{"title":"低水溶性甲氧基黄酮与PEG400和丙二醇的配方特性、生物相容性和渗透性的深入研究。","authors":"Fredrick Nwude Eze, Chaweewan Jansakul, Teerapol Srichana","doi":"10.2478/acph-2023-0030","DOIUrl":null,"url":null,"abstract":"<p><p>Herein, thermal and non-thermal techniques were used to elucidate the putative physical and chemical interactions between poorly water-soluble <i>Kaempferia</i> methoxyflavones and PEG400/propylene glycol. Additionally, the biocompatibility of methoxyflavone-glycol solutions was evaluated using Caco-2 cells whereas the absorptive transport was investigated by measuring the apparent permeability coefficient (<i>P</i> <sub>app</sub>) of the methoxyflavones and transepithelial electrical resistance (TEER) of the Caco-2 cell monolayer. Data from differential scanning calorimetry, Fourier-transform infrared (FTIR), and proton nuclear magnetic resonance (<sup>1</sup>H NMR) spectroscopic analysis revealed physico-chemical compatibility between the three methoxyflavones and PEG400/propylene glycol. Furthermore, PEG400 and propylene glycol solutions of the methoxyflavones were shown to be compatible with Caco-2 cells at pharmacologically effective concentrations. <i>In vitro</i> transport studies across the Caco-2 cell monolayer revealed high <i>P</i> <sub>app</sub> values of 24.07 × 10<sup>-6</sup> to 19.63 × 10<sup>-6</sup> cm s<sup>-1</sup> for PEG400 solutions of the methoxyflavones. The TEER values of the Caco-2 cell monolayers indicated that the increased drug transport was partly due to increased tight junction openings, but without compromising the epithelial barrier integrity. The good pharmaceutical and biocompatibility profiles, as well as improved transport of the methoxyflavones in PEG400 and propylene glycol solutions, are suggestive of the worthiness of this approach for further consideration pertaining to the development of these drugs into oral liquid dosage forms.</p>","PeriodicalId":7034,"journal":{"name":"Acta Pharmaceutica","volume":"73 3","pages":"385-404"},"PeriodicalIF":2.1000,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Insights into the formulation properties, biocompatibility, and permeability of poorly water-soluble methoxyflavones with PEG400 and propylene glycol.\",\"authors\":\"Fredrick Nwude Eze, Chaweewan Jansakul, Teerapol Srichana\",\"doi\":\"10.2478/acph-2023-0030\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Herein, thermal and non-thermal techniques were used to elucidate the putative physical and chemical interactions between poorly water-soluble <i>Kaempferia</i> methoxyflavones and PEG400/propylene glycol. Additionally, the biocompatibility of methoxyflavone-glycol solutions was evaluated using Caco-2 cells whereas the absorptive transport was investigated by measuring the apparent permeability coefficient (<i>P</i> <sub>app</sub>) of the methoxyflavones and transepithelial electrical resistance (TEER) of the Caco-2 cell monolayer. Data from differential scanning calorimetry, Fourier-transform infrared (FTIR), and proton nuclear magnetic resonance (<sup>1</sup>H NMR) spectroscopic analysis revealed physico-chemical compatibility between the three methoxyflavones and PEG400/propylene glycol. Furthermore, PEG400 and propylene glycol solutions of the methoxyflavones were shown to be compatible with Caco-2 cells at pharmacologically effective concentrations. <i>In vitro</i> transport studies across the Caco-2 cell monolayer revealed high <i>P</i> <sub>app</sub> values of 24.07 × 10<sup>-6</sup> to 19.63 × 10<sup>-6</sup> cm s<sup>-1</sup> for PEG400 solutions of the methoxyflavones. 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引用次数: 0
摘要
本研究采用热和非热技术对难水溶性山柰甲氧基黄酮与PEG400/丙二醇之间的物理和化学相互作用进行了研究。此外,利用Caco-2细胞评价了甲氧基黄酮-乙二醇溶液的生物相容性,并通过测量甲氧基黄酮的表观通透系数(P app)和Caco-2细胞单层的上皮传导电阻(TEER)来研究其吸收运输。差示扫描量热法、傅里叶变换红外(FTIR)和质子核磁共振(1H NMR)光谱分析的数据表明,这三种甲氧基黄酮与PEG400/丙二醇之间存在物理化学相容性。此外,PEG400和甲氧基黄酮的丙二醇溶液在药理学有效浓度下与Caco-2细胞相容。在Caco-2细胞单层的体外转运研究中,甲氧基黄酮PEG400溶液的P app值高达24.07 × 10-6至19.63 × 10-6 cm s-1。Caco-2细胞单层的TEER值表明,药物运输的增加部分是由于紧密连接开口的增加,但不影响上皮屏障的完整性。良好的药物和生物相容性,以及甲氧基黄酮在PEG400和丙二醇溶液中的运输能力的改善,表明了这种方法的价值,值得进一步考虑将这些药物开发成口服液剂型。
Insights into the formulation properties, biocompatibility, and permeability of poorly water-soluble methoxyflavones with PEG400 and propylene glycol.
Herein, thermal and non-thermal techniques were used to elucidate the putative physical and chemical interactions between poorly water-soluble Kaempferia methoxyflavones and PEG400/propylene glycol. Additionally, the biocompatibility of methoxyflavone-glycol solutions was evaluated using Caco-2 cells whereas the absorptive transport was investigated by measuring the apparent permeability coefficient (Papp) of the methoxyflavones and transepithelial electrical resistance (TEER) of the Caco-2 cell monolayer. Data from differential scanning calorimetry, Fourier-transform infrared (FTIR), and proton nuclear magnetic resonance (1H NMR) spectroscopic analysis revealed physico-chemical compatibility between the three methoxyflavones and PEG400/propylene glycol. Furthermore, PEG400 and propylene glycol solutions of the methoxyflavones were shown to be compatible with Caco-2 cells at pharmacologically effective concentrations. In vitro transport studies across the Caco-2 cell monolayer revealed high Papp values of 24.07 × 10-6 to 19.63 × 10-6 cm s-1 for PEG400 solutions of the methoxyflavones. The TEER values of the Caco-2 cell monolayers indicated that the increased drug transport was partly due to increased tight junction openings, but without compromising the epithelial barrier integrity. The good pharmaceutical and biocompatibility profiles, as well as improved transport of the methoxyflavones in PEG400 and propylene glycol solutions, are suggestive of the worthiness of this approach for further consideration pertaining to the development of these drugs into oral liquid dosage forms.
期刊介绍:
AP is an international, multidisciplinary journal devoted to pharmaceutical and allied sciences and contains articles predominantly on core biomedical and health subjects. The aim of AP is to increase the impact of pharmaceutical research in academia, industry and laboratories. With strong emphasis on quality and originality, AP publishes reports from the discovery of a drug up to clinical practice. Topics covered are: analytics, biochemistry, biopharmaceutics, biotechnology, cell biology, cell cultures, clinical pharmacy, drug design, drug delivery, drug disposition, drug stability, gene technology, medicine (including diagnostics and therapy), medicinal chemistry, metabolism, molecular modeling, pharmacology (clinical and animal), peptide and protein chemistry, pharmacognosy, pharmacoepidemiology, pharmacoeconomics, pharmacodynamics and pharmacokinetics, protein design, radiopharmaceuticals, and toxicology.