study of ginger-derived extracellular vesicles as a natural nanoscale drug carrier and their intestinal absorption in rats, AAPS PharmSciTech 23 (2022), 225.
    [137]
    M. Zhang, B. Xiao, H. Wang, et al., Edible ginger-derived nano-lipids loaded with doxorubicin as a novel drug-delivery approach for colon cancer therapy, Mol. Ther. 24 (2016) 1783-1796.
    [138]
    J. van Haasteren, J. Li, O.J. Scheideler, et al., The delivery challenge: Fulfilling the promise of therapeutic genome editing, Nat. Biotechnol. 38 (2020) 845-855.
    [139]
    Y. Liang, Z. Iqbal, J. Wang, et al., Cell-derived extracellular vesicles for CRISPR/Cas9 delivery: Engineering strategies for cargo packaging and loading, Biomater. Sci. 10 (2022) 4095-4106.
    [140]
    D. Mun, J.Y. Kang, H. Kim, et al., Small extracellular vesicle-mediated CRISPR-Cas9 RNP delivery for cardiac-specific genome editing, J. Control. Release 370 (2024) 798-810.
    [141]
    X. Han, Q. Wei, Y. Lv, et al., Ginseng-derived nanoparticles potentiate immune checkpoint antibody efficacy by reprogramming the cold tumor microenvironment, Mol. Ther. 30 (2022) 327-340.
    [142]
    T. Liu, Z. Qiu, Y. Qiu, et al., A preliminary study on protective mechanism of ginseng root exosomes against doxorubicin induced myocardial injury, Chin. Tradit. Herb. Drugs 52 (2021) 3514-3521.
    [143]
    S. Lu, S. Yang, L. Ren, et al., Panax ginseng exosomes promote HaCaT cell proliferation and wound healing, Chin. J. Biochem. Mol. Biol. 37 (2021) 1510-1519.
    [144]
    Z. Li, H. Wang, H. Yin, et al., Arrowtail RNA for ligand display on ginger exosome-like nanovesicles to systemic deliver siRNA for cancer suppression, Sci. Rep. 8 (2018), 14644.
    [145]
    Z. Qiao, K. Zhang, J. Liu, et al., Biomimetic electrodynamic nanoparticles comprising ginger-derived extracellular vesicles for synergistic anti-infective therapy, Nat. Commun. 13 (2022), 7164.
    [146]
    Y. Teng, Y. Ren, M. Sayed, et al., Plant-derived exosomal microRNAs shape the gut microbiota, Cell Host Microbe 24 (2018) 637-652.e8.
    [147]
    Y. Lu, J. Xu, R. Tang, et al., Edible Pueraria Lobata-derived exosome-like nanovesicles ameliorate dextran sulfate sodium-induced colitis associated lung inflammation through modulating macrophage polarization, Biomed. Pharmacother. 170 (2024), 116098.
    [148]
    W. Zhan, M. Deng, X. Huang, et al., Pueraria lobata-derived exosome-like nanovesicles alleviate osteoporosis by enhacning autophagy, J. Control. Release 364 (2023) 644-653.
    [149]
    Y.J. Liu, Regulatory effects of extracellular vesicles derived from Houttuynia cordata on mitochondrial metabolism and inflammatory response of macrophages [dissertation], Jiangsu: Nanjing University of Chinese Medicine, 2020.
    [150]
    Z. Zhou, X. Li, J. Liu, et al., Honeysuckle-encoded atypical microRNA2911 directly targets influenza A viruses, Cell Res. 25 (2015) 39-49.
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