M. Uhumwangho, K. Latha, S. Sunil, M. Srikanth, K. Murthy
{"title":"巴西棕榈蜡熔体造粒法制备盐酸地尔硫卓保胃浮剂","authors":"M. Uhumwangho, K. Latha, S. Sunil, M. Srikanth, K. Murthy","doi":"10.4314/JOPHAS.V7I2.63398","DOIUrl":null,"url":null,"abstract":"The study was carried out to investigate drug release profile of gastroretentive drug delivery system (GDDS) of diltiazem hydrochloride prepared with a hydrophilic polymer (hydroxylpropyl methyl cellulose), hydrophobic polymer (ethyl cellulose) and a waxy material (carnauba wax). Drug profiles were compared with a commercial formulation of the drug (MKT). Sodium bicarbonate (30%) was incorporated as gas generating agent. Formulations were either prepared alone with the individual polymer or admixed with carnauba wax. Formulations containing carnauba wax were prepared by melt granulation technique. Tablets were evaluated for tensile strength, in vitro buoyancy and drug release profiiles. Release data were subjected to analysis by four different mathematical models namely, – zero order flux, first order, Higuchi square root of time relationship and Korsmeyer equations. All formulated tablets and MKT had tensile strength values between 1.05 - 1.32 MNm -2 . One of the test formulations (F7) gave a comparable release profile with the commercial sample, MKT. For instance, the % maximum release (m∞) and time to attain this (t∞) for F7 and MKT were (96%, 99%) and (12, 12 h) respectively, while their dissolution rates (m∞/t∞) were 8 %h -1 and 8.3 %h -1 respectively. All the formulations fitted well into Korsmeyer and Peppas model (correlation coefficient r value ≥ 0.95). Release exponent (n) for F7 and MKT formulations were 0.150 and 0.286 respectively with a corresponding release rate constant values of 65.4 and 43.8. This showed that release of diltiazem hydrochloride from these formulations followed Fickian diffusion mechanism. An optimised GDDS of diltiazem hydrochloride using carnuba wax as a matrix, comparable with MKT has been developed. Keywords : Gastroretentive drug delivery system, melt granulation, floating, diltiazem hydrochloride, Carnauba wax Journal of Pharmaceutical and Allied Sciences , Vol. 7 No. 2 (2010)","PeriodicalId":16719,"journal":{"name":"Journal of Pharmaceutical and Allied Sciences","volume":"95 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2011-02-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"4","resultStr":"{\"title\":\"Formulation of gastro-retentive floating tables of Diltiazem Hydrochloride wtih carnauba wax by melt granulation technique\",\"authors\":\"M. Uhumwangho, K. Latha, S. Sunil, M. Srikanth, K. Murthy\",\"doi\":\"10.4314/JOPHAS.V7I2.63398\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The study was carried out to investigate drug release profile of gastroretentive drug delivery system (GDDS) of diltiazem hydrochloride prepared with a hydrophilic polymer (hydroxylpropyl methyl cellulose), hydrophobic polymer (ethyl cellulose) and a waxy material (carnauba wax). Drug profiles were compared with a commercial formulation of the drug (MKT). Sodium bicarbonate (30%) was incorporated as gas generating agent. Formulations were either prepared alone with the individual polymer or admixed with carnauba wax. Formulations containing carnauba wax were prepared by melt granulation technique. Tablets were evaluated for tensile strength, in vitro buoyancy and drug release profiiles. Release data were subjected to analysis by four different mathematical models namely, – zero order flux, first order, Higuchi square root of time relationship and Korsmeyer equations. All