Asmaa M Eldeeb, Dalia H Abdelkader, Gamal M El Maghraby
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引用次数: 0
摘要
本研究的目的是通过控制抗溶剂沉淀来提高替格瑞洛(TC)的溶出率和抗血小板活性。在不含波洛沙姆188或环氧树脂44/14的情况下制备了饱和乙醇溶液。在使用水或含水的波洛沙姆(1% w/v)控制沉淀之前加入Aerosil 200。对所得沉淀物进行干燥,并用傅里叶变换红外光谱(FTIR)、差示扫描量热法(DSC)、粉末x射线衍射(PXRD)和体外溶出度对其进行表征。红外光谱分析显示,TC加工后形成了氢键。DSC和PXRD反映了部分非晶化。与阴性对照组(3.43±0.46)和未处理TC组(5.78±2.18)相比,F6组(24.71±5.46)和F9组(30.06±1.63)显著增强(p p 0.05)。这些结果表明,TC的药理活性的增强可能是由于提高了生物利用度,提高了溶出率。采用可控抗溶剂沉淀法加速TC的溶解。
Controlled anti-solvent precipitation for enhanced dissolution rate and antiplatelet activity of ticagrelor.
The goal of our study is to augment ticagrelor (TC)'s dissolution rate and antiplatelet activity via controlled antisolvent precipitation. A saturated ethanolic solution of TC was prepared in the absence and presence of poloxamer 188 or gelucire 44/14. Aerosil 200 was added before controlled precipitation using water or water-containing poloxamer (1% w/v). The resulting precipitate was dried and characterized using Fourier transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), powder X-ray diffraction (PXRD), and in vitro dissolution. FTIR showed hydrogen bonding after the processing of TC. DSC and PXRD reflected partial amorphization. A significant enhancement (p < 0.05) in dissolution efficiency and TC amount released after five minutes was also shown. The most effective composition was F6, which comprised TC, poloxamer, and Aerosil (5:5:2.5), or F9, utilizing gelucire instead of poloxamer at a similar ratio. Assessment of tail bleeding time (min) exhibited a significant (p < 0.05) prolongation for rat groups treated with F6 (24.71 ± 5.46) and F9 (30.06 ± 1.63) compared with negative control (3.43 ± 0.46) and unprocessed TC (5.78 ± 2.18). These results suggest an enhancement of TC's pharmacological activity probably due to enhanced bioavailability imparted with an enhanced dissolution rate. The study introduced controlled antisolvent precipitation as a simple tool for hastened TC's dissolution.
期刊介绍:
Pharmaceutical Development & Technology publishes research on the design, development, manufacture, and evaluation of conventional and novel drug delivery systems, emphasizing practical solutions and applications to theoretical and research-based problems. The journal aims to publish significant, innovative and original research to advance the frontiers of pharmaceutical development and technology.
Through original articles, reviews (where prior discussion with the EIC is encouraged), short reports, book reviews and technical notes, Pharmaceutical Development & Technology covers aspects such as:
-Preformulation and pharmaceutical formulation studies
-Pharmaceutical materials selection and characterization
-Pharmaceutical process development, engineering, scale-up and industrialisation, and process validation
-QbD in the form a risk assessment and DoE driven approaches
-Design of dosage forms and drug delivery systems
-Emerging pharmaceutical formulation and drug delivery technologies with a focus on personalised therapies
-Drug delivery systems research and quality improvement
-Pharmaceutical regulatory affairs
This journal will not consider for publication manuscripts focusing purely on clinical evaluations, botanicals, or animal models.