Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add more filters










Database
Language
Publication year range
1.
Cells ; 11(20)2022 10 21.
Article in English | MEDLINE | ID: mdl-36291173

ABSTRACT

BNCT is a non-invasive cancer therapy that allows for cancer cell death without harming adjacent cells. However, the application is limited, owing to the challenges of working with clinically approved boron (B) compounds and drug delivery systems (DDS). To address the issues, we developed self-forming nanoparticles consisting of a biodegradable polymer, namely, "AB-type Lactosome (AB-Lac)" loaded with B compounds. Three carborane isomers (o-, m-, and p-carborane) and three related alkylated derivatives, i.e., 1,2-dimethy-o-carborane (diC1-Carb), 1,2-dihexyl-o-carborane (diC6-Carb), and 1,2-didodecyl-o-carborane (diC12-Carb), were separately loaded. diC6-Carb was highly loaded with AB-Lac particles, and their stability indicated the "molecular glue" effect. The efficiency of in vitro B uptake of diC6-Carb for BNCT was confirmed at non-cytotoxic concentration in several cancer cell lines. In vivo/ex vivo biodistribution studies indicated that the AB-Lac particles were remarkably accumulated within 72 h post-injection in the tumor lesions of mice bearing syngeneic breast cancer (4T1) cells, but the maximum accumulation was reached at 12 h. In ex vivo B biodistribution, the ratios of tumor/normal tissue (T/N) and tumor/blood (T/Bl) of the diC6-Carb-loaded particles remained stably high up to 72 h. Therefore, we propose the diC6-Carb-loaded AB-Lac particles as a promising candidate medicine for BNCT.


Subject(s)
Boron Neutron Capture Therapy , Boron , Animals , Mice , Boron/pharmacology , Boron/chemistry , Tissue Distribution , Cell Line, Tumor , Drug Delivery Systems , Polymers
2.
Cerebrovasc Dis ; 16(1): 31-5, 2003.
Article in English | MEDLINE | ID: mdl-12766359

ABSTRACT

To confirm that aspirin suppositories are an effective treatment for acute ischemic stroke, we examined the suppressive effects of 200-mg aspirin suppositories on platelet aggregation. Aspirin suppositories suppressed platelet aggregation induced by ADP or collagen, and the suppression continued for 24 h. There was no significant difference in suppression of platelet aggregation between aspirin administered by suppository and orally given aspirin. These results suggest that aspirin suppositories are a useful treatment for acute ischemic stroke.


Subject(s)
Aspirin/administration & dosage , Aspirin/therapeutic use , Platelet Aggregation Inhibitors/administration & dosage , Platelet Aggregation Inhibitors/therapeutic use , Adenosine Diphosphate/antagonists & inhibitors , Adenosine Diphosphate/pharmacology , Adult , Aspirin/pharmacokinetics , Collagen/antagonists & inhibitors , Collagen/pharmacology , Female , Gas Chromatography-Mass Spectrometry , Humans , Male , Platelet Aggregation/drug effects , Platelet Aggregation Inhibitors/pharmacokinetics , Sex Characteristics , Suppositories
SELECTION OF CITATIONS
SEARCH DETAIL
...