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影响可变形纳米囊泡用于胰岛素雾化吸入效果的因素研究

Investigation of Factors Influencing the Effectiveness of Deformable Nanovesicles for Insulin Nebulization Inhalation.

作者信息

Yu Jinghan, Meng Yingying, Wen Zhiyang, Jiang Yu, Guo Yiyue, Du Simeng, Liu Yuling, Xia Xuejun

机构信息

Beijing Key Laboratory of Drug Delivery Technology and Novel Formulations, State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Department of Pharmaceutics, Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100050, China.

Beijing Wehand-Bio Pharmaceutical Co., Ltd., Beijing 102600, China.

出版信息

Pharmaceutics. 2024 Jun 29;16(7):879. doi: 10.3390/pharmaceutics16070879.

DOI:10.3390/pharmaceutics16070879
PMID:39065576
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11280345/
Abstract

Nebulized inhalation offers a noninvasive method for delivering drugs to treat both local respiratory and systemic diseases. In this study, insulin was used as a model drug to design a series of deformable nanovesicles (DNVs) with key quality attributes, including particle size, deformability, and drug load capacity. We investigated the effects of these properties on aerosol generation, macrophage phagocytosis, and bloodstream penetration. The results showed that deformability improved nebulization performance and reduced macrophage phagocytosis, benefiting local and systemic delivery. However, the advantage of DNVs for transmembrane penetration was not evident in the alveolar epithelium. Within the size range of 80-490 nm, the smaller the particle size of IPC-DNVs, the easier it is to evade clearance by macrophages and the more effective the in vivo hypoglycemic efficacy will be. In the drug load range of 3-5 mg/mL, a lower drug load resulted in better hypoglycemic efficacy. The area above the blood glucose decline curve with time (AAC) of nebulized DNVs was 2.32 times higher than that of the insulin solution, demonstrating the feasibility and advantages of DNVs in the pulmonary delivery of biomacromolecule drugs. This study provides insights into the construction and formulation optimization of pulmonary delivery carriers.

摘要

雾化吸入提供了一种将药物递送至局部呼吸道和全身性疾病治疗的非侵入性方法。在本研究中,胰岛素被用作模型药物,以设计一系列具有关键质量属性的可变形纳米囊泡(DNV),包括粒径、可变形性和载药量。我们研究了这些性质对气溶胶生成、巨噬细胞吞噬作用和血流渗透的影响。结果表明,可变形性改善了雾化性能并减少了巨噬细胞吞噬作用,有利于局部和全身递送。然而,DNV在跨膜渗透方面的优势在肺泡上皮中并不明显。在80 - 490 nm的尺寸范围内,IPC-DNV的粒径越小,越容易逃避巨噬细胞的清除,体内降血糖效果也越有效。在3 - 5 mg/mL的载药范围内,较低的载药量导致更好的降血糖效果。雾化DNV的血糖随时间下降曲线(AAC)上方区域比胰岛素溶液高2.32倍,证明了DNV在肺部递送生物大分子药物方面的可行性和优势。本研究为肺部递送载体的构建和制剂优化提供了见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6531/11280345/54309e4aced2/pharmaceutics-16-00879-g012.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6531/11280345/441679048018/pharmaceutics-16-00879-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6531/11280345/623ae3786e5a/pharmaceutics-16-00879-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6531/11280345/f5fbb2a3eeaa/pharmaceutics-16-00879-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6531/11280345/0210bacac051/pharmaceutics-16-00879-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6531/11280345/c3fd4428e1f9/pharmaceutics-16-00879-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6531/11280345/d252b088dd15/pharmaceutics-16-00879-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6531/11280345/d5508725446a/pharmaceutics-16-00879-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6531/11280345/54309e4aced2/pharmaceutics-16-00879-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6531/11280345/dab0e7d8da3d/pharmaceutics-16-00879-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6531/11280345/bcff19c46891/pharmaceutics-16-00879-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6531/11280345/f028d5318f6d/pharmaceutics-16-00879-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6531/11280345/6d2510c2e98b/pharmaceutics-16-00879-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6531/11280345/441679048018/pharmaceutics-16-00879-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6531/11280345/623ae3786e5a/pharmaceutics-16-00879-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6531/11280345/f5fbb2a3eeaa/pharmaceutics-16-00879-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6531/11280345/0210bacac051/pharmaceutics-16-00879-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6531/11280345/c3fd4428e1f9/pharmaceutics-16-00879-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6531/11280345/d252b088dd15/pharmaceutics-16-00879-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6531/11280345/d5508725446a/pharmaceutics-16-00879-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6531/11280345/54309e4aced2/pharmaceutics-16-00879-g012.jpg

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