Metman L V, Hoff J, Mouradian M M, Chase T N
Experimental Therapeutics Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland 20892.
Mov Disord. 1994 Jul;9(4):463-5. doi: 10.1002/mds.870090416.
To evaluate the ability of orally administered liquid levodopa/carbidopa (LD/CD) to stabilize plasma levodopa levels and reduce motor response fluctuations in Parkinson's disease, five patients received LD/CD hourly, as standard tablets or as an aqueous solution on two separate days in a double-blind, placebo-controlled, cross-over design. Except for a slightly earlier peak plasma levodopa level, no significant advantage of the liquid formulation over tablet therapy was found. However, liquid LD/CD could be helpful in quickly resolving "off" states and by facilitating small dose adjustments that are not possible with tablets.
为评估口服左旋多巴/卡比多巴液体制剂(LD/CD)稳定帕金森病患者血浆左旋多巴水平及减少运动反应波动的能力,5例患者在双盲、安慰剂对照、交叉设计中,于两天内分别按标准片剂或水溶液形式每小时服用一次LD/CD。除血浆左旋多巴水平峰值稍早出现外,未发现液体制剂相对于片剂治疗有显著优势。然而,液体LD/CD可能有助于快速缓解“关”期状态,并便于进行片剂无法实现的小剂量调整。