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dc.contributor.author | GIBBENS BANDALA, BRENDA VIANEY | |
dc.contributor.author | MORALES AVILA, ENRIQUE | |
dc.contributor.author | FERRO FLORES, GUILLERMINA | |
dc.contributor.author | SANTOS CUEVAS, CLARA LETICIA | |
dc.contributor.author | MELENDEZ ALAFORT, LAURA | |
dc.contributor.author | TRUJILLO NOLASCO, ROSA MAYDELID | |
dc.contributor.author | OCAMPO GARCIA, BLANCA ELI | |
dc.creator | GIBBENS BANDALA, BRENDA VIANEY; 450667 | |
dc.creator | MORALES AVILA, ENRIQUE; 170668 | |
dc.creator | FERRO FLORES, GUILLERMINA; 19581 | |
dc.creator | SANTOS CUEVAS, CLARA LETICIA; 171596 | |
dc.creator | MELENDEZ ALAFORT, LAURA; 30308 | |
dc.creator | TRUJILLO NOLASCO, ROSA MAYDELID; 792262 | |
dc.creator | OCAMPO GARCIA, BLANCA ELI; 309879 | |
dc.date.accessioned | 2020-01-22T20:50:00Z | |
dc.date.available | 2020-01-22T20:50:00Z | |
dc.date.issued | 2019-08-01 | |
dc.identifier.issn | 0928-4931 | |
dc.identifier.uri | http://hdl.handle.net/20.500.11799/105353 | |
dc.description.abstract | The gastrin-releasing peptide receptor (GRPr) is overexpressed in>75% of breast cancers. 177Lu-Bombesin (177Lu-BN) has demonstrated the ability to target GRPr and facilitate efficient delivery of therapeutic radiation doses to malignant cells. Poly(D,L‑lactide‑co‑glycolide) acid (PLGA) nanoparticles can work as smart drug controlled- release systems activated through pH changes. Considering that paclitaxel (PTX) is a first-line drug for cancer treatment, this work aimed to synthesize and chemically characterize a novel polymeric PTX-loaded nanosystem with grafted 177Lu-BN and to evaluate its performance as a targeted controlled-release nanomedicine for concomitant radiotherapy and chemotherapy of breast cancer. PLGA(PTX) nanoparticles were synthesized using the single emulsification-solvent evaporation method with PVA as a stabilizer in the presence of PTX. Thereafter, the activation of PLGA carboxylic groups for BN attachment through the Lys1-amine group was performed. Results of the chemical characterization by FT-IR, DLS, HPLC and SEM/TEM demonstrated the successful synthesis of BN-PLGA(PTX) with a hydrodynamic diameter of 163.54 +- 33.25 nm. The entrapment efficiency of paclitaxel was 92.8 +- 3.6%. The nanosystem showed an adequate controlled release of the anticancer drug, which increased significantly due to the pH change from neutral (pH=7.4) to acidic conditions (pH=5.3). After labeling with 177Lu and purification by ultrafiltration, 177Lu-BN-PLGA(PTX) was obtained with a radiochemical purity of 99 +- 1%. In vitro and in vivo studies using MDA-MB-231 breast cancer cells (GRPr-positive) demonstrated a 177Lu-BNPLGA( PTX) specific uptake and a significantly higher cytotoxic effect for the radiolabeled nanosystem than the unlabeled BN-PLGA(PTX) nanoparticles. Using a pulmonary micrometastasis MDA-MB-231 model, the added value of 177Lu-BN-PLGA(PTX) for tumor imaging was confirmed. The 177Lu-BN-PLGA(PTX) nanomedicine is suitable as a targeted paclitaxel delivery system with concomitant radiotherapeutic effect for the treatment of GRPr-positive breast cancer. | es |
dc.description.sponsorship | This study was partially supported by the National Council of Science and Technology (CONACyT-CB-A1S38087) and the International Atomic Energy Agency (CRP-F22064, Contract 18358). It was carried out as part of the activities of the “Laboratorio Nacional de Investigación y Desarrollo de Radiofármacos, CONACyT. | es |
dc.language.iso | eng | es |
dc.publisher | Materials Science & Engineering C | es |
dc.rights | openAccess | es |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0 | |
dc.subject | Radiotherapy | es |
dc.subject | Targeted therapy | es |
dc.subject | Smart nanoparticles | es |
dc.subject | Drug delivery | es |
dc.subject | Cancer | es |
dc.subject | Concomitant cancer treatment | es |
dc.subject.classification | BIOLOGÍA Y QUÍMICA | |
dc.title | 177Lu-Bombesin-PLGA (paclitaxel): A targeted controlled-release nanomedicine for bimodal therapy of breast cancer | es |
dc.type | Artículo | es |
dc.provenance | Científica | es |
dc.road | Dorada | es |
dc.organismo | Química | es |
dc.ambito | Internacional | es |
dc.cve.CenCos | 20401 | es |
dc.cve.progEstudios | 6142 | es |
dc.audience | students | es |
dc.audience | researchers | es |
dc.type.conacyt | article | |
dc.identificator | 2 | |
dc.relation.doi | 10.1016/j.msec.2019.110043 |