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焦脱镁叶绿酸-a-己醚在犬体内的药代动力学

Pharmacokinetics of pyropheophorbide-a-hexyl ether in the dog.

作者信息

Payne J T, McCaw D L, Casteel S W, Frazier D, Rogers K, Tompson R V

机构信息

Department of Veterinary Medicine, University of Missouri-Columbia 65211, USA.

出版信息

Lasers Surg Med. 1996;18(4):406-9. doi: 10.1002/(SICI)1096-9101(1996)18:4<406::AID-LSM10>3.0.CO;2-1.

Abstract

BACKGROUND AND OBJECTIVES

Pyropheophorbide-a-hexyl ether (HPPH) is a new compound being investigated for use as a photosensitizer for photodynamic therapy; however, the pharmacokinetics are not known for any of the target species likely to be treated with this drug. The objective of this study was to determine the pharmacokinetic parameters of this drug prior to institution of a clinical trial in canine patients with various cancers.

STUDY DESIGN, MATERIALS AND METHODS: HPPH (0.3mg/kg i.v.) was administered to 12 dogs and blood samples were drawn at intervals for 24 hours and plasma HPPH concentrations were determined. Pharmacokinetic parameters were calculated for each dog.

RESULTS

No evidence of toxicity was noted in any dog. The mean half-life was calculated to be 26.98 +/- 2.35 hrs. The mean clearance was 5.061 +/- 0.214 ml/hr/kg. The mean volume of distribution of the central compartment was 0.069 +/- 0.003 L/kg, and the mean steady state volume of distribution was 4.47 +/- 0.25 L/kg.

CONCLUSION

The conclusion is that 0.3 mg/kg HPPH injected intravenously resulted in measurable plasma levels for 24 hrs, and resulted in no detectable adverse reactions.

摘要

背景与目的

焦脱镁叶绿酸-a-己醚(HPPH)是一种正在研究用作光动力疗法光敏剂的新化合物;然而,对于任何可能用该药物治疗的目标物种,其药代动力学尚不清楚。本研究的目的是在对患有各种癌症的犬类患者进行临床试验之前,确定该药物的药代动力学参数。

研究设计、材料与方法:对12只犬静脉注射HPPH(0.3mg/kg),并在24小时内定期采集血样,测定血浆中HPPH浓度。计算每只犬的药代动力学参数。

结果

未在任何犬中观察到毒性迹象。计算得出平均半衰期为26.98±2.35小时。平均清除率为5.061±0.214 ml/hr/kg。中央室的平均分布容积为0.069±0.003 L/kg,平均稳态分布容积为4.47±

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