Synthesis of Quarternized Chitosans and Their Potential Applications in the Solubility Enhancement of Indomethacin by Solid Dispersion

IF 3.4 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Sasikarn Sripetthong, Sirinporn Nalinbenjapun, Abdul Basit, Chitchamai Ovatlarnporn
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Abstract

This study was designed to synthesize quarternized chitosans (Q-CS) and explore their potential application in aqueous solubility enhancement of indomethacin (IND), a BCS class-II drug. Three different Q-CS; N,N,N-trimethyl chitosan chloride (TMC), N-(4-N‘-methylpyridinylmethyl) chitosan chloride (mPyCS), and N-(4-N’,N’,N’-trimethylaminobenzyl) chitosan chloride (TmBzCS) were synthesized and characterized through various spectroscopic analysis. Q-CS-based solid-dispersion (SD) composites of IND (Q-CS-IND) were prepared using the spray-drying method and characterized through Fourier transform infrared (FTIR), scanning electron microscopy (SEM), differential-scanning calorimetry (DSC), and powder X-ray diffraction (P-XRD). The solubility and dissolution profiles of SD-composites of IND were evaluated and compared with physical mixtures (PM). The IND contents were quantified and validated in the composites using UV-Vis spectrophotometer. FTIR and NMR analysis showed the successful preparation of Q-CS. TMC was found with the highest yield (55.13%) and mPyCS with the highest degree of quaternization (DQ) (63.37%). FT-IR analysis of IND-Q-CS composites demonstrated chemical interaction between carbonyl moieties of IND with functional groups of Q-CS. DSC and PXRD analyses demonstrated the transformation of IND in SD composites from crystalline to an amorphous form. All the IND-Q-CS composites were observed with a significant increase in the solubility and dissolution rate of the drug (1996.0 µg/min) compared to PM (1306.8 µg/min), which is higher than pure IND (791.6 µg/min). The contents of IND in TMC, mPyCS, and TmBzCS composites were 97.69–99.92%, 97.66-100.25%, and 97.18-100.11% respectively. Overall, the findings encourage the applications of Q-CS derivatives for increasing IND water solubility and warrant further in vivo biological profiling of IND composites.

Graphical Abstract

Abstract Image

四分之一化壳聚糖的合成及其在通过固体分散增强吲哚美辛溶解度中的潜在应用
本研究旨在合成四甲基化壳聚糖(Q-CS),并探索其在提高吲哚美辛(IND)(一种 BCS II 类药物)水溶性方面的潜在应用。研究人员合成了三种不同的 Q-CS:氯化 N,N,N-三甲基壳聚糖(TMC)、氯化 N-(4-N'-甲基吡啶基甲基)壳聚糖(mPyCS)和氯化 N-(4-N',N',N'-三甲基氨基苄基)壳聚糖(TmBzCS),并通过各种光谱分析对它们进行了表征。采用喷雾干燥法制备了基于 Q-CS 的 IND 固体分散(SD)复合材料(Q-CS-IND),并通过傅立叶变换红外(FTIR)、扫描电子显微镜(SEM)、差示扫描量热仪(DSC)和粉末 X 射线衍射(P-XRD)对其进行了表征。对 IND 的 SD 复合材料的溶解度和溶解曲线进行了评估,并与物理混合物(PM)进行了比较。使用紫外可见分光光度计对复合材料中的 IND 含量进行了定量和验证。傅立叶变换红外光谱和核磁共振分析表明成功制备了 Q-CS。TMC 的产率最高(55.13%),mPyCS 的季铵化程度(DQ)最高(63.37%)。IND-Q-CS 复合材料的傅立叶变换红外分析表明,IND 的羰基与 Q-CS 的官能团之间存在化学作用。DSC 和 PXRD 分析表明,SD 复合材料中的 IND 已从晶体状转变为无定形状。与 PM(1306.8 µg/min)相比,所有 IND-Q-CS 复合材料的药物溶解度和溶解速率(1996.0 µg/min)均显著提高,高于纯 IND(791.6 µg/min)。TMC、mPyCS 和 TmBzCS 复合物中 IND 的含量分别为 97.69%-99.92%、97.66%-100.25% 和 97.18%-100.11%。总之,研究结果鼓励应用 Q-CS 衍生物来增加 IND 的水溶性,并证明有必要进一步对 IND 复合材料进行体内生物分析。
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来源期刊
AAPS PharmSciTech
AAPS PharmSciTech 医学-药学
CiteScore
6.80
自引率
3.00%
发文量
264
审稿时长
2.4 months
期刊介绍: AAPS PharmSciTech is a peer-reviewed, online-only journal committed to serving those pharmaceutical scientists and engineers interested in the research, development, and evaluation of pharmaceutical dosage forms and delivery systems, including drugs derived from biotechnology and the manufacturing science pertaining to the commercialization of such dosage forms. Because of its electronic nature, AAPS PharmSciTech aspires to utilize evolving electronic technology to enable faster and diverse mechanisms of information delivery to its readership. Submission of uninvited expert reviews and research articles are welcomed.
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