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1.
J Diabetes Investig ; 9(2): 341-353, 2018 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-28644562

RESUMO

AIMS/INTRODUCTION: The aim of the present study was to evaluate the efficacy and safety of ipragliflozin in treating Japanese type 2 diabetes patients with inadequate glycemic control by investigating diurnal variations of blood glucose and body composition. MATERIALS AND METHODS: This was an investigator-initiated, multicenter, prospective study with a 6-month treatment period. The primary outcome investigated was change in hemoglobin A1c levels from baseline. Secondary outcomes included changes in fasting plasma glucose, insulin resistance, variations in 24-h glucose levels detected by continuous glucose monitoring, bodyweight, body composition, waist circumference and serum lipids. Adverse events were evaluated throughout the study. RESULTS: A total of 98 patients completed the study. Over the 6-month period, ipragliflozin-treated patients showed reduction in hemoglobin A1c levels by 0.3%, fasting plasma glucose levels by 13.0 mg/dL, bodyweight by 2.1 kg, body fat mass by 1.5 kg and extracellular water by 0.3 kg, as well as a decrease in systolic/diastolic blood pressures. Significant reductions from baseline in mean amplitude of glucose excursions and standard deviation, and the reduced frequency of hyperglycemia were confirmed. High-density lipoprotein cholesterol was also significantly improved. Notably, the subgroup analysis of hemoglobin A1c levels, bodyweight, waist circumference, and body composition based on age, sex and body mass index showed similar reductions within each subgroup. The incidences of adverse events and adverse drug reactions were 20.0% and 1.0%, respectively, over the 6-month period. CONCLUSIONS: Ipragliflozin is a useful oral antidiabetic medication for patients with a wide range of background characteristics.


Assuntos
Diabetes Mellitus Tipo 2/tratamento farmacológico , Glucosídeos/uso terapêutico , Hipoglicemiantes/uso terapêutico , Tiofenos/uso terapêutico , Administração Oral , Idoso , Povo Asiático , Glicemia/análise , Composição Corporal/efeitos dos fármacos , Peso Corporal/efeitos dos fármacos , Quimioterapia Combinada , Feminino , Glucosídeos/administração & dosagem , Glucosídeos/efeitos adversos , Hemoglobinas Glicadas/análise , Humanos , Hipoglicemiantes/administração & dosagem , Hipoglicemiantes/efeitos adversos , Japão , Masculino , Pessoa de Meia-Idade , Estudos Prospectivos , Tiofenos/administração & dosagem , Tiofenos/efeitos adversos , Resultado do Tratamento , Circunferência da Cintura/efeitos dos fármacos
2.
Anal Sci ; 25(2): 229-33, 2009 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-19212058

RESUMO

A layered manganese oxide film grown electrochemically was applied to remove methylene blue (MB), a cationic dye, from an aqueous solution. A layered MnO(x) film intercalated with tetraethylammonium (Et(4)N) cations was deposited potentiostatically at +1.0 V (vs. Ag/AgCl) from an aqueous Mn(2+) solution containing Et(4)NCl. Et(4)N cations were sandwiched between negatively charged MnO(x) layers. When the Et(4)N/MnO(x) film was immersed in a solution containing MB alone, the intercalated Et(4)N cations were replaced with MB in a solution phase by an ion-exchange mechanism. The uptake capacity of the Et(4)N/MnO(x) film for MB was estimated to be 45.3 mg per 1.0 g of MnO(2). In the presence of KCl, the MB sorption was seriously restricted because the interlayer space was occupied by K(+) ions. However, the MnO(x) film anodized at +0.8 V can selectively take up MB molecules from the KCl solution. This can be ascribed to an increase in the interlayer space available to the sorption of MB due to the extraction of K(+) ions, where the MnO(x) surface probably has a specific affinity toward MB molecules.

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