期刊文献+

高浓度吡喹酮溶液的透皮吸收及对日本血吸虫病鼠的治疗试验 被引量:4

Study on Transdermal Absorption of Praziquantel Solution at High Concentration and Its Worm-Reduction Effect on Schistosomiasis Japonicum in Mice
下载PDF
导出
摘要 目的制备高浓度吡喹酮溶液,初步考察其透皮吸收及对日本血吸虫病鼠的试验治疗效果。方法由试验考察了高浓度吡喹酮溶液的稳定性。用紫外可见分光光度计测定了吡喹酮在指定溶媒中不同温度下的溶解度。高效液相色谱法测定透皮到家兔血液中吡喹酮的浓度.用70,150,200g·L^-1的吡喹酮溶液对人工感染日本血吸虫病鼠进行治疗试验。结果高浓度吡喹酮溶液具有很好的稳定性。在35~40℃之间,吡喹酮在指定溶媒中的溶解度迅速提高(由284g·L^-1猛增到456g·L^-1)。透皮给药比灌胃给药吸收速度快,AUC及ρmax分别为灌胃的2.1和4.0倍。高浓度吡喹酮溶液透皮给药对日本血吸虫病鼠的治疗效果良好,减虫率可达100%。结论高浓度吡喹酮溶液有望成为吡喹酮的新型透皮给药制剂。 OBJECTIVE To prepare praziquantel solution at high concentration and to investigate its transdermal delivery and worm-reduction effect on Schistosomiasis japoricum in mice. METHODS The stability of the solution was evaluatad by experiments. The solubility of praziquantcl solution at different temperature was measured by UV spectrophotometer. The praziquantel concentrations in rabbit plasma were determined by HPLC. The praziquantel solution of 70,150,200 g·L^-1 ,were applied to the experimental therapy of Schistosomiasis japonicum in mice. RESULTS The praziquantel solution at high concentration showed good stability. From 35 to 45 ℃, there was a great change in the solubility of praziquantel in the solvent( 284 g·L^-1 →456 g·L^-1 ). The absorption rate of transdermal delivery was faster than that of oral administration. The AUC and ρmax of the former was as 2. 1 times and 4.0 times as oral administration. The praziquantel solution reached prefect therapy efficacy with the worm-reduction of 100%. CONCLUSION The solution containing high praziquantel concentration may be a promising vehicle for the transdermal delivery of praziquantel.
出处 《中国药学杂志》 CAS CSCD 北大核心 2007年第6期450-453,共4页 Chinese Pharmaceutical Journal
关键词 透皮吸收 吡喹酮 日本血吸虫病 transdermal absorption praziquantel schistosomiasis japonicum
  • 相关文献

参考文献5

二级参考文献25

  • 1李富荣,蒋次鹏,曹和洵,王琪.吡喹酮脂质体对泡球蚴病的治疗效果探讨[J].中国寄生虫学与寄生虫病杂志,1993,11(4):251-254. 被引量:18
  • 2钱明心 刘约翰.测定左旋吡喹酮血药浓度的反相高效液相色谱法[J].重庆医科大学学报,1988,13(1):67-67. 被引量:2
  • 3钱明心 刘约翰 等.左旋吡喹酮在体内的药物动力学[J].中国药理学通讯,1985,5:62-62. 被引量:4
  • 4[1]Weaver JC, Vaughan TE, Chizmadzhev YA. Theory of electrical creation of aqueous pathways across skin transport barriers. Adv Drug Deliv Rev, 1999;35(1):21~39 被引量:1
  • 5[2]Weaver JC, Chizmadzhev YA. Theory of electroporation: a review. Bioelectroc hem Bioenerg, 1996,41:135~160 被引量:1
  • 6[3]Chizmadzhev YA, Zamitsin VG, Weaver JC, Potts UO.Mechanism of electroinduced ionic species transport through a multilamellar lipid system. Biophysical J, 1995,68:749~765 被引量:1
  • 7[4]Chizmadzhev YA, Indenbom AV, Kuzmin PI, Galichenko SV,Weaver JC, Potts RO. Electrical properties of skin at moderate voltages: contribution of appendageal macropores.Biophys J, 1998,74:843~856 被引量:1
  • 8[5]Zewert T, Pliquett U, L anger R, Weaver JC. Transdermal transport of DNA antisense oligonucleotides by electroporation. Biochem Biophy Res Comm, 1995,212(2):286~292 被引量:1
  • 9[6]Pliquett UF, Vanbever R, Preat V, Weaver JC. Local transport regions LTRs in human stratum corneum due to long and short 'High Voltage' pulses. Bioelectrochem Bioenerg,1998,47:151~161 被引量:1
  • 10[7]Pliquett UF, Zewert TE, Chen T, Langer R, Weaver JC.Imaging of fluorescent molecule and small Ion transport through human stratum comeum during high voltage pulsing:local transport regions are involved. Biophys Chem, 1996,58:185~204 被引量:1

共引文献20

同被引文献62

引证文献4

二级引证文献24

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部