Silva Allana Carvalho, Costa Mirsiane Pascoal, Zacaron Thiago Medeiros, Ferreira Kézia Cristine Barbosa, Braz Wilson Rodrigues, Fabri Rodrigo Luiz, Frézard Frédéric Jean Georges, Pittella Frederico, Tavares Guilherme Diniz
Postgraduate Program in Pharmaceutical Science, Federal University of Juiz de Fora, Juiz de Fora 36036-900, Minas Gerais, Brazil.
Department of Biochemistry, Institute of Biological Sciences, Federal University of Juiz de Fora, Juiz de Fora 36036-900, Minas Gerais, Brazil.
Pharmaceutics. 2024 Jul 23;16(8):969. doi: 10.3390/pharmaceutics16080969.
Lung cancer is the leading cause of cancer-related mortality worldwide, largely due to the limited efficacy of anticancer drugs, which is primarily attributed to insufficient doses reaching the lungs. Additionally, patients undergoing treatment experience severe systemic adverse effects due to the distribution of anticancer drugs to non-targeted sites. In light of these challenges, there has been a growing interest in pulmonary administration of drugs for the treatment of lung cancer. This route allows drugs to be delivered directly to the lungs, resulting in high local concentrations that can enhance antitumor efficacy while mitigating systemic toxic effects. However, pulmonary administration poses the challenge of overcoming the mechanical, chemical, and immunological defenses of the respiratory tract that prevent the inhaled drug from properly penetrating the lungs. To overcome these drawbacks, the use of nanoparticles in inhaler formulations may be a promising strategy. Nanoparticles can assist in minimizing drug clearance, increasing penetration into the lung epithelium, and enhancing cellular uptake. They can also facilitate increased drug stability, promote controlled drug release, and delivery to target sites, such as the tumor environment. Among them, chitosan-based nanoparticles demonstrate advantages over other polymeric nanocarriers due to their unique biological properties, including antitumor activity and mucoadhesive capacity. These properties have the potential to enhance the efficacy of the drug when administered via the pulmonary route. In view of the above, this paper provides an overview of the research conducted on the delivery of anticancer drug-loaded chitosan-based nanoparticles incorporated into inhaled drug delivery devices for the treatment of lung cancer. Furthermore, the article addresses the use of emerging technologies, such as siRNA (small interfering RNA), in the context of lung cancer therapy. Particularly, recent studies employing chitosan-based nanoparticles for siRNA delivery via the pulmonary route are described.
肺癌是全球癌症相关死亡的主要原因,这主要归因于抗癌药物的疗效有限,而这主要是由于到达肺部的剂量不足。此外,接受治疗的患者会因抗癌药物分布到非靶向部位而出现严重的全身不良反应。鉴于这些挑战,通过肺部给药治疗肺癌的兴趣日益浓厚。这种给药途径可使药物直接输送到肺部,从而产生高局部浓度,既能增强抗肿瘤疗效,又能减轻全身毒性作用。然而,肺部给药面临着克服呼吸道机械、化学和免疫防御的挑战,这些防御会阻止吸入的药物正确穿透肺部。为了克服这些缺点,在吸入剂配方中使用纳米颗粒可能是一种有前景的策略。纳米颗粒有助于减少药物清除,增加对肺上皮的渗透,并增强细胞摄取。它们还能促进药物稳定性的提高,促进药物的控释,并将药物输送到靶部位,如肿瘤环境。其中,基于壳聚糖的纳米颗粒由于其独特的生物学特性,包括抗肿瘤活性和粘膜粘附能力,比其他聚合物纳米载体具有优势。这些特性有可能在通过肺部途径给药时提高药物疗效。鉴于上述情况,本文概述了关于将载有抗癌药物的基于壳聚糖的纳米颗粒纳入吸入式给药装置用于治疗肺癌的研究。此外,本文还探讨了新兴技术,如小干扰RNA(siRNA)在肺癌治疗中的应用。特别是描述了最近利用基于壳聚糖的纳米颗粒通过肺部途径递送siRNA的研究。