Department of Pharmaceutics, NGSM Institute of Pharmaceutical Sciences, Nitte (Deemed to be University), Mangaluru, Karnataka, India.
Formulation and Development, Viatris R&D Centre, Bengaluru, India.
Drug Dev Res. 2024 Dec;85(8):e70019. doi: 10.1002/ddr.70019.
Cell membrane-coated Nano-Liposomes (CM-NLPs) offer a promising approach that combines the advantages of both host cells and synthetic nano-liposomes (NLPs). This technique involves coating liposomes with red blood cell (RBC) membranes to enhance their functionality. In this study, novel carboplatin-loaded NLPs (CP-NLPs) were formulated using phospholipids (Soya Phosphatidyl Choline) and cholesterol through the thin-film hydration method, and optimized using a 3 full factorial design. The optimized CP-NLPs were coated with RBC membranes, resulting in the formulation "CP-RBCs-NLPs." These were characterized for particle size, zeta potential, entrapment efficiency, transmission electron microscopy (TEM), differential scanning calorimetry (DSC), protein content, in vitro drug release, cell viability, and stability. The optimized CP-RBCs-NLPs exhibited a particle size of 103.6 nm, with zeta potential values of -27.3 mV indicating good stability. The entrapment efficiency was approximately 56%, and the drug release profile showed sustained release for up to 8 h. Cytotoxicity studies in human triple-negative breast cancer (MDA-MB468) cell lines demonstrated that CP-RBCs-NLPs effectively delivered the drug into target cells, facilitating cell death due to their bilayer structure similar to cell membranes. Overall, CP-RBCs-NLPs outperformed both carboplatin-loaded conventional NLPs (CP-CNLPs) and carboplatin-conventional solution (CP-CNS), making it a superior formulation for drug delivery.
细胞膜包覆的纳米脂质体(CM-NLPs)提供了一种有前途的方法,结合了宿主细胞和合成纳米脂质体(NLPs)的优势。该技术涉及用红细胞(RBC)膜包覆脂质体,以增强其功能。在这项研究中,通过薄膜水化法用磷脂(大豆卵磷脂)和胆固醇制备了新型载卡铂的 NLPs(CP-NLPs),并通过 3 因子完全设计进行了优化。优化的 CP-NLPs 用 RBC 膜进行包覆,得到“CP-RBCs-NLPs”的配方。对其粒径、Zeta 电位、包封效率、透射电子显微镜(TEM)、差示扫描量热法(DSC)、蛋白含量、体外药物释放、细胞活力和稳定性进行了表征。优化的 CP-RBCs-NLPs 的粒径为 103.6nm,Zeta 电位值为-27.3mV,表明稳定性良好。包封效率约为 56%,药物释放曲线显示可长达 8 小时的持续释放。在人三阴性乳腺癌(MDA-MB468)细胞系中的细胞毒性研究表明,CP-RBCs-NLPs 可有效地将药物递送至靶细胞,由于其双层结构类似于细胞膜,从而促进细胞死亡。总的来说,CP-RBCs-NLPs 优于载卡铂的常规 NLPs(CP-CNLPs)和载卡铂常规溶液(CP-CNS),是一种优越的药物递送配方。