Laboratório de Tecnologia Farmacêutica, Programa de Pós-graduação em Ciências Farmacêuticas, Centro de Ciências da Saúde, Universidade Federal de Santa Maria, Santa Maria, 97105-900, Brazil.
Curso de Biomedicina, Centro Universitário Franciscano, Santa Maria, Brazil.
AAPS PharmSciTech. 2023 Jun 22;24(6):138. doi: 10.1208/s12249-023-02606-8.
In previous studies, we developed a hydrogel formulation containing silibinin-loaded pomegranate oil nanocapsules (HG-NCSB) that had improved in vivo anti-inflammatory action in comparison to non-encapsulated silibinin. To determine skin safety and whether the nanoencapsulation influences silibinin skin permeation, NCSB skin cytotoxicity, HG-NCSB permeation in human skin, and a biometric study with healthy volunteers were conducted. The formulation of nanocapsules was prepared by the preformed polymer method while the HG-NCSB was obtained by thickening the suspension of nanocarriers with gellan gum. The cytotoxicity and phototoxicity of nanocapsules were assessed in Keratinocytes (HaCaT) and fibroblast (HFF-1) using the MTT assay. The hydrogels were characterized regarding the rheological, occlusive, and bioadhesive properties, and silibinin permeation profile in human skin. The clinical safety of HG-NCSB was determined by cutaneous biometry in healthy human volunteers. NCSB yielded better cytotoxicity results than the blank nanocapsules (NCPO). NCSB did not cause photocytotoxicity, while NCPO and the non-encapsulated substances (SB and pomegranate oil) were phototoxic. The semisolids presented non-Newtonian pseudoplastic flow, adequate bioadhesiveness, and low occlusive potential. The skin permeation demonstrated that HG-NCSB retained a higher SB amount in the outermost layers than HG-SB. In addition, HG-SB reached the receptor medium and had a superior concentration of SB in the dermis layer. In the biometry assay, there was no significant cutaneous alteration after the administration of any of the HGs. Nanoencapsulation promoted greater SB retention in the skin, averted percutaneous absorption, and made the topical use of SB and pomegranate oil safer.
在之前的研究中,我们开发了一种水凝胶制剂,其中包含载有姜黄素的石榴籽油纳米胶囊(HG-NCSB),与未封装的姜黄素相比,其体内抗炎作用得到了改善。为了确定皮肤安全性以及纳米封装是否影响姜黄素的皮肤渗透,我们进行了 NCSB 皮肤细胞毒性、HG-NCSB 在人皮肤上的渗透以及健康志愿者的生物计量研究。纳米胶囊的配方是通过预形成聚合物的方法制备的,而 HG-NCSB 是通过用结冷胶增稠纳米载体悬浮液获得的。使用 MTT 测定法在角质细胞(HaCaT)和成纤维细胞(HFF-1)中评估纳米胶囊的细胞毒性和光毒性。水凝胶的流变学、闭塞性和生物粘附特性以及姜黄素在人皮肤上的渗透特性进行了表征。通过健康人体志愿者的皮肤生物计量学确定 HG-NCSB 的临床安全性。NCSB 的细胞毒性结果优于空白纳米胶囊(NCPO)。NCSB 没有引起光细胞毒性,而 NCPO 和未封装的物质(SB 和石榴籽油)则具有光毒性。半固体呈非牛顿假塑性流动,具有适当的生物粘附性和低闭塞潜力。皮肤渗透表明,HG-NCSB 在最外层保留了更高量的 SB,而 HG-SB 则保留了更多的 SB。此外,HG-SB 到达受体介质,并且在真皮层中具有更高浓度的 SB。在生物计量学测定中,任何 HG 的给药后皮肤均未发生明显改变。纳米封装促进了 SB 在皮肤中的更好保留,避免了经皮吸收,并使 SB 和石榴籽油的局部使用更加安全。