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作 者:赵林[1,2] 谢艳招[1] 潘剑茹[2] 刘树滔[2]
机构地区:[1]福建师范大学闽南科技学院,泉州362332 [2]福州大学生物工程研究所,福州350002
出 处:《辐射研究与辐射工艺学报》2011年第2期99-103,共5页Journal of Radiation Research and Radiation Processing
基 金:福建省教育厅B类项目(JB09079)资助
摘 要:通过小鼠的离体皮肤渗透,研究了低频超声(40 kHz)辐射对融合了蛋白转导域的超氧化物歧化酶(Protein transduction domain-superoxide dismutase,PTD-SOD)体外经皮渗透的影响。结果表明,透皮8 h时,低频超声与氮酮(Azone)的增渗比分别为3.40和2.52;低频超声作用下,药物初始pH=6.0时,接收池中的SOD活性最高,可达1598.00 U;药物浓度效应符合Fick扩散定律,且药物渗透系数为0.011。这些结果说明,低频超声能显著提高PTD-SOD的经皮渗透速率,且效果优于Azone;药物溶液的初始pH值及药物初始浓度均能影响PTD-SOD的透皮速率,其最佳pH值及最佳给药浓度分别为6.0和15.00 kU·mL-1。By means of trans-dermal permeation on rat skin in vitro,the effect of low-frequency ultrasound(40 kHz) on trans-dermal permeation of(Protein transduction domain-superoxide dismutase,PTD-SOD) has been inves-tigated.The results show that the enhancement ratios of ultrasound and Azone are 3.40 and 2.52,respectively,when the trans-dermal permeation time is 8 h.In the presence of low-frequency ultrasound,when the initial pH value of drug solution is 6.0,the activity of PTD-SOD in receiver cell reaches 1598.00 U,the maximum value.Under the ac-tion of low-frequency ultrasound,the trans-dermal permeation of drug varies as a function of the initial PTD-SOD concentration according with a Fick-type scattering law,and the coefficient of permeation is 0.011.These results demonstrate that Low-frequency ultrasound can significantly improve trans-dermal transport of PTD-SOD,and the effect is superior to Azone.Both of the initial pH value of drug solution and the initial PTD-SOD concentration can affect the permeation rate of the PTD-SOD.And the best initial pH value and drug concentration is 6.0 and 15.00kU·mL-1,respectively.
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