提高溶出度的环糊精络合片的研制及评价

Gowtham Mandadapu, Prachetha Kolli, Venkata Gopaiah Kurra
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摘要

本文对雷卡尼地平包合物速释片的设计、处方开发和评价进行了研究,以期提高其水溶性、溶出度和口服生物利用度。以β-环糊精为原料,采用物理混合、捏合法和溶剂蒸发法制备来卡尼地平包合物。以药物与β-环糊精的摩尔比为1:1M, β-环糊精为1:2M制备配合物。莱卡尼地平与β-环糊精在水中形成络合物的相溶解度图为AL型。来卡尼地平与β-环糊精的相溶解度图说明了环糊精的增溶能力。来卡尼地平的溶解度随β-环糊精浓度的增加呈线性增加(R2=0.989)。稳定常数Kc为164.557M-1。采用USP II桨式溶出度仪对纯药、包合物及制剂在900 ml 0.1 HCL中进行体外溶出度研究。显然,与纯药物溶出度数据相比,所制备的配合物和片剂具有更快的溶出度。用捏合法制备的LK2明显提高了溶解速率。包合物和揉制片剂溶出率较高,可能是由于药物β-环糊精相互作用较好。用FT-IR对所制备的配合物进行了表征。莱卡尼替尼的包合物。将LK2配合物和含LK2配合物的F6片分别保存在室温和400C、75%RH相对湿度下进行短期稳定性研究。每隔一周、三周和六周对样品进行物理外观、药物含量值和溶出度分析。上述参数未见明显变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Formulation & evaluation of cyclodextrin complexed tablets by enhancing the dissolution rate
In the present work, studies design, formulation development and evaluation of immediate release tablets of Lercanidipine inclusion complex with a view to improve its aqueous solubility, dissolution rate and oral bioavailability.The inclusion complexes of Lercanidipine were prepared with β-cyclodextrin by physical mixture, Kneading method and solvent evaporation method. The complexes were prepared in different molar ratios of drug and β-cyclodextrin namely 1:1M, 1:2M with β-cyclodextrin.The phase solubility diagram for the complex formation between Lercanidipine and β-cyclodextrin in water are AL type. Phase solubility diagram of Lercanidipine with β-cyclodextrin illustrate the solubility enhancement capacity of cyclodextrin.  The aqueous solubility of Lercanidipine increased linearly (R2=0.989) as the function of β-cyclodextrin concentration. The stability constant “Kc” was found to be 164.557M-1.Invitro dissolution studies for pure drug and inclusion complexes and prepared tablets were carried out in 900 ml of 0.1N HCL using USP II paddle type dissolution apparatus.It is evident that the complex and tablets prepared were exhibited a faster dissolution when compared to pure drug dissolution data.A marked improvement in the dissolution rates observed with LK2 prepared by Kneading method. The higher dissolution rates observed with inclusion complexes and tablets prepared by Kneading may be due to better interaction of drug β- cyclodextrin. The prepared complexes were characterized by FT-IR Studies.The inclusion complex of Lercanidipinei.e.LK2 complex and F6 tablets containing LK2 complex were subjected to short-term stability studies by storing them at room temperature and at 400C and relative Humidity of 75%RH. The samples were analyzed at an interval of one week, three weeks and six weeks for their physical appearance, drug content values and dissolution profiles. No appreciable changes observed with the above parameters.
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