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载药量高的 提取物纳米混悬剂,经皮递送效果好且无刺激性。

High-Payload Nanosuspension of Extract for Improved Skin Delivery with No Irritation.

机构信息

College of Pharmacy, Dankook University, Cheonan, Chungnam, 330-714, Korea.

出版信息

Int J Nanomedicine. 2021 Nov 3;16:7417-7432. doi: 10.2147/IJN.S335039. eCollection 2021.

Abstract

BACKGROUND

The titrated extract of (CA) has received much attention as a cosmeceutical ingredient owing to its anti-wrinkle effect. However, due to the low solubility and high molecular weight of pharmacologically active constituents, including asiatic acid (AA), madecassic acid (MA), and asiaticoside (AS), it is challenging to fabricate high-payload topical preparations of CA with satisfactory skin absorption profiles.

PURPOSE

This study aimed to design a high-payload topical preparation of CA using nanocrystallization technique and to evaluate its skin absorption profile and local tolerability.

METHODS

High-payload nanocrystal suspensions (NSs) were prepared using lab-scale bead-milling technology, by adjusting the type and amount of suspending agent, CA content, type of vehicle, and milling speed. CA-loaded NSs were characterized in terms of morphology, particle size, crystallinity, and in vitro dissolution pattern. Skin absorption of CA nanocrystals was evaluated using a vertical Franz diffusion cell mounted with porcine skin. In vivo skin irritation following topical application of high-payload NS was assessed in normal rats.

RESULTS

The optimized NS system, composed of 10% (w/v) CA, 0.5% polyvinylpyrrolidone (PVP) K30 as steric stabilizer, and 89.5% of distilled water, was characterized as follows: spherical or elliptical in shape, 200 nm in size, with low crystallinity. The in vitro dissolution of AA or MA from NSs was markedly faster compared to raw material, under sink condition. Penetration of AA, MA, and AS in the porcine skin was markedly elevated using the high-payload NS formula, providing 5-, 4-, and 4.5-fold higher accumulation in skin layer, compared to that of the marketed cream formula (CA 1%, Madeca cream). Moreover, topical application of high-payload NS was tolerable, showing neither erythema nor oedema in normal rats.

CONCLUSION

The novel NS system is expected to be a virtuous approach for offering a better skin absorption of CA, without using an excess quantity of solubilizers.

摘要

背景

(CA)的经滴定提取物因其抗皱效果而作为一种化妆品成分受到广泛关注。然而,由于包括亚洲酸(AA)、马卡因酸(MA)和亚洲苷(AS)在内的具有药理活性的成分溶解度低、分子量高,因此很难制备具有令人满意的皮肤吸收特征的高载药量 CA 局部制剂。

目的

本研究旨在使用纳米结晶技术设计 CA 的高载药量局部制剂,并评估其皮肤吸收特征和局部耐受性。

方法

使用实验室规模的珠磨技术,通过调整悬浮剂的类型和用量、CA 含量、载体类型和研磨速度,制备高载药量纳米混悬剂(NS)。通过形态学、粒径、结晶度和体外溶解模式对 CA 负载 NS 进行了表征。使用垂直 Franz 扩散池和猪皮评估 CA 纳米晶体的皮肤吸收。在正常大鼠中评估高载量 NS 经皮应用后的局部刺激性。

结果

由 10%(w/v)CA、0.5%聚乙烯吡咯烷酮(PVP)K30 作为空间稳定剂和 89.5%蒸馏水组成的优化 NS 系统,其特点如下:形状为球形或椭圆形,大小为 200nm,结晶度低。在溶出条件下,AA 或 MA 从 NS 中的体外溶出明显快于原料药。使用高载量 NS 配方,AA、MA 和 AS 在猪皮中的渗透明显增加,与市售乳膏配方(CA1%,Madeca 乳膏)相比,皮肤层中的累积量分别提高了 5 倍、4 倍和 4.5 倍。此外,高载量 NS 的经皮应用是耐受的,在正常大鼠中既没有红斑也没有水肿。

结论

新型 NS 系统有望成为提供 CA 更好皮肤吸收的良性方法,而无需使用过量的增溶剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bd7/8573141/05f1badd2a4d/IJN-16-7417-g0001.jpg

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