吲达帕胺含片的制备、评估和表征

Archana B, Sahithi Sri Charani Yallapragada, Sony Pawar, Sathvika D, Sathwika Gotham
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摘要

Niosomes 也称为非离子表面活性剂囊泡,是将药物分子运送到目标部位的众多载体之一。它们既可以容纳亲水性药物,也可以容纳疏水性药物。吲达帕胺是一种血管紧张素 II 1 型受体(AT1)拮抗剂,主要用于治疗高血压。利用不同浓度的胆固醇和非离子表面活性剂(span 60)的薄膜水合工艺制成了含有吲达帕胺的niosomes。对所有niosome制剂进行了夹持效率、药物含量、重现性、囊泡直径、形状和大小分布显微照相术、傅立叶变换红外分析和体外释放实验评估。结果表明,随着表面活性剂含量的增加,所有已制备的尼泊金制剂的夹持效率也随之提高。药物含量在 90.06±0.57 和 96.15±0.42 之间,标准偏差较小。Niosomes 的大小从 0.280±0.098µm 到 0.299±0.044µm,呈球形。红外光谱分析表明,药物与制剂成分之间没有相互作用。使用膜扩散细胞研究体外溶解参数。结果表明,与其他制剂相比,制剂 F6 具有更好的控制释放作用,"n "值为 0.917,表明药物是通过零阶动力学释放的。
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Formulation, Evaluation, and Characterization of Indapamide Niosomes
Niosomes, also known as nonionic surfactant vesicles, are one of the many carriers used to carry drug molecules to their target sites. They can hold both hydrophilic and hydrophobic medicines. Indapamide is an angiotensin II type 1 receptor (AT1) antagonist medication primarily used to treat high blood pressure. Niosomes containing Indapamide were created utilizing the thin film hydration process with various cholesterol concentrations and nonionic surfactants (span 60). All noisome formulations were assessed for entrapment efficiency, drug content, reproducibility, vesicular diameter, shape and size distribution microphotography, FTIR analysis, and in vitro release experiments. The results indicate that in all of the created niosomal formulations, as the surfactant content increases, the entrapment efficiency also increases. The drug content ranged between 90.06±0.57 and 96.15±0.42, with a low standard deviation. Niosomes range in size from 0.280±0.098µm to 0.299±0.044µm and have a spherical shape. The IR spectrum analysis indicated no interaction between the medication and the formulation ingredients. Membrane diffusion cells were used to study the in vitro dissolution parameters. The results demonstrate that formulation F6 had a better-controlled release action than other formulations, with an 'n' value of 0.917, indicating that the medication was released using zero-order kinetics.
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