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[经皮吸收猪耳原位灌注模型的建立与应用]

[Establishment and application of in situ perfused pig ear model for percutaneous absorption].

作者信息

Hu Jin-hong, Zhu Quan-gang, Shen Qi

机构信息

Department of Pharmacy, Changhai Hospital, Second Military Medical University, Shanghai 200433, China.

出版信息

Yao Xue Xue Bao. 2003 Oct;38(10):783-6.

Abstract

AIM

To establish an in situ perfused pig ear model for percutaneous absorption.

METHODS

The in situ perfused pig ear model for percutaneous absorption consisted of artificial gas, sample chamber, constant flow pump, constant temperature system, polytetrafluorethylene connective tube, porcine ear vein, porcine ear skin and special laminar flow apparatus. The perfused system viability was assessed by glucose utilization and lactate production. Ketoprofen isopropyl ester and methyl salicylate was used for validating this model. The concentrations of perfused sample were measured by HPLC.

RESULTS

Glucose utilization and lactate production showed that this model was viable till 7 h. Ketoprofen isopropyl ester was completely metabolized to ketoprofen in situ in perfused pig ear model. The steady cumulative amount (Q) of ketoprofen from permeation and metabolism was linear with time (t), the equation of ketoprofen formation was Q = -0.024 + 0.120t, the rate of ketoprofen formation was 0.120 microgram.cm-2.h-1. Methyl salicylate was partially metabolized to salicylic acid. The steady cumulative amount (Q) of methyl salicylate from permeation was linear with time (t), the permeation equation of methyl salicylate was Q = -3.809 + 6.129t, the permeation rate of metyl salicylate was 6.129 micrograms.cm-2.h-1. The steady cumulative amount (Q) of salicylic acid from metabolism was also linear with time (t), the formation equation of salicylic acid was Q = -1.785 + 0.879t, the formation rate of salicylic acid was 0.879 microgram.cm-2.h-1.

CONCLUSION

The in situ pig ear vein perfused model is a novel easy-handing and cost-efficient technique for percutaneous absorption and skin metabolism.

摘要

目的

建立一种用于经皮吸收的原位灌注猪耳模型。

方法

用于经皮吸收的原位灌注猪耳模型由人工气体、样品室、恒流泵、恒温系统、聚四氟乙烯连接管、猪耳静脉、猪耳皮肤和特殊层流装置组成。通过葡萄糖利用和乳酸生成评估灌注系统的活力。使用酮洛芬异丙酯和水杨酸甲酯对该模型进行验证。通过高效液相色谱法测定灌注样品的浓度。

结果

葡萄糖利用和乳酸生成表明该模型在7小时内保持活力。在原位灌注猪耳模型中,酮洛芬异丙酯完全代谢为酮洛芬。酮洛芬经渗透和代谢的稳态累积量(Q)与时间(t)呈线性关系,酮洛芬生成方程为Q = -0.024 + 0.120t,酮洛芬生成速率为0.120微克·厘米⁻²·小时⁻¹。水杨酸甲酯部分代谢为水杨酸。水杨酸甲酯经渗透的稳态累积量(Q)与时间(t)呈线性关系,水杨酸甲酯的渗透方程为Q = -3.809 + 6.129t,水杨酸甲酯的渗透速率为6.129微克·厘米⁻²·小时⁻¹。水杨酸经代谢的稳态累积量(Q)也与时间(t)呈线性关系,水杨酸的生成方程为Q = -1.785 + 0.879t,水杨酸的生成速率为0.879微克·厘米⁻²·小时⁻¹。

结论

原位猪耳静脉灌注模型是一种用于经皮吸收和皮肤代谢的新型、易于操作且成本效益高的技术。

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