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Controlled release formulation of tramadol hydrochloride using hydrophilic and hydrophobic matrix system

机译:使用亲水和疏水基质系统的盐酸曲马多控释制剂

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摘要

The effect of concentration of hydrophilic (hydroxypropyl methylcellulose [HPMC]) and hydrophobic polymers (hydrogenated castor oil [HCO], ethylcellulose) on the release rate of tramadol was studied. Hydrophilic matrix tablets were prepared by wet granulation technique, while hydrophobic (wax) matrix tablets were prepared by melt granulation technique and in vitro dissolution studies were performed using United States Pharmacopeia (USP) apparatus type II. Hydrophobic matrix tablets resulted in sustained in vitro drug release (>20 hours) as compared with hydrophilic matrix tablets (<14 hours). The presence of ethylcellulose in either of the matrix systems prolonged the release rate of the drug. Tablets prepared by combination of hydrophilic and hydrophobic polymers failed to prolong the drug release beyond 12 hours. The effect of ethylcellulose coating (Surelease) and the presence of lactose and HPMC in the coating composition on the drug release was also investigated. Hydrophobic matrix tablets prepared using HCO were found to be best suited for modulating the delivery of the highly water-soluble drug, tramadol hydrochloride.
机译:研究了亲水性(羟丙基甲基纤维素[HPMC])和疏水性聚合物(氢化蓖麻油[HCO],乙基纤维素)的浓度对曲马多释放速率的影响。通过湿法制粒技术制备亲水性基质片剂,而通过熔体制粒技术制备疏水性(蜡)基质片剂,并使用美国药典(USP)II型装置进行体外溶出研究。与亲水性基质片剂(<14小时)相比,疏水性基质片剂导致持续的体外药物释放(> 20小时)。任一基质系统中乙基纤维素的存在均延长了药物的释放速率。通过亲水和疏水聚合物的组合制备的片剂不能将药物释放延长超过12小时。还研究了乙基纤维素包衣(Surelease)以及包衣组合物中乳糖和HPMC的存在对药物释放的影响。发现使用HCO制备的疏水性基质片剂最适合调节高水溶性药物曲马多盐酸盐的递送。

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