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A novel multi-stage enrichment workflow and comprehensive characterization for HEK293F-derived extracellular vesicles.
Vo, Nhan; Tran, Chau; Tran, Nam H B; Nguyen, Nhat T; Nguyen, Thieu; Ho, Duyen T K; Nguyen, Diem D N; Pham, Tran; Nguyen, Tien Anh; Phan, Hoa T N; Nguyen, Hoai-Nghia; Tu, Lan N.
Afiliación
  • Vo N; Medical Genetics Institute, Ho Chi Minh City, Vietnam.
  • Tran C; Medical Genetics Institute, Ho Chi Minh City, Vietnam.
  • Tran NHB; Medical Genetics Institute, Ho Chi Minh City, Vietnam.
  • Nguyen NT; Medical Genetics Institute, Ho Chi Minh City, Vietnam.
  • Nguyen T; Medical Genetics Institute, Ho Chi Minh City, Vietnam.
  • Ho DTK; Medical Genetics Institute, Ho Chi Minh City, Vietnam.
  • Nguyen DDN; Medical Genetics Institute, Ho Chi Minh City, Vietnam.
  • Pham T; Medical Genetics Institute, Ho Chi Minh City, Vietnam.
  • Nguyen TA; Medical Genetics Institute, Ho Chi Minh City, Vietnam.
  • Phan HTN; Medical Genetics Institute, Ho Chi Minh City, Vietnam.
  • Nguyen HN; Medical Genetics Institute, Ho Chi Minh City, Vietnam.
  • Tu LN; Medical Genetics Institute, Ho Chi Minh City, Vietnam.
J Extracell Vesicles ; 13(5): e12454, 2024 May.
Article en En | MEDLINE | ID: mdl-38760878
ABSTRACT
Extracellular vesicles (EVs) are emerging as a promising drug delivery vehicle as they are biocompatible and capable of targeted delivery. However, clinical translation of EVs remains challenging due to the lack of standardized and scalable manufacturing protocols to consistently isolate small EVs (sEVs) with both high yield and high purity. The heterogenous nature of sEVs leading to unknown composition of biocargos causes further pushback due to safety concerns. In order to address these issues, we developed a robust quality-controlled multi-stage process to produce and isolate sEVs from human embryonic kidney HEK293F cells. We then compared different 2-step and 3-step workflows for eliminating protein impurities and cell-free nucleic acids to meet acceptable limits of regulatory authorities. Our results showed that sEV production was maximized when HEK293F cells were grown at high-density stationary phase in semi-continuous culture. The novel 3-step workflow combining tangential flow filtration, sucrose-cushion ultracentrifugation and bind-elute size-exclusion chromatography outperformed other methods in sEV purity while still preserved high yield and particle integrity. The purified HEK293F-derived sEVs were thoroughly characterized for identity including sub-population analysis, content profiling including proteomics and miRNA sequencing, and demonstrated excellent preclinical safety profile in both in-vitro and in-vivo testing. Our rigorous enrichment workflow and comprehensive characterization will help advance the development of EVs, particularly HEK293F-derived sEVs, to be safe and reliable drug carriers for therapeutic applications.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Vesículas Extracelulares Límite: Humans Idioma: En Revista: J Extracell Vesicles Año: 2024 Tipo del documento: Article País de afiliación: Vietnam Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Vesículas Extracelulares Límite: Humans Idioma: En Revista: J Extracell Vesicles Año: 2024 Tipo del documento: Article País de afiliación: Vietnam Pais de publicación: Estados Unidos