FORMULATION DEVELOPMENT OF ROSUVASTATIN CALCIUM DRUG IN ADHESIVE TRANSDERMAL SYSTEM

被引:1
作者
Geevarghese, Rachel B. [1 ]
Shirolkar, Satish, V [1 ]
机构
[1] Dr DY Patil Inst Pharmaceut Sci & Res, Dept Pharmaceut, Pune 411018, Maharashtra, India
关键词
Rosuvastatin calcium; Drug-; in-; adhesive; % cumulative release; Peel adhesion strength; Tensile strength; THERAPEUTIC SYSTEM; PATCH; DESIGN; DELIVERY; STATINS;
D O I
10.13040/IJPSR.0975-8232.11(8).3902-11
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Current investigation was aimed at designing a Rosuvastatin calcium loaded drug - in- adhesive patch (DIAP) to overcome the problems associated with the daily oral administration of the drug. The patches were prepared by solvent casting method using acrylate emulsion polymers like Covinax 525-78, Mowinyl 461 and Novacryl PSR 3(2,) which served as sustained release matrix polymer and adhesive. Methocel K100M was added as a solubilizer whereas propylene glycol (PG), labrasol, transcutol, and polyethylene glycol 400 (PEG400) were tried as permeation enhancers for the drug- in- adhesive film. The combination of Novacryl -PEG 400 and Novacryl-Transcutol was further optimized by 3(2) factorial design to study the effect of two independent variables i.e. concentration of solubilizer and permeation enhancer on responses i.e. % drug release, tensile strength and peel adhesion strength. The effect of the solubilizer and permeation enhancer on the final formulation was studied. The % cumulative release of drug at the end of 24 h was found to be between 90-93%. The formulations also show tensile strength in the range of 6-11 kg/cm(2) and peel adhesion strength of 14-16 N/25 mm. Hence the developed transdermal patch could be acceptable for transdermal use.
引用
收藏
页码:3902 / 3911
页数:10
相关论文
共 26 条
[1]  
Anod H.V., 2018, Int. J. Appl. Pharm, V10, P235, DOI [10.22159/ijap.2018v10i5.26657, DOI 10.22159/IJAP.2018V10I5.26657]
[2]  
Bhaskar VN, 2015, CHEM PHARM RES, V7, P1084
[3]  
Cantor A.S., 2002, Pharmaceutical Technology North America, V26, P28
[4]   RP-HPLC METHOD FOR ESTIMATION OF ROSUVASTATIN CALCIUM FROM BULK AND TRANSDERMAL DOSAGE FORM [J].
Geevarghese, Rachel B. ;
Shirolkar, Satish V. .
INTERNATIONAL JOURNAL OF PHARMACEUTICAL SCIENCES AND RESEARCH, 2018, 9 (11) :4875-4879
[5]   Drug crystallization - implications for topical and transdermal delivery [J].
Hadgraft, Jonathan ;
Lane, Majella E. .
EXPERT OPINION ON DRUG DELIVERY, 2016, 13 (06) :817-830
[6]   Transdermal delivery of fluvastatin loaded nanoemulsion gel: Preparation, characterization and in vivo anti-osteoporosis activity [J].
Kaur, Ramandeep ;
Ajitha, Makula .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2019, 136
[7]   FORMULATION AND EVALUATION OF TRANSDERMAL PATCH FOR TREATMENT OF INFLAMMATION [J].
Kharia, A. ;
Gilhotra, R. ;
Singhai, A. K. .
INTERNATIONAL JOURNAL OF PHARMACEUTICAL SCIENCES AND RESEARCH, 2019, 10 (05) :2375-2384
[8]   Trans-ungual Delivery of AR-12, a Novel Antifungal Drug [J].
Kushwaha, Avadhesh Singh ;
Sharma, P. ;
Shivakumar, H. N. ;
Rappleye, C. ;
Zukiwski, A. ;
Proniuk, S. ;
Murthy, S. Narasimha .
AAPS PHARMSCITECH, 2017, 18 (07) :2702-2705
[9]  
Lewis G.A., 1999, PHARM EXPT DESIGN
[10]   Enhanced oral bioavailability of fluvastatin by using nanosuspensions containing cyclodextrin [J].
Li, Jun ;
Yang, Min ;
Xu, Wen-Rong .
DRUG DESIGN DEVELOPMENT AND THERAPY, 2018, 12 :3491-3499