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蛋清蛋白载体辅助固体分散体的开发,以提高难溶性盐酸氢氯噻嗪的水溶解度和渗透性。

Egg White Protein Carrier-Assisted Development of Solid Dispersion for Improved Aqueous Solubility and Permeability of Poorly Water Soluble Hydrochlorothiazide.

机构信息

Rajarshi Shahu College of Pharmacy, Malvihir, Botha Road, Buldhana, Maharashtra, India.

School of Pharmacy & Technology Management, NMIMS (Deemed to be University), Hyderabad Campus, Hyderabad, Telangana, India.

出版信息

AAPS PharmSciTech. 2021 Mar 8;22(3):94. doi: 10.1208/s12249-021-01967-2.

DOI:10.1208/s12249-021-01967-2
PMID:33683493
Abstract

Hydrochlorothiazide (HTZ) is a first-line drug used in the treatment of hypertension suffered from low oral bioavailability due to poor aqueous solubility and permeability. Hence, lyophilized egg white protein-based solid dispersion (HTZ-EWP SD) was developed to explore its feasibility as a solid dispersion carrier for enhanced aqueous solubility and permeability of HTZ. The HTZ-EWP SD was prepared using the kneading method. HTZ-EWP SD was characterized using scanning electron microscopy (SEM), differential scanning calorimetry (DSC), Fourier transforms infrared spectroscopy (FT-IR), powder X-ray diffractometer (PXRD), solubility, in vitro dissolution, and ex vivo permeation studies. The physico-chemical evaluation suggested the formation of the solid dispersion. Optimized HTZ-EWP SD4 drastically enhanced (32-fold) aqueous solubility (16.12 ± 0.08 mg/mL) over to pure HTZ (~ 0.51 ± 0.03 mg/mL). The dissolution study in phosphate buffer media (pH 6.8) revealed that HTZ-EWP SD4 significantly enhanced the release rate of HTZ (~ 87 %) over to HTZ (~ 25 %). The permeation rate of HTZ from optimized HTZ-EWP SD4 was enhanced significantly (~ 84 %) compared to pure HTZ (~ 24 %). Optimized HTZ-EWP-SD4 enhanced the rate of HTZ dissolution (~ 86 %) in FeSSIF (fed state simulated intestinal fluid), compared to a low dissolution rate (~ 72 %) in FaSSIF (fasted state simulated intestinal fluid) state after 2-h study. Obtained results conclude that lyophilized egg white protein can be utilized as an alternative solid dispersion carrier for enhancing the solubility and permeability of HTZ.

摘要

氢氯噻嗪(HTZ)是治疗高血压的一线药物,但由于其水溶性和渗透性差,口服生物利用度低。因此,开发了冻干蛋清蛋白固体分散体(HTZ-EWP SD),以探索其作为固体分散体载体增强 HTZ 水溶性和渗透性的可行性。HTZ-EWP SD 采用捏合法制备。采用扫描电子显微镜(SEM)、差示扫描量热法(DSC)、傅里叶变换红外光谱(FT-IR)、粉末 X 射线衍射仪(PXRD)、溶解度、体外溶出度和离体渗透研究对 HTZ-EWP SD 进行了表征。物理化学评价表明形成了固体分散体。优化的 HTZ-EWP SD4 显著提高了 HTZ 的水溶性(16.12±0.08mg/mL)(0.51±0.03mg/mL)。在磷酸盐缓冲介质(pH6.8)中的溶解研究表明,HTZ-EWP SD4 显著提高了 HTZ 的释放速率(87%)(25%)。与纯 HTZ 相比,HTZ-EWP SD4 中 HTZ 的渗透速率显著提高(84%)(24%)。与 FaSSIF(禁食状态模拟肠液)相比,优化后的 HTZ-EWP-SD4 在 2 小时的研究中,HTZ 在 FeSSIF(进食状态模拟肠液)中的溶解速率提高了(86%),而 FaSSIF 中的溶解速率较低(72%)。结果表明,冻干蛋清蛋白可用作增强 HTZ 溶解度和渗透性的替代固体分散体载体。

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