著者

宗 村盛 鈴木 豊史 高野 賢児 島田 侯陛 井上 真由美 川井 龍美 深水 啓朗 伴野 和夫

出版者

公益社団法人 日本薬学会

雑誌

YAKUGAKU ZASSHI (ISSN:00316903)

巻号頁・発行日

vol.133, no.5, pp.587-595, 2013-05-01 (Released:2013-05-01)

参考文献数

28

被引用文献数

1 2

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Japanese patients with normal renal function were retrospectively analyzed to characterize increases in serum creatinine (SCr) observed following the use of a sulfamethoxazole-trimethoprim (SMX-TMP) combination product and identify factors affecting these increases. In the patients studied (n=49), an individual comparison was conducted for the three factors of age group [≤74 years (n=21) vs. ≥75 years (n=28)], sex [male (n=24) vs. female (n=25)], and total dose throughout the treatment period [≤7 g (n=24) vs. ≥8 g (n=25)] to determine the extent of SCr increase following SMX-TMP combination product use. SCr increased significantly following SMX-TMP combination product use in patients ≤74 years of age and ≥75 years of age, in both males and females, and in patients with a total dose of ≥8 g (8 to 96 g) (p<0.05). Multivariate logistic regression analysis was used to determine the independence of these factors. Total dose was identified as an independent factor and had an odds ratio of 6.571 [95% confidence interval=1.735-24.882, p=0.006]. Post-treatment percent increases in SCr were compared using pre-treatment levels as the baseline. The group with a total dose of ≥8 g (mean 29.8 g) had a significant SCr increase of 18.4% (p=0.002), while the increase in the ≤7 g (mean 5.3 g) group was only 4.5%. The data showed that SCr increased by about 20% when the total dose taken over the treatment period was around 30 g (about 2.4 g as TMP) and indicated that total dose contributes more than age and sex to the post-treatment increase in SCr.

著者

山本 佳久 鎌野 衛 深水 啓朗 古石 誉之 鈴木 豊史 梅田 由紀子 牧村 瑞恵 伴野 和夫

出版者

一般社団法人日本医療薬学会

雑誌

医療薬学 (ISSN:1346342X)

巻号頁・発行日

vol.31, no.8, pp.625-631, 2005-08-10 (Released:2011-03-04)

参考文献数

8

被引用文献数

2 1

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A general method of administering powdered medicines to infants is to add a spoonful of water to the powder to make a paste and then making the paste into small dumpling-sized balls. We investigated the optimal amount of water for making a paste for 35 kinds of powdered medicine which included fine granules, granules and dry syrups. The optimal water amount was expressed as an amount per gram of powder. Approximately 80% of the powders examined in this study required 0.2-0.4 mL of water per gram of powder to make a paste that would form small balls. Optimal water amounts were calculated for amounts of powder ranging between 0.1 and 1.5 grams by proportion and when the calculated amounts of water were added, small dumpling sized balls could be formed. In the same way, we also calculated amounts of water required for powdered mixtures of several medicines for 6 prescriptions often prescribed in our pharmacy from corrected standard volumes for each medicine in the mixture. The amounts of water added on this basis achieved the required paste state for all of the powder mixtures used. These results suggest that the optimal water amount for powdered medicines of various weights can be estimated from standard volumes of water by proportion. Thus, optimal water amounts determined by our method may be useful for the administration of mixed powdered medicines to infants.

著者

深水 啓朗 山本 佳久 中村 裕美子 鎌野 衛 梅田 由紀子 牧村 瑞恵 古石 誉之 鈴木 豊史 伴野 和夫

出版者

一般社団法人日本医療薬学会

雑誌

医療薬学 (ISSN:1346342X)

巻号頁・発行日

vol.32, no.9, pp.964-969, 2006-09-10 (Released:2007-11-09)

参考文献数

17

被引用文献数

17 15

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We investigated the uniformity of content, rheological properties and chemical stability for prescription of Kindavate® ointment diluted with white petrolatum. When the ointment was levigated with white petrolatum (Propeto® for dilution) by a pharmacist or mixed by an autorotation/orbital mechanical mixer, a uniform ointment having the precise drug content could be prepared for all conditions. However, as the dilution ratio increased, the hardness of the ointment seemed to decrease based on the yield point measured with a spread meter and apparent absolute viscosity. Also, using a polarizing microscope, we observed a dispersion of oil droplets (consisting of liquid paraffin in clobetasone butyrate) in petrolatum for both Kindavate® ointment and the diluted ointment showing that the internal structure of ointment had not been affected by preparation of the diluted ointment either manually by pharmacists or using the mechanical mixer. When the diluted ointment was stored at 4 or 25°C in tight container in the absence of light, it was chemically stable for at least a month.Since our results showed that Kindavate® ointment diluted with petrolatum had a precise drug content and was stable over time, it should be feasible to prepare the ointment in advance of use.

著者

山本 佳久 鈴木 豊史 深水 啓朗 鎌野 衛 伴野 和夫

出版者

一般社団法人日本医療薬学会

雑誌

医療薬学 (ISSN:1346342X)

巻号頁・発行日

vol.34, no.7, pp.691-698, 2008 (Released:2010-02-07)

参考文献数

22

被引用文献数

1 2

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We determined the adhesion loss in a metering glass for 9 types of syrup for infants,and investigated the relationship between the adhesion loss and the rheological properties of the syrups.There was a good correlation (r2=0.981)between the viscosity of the syrups and percentage syrup residues on the metering glass.Further,from the viewpoints of accuracy and efficiency in dispensing,our finding that percentage residues for a dispenser were much lower (<0.15%) than for the metering glass suggested that it was better to use a dispenser for dispensing viscous syrups with a viscosity of at least 50-60 mPa·s.The results of our examination of syrup viscosities in the present study are expected to be useful information for their administration,and to contribute to the establishment of dispensing procedures based on scientific evidence.

著者

太田 美鈴 高橋 由里 深水 啓朗 伴野 和夫 岩田 政則 日高 慎二

出版者

一般社団法人日本医療薬学会

雑誌

医療薬学 (ISSN:1346342X)

巻号頁・発行日

vol.36, no.6, pp.425-435, 2010 (Released:2012-03-09)

参考文献数

8

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Very little information is provided with OTC drugs and unlike prescription products,they do not have package inserts or interview forms.The purpose of this study was to examine the stability of 5 acetaminophen-containing OTC drugs by observing temporal changes in their characteristic physico-pharmaceutical parameters (hardness,mass,elution,drug migration) when they were preserved under conditions in which temperature and humidity were altered.From the results,it was assumed that 3 of the 5 drugs were affected by temperature and humidity,and that it was difficult to maintain stability when they were taken out of their packages.In particular,the drugs seemed to be more adversely affected the higher the temperature was and changes in parameters were greater.Also,the results of an elution test conducted after 24 hours of storage suggested that there was deterioration in 3 of the products.In conclusion,our findings clearly showed that patients need adequate explanation on how to keep OTC drugs.