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水飞蓟宾制剂的研制:水飞蓟宾的体外和离体经皮药代动力学。

Development of silymarin topical formulation: In vitro and ex vivo dermal kinetics of silymarin.

机构信息

Department of Pharmaceutics and Drug Delivery, School of Pharmacy, The University of Mississippi, University, MS 38677, USA.

出版信息

Int J Pharm. 2023 Jan 5;630:122431. doi: 10.1016/j.ijpharm.2022.122431. Epub 2022 Nov 24.

DOI:10.1016/j.ijpharm.2022.122431
PMID:36436747
Abstract

Silymarin constituents are extensively investigated in the treatment of skin disorders. The main constituents of silymarin include taxifolin (TX), silychristin (ST), silydianin (SDN), silybin A (SA), silybin B (SB), isosilybin A (ISA) and isosilybin B (ISB). The objective of the present study was to determine in-vitro dermal kinetics of individual silymarin constituents in human skin models and to develop a silymarin topical formulation. In-vitro studies indicate human skin binding of silymarin was in the range of 2.09 to 12.3% and half-life of silymarin constituents was > 15.5 h in epidermal and dermal cells. Topical silymarin cream was prepared using sulfobutylether-β-cyclodextrins as solubilizer and propylene glycol as permeation enhancer. The cream was subjected to ex-vivo human skin permeation studies. In ex-vivo studies, cumulative amount of TX, ST, SDN, SA, SB, ISA and ISB permeated across human cadaver skin at 24 h was 921 ± 13.5, 1992 ± 67.6, 345 ± 39.2, 1089 ± 45.0, 1770 ± 100, 1469 ± 81.5 and 1285 ± 33.1 ng/cm, respectively. The amount TX, ST, SDN, SA, SB, ISA and ISB retained after 24 h was 60.7 ± 8.2, 376 ± 45.5, 72.3 ± 6.9, 66.4 ± 8.0, 208 ± 31.3, 154 ± 12.4 and 102 ± 6.3 ng/mg of human cadaver skin, respectively. The study results demonstrate silymarin topical formulation could deliver significant amount of silymarin constituents into skin. The developed silymarin formulation could be beneficial for treatment or management of a broad spectrum of dermatological disorders.

摘要

水飞蓟素的成分在治疗皮肤疾病方面得到了广泛的研究。水飞蓟素的主要成分包括水飞蓟宾(TX)、水飞蓟宾甲(ST)、水飞蓟宁(SDN)、水飞蓟宾 A(SA)、水飞蓟宾 B(SB)、异水飞蓟宾 A(ISA)和异水飞蓟宾 B(ISB)。本研究的目的是确定水飞蓟素成分在人体皮肤模型中的体外皮肤动力学,并开发水飞蓟素的局部制剂。体外研究表明,水飞蓟素在人体皮肤中的结合率为 2.09%至 12.3%,其成分在表皮和真皮细胞中的半衰期均大于 15.5 小时。水飞蓟素乳膏采用磺丁基醚-β-环糊精作为增溶剂,丙二醇作为渗透促进剂制备。乳膏进行了离体人体皮肤渗透研究。在离体研究中,TX、ST、SDN、SA、SB、ISA 和 ISB 在 24 小时内透过人体尸体皮肤的累积量分别为 921±13.5、1992±67.6、345±39.2、1089±45.0、1770±100.0、1469±81.5 和 1285±33.1ng/cm。24 小时后,TX、ST、SDN、SA、SB、ISA 和 ISB 的保留量分别为 60.7±8.2、376±45.5、72.3±6.9、66.4±8.0、208±31.3、154±12.4 和 102±6.3ng/mg 人体尸体皮肤。研究结果表明,水飞蓟素局部制剂可将大量水飞蓟素成分递送至皮肤。开发的水飞蓟素制剂可用于治疗或管理广泛的皮肤科疾病。

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