工业可持续脱晶配方,以提高坎地沙坦西莱西地酯的溶解:克服传统固体分散方法的局限性。

IF 5.5 3区 医学 Q1 PHARMACOLOGY & PHARMACY
Mohamed A Ibrahim, Abdelrahman Y Sherif, Doaa Hasan Alshora
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引用次数: 0

摘要

背景/目的:传统的固体分散方法面临着显著的工业局限性,包括热降解、残留有机溶剂和复杂的制备工艺。本研究提出了一种使用波洛沙姆和丙二醇的新型脱晶配方,该配方在储存期间保持固体状态,但在生理温度(37°C)下液化。方法:制备不同波洛沙姆类型(407和188)不同浓度(5 ~ 25% w/w)的解晶配方,并对解晶温度、解晶时间和药物溶解度进行评价。通过FTIR分析、体外液化性能和溶出度研究对最佳配方进行了进一步表征。最后,对比常规方法对脱结晶配方的工业可持续性进行了评估。结果:与波洛沙姆188相比,波洛沙姆407具有更高的脱晶温度、更长的脱晶时间和更强的增溶能力。波洛沙姆407的溶解度为5.51±0.08 mg/g,浓度为20% w/w,脱晶温度为37℃,脱晶时间为216 s。FTIR光谱证实了氢键相互作用,这是温度依赖性相变的原因。与原料药(1.8±0.8%)、物理合剂(11.1±6.0%)和市售片剂(30.8±2.2%)相比,该解结晶制剂溶出效率(80.6±3.9%)显著提高。结论:该方法为提高水溶性较差药物的生物利用度和解决传统方法的局限性提供了一种有前途的方法。此外,与传统方法相比,它在连续生产的工业可持续性方面提供了额外的优势。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Industrial Sustainable Decrystallizing Formulation to Enhance Dissolution of Candesartan Cilexetil: Overcoming Limitations of Traditional Solid Dispersion Approaches.

Industrial Sustainable Decrystallizing Formulation to Enhance Dissolution of Candesartan Cilexetil: Overcoming Limitations of Traditional Solid Dispersion Approaches.

Industrial Sustainable Decrystallizing Formulation to Enhance Dissolution of Candesartan Cilexetil: Overcoming Limitations of Traditional Solid Dispersion Approaches.

Industrial Sustainable Decrystallizing Formulation to Enhance Dissolution of Candesartan Cilexetil: Overcoming Limitations of Traditional Solid Dispersion Approaches.

Background/Objectives: Conventional solid dispersion methods face significant industrial limitations, including thermal degradation, residual organic solvents, and complex preparation processes. This study presents a novel decrystallizing formulation using poloxamer and propylene glycol that remains solid during storage but liquefies at physiological temperature (37 °C). Methods: Decrystallizing formulations containing various poloxamer types (407 and 188) at different concentrations (5-25% w/w) were prepared and assessed for decrystallization temperature, decrystallization time, and drug solubility. The optimal formulation was further characterized using FTIR analysis, as well as in vitro liquefaction performance and dissolution studies. Finally, the industrial sustainability of the decrystallizing formulation was assessed against conventional methods. Results: Poloxamer 407 exhibited higher decrystallization temperature, longer decrystallization time, and superior solubilization capacity compared to Poloxamer 188. Maximum drug solubility (5.51 ± 0.08 mg/g) was achieved at 20% w/w of poloxamer 407 with a decrystallization temperature of 37 °C, and it took 216 s for decrystallization. FTIR spectroscopy confirmed hydrogen bonding interactions, which are responsible for temperature-dependent phase transitions. The decrystallizing formulation showed remarkable improvement in dissolution efficiency (80.6 ± 3.9%) compared to the raw drug (1.8 ± 0.8%), a physical mixture (11.1 ± 6.0%), and a marketed tablet (30.8 ± 2.2%). Conclusions: The current decrystallizing formulation offers a promising approach for improving the bioavailability of poorly water-soluble drugs and tackling the limitations of conventional methods. Moreover, it provides additional advantages in terms of industrial sustainability for continuous production compared to conventional approaches.

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来源期刊
Pharmaceutics
Pharmaceutics Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
7.90
自引率
11.10%
发文量
2379
审稿时长
16.41 days
期刊介绍: Pharmaceutics (ISSN 1999-4923) is an open access journal which provides an advanced forum for the science and technology of pharmaceutics and biopharmaceutics. It publishes reviews, regular research papers, communications,  and short notes. Covered topics include pharmacokinetics, toxicokinetics, pharmacodynamics, pharmacogenetics and pharmacogenomics, and pharmaceutical formulation. Our aim is to encourage scientists to publish their experimental and theoretical details in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.
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