Kazmi Imran, Yadav Hemant K S, Al-Abbasi Fahad A, Afzal Muhammad, Nadeem Muhammad Shahid, Altayb Hisham N, Raizaday Abhay, Hussain Md Sadique, Ali Haider, Imam Faisal, Gupta Gaurav
Department of Biochemistry, Faculty of Science, King Abdulaziz University, Jeddah, Saudi Arabia.
School of Pharmacy, Suresh Gyan Vihar University, Jagatpura, Mahal Road, Jaipur, India.
Ann Pharm Fr. 2025 Jan;83(1):68-80. doi: 10.1016/j.pharma.2024.10.004. Epub 2024 Oct 16.
The analysis aimed to prepare an in-situ implant (ISFI) formulation holding dimethyl fumarate as (a model drug) using cross-linked gellan gum by homogenization method. Cross-linking of gellan gum was done with L-cysteine to improve its gelation properties. Fourier transform infrared spectroscopy (FTIR) and (DSC) Differential scanning calorimetry were used to test the compatibility of the drug-polymer. The diverse formulations were prepared and tested using Design Expert® ver 8.0.1 software to optimize the experiment technique and employ the response surface. The tissue compatibility of the test verified the existence of non-irritants in the established formulation. All preparations contained the drug content from approximately 97.98 to 99.88%. Viscosities are ideal for injection in the optimized formulation (1,55 percent w/w in water). The optimized formula was monitored, and up to 156hours, it was found to be 95.7%. The result was that ISFI can effectively monitor and control the delivery of several powerful drug products.
该分析旨在通过均质法使用交联结冷胶制备一种含有富马酸二甲酯(作为模型药物)的原位植入剂(ISFI)制剂。结冷胶与L-半胱氨酸进行交联以改善其凝胶化特性。使用傅里叶变换红外光谱(FTIR)和差示扫描量热法(DSC)测试药物-聚合物的相容性。使用Design Expert® ver 8.0.1软件制备并测试了多种制剂,以优化实验技术并应用响应面。测试的组织相容性证实了既定制剂中不存在刺激性物质。所有制剂的药物含量约为97.98%至99.88%。在优化制剂(在水中为1.55% w/w)中,粘度适合注射。对优化配方进行了监测,发现长达156小时时,其含量为95.7%。结果表明,ISFI可以有效地监测和控制几种强效药物产品的递送。