负载acclofenac的pluronic F108/L81混合聚合物胶束:HLB对增溶作用的影响。

IF 1.8 4区 化学 Q3 POLYMER SCIENCE Designed Monomers and Polymers Pub Date : 2022-01-28 eCollection Date: 2022-01-01 DOI:10.1080/15685551.2022.2028373
M Senthilkumar, Sasmita Dash, R Vigneshwari, E Paulraj
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引用次数: 6

摘要

Pluronic嵌段共聚物具有相行为特征,被广泛研究用于药物输送应用。本研究探索亲水性pluronic F108 (HLB = 27)、疏水性pluronic L81 (HLB = 2)及其混合胶束作为模型药物乙酰氯芬酸的增溶介质。利用紫外可见光谱、荧光光谱、流变学研究、傅里叶变换红外光谱、扫描电子显微镜、动态光散射、云点和分配系数测量分析了药物的溶解和相互作用。紫外分光光度法研究表明,在相同浓度下,混合pluronics比两种纯pluronics捕获更多的乙酰氯芬酸分子。以芘为探针的荧光光谱证实了准分子的形成。流变学研究表明,在低剪切范围内粘度存在差异。FTIR研究表明,acclofenac与混合pluronic分子之间可能存在键合。混合pluronic的DLS研究显示胶束直径从317.6 nm膨胀到413.5 nm。该体系的热力学参数表明,该体系对药物的混合多元溶和自发溶具有较高的分配系数值。本研究可以利用疏水共聚胶束在混合多元离子配方中更好地增溶药物。
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Aceclofenac-loaded pluronic F108/L81 mixed polymeric micelles: effect of HLB on solubilization.

Pluronic block copolymers have phase behavioural characteristics which are extensively studied for drug delivery applications. In this study, we explored hydrophilic pluronic F108 (HLB = 27), hydrophobic pluronic L81 (HLB = 2) and their mixed micelles acting as solubilising mediums for model drug aceclofenac. The drug solubilisation and interactions have been analysed using UV-visible spectroscopy, Fluorescence spectroscopy, Rheology studies, Fourier-transform infrared spectroscopy, Scanning electron microscope, Dynamic light scattering, Cloud point and partition coefficient measurements. The investigation from UV-spectrophotometry demonstrated that mixed pluronic entrapped greater number of aceclofenac molecules than both the neat pluronics at same concentration. Excimer formation was evidenced from fluorescence spectra with pyrene as a probe. The rheological studies showed difference in viscosity over low shear range. Studies on FTIR demonstrated probable bonding between the aceclofenac and mixed pluronic molecules. The DLS studies on mixed pluronic showed swelling of micellar diameter from 317.6 nm to 413.5 nm. Thermodynamic parameters of the above system revealed higher partition coefficient value for mixed pluronic and spontaneity in drug solubilisation. This study can be exploited to use a hydrophobic copolymeric micelle in mixed pluronic formulation for better drug solubilisation.

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来源期刊
Designed Monomers and Polymers
Designed Monomers and Polymers 化学-高分子科学
CiteScore
3.30
自引率
0.00%
发文量
28
审稿时长
2.1 months
期刊介绍: Designed Monomers and Polymers ( DMP) publishes prompt peer-reviewed papers and short topical reviews on all areas of macromolecular design and applications. Emphasis is placed on the preparations of new monomers, including characterization and applications. Experiments should be presented in sufficient detail (including specific observations, precautionary notes, use of new materials, techniques, and their possible problems) that they could be reproduced by any researcher wishing to repeat the work. The journal also includes macromolecular design of polymeric materials (such as polymeric biomaterials, biomedical polymers, etc.) with medical applications. DMP provides an interface between organic and polymer chemistries and aims to bridge the gap between monomer synthesis and the design of new polymers. Submssions are invited in the areas including, but not limited to: -macromolecular science, initiators, macroinitiators for macromolecular design -kinetics, mechanism and modelling aspects of polymerization -new methods of synthesis of known monomers -new monomers (must show evidence for polymerization, e.g. polycondensation, sequential combination, oxidative coupling, radiation, plasma polymerization) -functional prepolymers of various architectures such as hyperbranched polymers, telechelic polymers, macromonomers, or dendrimers -new polymeric materials with biomedical applications
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