Park Jung-Hwan, Lee Jeong-Woo, Kim Yeu-Chun, Prausnitz Mark R
Department of BioNano Technology and Gachon BioNano Research Institute, Kyungwon University, Seongnam, Geonggi-do 461-701, Republic of Korea.
Int J Pharm. 2008 Jul 9;359(1-2):94-103. doi: 10.1016/j.ijpharm.2008.03.032. Epub 2008 Mar 29.
Although the effects of long exposure (>>1s) to moderate temperatures (< or =100 degrees C) have been well characterized, recent studies suggest that shorter exposure (<1s) to higher temperatures (>100 degrees C) can dramatically increase skin permeability. Previous studies suggest that by keeping exposures short, thermal damage can be localized to the stratum corneum without damaging deeper tissue. Initial clinical trials have progressed to Phase II (see http://clinicaltrials.gov), which indicates the procedure can be safe. Because the effect of heating under these conditions has received little systematic or mechanistic study, we heated full-thickness skin, epidermis and stratum corneum samples from human and porcine cadavers to temperatures ranging from 100 to 315 degrees C for times ranging from 100ms to 5s. Tissue samples were analyzed using skin permeability measurements, differential scanning calorimetry, thermomechanical analysis, thermal gravimetric analysis, brightfield and confocal microscopy, and histology. Skin permeability was shown to be a very strong function of temperature and a less strong function of the duration of heating. At optimal conditions used in this study, transdermal delivery of calcein was increased up to 760-fold by rapidly heating the skin at high temperature. More specifically, skin permeability was increased (I) by a few fold after heating to approximately 100-150 degrees C, (II) by one to two orders of magnitude after heating to approximately 150-250 degrees C and (III) by three orders of magnitude after heating above 300 degrees C. These permeability changes were attributed to (I) disordering of stratum corneum lipid structure, (II) disruption of stratum corneum keratin network structure and (III) decomposition and vaporization of keratin to create micron-scale holes in the stratum corneum, respectively. We conclude that heating the skin with short, high temperature pulses can increase skin permeability by orders of magnitude due to structural disruption and removal of stratum corneum.
尽管长时间(>>1秒)暴露于适度温度(≤100摄氏度)的影响已得到充分表征,但最近的研究表明,较短时间(<1秒)暴露于更高温度(>100摄氏度)会显著增加皮肤通透性。先前的研究表明,通过保持暴露时间短,热损伤可局限于角质层,而不会损伤更深层组织。初步临床试验已进入二期(见http://clinicaltrials.gov),这表明该程序可能是安全的。由于在这些条件下加热的效果很少受到系统或机制研究,我们将来自人类和猪尸体的全层皮肤、表皮和角质层样本加热到100至315摄氏度,持续时间为100毫秒至5秒。使用皮肤通透性测量、差示扫描量热法、热机械分析、热重分析、明场和共聚焦显微镜以及组织学对组织样本进行分析。结果表明,皮肤通透性是温度的极强函数,而加热持续时间的函数较弱。在本研究使用的最佳条件下,通过在高温下快速加热皮肤,钙黄绿素的透皮递送增加了760倍。更具体地说,加热到约100-150摄氏度后,皮肤通透性增加了几倍;加热到约150-250摄氏度后,增加了一到两个数量级;加热到300摄氏度以上后,增加了三个数量级。这些通透性变化分别归因于:(I)角质层脂质结构的无序化;(II)角质层角蛋白网络结构的破坏;(III)角蛋白的分解和汽化,从而在角质层中形成微米级孔洞。我们得出结论,用短时间高温脉冲加热皮肤可因角质层的结构破坏和去除而使皮肤通透性增加几个数量级。