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1.
Theranostics ; 14(8): 3193-3212, 2024.
Artigo em Inglês | MEDLINE | ID: mdl-38855185

RESUMO

As a developing radiation treatment for tumors, neutron capture therapy (NCT) has less side effects and a higher efficacy than conventional radiation therapy. Drugs with specific isotopes are indispensable counterparts of NCT, as they are the indespensable part of the neutron capture reaction. Since the creation of the first and second generations of boron-containing reagents, NCT has significantly advanced. Notwithstanding, the extant NCT medications, predominantly comprised of small molecule boron medicines, have encountered challenges such monofunctionality, inadequate targeting of tumors, and hypermetabolism. There is an urgent need to promote the research and development of new types of NCT drugs. Bio-nanomaterials can be introduced into the realm of NCT, and nanotechnology can give conventional medications richer functionality and significant adaptability. This can complement the advantages of each other and is expected to develop more new drugs with less toxicity, low side effects, better tumor targeting, and high biocompatibility. In this review, we summarized the research progress of nano-drugs in NCT based on the different types and sources of isotopes used, and introduced the attempts and efforts made by relevant researchers in combining nanomaterials with NCT, hoping to provide pivotal references for promoting the development of the field of tumor radiotherapy.


Assuntos
Neoplasias , Humanos , Neoplasias/radioterapia , Neoplasias/tratamento farmacológico , Animais , Terapia por Captura de Nêutron/métodos , Nanopartículas/química , Nanoestruturas/uso terapêutico , Nanoestruturas/química , Nanotecnologia/métodos , Terapia por Captura de Nêutron de Boro/métodos , Compostos de Boro/uso terapêutico , Compostos de Boro/química , Compostos de Boro/farmacologia
2.
Sci Total Environ ; 935: 173303, 2024 Jul 20.
Artigo em Inglês | MEDLINE | ID: mdl-38761948

RESUMO

Cadmium (Cd) and sulfamethoxazole (SMX) frequently coexist in farmlands, yet their synergistic toxicological impacts on terrestrial invertebrates remain unexplored. In this study, earthworms were exposed to artificial soils percolated with Cd (5 mg/kg), SMX (5 mg/kg) or combination of them for 7 days, followed by a 12-day elimination phase in uncontaminated soil. The uptake of Cd and SMX by the earthworms, along with their subcellular distribution, was meticulously analyzed. Additionally, a suite of biomarkers-including superoxide dismutase (SOD), catalase (CAT), malondialdehyde (MDA), and weight loss-were evaluated to assess the health status of the earthworms and the toxicological effects of the Cd and SMX mixture. Notably, the cotreatment with Cd and SMX resulted in a significantly higher weight loss in Eisenia fetida (41.25 %) compared to exposure to Cd alone (26.84 %). Moreover, the cotreatment group exhibited substantially higher concentrations of Cd in the total internal body, fraction C (cytosol), and fraction E (tissue fragments and cell membranes) in Eisenia fetida compared to Cd alone counterparts. The combined exposure also significantly elevated the SMX levels in the total body and fraction C compared with the SMX-only treated earthworms. Additionally, Eisenia fetida subjected to the combined treatment showed markedly increased activities of SOD, CAT, and MDA compared to those treated with Cd alone. The effect addition indices (EAIs), ranging from 1.00 to 2.23, unequivocally demonstrated a synergistic effect of the combined treatments. Interestingly, relocating the earthworms to clean soil did not mitigate the observed adverse effects. These findings underscore the increased risk posed by the Cd-SMX complex to terrestrial invertebrates in agricultural areas.


Assuntos
Biomarcadores , Cádmio , Oligoquetos , Poluentes do Solo , Sulfametoxazol , Oligoquetos/efeitos dos fármacos , Oligoquetos/fisiologia , Animais , Sulfametoxazol/toxicidade , Cádmio/toxicidade , Poluentes do Solo/toxicidade , Biomarcadores/metabolismo , Malondialdeído/metabolismo , Superóxido Dismutase/metabolismo , Catalase/metabolismo
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