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微波技术对甲芬那酸和氟芬那酸固体分散体的影响。

Influence of the microwave technology on solid dispersions of mefenamic acid and flufenamic acid.

作者信息

Alshehri Sultan, Shakeel Faiyaz, Ibrahim Mohamed, Elzayat Ehab, Altamimi Mohammad, Shazly Gamal, Mohsin Kazi, Alkholief Musaed, Alsulays Bader, Alshetaili Abdullah, Alshahrani Abdulaziz, Almalki Bander, Alanazi Fars

机构信息

Department of Pharmaceutics, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia.

Department of Pharmaceutics, Faculty of Pharmacy, Assiut University, Assiut, Egypt.

出版信息

PLoS One. 2017 Jul 31;12(7):e0182011. doi: 10.1371/journal.pone.0182011. eCollection 2017.

Abstract

The present studies were undertaken to develop solvent-free solid dispersions (SDs) for poorly soluble anti-inflammatory drugs mefenamic acid (MA) and flufenamic acid (FFA) in order to enhance their in vitro dissolution rate and in vivo anti-inflammatory effects. The SDs of MA and FFA were prepared using microwaves irradiation (MW) technique. Different carriers such as Pluronic F127® (PL), Eudragit EPO® (EPO), polyethylene glycol 4000 (PEG 4000) and Gelucire 50/13 (GLU) were used for the preparation of SDs. Prepared MW irradiated SDs were characterized physicochemically using differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), Fourier transform infra-red (FT-IR) spectroscopy, powder X-ray diffraction (PXRD) and scanning electron microscopy (SEM). The physicochemical characteristics and drug release profile of SDs were compared with pure drugs. The results of DSC, TGA, FT-IR, PXRD and SEM showed that SDs were successfully prepared. In vitro dissolution rate of MA and FFA was remarkably enhanced by SDs in comparison with pure MA and FFA. The SDs of MA and FFA prepared using PEG 400 showed higher drug release profile in comparison with those prepared using PL, EPO or GLU. The dissolution efficiency for MA-PEG SD and FFA-PEG SD was obtained as 61.40 and 59.18%, respectively. Optimized SDs were also evaluated for in vivo anti-inflammatory effects in male Wistar rats. The results showed significant % inhibition by MA-PEG (87.74% after 4 h) and FFA-PEG SDs (81.76% after 4 h) in comparison with pure MA (68.09% after 4 h) and pure FFA (55.27% after 4 h) (P<0.05). These results suggested that MW irradiated SDs of MA and FFA could be successfully used for the enhancement of in vitro dissolution rate and in vivo therapeutic efficacy of both drugs.

摘要

开展本研究是为了开发难溶性抗炎药物甲芬那酸(MA)和氟芬那酸(FFA)的无溶剂固体分散体(SDs),以提高它们的体外溶出速率和体内抗炎效果。采用微波辐射(MW)技术制备MA和FFA的固体分散体。使用不同的载体,如普朗尼克F127®(PL)、尤特奇EPO®(EPO)、聚乙二醇4000(PEG 4000)和Gelucire 50/13(GLU)来制备固体分散体。使用差示扫描量热法(DSC)、热重分析(TGA)、傅里叶变换红外(FT-IR)光谱、粉末X射线衍射(PXRD)和扫描电子显微镜(SEM)对制备的微波辐射固体分散体进行物理化学表征。将固体分散体的物理化学特性和药物释放曲线与纯药物进行比较。DSC、TGA、FT-IR、PXRD和SEM的结果表明成功制备了固体分散体。与纯MA和FFA相比,固体分散体显著提高了MA和FFA的体外溶出速率。与使用PL、EPO或GLU制备的固体分散体相比,使用PEG 400制备的MA和FFA的固体分散体显示出更高的药物释放曲线。MA-PEG SD和FFA-PEG SD的溶出效率分别为61.40%和59.18%。还评估了优化后的固体分散体对雄性Wistar大鼠的体内抗炎效果。结果显示,与纯MA(4小时后为68.09%)和纯FFA(4小时后为55.27%)相比,MA-PEG(4小时后为87.74%)和FFA-PEG SDs(4小时后为81.76%)具有显著的抑制百分比(P<0.05)。这些结果表明,微波辐射的MA和FFA固体分散体可成功用于提高两种药物的体外溶出速率和体内治疗效果。

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