カワシマ アキツグ
Kawashima Akitsugu
川島 明次 所属 医学部 医学科(東京女子医科大学病院) 職種 准教授 |
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論文種別 | 原著 |
言語種別 | 英語 |
査読の有無 | 査読あり |
表題 | Prevention of cerebral vasospasm by nicardipine prolonged-release implants in dogs. |
掲載誌名 | 正式名:Neurological research 略 称:Neurol Res ISSNコード:01616412/01616412 |
掲載区分 | 国外 |
巻・号・頁 | 22(6),pp.634-41 |
著者・共著者 | Kawashima A, Kasuya H, Sasahara A, Miyajima M, Izawa M, Hori T |
担当区分 | 筆頭著者 |
発行年月 | 2000/09 |
概要 | The purpose of this study was to determine the efficacy of nicardipine prolonged-release implants for preventing vasospasm in a canine SAH model in a dose-escalating placebo-controlled blind fashion. Drug-release kinetics of copoly(lactic/glycolic acid) pellet containing nicardipine were evaluated in vitro. In vivo, 18 dogs were randomly assigned to one of three groups, i.e. placebo, low-dose (0.8 mg), or high-dose (8 mg) nicardipine. Angiography was performed, followed by right craniectomy, the induction of subarachnoid hemorrhage, and the placement of the pellets in the Sylvian fissure. On Day 7 and Day 14, the angiography was repeated. In the first four days, 61.9% of the actual nicardipine loaded was released and within 10 days, 96%. The average percent reductions of vessel diameters in the middle cerebral artery on Day 7 were 43%, 14% and 7% in the placebo, low-dose, and high-dose groups, respectively (p = 0.0319). The mean concentration of nicardipine in the clots on Day 14 was 9.7 x 10(-7) mol-1 l-1 and 5.1 x 10(-6) mol-1 l-1 in the low-dose and high-dose group, respectively. This drug delivery system prevented vasospasm in dogs significantly even at low dose, while maintaining an appropriate concentration of nicardipine in the clot adjacent to the arteries. |
DOI | 10.1080/01616412.2000.11740733 |
PMID | 11045030 |