Aug 2026· International Journal of Pharmaceutics: X· Vol 12, pp. 100634· 0 citations· 102 references
Medicine
TL;DR
This review systematically summarizes the mechanisms, delivery methods, key challenges, safety considerations, and translational gaps associated with mRNA-LNP therapeutics for pulmonary disorders.
Abstract
The success of mRNA vaccines has established lipid nanoparticles (LNPs) as a clinically validated delivery platform, yet their application to pulmonary therapeutics presents formidable challenges. This review systematically summarizes the mechanisms, delivery methods, key challenges, safety considerations, and translational gaps associated with mRNA-LNP therapeutics for pulmonary disorders. It surveys LNP-mediated delivery to pulmonary cell populations, distinguishing readily accessible targets (such as alveolar type II cells, bronchial epithelia, and macrophages) from refractory cell types (including T cells and rare fibroblast subsets). The evolution of LNPs is traced through three generations: from initial hepatic-optimized carriers, to lung-tropic selective organ targeting (SORT) formulations, and onward to contemporary precision-engineered aerosol systems. These advances have enabled diverse mRNA-based therapeutic modalities, encompassing protein replacement, gene editing, cell reprogramming, and cancer immunotherapy, each of which is examined with emphasis on their distinct mechanisms of action and safety profiles. Lung cancer represents a particularly intractable therapeutic challenge. Stromal barriers and tumor-associated macrophages render most lung-selective LNPs ineffective in orthotopic models, necessitating development strategies decoupled from those for non-malignant indications. Significant translational gaps persist, including a limited understanding of inhaled delivery barriers, insufficient long-term safety data for repeated dosing regimens, and the poor predictive value of healthy rodent models. While AI-guided lipid discovery, biodegradable formulations, and active targeting strategies offer considerable promise, clinical success will demand rigorous validation in disease-relevant preclinical models.
The pulmonary system is a vital interface between the body and the external environment, making it highly vulnerable to environmental, infectious, and genetic insults. Precision nanomedicine offers a promising strategy to overcome the limitations of conventional gene and drug therapies, including safety concerns associated with viral vectors, instability of therapeutic agents, suboptimal cellular internalization, and a critical lack of tissue- and cell-specific targeting. Nanoparticle-based delivery platforms address these challenges by enhancing therapeutic stability and bioavailability, enabling controlled release, facilitating cellular uptake and endosomal escape, and achieving targeted delivery to specific lung compartments. While recent literature often focuses on specific nanoparticle types or isolated pathologies, this work provides a comprehensive overview of the current state of respiratory nanomedicine, bridging fundamental nanoparticle bioengineering with a wide range of pulmonary pathologies and the obstacles to clinical translation. We discuss the key physicochemical properties of nanoparticles for pulmonary biomedical applications, along with advanced design strategies for targeted delivery. Given the unique architecture and physiology of the lung, we compare the advantages and limitations of pulmonary versus systemic administration routes, emphasizing context-specific delivery strategies. Nanoparticle design and therapeutic applications are explored across a broad spectrum of diseases, including pulmonary fibrosis, chronic obstructive pulmonary disease, infections, pulmonary vascular disease, cystic fibrosis, asthma, lung cancers, and neonatal pulmonary disorders. Finally, we evaluate the current status of clinical trials, highlighting translational challenges such as biological barriers, long-term safety, and manufacturing. Future perspectives and interdisciplinary strategies are proposed to advance the clinical translation of nanocarriers for respiratory diseases.
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Organ-selective immunomodulation is increasingly viewed as a route to improve the therapeutic index of cancer immunotherapy, yet most agents are still delivered systemically, where limited tumor exposure and immune-related toxicities remain common. The lung is an attractive site for local intervention because it is directly accessible and immunologically specialized. However, effective pulmonary delivery is constrained by mucociliary clearance, airway mucus, alveolar macrophage uptake, and epithelial barriers. Nanomaterials can be rationally engineered to address these constraints, increasing pulmonary retention and concentrating immunotherapeutics within the lung tumor microenvironment while reducing systemic burden. This Review summarized the key physiological barriers for pulmonary immunotherapeutic delivery and discusses how nanomaterial properties shape deposition, retention, cellular partitioning, and downstream immune activation. We critically evaluate representative inhalable platforms across major immunotherapeutic modalities, including vaccines, immune checkpoint blockade, innate immune agonists (e.g., STING agonists), cytokine regulation, and emerging in situ immune-cell engineering strategies. We also highlight translational considerations. Together, these advances support inhalable immunotherapeutic nanomedicines as a complementary approach to current lung cancer treatment and a broader framework for pulmonary immune modulation.
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