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Engineered Hybrid Vesicles and Cellular Internalization in Mammary Cancer Cells.
Kim, So Yun; Guk, Dagyeong; Jeong, Youngdo; Kim, Eunji; Kim, Hansol; Kim, Sung Tae.
Affiliation
  • Kim SY; Department of Nanoscience and Engineering, Inje University, Gimhae 50834, Republic of Korea.
  • Guk D; Center for Advanced Biomolecular Recognition, KIST Biomedical Research Division, Korea Institute of Science and Technology, Seoul 02792, Republic of Korea.
  • Jeong Y; KU-KIST Graduate School of Converging Science and Technology, Korea University, Seoul 02841, Republic of Korea.
  • Kim E; Center for Advanced Biomolecular Recognition, KIST Biomedical Research Division, Korea Institute of Science and Technology, Seoul 02792, Republic of Korea.
  • Kim H; HY-KIST Department of Bioconvergence, Hanyang University, Seoul 04763, Republic of Korea.
  • Kim ST; Department of Nanoscience and Engineering, Inje University, Gimhae 50834, Republic of Korea.
Pharmaceutics ; 16(4)2024 Mar 22.
Article in En | MEDLINE | ID: mdl-38675102
ABSTRACT
Extracellular vesicles play an important role in intercellular communication, with the potential to serve as biomaterials for nanocarriers. Combining such extracellular vesicles and liposomes results in advanced drug delivery carriers. In this study, we attempted to fabricate hybrid vesicles using a membrane fusion method and incorporated an anticancer drug. As a result, we successfully prepared nanosized uniform hybrid vesicles and evaluated their physicochemical characteristics and intracellular uptake mechanisms via endocytosis in various cell lines. Compared to liposomes, the hybrid vesicles showed better physical properties and a relatively higher reduction in cell viability, which was presumably dependent on the specific cell type. These findings suggest that fusion-based hybrid vesicles offer a novel strategy for delivering therapeutic agents and provide insights into the types of extracellular vesicles that are useful in fabricating hybrid vesicles to develop an advanced drug delivery system.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Pharmaceutics Year: 2024 Document type: Article Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Pharmaceutics Year: 2024 Document type: Article Country of publication: