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http://www.alice.cnptia.embrapa.br/alice/handle/doc/1180498| Título: | Red blood cell-based celivery xystems for the release of hemoglobin-derived peptides with in vitro antitumor activities. |
| Autoria: | BONATTO, C. C.![]() ![]() JOANITTI, G. A. ![]() ![]() SILVA, L. P. da ![]() ![]() |
| Afiliação: | CÍNTHIA CAETANO BONATTO, UNIVERSITY OF BRASILIA (UNB); GRAZIELLA ANSELMO JOANITTI, UNIVERSITY OF BRASILIA; LUCIANO PAULINO DA SILVA, CENARGEN. |
| Ano de publicação: | 2025 |
| Referência: | Pharmaceuticals, v. 18, n. 4, 570, 2025. |
| Conteúdo: | This study aimed to develop liposomes derived from lipids obtained from red blood cell membranes for potential use in antitumor applications. Hemoglobin hydrolysates exhibiting peptides with known antitumor activities were encapsulated within these liposomes. Methods: The developed liposomal systems were characterized by their physicochemical properties, including size, surface charge, and encapsulation efficiency, and tested in vitro against 4T1 breast cancer cells and NIH3T3 fibroblasts. Results: Results indicated that the liposomes achieved effective encapsulation (88.9%), with nanometer-scale sizes (ranging from 140.7 nm for Blank-Liposomes to 658.3 nm for Pep-Liposomes) and stable colloidal properties. Conclusions: Although cytotoxicity was limited, the use of liposomes from endogenous components, such as red blood cells, demonstrates promise as a complementary approach in anticancer therapy. |
| NAL Thesaurus: | Peptides |
| Palavras-chave: | Liposome Red blood cell Antitumor In vitro Cell mimetics Nanosystems Mammalian cell |
| Digital Object Identifier: | https://doi.org/10.3390/ph18040570 |
| Notas: | Na publicação: Luciano Paulino Silva. |
| Tipo do material: | Artigo de periódico |
| Acesso: | openAccess |
| Aparece nas coleções: | Artigo em periódico indexado (CENARGEN)![]() ![]() |
Arquivos associados a este item:
| Arquivo | Descrição | Tamanho | Formato | |
|---|---|---|---|---|
| pharmaceuticals-18-00570-v2.pdf | 3.2 MB | Adobe PDF | ![]() Visualizar/Abrir |








