Busca avançada
Ano de início
Entree


Sugar-decorated cholesterol-core nanoparticles as potential targeting nanomedicines for the delivery of lipophilic drugs

Texto completo
Autor(es):
de Barros, Lais Rossetto Ferraz ; de Castro, Carlos Eduardo ; Rosso, Anabella Patricia ; da Costa Duarte, Rodrigo ; Dal-Bo, Alexandre Goncalves ; Alves, Wendel Andrade ; Giacomelli, Fernando Carlos
Número total de Autores: 7
Tipo de documento: Artigo Científico
Fonte: RSC PHARMACEUTICS; v. 2, n. 2, p. 11-pg., 2025-03-18.
Resumo

Targeted drug delivery is a precise and effective strategy in oncotherapy and can be achieved through sugar-decorated assemblies since glucose receptors are overexpressed on cancer cell membranes to compensate for their increased glucose demands. In this study, core-shell nanoparticles (NPs) were synthesized using amphiphilic macromolecules comprising hydrophobic cholesterol (Chol) segments conjugated to hydrophilic polyethylene oxide containing azide group (Chol-PEO22-N3) or substituted with the carbohydrate N-acetyl-d-glucosamine (Chol-PEO22-GlcNAc) via a click chemistry reaction. These self-assemblies, which are smaller than 100 nm and suitable for cancer treatment, demonstrated efficient loading efficiency (exceeding 70%) with ursolic acid (UA), a hydrophobic drug, serving as a proof-of-concept for targeted therapy using natural compounds against non-small cell lung cancer. The incorporation of sugar molecules modified the structural characteristics of the nanocarriers, resulting in larger and presumably less dense particles. This modification influenced the UA release mechanism, leading to a faster and nearly complete release over a week, whereas approximately 60% of the encapsulated UA remained entrapped in the Chol-PEO22-N3 NPs. Enhanced cell cytotoxicity was achieved with UA-loaded NPs with in vitro cell viability assays indicating at least two-fold increase in the inhibitory effect of the drug-loaded nanocarriers. The targeted delivery was also demonstrated as UA-loaded Chol-PEO22-GlcNAc NPs showed greater internalization by cancer cells than their healthy counterparts. (AU)

Processo FAPESP: 21/12071-6 - Arquitetando coloides via interações supramoleculares: de fundamentos a aplicações
Beneficiário:Watson Loh
Modalidade de apoio: Auxílio à Pesquisa - Temático
Processo FAPESP: 23/00558-3 - Polimerossomos contendo nanocanais biomiméticos para reações enzimáticas em espaços confinados
Beneficiário:Fernando Carlos Giacomelli
Modalidade de apoio: Auxílio à Pesquisa - Regular
Processo FAPESP: 22/14668-2 - Manufatura de polimerossomos com permeabilidade seletiva para utilização como nanoreatores para biocatálise
Beneficiário:Anabella Patricia Rosso
Modalidade de apoio: Bolsas no Brasil - Pós-Doutorado
Processo FAPESP: 22/14753-0 - Tecnologias de biossensores e sistemas de liberação controlada baseadas em microagulhas para diagnóstico e tratamento de doenças
Beneficiário:Wendel Andrade Alves
Modalidade de apoio: Auxílio à Pesquisa - Temático
Processo FAPESP: 14/50867-3 - INCT 2014: Instituto Nacional de Ciência e Tecnologia de Bioanalítica
Beneficiário:Marco Aurelio Zezzi Arruda
Modalidade de apoio: Auxílio à Pesquisa - Temático