Centre for Advanced Formulation & Technology, Delhi Pharmaceutical Sciences and Research University, New Delhi, 110017, India.
Department of Pharmaceutics, College of Pharmacy, Jazan University, PO box no. 114, Jazan, Saudi Arabia.
Nanomedicine (Lond). 2024 Apr;19(10):855-874. doi: 10.2217/nnm-2023-0260. Epub 2024 Mar 5.
This study was aimed to formulate erlotinib (ERL)-loaded transferosomal gel (ERL@TG) intended for topical application for the treatment of ductal carcinoma . The optimized process involved a thin-film hydration method to generate ERL-loaded transferosomes (ERL@TFS), which was incorporated into a carbopol gel matrix to generate ERL@TG. The optimized formulation was characterized followed by cytotoxicity evaluation on MCF-7 breast cancer cell lines and acute toxicity and skin irritation studies was performed . In a comparative assessment against plain ERL, ERL@TG displayed enhanced efficacy against MCF-7 cell lines, reflected in considerably lower IC values with an enhanced safety profile. Optimized ERL@TG was identified as a promising avenue for addressing ductal carcinoma breast cancer.
本研究旨在制备用于治疗导管癌的外用埃罗替尼(ERL)载转移体凝胶(ERL@TG)。优化工艺涉及薄膜水化法生成 ERL 载转移体(ERL@TFS),将其掺入卡波姆凝胶基质中生成 ERL@TG。对优化的配方进行了表征,随后对 MCF-7 乳腺癌细胞系进行了细胞毒性评价,并进行了急性毒性和皮肤刺激性研究。与普通 ERL 进行比较评估时,ERL@TG 对 MCF-7 细胞系显示出增强的疗效,反映在 IC 值明显降低且安全性更高。优化的 ERL@TG 被确定为治疗导管癌乳腺癌的有前途的途径。