设计、评估和优化用于哮喘慢性期治疗的硫酸阿布特罗和茶碱脉冲帽给药系统

Govinda Reddy G., R. Jat, K. M. Manjanna
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引用次数: 0

摘要

本研究旨在设计、开发和评估用于治疗哮喘的硫酸阿布特罗和茶碱脉冲给药系统。胶囊体通过与甲醛沃普交联而变得不溶于水。采用福尔马林处理来改变明胶胶囊的溶解性。福尔马林残留量采用定量检测。通过傅立叶变换红外光谱(FTIR)和紫外光谱(UV)检测药物与辅料的相容性。使用不同成分的水凝胶塞制备了 pulsincap 制剂。结果表明,pulsincap 配方的药物含量在一般范围内。在 ph1.2 、6.2 和 7.4 缓冲溶液中进行的体外药物释放研究发现,药物释放率为零,胶囊在 2 小时内保持稳定。可以采用 Pulsincap 配方,根据慢性病疗法优化颗粒给药: 茶碱;定量试验;体外药物释放研究;磷酸盐缓冲液6.2和7.4。
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Design, Evaluation and Optimization of Albuterol Sulphate and Theophylline Pulsincap drug delivery system for chronotherapy of Asthma
The aim of the current study was to design and develop and evaluate pulsatile drug delivery system of Albuterol Sulphate and Theophylline for the treatment of Asthma. The capsule body was made water insoluble by cross linked with formaldehyde vaopur. The treatment of Formalin was adopted to modify the gelatin capsule solubility. The formalin residue was carried out by quantitative test. The drug-excipient compatibility is done by FTIR and UV . The pulsincap formulation were prepared by using hydrogel plug of various components. The drug content of the formulation of pulsincap was found to be in the general range. The invitro drug release studies in ph1.2 .6.2 and 7.4 buffern was noticed to be zero percent and capsule was stable for 2 hours drug the studyF5 formulation batch was selected which was best and good formulation and promoted maximum drug release of  96.29%   percentage at  phosphate buffers when compared with other formulation. Pulsincap formulation can be adopted for optimum delivery of pellets in the treatment as per chronotherapy Keywords:  Theophylline, quantitative test, invitro drug release studies, phosphate buffers6.2 and 7.4.
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