首页> 外文期刊>Journal of drug targeting >Identification of a novel peptide ligand targeting visceral adipose tissue via transdermal route by in vivo phage display.
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Identification of a novel peptide ligand targeting visceral adipose tissue via transdermal route by in vivo phage display.

机译:通过体内噬菌体展示通过透皮途径鉴定靶向内脏脂肪组织的新型肽配体。

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摘要

To find novel peptide ligands targeting visceral adipose tissue (visceral fat) via transdermal route, in vivo phage display screening was conducted by dermal administration of a phage-peptide library to rats and a peptide sequence, CGLHPAFQC (designated as TDA1), was identified as a targeting ligand to visceral adipose tissue through the consecutive transdermal biopannings. Adipocyte-specific affinity and transdermal activity of the TDA1 were validated in vitro and targeting ability of the dermally administered TDA1 to visceral adipose tissue was also confirmed in vivo. TDA1 was effectively translocated into systemic circulation after dermal administration and selectively targeted visceral adipose tissue without any preference to other organs tested. Fluorescent microscopic analysis revealed that the TDA1 could be specifically localized in the hair follicles of the skin, as well as in the visceral adipose tissue. Thus, we inferred that dermally administered TDA1 would first access systemic circulation via hair follicles as its transdermal route and then could target visceral fat effectively. The overall results suggest that the TDA1 peptide could be potentially applied as a homing moiety for delivery of anti-obesity therapeutics to visceral fat through the convenient transdermal pathway.
机译:为了通过透皮途径找到靶向内脏脂肪组织(内脏脂肪)的新型肽配体,通过对大鼠皮肤施用噬菌体-肽文库进行体内噬菌体展示筛选,并将肽序列CGLHPAFQC(称为TDA1)鉴定为通过连续的透皮生物淘选来靶向内脏脂肪组织的靶向配体。在体外验证了TDA1的脂肪细胞特异性亲和力和透皮活性,并且在体内也证实了经皮给药的TDA1对内脏脂肪组织的靶向能力。皮肤给药后,TDA1有效地转移到全身循环中,并且选择性靶向内脏脂肪组织,而没有其他测试器官的任何优先选择。荧光显微镜分析表明,TDA1可以特异性地定位在皮肤的毛囊以及内脏脂肪组织中。因此,我们推断经皮给药的TDA1将首先通过毛囊进入全身循环,作为其透皮途径,然后才能有效地靶向内脏脂肪。总体结果表明,TDA1肽可潜在地用作归巢部分,通过便利的透皮途径将抗肥胖症治疗剂输送至内脏脂肪。

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