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采用中心组合设计和响应面法优化并表征了去氧鬼臼毒素载 mPEG-PDLLA 胶束。

Optimization and characterization of deoxypodophyllotoxin loaded mPEG-PDLLA micelles by central composite design with response surface methodology.

机构信息

Department of Pharmaceutics, School of Pharmacy, China Pharmaceutical University, Nanjing 210009, China.

Children's Hospital of Nanjing Medical University, Nanjing 210008, China.

出版信息

Chin J Nat Med. 2018 Jun;16(6):471-480. doi: 10.1016/S1875-5364(18)30081-5.

Abstract

The therapeutic application of deoxypodophyllotoxin (DPT) is limited due to its poor water solubility and stability. In the present study, the micelles assembled by the amphiphilic block copolymers (mPEG-PDLLA) were constructed to improve the solubility and safety of DPT for their in vitro and in vivo application. The central composite design was utilized to develop the optimal formulation composed of 1221.41 mg mPEG-PDLLA, the weight ratio of 1 : 4 (mPEG-PDLLA : DPT), 30 mL hydration volume and the hydration temperature at 40 °C. The results showed that the micelles exhibited uniformly spherical shape with the diameter of 20 nm. The drug-loading and entrapment efficiency of deoxypodophyllotoxin-polymeric micelles (DPT-PM) were about (20 ± 2.84)% and (98 ± 0.79)%, respectively, indicating that the mathematical models predicted well for the results. Compared to the free DPT, the cytotoxicity showed that blank micelles possessed great safety for Hela cells. In addition, the DPT loaded micelle formulation achieved stronger cytotoxicity at the concentration of 1 × 10 mol·L, which showed significant difference from free DPT (P < 0.05). In conclusion, the micelles were highly promising nano-carriers for the anti-tumor therapy with DPT.

摘要

脱氧鬼臼毒素(DPT)的治疗应用受到其较差的水溶性和稳定性的限制。在本研究中,通过两亲性嵌段共聚物(mPEG-PDLLA)组装胶束,以提高 DPT 的溶解度和安全性,用于其体外和体内应用。采用中心复合设计开发由 1221.41 mg mPEG-PDLLA、质量比为 1:4(mPEG-PDLLA:DPT)、30 mL 水合体积和 40°C 水合温度组成的最佳配方。结果表明,胶束呈现出均匀的球形,粒径为 20nm。载药和包封效率约为(20±2.84)%和(98±0.79)%,表明数学模型很好地预测了结果。与游离 DPT 相比,空白胶束对 Hela 细胞表现出良好的安全性。此外,载药胶束制剂在浓度为 1×10 mol·L 时表现出更强的细胞毒性,与游离 DPT 相比具有显著差异(P<0.05)。总之,载药胶束是具有应用前景的抗肿瘤治疗 DPT 的纳米载体。

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