表面活性剂类型对含羊膜间充质干细胞代谢物转移体的特性、皮肤渗透及抗衰老作用的影响。

IF 6.5 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Andang Miatmoko, Nurul Ailda Marufah, Qothrin Nada, Noorma Rosita, Tristiana Erawati, Joni Susanto, Kusuma Eko Purwantari, Arif Nurkanto, Widji Soeratri
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引用次数: 5

摘要

Transfersome已被开发用于增强羊膜间充质干细胞代谢物(AMSC-MP)的真皮递送。AMSC-MP含有许多管理皮肤老化的生长因子,从而提高调整生命年的质量。本研究旨在确定表面活性剂类型作为边缘活化剂对转移体负载的影响。采用薄层水合法制备了转移体,该转移体由1 -α-磷脂酰胆碱和3种表面活性剂组成,即;阳离子(硬脂胺)、阴离子(胆酸钠)和非离子表面活性剂(Tween 80)的重量比分别为85:15。对转移体的物理特性、穿透性、有效性和安全性进行评估。结果表明,阴离子表面活性剂胆酸钠的转移体粒径最小,为144.2±3.2 nm。含有硬脂胺的Trans-SA的正电荷为41.53±6.03 mV,而Trans-SC和Trans-TW的正电荷分别为-56.9±0.55 mV和-41.73±0.86 mV。含有AMSC-MP的转移体具有较小的粒径和较低的zeta电位负值,因此具有较高的渗透能力,而硬脂胺的正电荷则阻碍了其对深层皮肤的渗透。Trans-SC和Trans-TW的胶原密度值分别为77.11±4.15%和70.05±6.95%,高于Trans-SA。所有的AMSC-MP转移体都是相对安全的,每视野0.5-1.0个巨噬细胞数量侵入真皮。综上所述,阴离子表面活性剂胆酸钠作为转运体负载的AMSC-MP的边缘活化剂具有相当大的抗衰老能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The effect of surfactant type on characteristics, skin penetration and anti-aging effectiveness of transfersomes containing amniotic mesenchymal stem cells metabolite products in UV-aging induced mice.

The effect of surfactant type on characteristics, skin penetration and anti-aging effectiveness of transfersomes containing amniotic mesenchymal stem cells metabolite products in UV-aging induced mice.

The effect of surfactant type on characteristics, skin penetration and anti-aging effectiveness of transfersomes containing amniotic mesenchymal stem cells metabolite products in UV-aging induced mice.

The effect of surfactant type on characteristics, skin penetration and anti-aging effectiveness of transfersomes containing amniotic mesenchymal stem cells metabolite products in UV-aging induced mice.

Transfersome has been developed to enhance dermal delivery of amniotic mesenchymal stem cell metabolite products (AMSC-MP). AMSC-MP contains many growth factors for managing skin aging, thus improving the quality of an adjusted life year. This study aims to determine the effect of surfactant types acting as the edge activator on transfersome-loading AMSC-MP. Transfersome was prepared by thin-layer hydration method and composed of l-α-phosphatidylcholine as a phospholipid and three types of surfactants, namely; cationic (stearylamine), anionic (sodium cholate), and nonionic surfactant (Tween 80) at a weight ratio of 85:15, respectively. Transfersomes were evaluated for physical characteristics, penetration, effectiveness, and safety. The results showed that sodium cholate, an anionic surfactant, produced the smallest transfersome particle size, i.e., 144.2 ± 3.2 nm, among all formulas. Trans-SA containing stearylamine had a positive charge of 41.53 ± 6.03 mV compared to Trans-SC and Trans-TW, whose respective charges were -56.9 ± 0.55 mV and -41.73 ± 0.86 mV. The small particle size and low negative value of zeta potential enabled high dermal penetration by transfersomes containing AMSC-MP, while the positive charge of stearylamine hindered its penetration of deeper skin layers. Trans-SC and Trans-TW produced higher collagen density values at 77.11 ± of 4.15% and 70.05 ± of 6.95%, than that of Trans-SA. All the AMSC-MP transfersomes were relatively safe with 0.5-1.0 macrophage cell numbers invaded the dermis per field of view. In conclusion, sodium cholate, an anionic surfactant, demonstrated considerable capacity as the edge activator of transfersome-loading AMSC-MP for skin anti-aging therapy.

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来源期刊
Drug Delivery
Drug Delivery 医学-药学
CiteScore
11.80
自引率
5.00%
发文量
250
审稿时长
3.3 months
期刊介绍: Drug Delivery is an open access journal serving the academic and industrial communities with peer reviewed coverage of basic research, development, and application principles of drug delivery and targeting at molecular, cellular, and higher levels. Topics covered include all delivery systems including oral, pulmonary, nasal, parenteral and transdermal, and modes of entry such as controlled release systems; microcapsules, liposomes, vesicles, and macromolecular conjugates; antibody targeting; protein/peptide delivery; DNA, oligonucleotide and siRNA delivery. Papers on drug dosage forms and their optimization will not be considered unless they directly relate to the original drug delivery issues. Published articles present original research and critical reviews.
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