TY - JOUR
T1 - Physicochemical Characterization of PHBV Nanoparticles Functionalized with Multiple Bioactives Designed to be Theranostics for Lung Cancer
AU - Solar, Paula
AU - Herrera, Natalia
AU - Cea, Diego
AU - Devis, Sindy
AU - Gonzalez-Nilo, Fernando
AU - Juica, Natalia
AU - Moreno, Mabel
AU - Gai, Maria Nella
AU - Brescia, Ignacio
AU - Henríquez, Soledad
AU - Velasquez, Luis
N1 - Funding Information:
This work was supported by CONICYT—PCHA/ Doctorado nacional/2013–21130869, and SEK University, SEK1905. Acknowledgements
Publisher Copyright:
© 2020, Springer Science+Business Media, LLC, part of Springer Nature.
Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2020
Y1 - 2020
N2 - Lung cancer is a neoplasm associated with bacterial infections, main reason, to design a combined chemotherapy and antimicrobial treatment. Due to adverse drug reactions, we designed and synthetized polymer Poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) nanoparticles loaded with clarithromycin and paclitaxel and Superparamagnetic Iron Oxide Nanoparticles (SPION). Spherical nanoparticles with diameters ranging between 176 ± 19 and 222 ± 68 nm, hydrophilic and had a net negative surface charge were obtained. These nanoparticles can be lyophilized and resuspended in polar environments without affecting their physicochemical characteristics and maintaining their antibacterial activity. Both drugs interacted differently with the polymer, avoiding competition between them and facilitating the simultaneous encapsulation. The paclitaxel loaded in these nanoparticles remains almost completely encapsulated during the first 24 h under physiological conditions, allowing its accumulation and release in sites of high permeability and retention, such as tumors. In summary, these PHBV nanoparticles loaded with clarithromycin, paclitaxel and SPION are a promising drug delivery system for use in theranostics against lung cancer. [Figure not available: see fulltext.]
AB - Lung cancer is a neoplasm associated with bacterial infections, main reason, to design a combined chemotherapy and antimicrobial treatment. Due to adverse drug reactions, we designed and synthetized polymer Poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) nanoparticles loaded with clarithromycin and paclitaxel and Superparamagnetic Iron Oxide Nanoparticles (SPION). Spherical nanoparticles with diameters ranging between 176 ± 19 and 222 ± 68 nm, hydrophilic and had a net negative surface charge were obtained. These nanoparticles can be lyophilized and resuspended in polar environments without affecting their physicochemical characteristics and maintaining their antibacterial activity. Both drugs interacted differently with the polymer, avoiding competition between them and facilitating the simultaneous encapsulation. The paclitaxel loaded in these nanoparticles remains almost completely encapsulated during the first 24 h under physiological conditions, allowing its accumulation and release in sites of high permeability and retention, such as tumors. In summary, these PHBV nanoparticles loaded with clarithromycin, paclitaxel and SPION are a promising drug delivery system for use in theranostics against lung cancer. [Figure not available: see fulltext.]
KW - Biopolymer nanoparticles
KW - Clarithromycin
KW - Paclitaxel
KW - PHBV
KW - SPION
UR - http://www.scopus.com/inward/record.url?scp=85092924874&partnerID=8YFLogxK
U2 - 10.1007/s10876-020-01912-6
DO - 10.1007/s10876-020-01912-6
M3 - Article
AN - SCOPUS:85092924874
SN - 1040-7278
VL - 32
SP - 1563
EP - 1574
JO - Journal of Cluster Science
JF - Journal of Cluster Science
IS - 6
ER -