formulated tablets and MKT had tensile strength values between 1.05 - 1.32 MNm -2 . One of the test formulations (F7) gave a comparable release profile with the commercial sample, MKT. For instance, the % maximum release (m∞) and time to attain this (t∞) for F7 and MKT were (96%, 99%) and (12, 12 h) respectively, while their dissolution rates (m∞/t∞) were 8 %h -1 and 8.3 %h -1 respectively. All the formulations fitted well into Korsmeyer and Peppas model (correlation coefficient r value ≥ 0.95). Release exponent (n) for F7 and MKT formulations were 0.150 and 0.286 respectively with a corresponding release rate constant values of 65.4 and 43.8. This showed that release of diltiazem hydrochloride from these formulations followed Fickian diffusion mechanism. An optimised GDDS of diltiazem hydrochloride using carnuba wax as a matrix, comparable with MKT has been developed. 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引用次数: 4
摘要
采用亲水性聚合物(羟丙基甲基纤维素)、疏水性聚合物(乙基纤维素)和蜡质材料(巴西棕榈蜡)制备盐酸地尔硫卓胃保留型给药系统(GDDS),研究其药物释放特性。将药物概况与该药物的商业配方(MKT)进行比较。加入碳酸氢钠(30%)作为生气剂。配方要么单独与单个聚合物制备,要么与巴西棕榈蜡混合。采用熔融造粒技术制备了含有巴西棕榈蜡的配方。评估片剂的抗拉强度、体外浮力和药物释放特性。发布数据采用四种不同的数学模型进行分析,即-零阶通量、一阶通量、Higuchi平方根时间关系和Korsmeyer方程。所有配方片剂和MKT的抗拉强度值在1.05 ~ 1.32 MNm -2之间。其中一个测试配方(F7)给出了与商业样品(MKT)相当的释放概况。例如,F7和MKT的最大释放% (m∞)和达到该(t∞)的时间分别为(96%,99%)和(12,12 h),而它们的溶出率(m∞/t∞)分别为8% h -1和8.3% h -1。各配方均符合Korsmeyer和Peppas模型(相关系数r值≥0.95)。F7和MKT的释放指数(n)分别为0.150和0.286,相应的释放速率常数分别为65.4和43.8。结果表明,盐酸地尔硫卓的释放符合菲克扩散机制。以卡鲁巴蜡为基体,优选出与MKT相当的盐酸地尔硫卓GDDS。关键词:胃保留给药系统,熔融造粒,漂浮,盐酸地尔硫卓,巴西棕榈蜡
Formulation of gastro-retentive floating tables of Diltiazem Hydrochloride wtih carnauba wax by melt granulation technique
The study was carried out to investigate drug release profile of gastroretentive drug delivery system (GDDS) of diltiazem hydrochloride prepared with a hydrophilic polymer (hydroxylpropyl methyl cellulose), hydrophobic polymer (ethyl cellulose) and a waxy material (carnauba wax). Drug profiles were compared with a commercial formulation of the drug (MKT). Sodium bicarbonate (30%) was incorporated as gas generating agent. Formulations were either prepared alone with the individual polymer or admixed with carnauba wax. Formulations containing carnauba wax were prepared by melt granulation technique. Tablets were evaluated for tensile strength, in vitro buoyancy and drug release profiiles. Release data were subjected to analysis by four different mathematical models namely, – zero order flux, first order, Higuchi square root of time relationship and Korsmeyer equations. All formulated tablets and MKT had tensile strength values between 1.05 - 1.32 MNm -2 . One of the test formulations (F7) gave a comparable release profile with the commercial sample, MKT. For instance, the % maximum release (m∞) and time to attain this (t∞) for F7 and MKT were (96%, 99%) and (12, 12 h) respectively, while their dissolution rates (m∞/t∞) were 8 %h -1 and 8.3 %h -1 respectively. All the formulations fitted well into Korsmeyer and Peppas model (correlation coefficient r value ≥ 0.95). Release exponent (n) for F7 and MKT formulations were 0.150 and 0.286 respectively with a corresponding release rate constant values of 65.4 and 43.8. This showed that release of diltiazem hydrochloride from these formulations followed Fickian diffusion mechanism. An optimised GDDS of diltiazem hydrochloride using carnuba wax as a matrix, comparable with MKT has been developed. Keywords : Gastroretentive drug delivery system, melt granulation, floating, diltiazem hydrochloride, Carnauba wax Journal of Pharmaceutical and Allied Sciences , Vol. 7 No. 2 (2010)