{"title":"硝酸异山梨酯舌下膜的配方研制及体外评价","authors":"S. Rajbongshi","doi":"10.20959/WJPR201711-9426","DOIUrl":null,"url":null,"abstract":"Objective: To formulate and evaluated sublingual film containing an antianginal drug. Experimental work: Sublingual film of Isosorbide dinitrate was formulated using film coating polymer pullulan and inert plasticizer PEG-400 by solving casting method. 3 2 full factorial design was applied to optimize the formulation. The lower concentration of film forming polymer and higher concentration of plasticizer showing best results were selected as independent variables. Disintegration time (Y1) and % drug release at 1 minute (Y2) and folding endurance (Y3) were selected as dependent variables. The prepared films were evaluated for, disintegration time in vitro drug release, folding endurance and mechanical strength and further optimized batch compared with marketed sublingual tablet. Results: Isosorbide dinitrate sublingual film prepared was found to be fulfilling all the film dosage form. The film compared to sublingual tablet concentration of pullulan (X1) and PEG-400 (X2) significantly affected the disintegration time (Y1) and % of drug release at 1 minute(Y2) and folding endurance (Y3). Regression analysis and numerical optimization were performed to identify the best formulation. Formulation F10 prepared with 223 mg, pullulan 19.5%, PEGWorld Journal of Pharmaceutical Research SJIF Impact Factor 7.523 Volume 6, Issue 11, 493-507. Research Article ISSN 2277– 7105 *Corresponding Author Hardik R. Joshi Master of Pharmacy, LM","PeriodicalId":23796,"journal":{"name":"World journal of pharmaceutical research","volume":"19 1","pages":"493-507"},"PeriodicalIF":0.0000,"publicationDate":"2017-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"FORMULATION DEVELOPMENT AND IN VITRO EVALUATION OF SUBLINGUAL FILM OF ISOSORBIDE DINITRATE\",\"authors\":\"S. Rajbongshi\",\"doi\":\"10.20959/WJPR201711-9426\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Objective: To formulate and evaluated sublingual film containing an antianginal drug. Experimental work: Sublingual film of Isosorbide dinitrate was formulated using film coating polymer pullulan and inert plasticizer PEG-400 by solving casting method. 3 2 full factorial design was applied to optimize the formulation. The lower concentration of film forming polymer and higher concentration of plasticizer showing best results were selected as independent variables. Disintegration time (Y1) and % drug release at 1 minute (Y2) and folding endurance (Y3) were selected as dependent variables. The prepared films were evaluated for, disintegration time in vitro drug release, folding endurance and mechanical strength and further optimized batch compared with marketed sublingual tablet. Results: Isosorbide dinitrate sublingual film prepared was found to be fulfilling all the film dosage form. The film compared to sublingual tablet concentration of pullulan (X1) and PEG-400 (X2) significantly affected the disintegration time (Y1) and % of drug release at 1 minute(Y2) and folding endurance (Y3). Regression analysis and numerical optimization were performed to identify the best formulation. Formulation F10 prepared with 223 mg, pullulan 19.5%, PEGWorld Journal of Pharmaceutical Research SJIF Impact Factor 7.523 Volume 6, Issue 11, 493-507. Research Article ISSN 2277– 7105 *Corresponding Author Hardik R. Joshi Master of Pharmacy, LM\",\"PeriodicalId\":23796,\"journal\":{\"name\":\"World journal of pharmaceutical research\",\"volume\":\"19 1\",\"pages\":\"493-507\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2017-11-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"World journal of pharmaceutical research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.20959/WJPR201711-9426\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"World journal of pharmaceutical research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.20959/WJPR201711-9426","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
目的:研制并评价含抗心绞痛药物舌下膜。实验工作:采用溶铸法制备涂膜聚合物普鲁兰和惰性增塑剂PEG-400配制硝酸异山梨酯舌下膜。采用全因子设计对配方进行优化。选取低浓度成膜聚合物和高浓度增塑剂作为自变量。以崩解时间(Y1)、1分钟释药% (Y2)和折叠时间(Y3)为因变量。对制备的膜进行体外崩解时间、药物释放、折叠耐力和机械强度的评价,并与市售舌下片进行优化。结果:所制备的硝酸异山梨酯舌下膜符合所有膜剂型要求。普兰兰(X1)和PEG-400 (X2)舌下片浓度对其崩解时间(Y1)、1分钟释药率(Y2)和折叠时间(Y3)有显著影响。通过回归分析和数值优化确定了最佳配方。配方F10以223 mg, 19.5%的普鲁兰配制,世界药物研究杂志SJIF影响因子7.523卷6,第11期,493-507。通讯作者:Hardik R. Joshi,药学硕士,硕士
FORMULATION DEVELOPMENT AND IN VITRO EVALUATION OF SUBLINGUAL FILM OF ISOSORBIDE DINITRATE
Objective: To formulate and evaluated sublingual film containing an antianginal drug. Experimental work: Sublingual film of Isosorbide dinitrate was formulated using film coating polymer pullulan and inert plasticizer PEG-400 by solving casting method. 3 2 full factorial design was applied to optimize the formulation. The lower concentration of film forming polymer and higher concentration of plasticizer showing best results were selected as independent variables. Disintegration time (Y1) and % drug release at 1 minute (Y2) and folding endurance (Y3) were selected as dependent variables. The prepared films were evaluated for, disintegration time in vitro drug release, folding endurance and mechanical strength and further optimized batch compared with marketed sublingual tablet. Results: Isosorbide dinitrate sublingual film prepared was found to be fulfilling all the film dosage form. The film compared to sublingual tablet concentration of pullulan (X1) and PEG-400 (X2) significantly affected the disintegration time (Y1) and % of drug release at 1 minute(Y2) and folding endurance (Y3). Regression analysis and numerical optimization were performed to identify the best formulation. Formulation F10 prepared with 223 mg, pullulan 19.5%, PEGWorld Journal of Pharmaceutical Research SJIF Impact Factor 7.523 Volume 6, Issue 11, 493-507. Research Article ISSN 2277– 7105 *Corresponding Author Hardik R. Joshi Master of Pharmacy, LM