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通过射频微通道进行人生长激素的透皮给药。

Transdermal delivery of human growth hormone through RF-microchannels.

作者信息

Levin Galit, Gershonowitz Amikam, Sacks Hagit, Stern Meir, Sherman Amir, Rudaev Sergey, Zivin Inna, Phillip Moshe

机构信息

TransPharma Medical, Lod 71291, Israel.

出版信息

Pharm Res. 2005 Apr;22(4):550-5. doi: 10.1007/s11095-005-2498-6. Epub 2005 Apr 7.

Abstract

PURPOSE

To evaluate the bioavailability and bioactivity of human growth hormone (hGH) delivered transdermally through microchannels (MCs) in the skin created by radio-frequency (RF) ablation.

METHODS

The creation of MCs was observed in magnified rat and guinea pig skin after staining by methylene blue. Various doses of hGH in a dry form were applied on rat or guinea pig (GP) skin after the formation of MCs. The pharmacokinetic profile of systemic hGH in both animal models was monitored for 15 h post patch application. Bioactivity of the transdermally delivered hGH was verified by measuring IGF-I levels in hypophysectomized rats.

RESULTS

The ordered array of MCs was clearly visible in the magnified rat and guinea pig skin. The MCs were very uniform in diameter and of equal separation. Creation of MCs in the outer layers of the skin enabled efficient delivery of hGH, with a bioavailability of 75% (rats) or 33% (GPs) relative to subcutaneous (s.c.) injection with plasma profiles resembling that of s.c. injection. Elevated levels of systemic insulin-like growth factor-1 (IGF-I) were observed after transdermal delivery of hGH to hypophysectomized rats indicative of the bioactivity of the transdermally delivered hGH in vivo.

CONCLUSIONS

Formation of RF-microchannels is a well-controlled process. These MCs permitted the transdermal delivery of bioactive hGH in rats and GPs with high bioavailability.

摘要

目的

评估通过射频(RF)消融在皮肤中创建的微通道(MCs)经皮递送人生长激素(hGH)的生物利用度和生物活性。

方法

用亚甲蓝染色后,在放大的大鼠和豚鼠皮肤中观察MCs的创建情况。在MCs形成后,将不同剂量的干燥形式的hGH应用于大鼠或豚鼠皮肤。在贴片应用后15小时监测两种动物模型中全身hGH的药代动力学概况。通过测量垂体切除大鼠的IGF-I水平来验证经皮递送的hGH的生物活性。

结果

在放大的大鼠和豚鼠皮肤中可以清楚地看到MCs的有序排列。MCs的直径非常均匀且间距相等。在皮肤外层创建MCs能够有效地递送hGH,相对于皮下注射,生物利用度为75%(大鼠)或33%(豚鼠),血浆曲线类似于皮下注射。在将hGH经皮递送至垂体切除大鼠后,观察到全身胰岛素样生长因子-1(IGF-I)水平升高,这表明经皮递送的hGH在体内具有生物活性。

结论

射频微通道的形成是一个可控的过程。这些MCs允许在大鼠和豚鼠中经皮递送具有高生物利用度的生物活性hGH。

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