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基于硝苯地平-植烷三醇的立方液晶纳米粒的研制及经儿科喂食管给药的体外模拟

Development of Nifedipine Phytantriol-Based Cubosomes and In Vitro Simulation of Administration Through Pediatric Feeding Tubes.

作者信息

Lima Lorena Almeida, Moura Euler Eduardo Lisboa de, Fraga Schauana Freitas, Contri Renata Vidor, Külkamp-Guerreiro Irene Clemes

机构信息

Programa de Pós-Graduação em Ciências Farmacêuticas, Universidade Federal do Rio Grande do Sul, Porto Alegre 90610-000, Brazil.

Graduação em Química Bacharelado, Universidade Federal do Rio Grande do Sul, Porto Alegre 90610-000, Brazil.

出版信息

Pharmaceutics. 2025 Jun 25;17(7):828. doi: 10.3390/pharmaceutics17070828.

DOI:10.3390/pharmaceutics17070828
PMID:40733036
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12299420/
Abstract

This study focused on developing an organic solvent-free formulation of phytantriol-based cubosomes for nifedipine delivery. It assessed the physicochemical properties and in vitro administration performance in pediatric nasogastric tubes and preliminarily evaluated toxicity in a brine shrimp lethality model. The nanocarrier formulation was characterized in terms of the particle size and drug release properties and was compared with extemporaneous formulations prepared using nifedipine tablets in flow rate tests through pediatric feeding tubes. The recovery efficiency was evaluated across different tube sizes and rinsing volumes. A preliminary toxicity study was conducted using a brine shrimp lethality model. Compared with nifedipine tablets, the nanocarrier formulation demonstrated favorable physicochemical properties, including controlled release and superior flow rates, in the pediatric tubes. Full recovery of the nifedipine content was achieved with the nanocarrier formulation, whereas extemporaneous formulation of the nifedipine recovery depended on the tube dimensions and rinsing protocols. Compared with the traditional formulations, the nanocarrier formulation represents a promising alternative for administering nifedipine via pediatric feeding tubes, offering an enhanced administration recovery.

摘要

本研究聚焦于开发一种用于硝苯地平递送的基于植烷三醇的无有机溶剂立方液晶纳米粒制剂。评估了其理化性质以及在小儿鼻胃管中的体外给药性能,并在卤虫致死模型中初步评估了毒性。对纳米载体制剂的粒径和药物释放特性进行了表征,并在通过小儿喂食管的流速测试中与使用硝苯地平片制备的临时制剂进行了比较。在不同管径和冲洗体积下评估了回收效率。使用卤虫致死模型进行了初步毒性研究。与硝苯地平片相比,纳米载体制剂在小儿喂食管中表现出良好的理化性质,包括控释和优异的流速。纳米载体制剂可实现硝苯地平含量的完全回收,而硝苯地平临时制剂的回收则取决于管径和冲洗方案。与传统制剂相比,纳米载体制剂是通过小儿喂食管给药硝苯地平的一种有前景的替代方案,可提高给药回收率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82a0/12299420/88591fef89f3/pharmaceutics-17-00828-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82a0/12299420/4e6b0e728459/pharmaceutics-17-00828-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82a0/12299420/558968bb0091/pharmaceutics-17-00828-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82a0/12299420/5b76dbbf46cc/pharmaceutics-17-00828-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82a0/12299420/88591fef89f3/pharmaceutics-17-00828-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82a0/12299420/4e6b0e728459/pharmaceutics-17-00828-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82a0/12299420/558968bb0091/pharmaceutics-17-00828-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82a0/12299420/5b76dbbf46cc/pharmaceutics-17-00828-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82a0/12299420/88591fef89f3/pharmaceutics-17-00828-g004.jpg

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Nanomaterials (Basel). 2023 Feb 18;13(4):770. doi: 10.3390/nano13040770.
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Pediatric hypertension: Review of the definition, diagnosis, and initial management.小儿高血压:定义、诊断及初始治疗综述
Int J Pediatr Adolesc Med. 2022 Mar;9(1):1-6. doi: 10.1016/j.ijpam.2020.09.005. Epub 2020 Oct 15.
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Intratracheally Inhalable Nifedipine-Loaded Chitosan-PLGA Nanocomposites as a Promising Nanoplatform for Lung Targeting: Snowballed Protection Regulation of TGF-β/β-Catenin Pathway in Bleomycin-Induced Pulmonary Fibrosis.
气管内可吸入的载硝苯地平壳聚糖-聚乳酸-羟基乙酸共聚物纳米复合材料作为一种有前景的肺靶向纳米平台:对博来霉素诱导的肺纤维化中TGF-β/β-连环蛋白信号通路的累积保护调控
Pharmaceuticals (Basel). 2021 Nov 26;14(12):1225. doi: 10.3390/ph14121225.
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Neonatal and pediatric oral drug delivery: Hopes and hurdles.新生儿和儿科口腔药物传递:希望与障碍。
Int J Pharm. 2021 Mar 15;597:120296. doi: 10.1016/j.ijpharm.2021.120296. Epub 2021 Jan 29.
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