The design of ibuprofen-loaded microbeads using polymers obtained from Xanthosoma sagittifolium and Dillenia indica.

Q3 Medicine
Tolulope Omolola Ajala, Boladale Olanrewaju Silva
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引用次数: 9

Abstract

Background: Ibuprofen is used both for acute and chronic disorders, such as ankylosing spondylitis, osteoarthritis and rheumatoid arthritis; however, ibuprofen causes gastrointestinal disturbances. Therefore, it would be desirable to design it as a sustained-release preparation.

Objectives: To design ibuprofen microbeads using polymers obtained from Xanthosoma sagittifolium starch and Dillenia indica mucilage to provide sustained-release delivery of ibuprofen.

Material and methods: The polymers were extracted using standard methods and characterized by their material, physicochemical, elemental, and rheological profiles. Microbeads loaded with ibuprofen were prepared using the ionotropic gelation method utilizing blends of the polymers and sodium alginate. The microbeads were evaluated using particle shape, particle size, swelling index, entrapment efficiency, and release assays.

Results: The results showed that the polymers have distinct material and physicochemical properties unique to their botanical sources. The microbeads were spherical and free-flowing, and they rolled without friction. The swelling properties ranged from 47.62 ±2.74% to 79.49 ±3.66%. The particle size of the microbeads ranged from 88.14 ±68.57 μm to 214.90 ±66.95 μm, while the encapsulation efficiencies ranged from 20.67 ±4.66% to 83.61 ±6.35%. The dissolution times suggested that the concentration of the natural polymers in the bead formulation could be used to modulate the dissolution properties. Generally, formulations containing the mucilage yielded higher dissolution times than those containing the starch. The kinetics of drug release from the microbeads containing the polymer blends generally fitted the Korsmeyer-Peppas model. The highest similarity was found between formulations C6 and D4 with f2 of 81.07.

Conclusions: The microbeads prepared with polymers obtained from Xanthosoma and Dillenia showed acceptable physicochemical properties, dependent upon polymer type, blend and concentration.

利用从矢状叶黄索和刺叶黄索中获得的聚合物设计负载布洛芬的微球。
背景:布洛芬可用于急性和慢性疾病,如强直性脊柱炎、骨关节炎和类风湿性关节炎;然而,布洛芬会引起胃肠道紊乱。因此,将其设计为缓释制剂是可取的。目的:利用矢状叶淀粉和白莲胶制备的聚合物设计布洛芬微球,以实现布洛芬的缓释。材料和方法:采用标准方法提取聚合物,并对其材料、物理化学、元素和流变特性进行表征。利用海藻酸钠和聚合物的共混物,采用离子化凝胶法制备了负载布洛芬的微球。采用颗粒形状、粒径、膨胀指数、包封效率和释放度等方法对微珠进行评价。结果:该聚合物具有其植物源所特有的物质和物理化学性质。微珠呈球形,自由流动,滚动时没有摩擦。溶胀性能范围为47.62±2.74% ~ 79.49±3.66%。微球粒径范围为88.14±68.57 μm ~ 214.90±66.95 μm,包封效率范围为20.67±4.66% ~ 83.61±6.35%。溶出次数表明,天然聚合物在珠粒配方中的浓度可以调节其溶出性能。通常,含有黏液的配方比含有淀粉的配方产生更高的溶解时间。从含有聚合物混合物的微珠中释放药物的动力学通常符合Korsmeyer-Peppas模型。C6与D4的相似度最高,f2为81.07。结论:用黄原菌和白原菌的聚合物制备的微球具有良好的理化性能,但与聚合物类型、共混物和浓度有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Polimery w medycynie
Polimery w medycynie Medicine-Medicine (all)
CiteScore
3.30
自引率
0.00%
发文量
9
审稿时长
53 weeks
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