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首页> 外文期刊>Journal of Photochemistry and Photobiology, B. Biology: Official Journal of the European Society for Photobiology >Desonide nanoencapsulation with acai oil as oil core: Physicochemical characterization, photostability study and in vitro phototoxicity evaluation
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Desonide nanoencapsulation with acai oil as oil core: Physicochemical characterization, photostability study and in vitro phototoxicity evaluation

机译:用Acai油脱落纳米型含油作为油芯:物理化学表征,光稳定性研究和体外光毒性评价

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This study aimed to develop Eudragit (R) RL 100 nanocapsules loaded with desonide (DES) using acai oil (AO) or medium chain triglycerides (MCT) as oil core. Pre-formulation study showed that AO and MCT are suitable for nanocapsules preparation. The nanocapsules prepared with AO and MCT presented mean particle size around 165 and 131 nm, respectively; polydispersity index values < 0.20, positive zeta potential values, drug content close to the theoretical value (0.25 mg mL(-1)), and DES encapsulation efficiency around 81%, regardless of the oil core (AO or MCT). Considering the photoinstability reported to DES, photodegradation studies were performed. The UV-A (365 nm) and UV-C (254 nm) photodegradation studies revealed less DES degradation when associated to the nanocapsules containing AO in comparison to those with MCT. The in vitro release study showed a biphasic release profile for both nanocapsule suspensions: an initial burst effect followed by a prolonged DES release. In addition, the formulations were considered non-phototoxic at 0.5 mg mL(-1) when tested on 3 T3 murine fibroblasts and HaCaT human keratinocytes using the MTT and NRU viability assays. The irritant potential of the prepared nanocapsules and DES in free form were evaluated by HET-CAM method. All formulations were classified as slightly irritant, including the non-associate DES. In conclusion, the nanocapsule formulations developed in this study may be promising for therapeutic applications.
机译:本研究旨在使用Acai油(AO)或中链甘油三酯(MCT)作为油芯,开发用脱盐(DES)负载的Eudragit(R)R100纳米胶囊。预制剂研究表明,AO和MCT适用于纳米胶囊制剂。用AO和MCT制备的纳米胶囊分别呈现为165和131nm的平均粒度;多分散指数值<0.20,阳性Zeta电位值,靠近理论值的药物含量(0.25mg ml(-1)),并且DES封装效率约为81%,而不管油芯(AO或MCT)。考虑到DES报告的光突显性,进行光降解研究。 UV-A(365nm)和UV-C(254nm)光降解研究显示与含有AO的纳米胶囊相比,与用MCT的纳米胶囊相关联。体外释放研究显示纳米胶囊悬浮液的双相释放曲线:初始突发效应,然后延长DES释放。此外,当使用MTT和NRU活力测定在3 T3鼠成纤维细胞和HaCAT人角质形成细胞上测试时,将制剂被认为是0.5mg mL(-1)的非光毒性。通过HET-CAM方法评估制备的纳米胶囊和以自由形式的刺激性潜力。所有制剂均分为略微刺激物,包括非助理DES。总之,本研究中开发的纳米胶囊配方可能对治疗应用有望。

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