Development and Charecterization of Caffeine and Quercetin Loaded Nasal Niosomal In-Situ Gel for Treatment of Depression

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Abstract

Caffeine and Quercetin both are used in combination for the treatment of patient with depression as they are adenosine antagonist due to which they elevate the level of neurotransmitters. The study was designed with two aims. First, is to enhance the solubility and bioavailability of BCS Class II i.e. Quercetin; secondly to ease administration of the formulation to the patient with depression. The culmination of this study, the caffeine and quercetin loaded niosomal in-situ gel for nose-to-brain delivery was formulated. Niosomes were prepared and optimized by using definitive screening design whereas, the Niosomal in-situ gel were prepared and optimized using central composite design. The vesicle size of the optimized batch was found to be 0.281±0.26µm. The % EE of all niosomal batches was found to be in a range of 81.52±0.21% to 98.72±0.16% for Caffeine and 94.3±0.31 to 99.73±0.23 for Quercetin and the cumulative % release was found to be in a range of 72.09±0.18% to 103.3±0.26% for Caffeine and 10.9±0.31% to 37.06±0.15% for Quercetin at 4hrs. DSC, FTIR studies were performed for pure drug and optimized niosomal batch. All the gels as per design were formulated, where the Spreadability was found to be in range of 5.1±0.26cm to 7.9±0.16cm and viscosity after gelation in range of 1800±0.11cps to 4780±0.26cps. The % drug permeated was found to be in range of 85.86±0.015% to 98.61±0.024% for Caffeine and 22.65±0.19% to 33.23±0.34% for Quercetin at 6hrs. These results indicated that niosomal In-situ gel can be used to enhance the bioavailability of drug by directly delivering the drug to the brain by avoiding first pass effect
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咖啡因和槲皮素负载鼻腔Niosomal原位凝胶治疗抑郁症的研制与表征
咖啡因和槲皮素都是腺苷拮抗剂,可以提高神经递质水平,因此可以联合用于抑郁症患者的治疗。这项研究有两个目的。一是提高BCSⅱ类即槲皮素的溶解度和生物利用度;二是方便抑郁症患者的用药。这项研究的高潮,咖啡因和槲皮素负载的niosomal原位凝胶用于鼻到脑输送的配方。采用确定性筛选设计制备和优化乳质体,采用中心复合设计制备和优化乳质体原位凝胶。优化后的微泡大小为0.281±0.26µm。结果表明,4h时,咖啡因的EE为81.52±0.21% ~ 98.72±0.16%,槲皮素的EE为94.3±0.31 ~ 99.73±0.23,槲皮素的累积释放量为72.09±0.18% ~ 103.3±0.26%,槲皮素的释放量为10.9±0.31% ~ 37.06±0.15%。采用DSC、FTIR对纯药和优化后的niosomal batch进行研究。根据设计配制了所有凝胶,其中展布性范围为5.1±0.26cm至7.9±0.16cm,凝胶后粘度范围为1800±0.11cps至4780±0.26cps。6h时,咖啡因的渗透率为85.86±0.015% ~ 98.61±0.024%,槲皮素的渗透率为22.65±0.19% ~ 33.23±0.34%。这些结果表明,niosomal原位凝胶可以避免首过效应,直接将药物传递到大脑,从而提高药物的生物利用度
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