4.8 Article

Dissolving microneedles for long-term storage and transdermal delivery of extracellular vesicles

期刊

BIOMATERIALS
卷 287, 期 -, 页码 -

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2022.121644

关键词

Extracellular vesicle; Microneedle; Long-term storage; Transdermal delivery; Fibroblast

资金

  1. National Research Foundation (NRF), Republic of Korea, under the Korea Research Fellowship (KRF) Program [2019H1D3A1A01071101]
  2. Basic Science Research Programs [2019R1I1A1A01061426, 2018R1A2B3006080]
  3. Basic Research Laboratory [2021R1A4A1032782]
  4. Ministry of Science and ICT (MSIT)
  5. Ministry of Health and Welfare, Republic of Korea, under the Korean Fund for Regenerative Medicine [2021M3E5E5096677]
  6. Basic Research Laboratory [2021R1A4A1032782]
  7. Ministry of Science and ICT (MSIT)
  8. Ministry of Health and Welfare, Republic of Korea, under the Korean Fund for Regenerative Medicine [2021M3E5E5096677]
  9. National Research Foundation of Korea [2021M3E5E5096677, 2019H1D3A1A01071101] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

This study investigated the feasibility of extracellular vesicles (EVs) for clinical applications and prepared hyaluronic acid dissolving microneedles loaded with human adipose stem cell-derived EVs (EV@MN) with long-term stability. The EV@MN enabled precise and convenient intradermal delivery of EVs, significantly improving the biological functions of dermal fibroblasts.
Extracellular vesicles (EVs) have shown great potential in disease diagnosis and treatment; however, their clinical applications remain challenging due to their unsatisfactory long-term stability and the lack of effective delivery strategies. In this study, we prepared human adipose stem cell-derived EV (hASC-EV)-loaded hyaluronic acid dissolving microneedles (EV@MN) to investigate the feasibility of EVs for their clinical applications. The biological activities of the EVs in this formulation were maintained for more than six months under mild storage conditions, especially at temperatures lower than 4 degrees C. Moreover, the EV@MN enabled precise and convenient intradermal delivery for sustained release of EVs in the dermis layer. Therefore, EV@MN significantly improved the biological functions of hASC-EVs on dermal fibroblasts by promoting syntheses of proteins for the extracellular matrix such as collagen and elastin, enhancing fibroblast proliferation, and regulating the phenotype of fibroblast, compared with other administration methods. This research revealed a possible and feasible formulation for the clinical application of EVs.

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