Jiang Chengwei, Bai Rongjun, Somavarapu Satyanarayana
Department of Pharmaceutics, School of Pharmacy, University College London, 29-39 Brunswick Square, London WC1N 1AX, U.K.
ACS Omega. 2025 Apr 11;10(15):15400-15411. doi: 10.1021/acsomega.5c00008. eCollection 2025 Apr 22.
Lung cancer, particularly NSCLC, poses a major therapeutic challenge due to drug resistance and the poor aqueous solubility of chemotherapeutic agents, limiting treatment efficacy. This study investigates inhalable micelles for the codelivery of curcumin (CUR) and icariin (ICA), two hydrophobic bioactive compounds with anticancer potential, as a targeted therapeutic approach for NSCLC. The optimized micellar formulation (9:1 TPGS/DPPC) yielded nanomicelles (∼18 nm) with high encapsulation efficiency (∼90%) and a zeta potential of -1.24 mV, demonstrating stability for pulmonary administration. cytotoxicity studies demonstrated enhanced anticancer activity of CUR- and ICA-loaded micelles against A549 lung cancer cells (IC = 3.0 μg/mL), lower than doxorubicin (30 μg/mL), suggesting enhanced cytotoxic potential. Additionally, DPPH assays confirmed that encapsulation preserved curcumin's functionality. Aerosolization studies demonstrated a high fine particle fraction (67 ± 3%) and emitted fraction (95 ± 1.0%), confirming the micelles' suitability for deep lung deposition and effective pulmonary drug delivery. These findings highlight the potential of CUR- and ICA-loaded micelles as an inhalable NSCLC treatment, requiring further preclinical investigation.
肺癌,尤其是非小细胞肺癌(NSCLC),由于耐药性和化疗药物水溶性差,构成了重大的治疗挑战,限制了治疗效果。本研究调查了可吸入胶束用于姜黄素(CUR)和淫羊藿苷(ICA)的共递送,这两种具有抗癌潜力的疏水性生物活性化合物,作为NSCLC的靶向治疗方法。优化后的胶束配方(9:1 TPGS/DPPC)产生了纳米胶束(约18纳米),具有高包封效率(约90%)和-1.24 mV的zeta电位,证明了肺部给药的稳定性。细胞毒性研究表明,负载CUR和ICA的胶束对A549肺癌细胞具有增强的抗癌活性(IC = 3.0 μg/mL),低于阿霉素(30 μg/mL),表明细胞毒性潜力增强。此外,DPPH测定证实包封保留了姜黄素的功能。雾化研究表明细颗粒分数高(67 ± 3%)和发射分数高(95 ± 1.0%),证实了胶束适用于肺部深部沉积和有效的肺部药物递送。这些发现突出了负载CUR和ICA的胶束作为可吸入NSCLC治疗方法的潜力,需要进一步的临床前研究。