医療薬学
Online ISSN : 1882-1499
Print ISSN : 1346-342X
ISSN-L : 1346-342X
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バルガンシクロビルの簡易懸濁法適応に向けての基礎的研究―他剤同時懸濁時の安定性の検討―
小川 敦河崎 陽一正岡 康幸山路 和彦名和 秀起佐藤 智昭松永 尚千堂 年昭
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ジャーナル フリー

2012 年 38 巻 8 号 p. 534-539

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A simple suspension method has been developed for the administration of tablets and capsules through a nasogastric tube. Tablets or capsules were suspended in hot water (55℃) without grinding or opening. Valganciclovir hydrochloride (VALIXA®), a drug often prescribed to protect patients from cytomegalovirus infection after organ transplantation, was dispensed via a crushing method to recipients unable to take food or liquids by oral administration.
The interaction of VALIXA® tablets with other medicines in a simple suspension has not been investigated, even though VALIXA® is commonly used in combination with immune-suppressant drugs and several other medicines. Thus, we sought to examine the effect of co-administering suspensions of drugs combined with VALIXA® tablets prescribed for transplant recipients. Valganciclovir hydrochloride was mixed with a variety of other therapeutics including prednisolone (PREDONINE® tablets), ursodeoxycholic acid (URSO® granules), sulfamethoxazole-trimethoprim (BAKTAR® granules), mycophenolate mofetil (CELLCEPT® capsules), tacrolimus (PROGRAF® capsules), sucralfate (ULCERLMIN® fine granule), and fluconazole (DIFLUCAN® capsules), and the residual content of valganciclovir was evaluated by a high performance liquid chromatography assay. Our results indicated that over 90% of the original valganciclovir remained in the drug mixture suspension. In a practical test of delivering such suspensions by nasogastric tube, we observed that suspensions did not block either the catheter or injection syringe, and upon flushing, no residual drug suspension remained in the device.
In conclusion, this study suggests that VALIXA® tablets in combination with a variety of other medicines may be administered to patients by a simple suspension method.
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© 2012 日本医療薬学会
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