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出 处:《中南药学》2008年第1期58-60,共3页Central South Pharmacy
摘 要:目的 建立反相高效液相色谱法测定血浆中司帕沙星浓度,并研究其片剂与胶囊的人体相对生物利用度。方法 采用随机交叉、自身对照试验设计,20例健康男性志愿受试者单剂口服国产司帕沙星片剂或胶囊剂400mg后在不同时间点采血。用反相高效液相色谱法测定血清中司帕沙星浓度,以方差分析对主要药动学参数进行差别检验,双单侧t检验进行生物等效性判定。结果单剂量口服用400mg司帕沙星胶囊剂和片剂后的药物动力学参数AUC0~96分别为(50.50±6.78)和(50.82±11.57)μg·h·mL^-1,AUC0~∞。分别为(53.44±7.79)和(54.25±12.96)μg·h·mL^-1、tmax分别为(4.22±1.59)和(5.06±2.13)h、Cmax别为(1.46±0.23)和(1.46±0.31)μg·h·mL^-1、t1/2分别为(22.03±4.57)和(23.01±2.94)h。胶囊剂和片剂的相对生物利用度为102.41%±16.77%。2种制剂的药物动力学参数无明显差异。结论RP-HPLC法能快速、准确地测定人血浆中的司帕沙星,受试制剂与参比制剂具有生物等效性。Objective To determine the concentration of sparfloxacin in the human plasma by High Performance Liquid Chro- matography (HPLC), and to study its bioequivalence. Methods The pharmaeokinetics of sparfloxacin tablets and capsules were determined following a single oral dose of 400 mg given to 20 healthy volunteers in an open randomized crossover study. The sparfloxacin concentrations in the serum were measured by RP-HPLC. The pharmacokinetic parameters were calculated on the basis of one compartment model using 3P97 program. Results The pharmacokinetic parameters, after the volunteers taking a single dose of 400 mg of the trial preparation or the comparison preparation were as follows: tmax was (4. 22± 1.59) and (5.06±2. 13)h; Cmax was (1.46±0.23) and (1.46±0. 31)μg· mL^-1 ; AUC0~96 was (50. 50±6.78) and (50. 82±11.57) μg·h·mL^-1; AUC0~x was (53. 44±7. 79) and (54. 25±12. 96)μg·h·mL^-1; and t12 was (22. 03 ± 4. 57) and (23.01±2.94) h respectively. The pharmacokinetic parameters obtained from our studies showed no significant differences between the two products. The relative bioavailability of sparfloxacin capsule to tablet was 102. 41%±16. 77%. Conclusion The method can determine sparfloxacin in the plasma quickly and correctly. The two preparations are bioequivalent.
关 键 词:司帕沙星 生物等效性 反相高效液相色谱法 药物动力学
分 类 号:R917[医药卫生—药物分析学] R969.1[医药卫生—药学]
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