College of Pharmacy and Nutrition, University of Saskatchewan, 107 Wiggins Road, Health Sciences Building, Saskatoon, S7N 5E5 Saskatchewan, Canada.
Mol Pharm. 2024 Jul 1;21(7):3084-3102. doi: 10.1021/acs.molpharmaceut.4c00128. Epub 2024 Jun 3.
Biopharmaceuticals such as nucleic acids, proteins, and peptides constitute a new array of treatment modalities for chronic ailments. Invasive routes remain the mainstay of administering biopharmaceuticals due to their labile nature in the biological environment. However, it is not preferred for long-term therapy due to the lack of patient adherence and clinical suitability. Therefore, alternative routes of administration are sought to utilize novel biopharmaceutical therapies to their utmost potential. Nanoparticle-mediated pulmonary delivery of biologics can facilitate both local and systemic disorders. Solid lipid nanoparticles (SLNs) afford many opportunities as pulmonary carriers due to their physicochemical stability and ability to incorporate both hydrophilic and hydrophobic moieties, thus allowing novel combinatorial drug/gene therapies. These applications include pulmonary infections, lung cancer, and cystic fibrosis, while systemic delivery of biomolecules, like insulin, is also attractive for the treatment of chronic ailments. This Review explores physiological and particle-associated factors affecting pulmonary delivery of biopharmaceuticals. It compares the advantages and limitations of SLNs as pulmonary nanocarriers along with design improvements underway to overcome these limitations. Current research illustrating various SLN designs to deliver proteins, peptides, plasmids, oligonucleotides, siRNA, and mRNA is also summarized.
生物制药,如核酸、蛋白质和肽,构成了治疗慢性疾病的新治疗方式。由于其在生物环境中的不稳定性,侵入性途径仍然是生物制药给药的主要途径。然而,由于缺乏患者依从性和临床适用性,它并不适合长期治疗。因此,人们正在寻找替代给药途径,以充分利用新型生物制药疗法。纳米颗粒介导的生物制剂肺部给药可以促进局部和全身疾病的治疗。固体脂质纳米粒 (SLN) 由于其物理化学稳定性和能够结合亲水性和疏水性部分的能力,为肺部载体提供了许多机会,从而允许新的组合药物/基因治疗。这些应用包括肺部感染、肺癌和囊性纤维化,而生物分子如胰岛素的全身递送也吸引人们用于治疗慢性疾病。本文综述了影响生物制药肺部递释的生理和颗粒相关因素。它比较了 SLN 作为肺部纳米载体的优缺点以及正在进行的设计改进以克服这些限制。还总结了目前研究中各种 SLN 设计用于递送蛋白质、肽、质粒、寡核苷酸、siRNA 和 mRNA 的情况。