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Construction of cryomicroneedles loaded with milk-derived exosomes encapsulated TNF-α siRNA and efficacy of percutaneous acupoint administration in rheumatoid arthritis.
Wen, Wulong; Yang, Jing; Liang, Xiao; Li, Yalan; Zhang, Weiye; Sun, Xin; Wang, Rui.
Afiliación
  • Wen W; College of Pharmacy, Heilongjiang University of Chinese Medicine, Harbin, China.
  • Yang J; Basic Medical College of Heilongjiang University of Chinese Medicine, Harbin, China.
  • Liang X; College of Pharmacy, Heilongjiang University of Chinese Medicine, Harbin, China.
  • Li Y; College of Pharmacy, Heilongjiang University of Chinese Medicine, Harbin, China.
  • Zhang W; College of Pharmacy, Heilongjiang University of Chinese Medicine, Harbin, China.
  • Sun X; College of Pharmacy, Heilongjiang University of Chinese Medicine, Harbin, China.
  • Wang R; College of Pharmacy, Heilongjiang University of Chinese Medicine, Harbin, China; Key Laboratory of Basic and Application Research of Beiyao (Heilongjiang University of Chinese Medicine), Ministry of Education, Harbin, China. Electronic address: wrdx@sina.com.
Int J Pharm ; 657: 124159, 2024 May 25.
Article en En | MEDLINE | ID: mdl-38701907
ABSTRACT
Inhibiting the expression of tumor necrosis factor-α (TNF-α), a pro-inflammatory cytokine widely distributed in the serum and synovial fluid, is important for managing rheumatoid arthritis (RA). Despite the good therapeutic effects of TNF-α small interfering RNA (TNF-α siRNA) in RA animal models, safe and efficient siRNA delivery systems that retain stability are lacking. We introduced a novel therapy using milk-derived exosomes(mEXOs)-encapsulated TNF-α siRNA-coated cryomicroneedle (cryoMN) patch and evaluated its efficacy via local transdermal administration through acupoints in RA treatment. The loading of TNF-α siRNAs into mEXOs was achieved by sonication, the loading rate, stability, and in vitro release of mEXOs-TNF-α siRNA were determined. The cryoMNs were prepared by micromolding, morphology, drug loading, and mechanical strength of the cryoMN array were analyzed. The loading efficiency of TNF-α siRNA was up to 21% and each cryoMN contained 39.6 ± 1.29 µg of TNF-α siRNA. Frozen sections penetrated 523 ± 63 µm deep. In vitro experiments have shown that mEXOs-TNF-α siRNA cryoMNs have good biocompatibility and inhibit the proliferation of HFLS-RA cells. In vivo pharmacodynamics studies found that general conditions, changes in microcirculation indexes, synovial histopathological changes, and expression of related proteins in the synovial tissue in RA rabbits were effectively alleviated by mEXOs-TNF-α siRNA cryoMNs. Improvement of each index at acupoints was greater than that at non-acupoints. Our findings facilitate the development of cryoMNs combined with exosomes and acupoints drug delivery for the treatment of RA. The combination of exosomes and cryoMNs will enable the development of new-generation microneedle-based treatments.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Artritis Reumatoide / Administración Cutánea / Factor de Necrosis Tumoral alfa / ARN Interferente Pequeño / Leche / Exosomas Límite: Animals / Humans / Male Idioma: En Revista: Int J Pharm Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Países Bajos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Artritis Reumatoide / Administración Cutánea / Factor de Necrosis Tumoral alfa / ARN Interferente Pequeño / Leche / Exosomas Límite: Animals / Humans / Male Idioma: En Revista: Int J Pharm Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Países Bajos